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(1)

A

Abscissic acid, 209

Absorbance spectra, allosteric binding and, 15

Acetic anhydride, 28 Acetokinase, 19

3-(a-Acetonylbenzyl)-4-hydroxycoum- arin, 262

Acetylation, 28 O-Acetylation, 28

(-f)-Acetylcarnitine, 317 Acetylcholine

adenyl cyclase and, 404, 408 inositol phosphatides and, 368 Acetylcholine hydrolase, 21 Acetyl-CoA acetyltransferase, 319 Acetyl-CoA carboxylase, 21, 324

inhibitors of, 331-332 A^-Acetylglucosamine kinase, 19 N-Acetyl glutamate 5-phosphotrans-

ferase, 20

Af-Acetylhexosamines, 364

iV-Acetylhexosaminidase, inhibitors of, 363-364

N-Acetylhistidine, 360 iV-Acetylimidazole, 28, 235 iV-Aeetylneuraminie acid, 364 Acetylpantetheine, 329 Acetylsalicyclic acid, 279 Acid shock, 234

Ac-Phe-puromycin, 161 Acriflavin, 121

Acrylylcarnitine, 316 Acrylyl-CoA, 316

A C T H , see Adrenocorticotropic hormone Actinomycetes, 232

Actinomycin D , 86, 88, 127, 263, 288 adenyl cyclase and, 406

Activators, allosteric, 2 iV-Acylaminoacyl-tRNA, 155

( + )-Acylcarnitine, 317-319 Acylchloroanilides, 190

A c y l - C o A hydrolase, 366

Acyl dihydroxyacetone phosphate path­

way, inhibitors of, 369 1-Acyl glycerol 3-phosphate, 366 AT-Acylsphingosine, 356, 362

Adenine nucleotides, relative concentra­

tions of, 3 Adenohypophysis, 410

Adenosine 5'-0-(l-thiotriphosphate), 114 Adenosinetriphosphatase, see ATPase Adenosine triphosphate, see also A T P

competitive inhibitors of, 114-115 Adenyl cyclase

activation, role of lipids, 421 activators of, 396-415

distribution and subcellular location, 391-392

effect of age on, 420-421 inhibitors of, 415-417 lipolysis and, 312

purification and properties, 392-393 5-Adenylyl imidodiphosphate, 405 Adhesions, peritoneal, 275 Adipocytes, 312

Adipose tissue, adenyl cyclase and, 404 Adrenal carcinoma, 406

Adrenal tumor cells, 391

Adrenalectomized animals, adenyl c y ­ clase in, 399

Adrenochrome, 64 Adrenocorticosteroids, 86

Adrenocorticotropic hormone, 87, 312 adenyl cyclase and, 396, 406 Aesculus californica, 117

A F I F , see Anticoagulant fraction of in­

cubated fibrinogen

Age, effect on adenyl cyclase and phos­

phodiesterase, 420-421 Aggression, 78

Agkistrodon rhodostoma, 220 A H F , see Antihemophilic factor Alanine dehydrogenase, 29

487

(2)

Albumin, 274

effects on lipid metabolism, 381-382 Algae

blue-green, 180 red, 183

Alk-l-enyl-2-acyl-sn-glycero-3-phos- phorylethanolamine, 361 l-Alkenylglycero-3-phosphorylcholine,

360

2-Alkyl-4-hydroxyquinoline oxides, 190 Allantoin, 21

Alloisoleucine, 115

Allosteric properties, variation among source organisms, 16-17

Alloxan, adenyl cyclase and, 405, 416 A M B A , see 4-Aminomethylbenzoic acid A M B O A , see 4-Aminobicyelo[2.2.2.]oc-

tane-l-carboxylic acid

A M C H A , see £raws-4-Aminomethylcy- clohexanecarboxylic acid Amethopterin, 56, 57, 83 Amicetin, 156-157, 165 Amidines

bifunctional, 253-254 competitive inhibition by, 253 p-Amidinophenylpyruvie acid, 253 Amines, 252-259

aliphatic, uncoupling by, 194 alkyl, 253

aromatic, 199 aryl, 253

bifunctional, 253-254 biogenic, 390

cyclic A M P formation and, 413 complex, uncoupling and, 195 Aminoacetocatechol, 61 Amino acid(s)

as allosteric inhibitors, 22 competitive inhibitors of, 115-118 Amino acid activation

dual paths to, 108-111 inhibitors of, 107-127

noncompetitive inhibitors of, 111-114 therapy, 126-127

Amino acid analogs

competitive inhibitors of, 115-118 hydroxylases and, 65-71

phenylalanine hydroxylase and, 81-83

tryptophan hydroxylase inhibitors, 80-81

tyrosine hydroxylase inhibitors, 74-80

L-Amino acid decarboxylase, 54 w-Amino acid hexyl esters, 254

Amino acid hydroxylase inhibitors, 45-90 Amino a c i d : t R N A ligases, 108

Aminoacyl adenylate, 108 ferrous ion and, 109 synthesis of, 109

Aminoacyl-tRNA binding, 144-150 A m i n o a c y l - t R N A formation

pyrophosphate and, 125

synthetic oligonucleotides and, 120 Aminoacyl-tRNA production, 110 A m i n o a c y l - t R N A synthetases, 108 2-Aminoadipate, 338

Aminoalkyl alcohols, 118 4-Aminobenzamidine, 253 a-Aminobutyric acid, 115 a-Aminobutyric hydroxamate, 115 e-Aminocaproic acid, 254

6-Amino-7-chloroquinoline-5,8-quinone, 64

Aminoglycoside antibiotic, 142 Aminohexose antibiotics, 156-157 2-Amino-3-hydroxypteridine, 57 DL-a-Amino-j3-hydroxyvaleric acid, 20 4-Aminomethylbenzoic acid, 254 4-Aminomethylbicy clo [2.2.2] octane-1-

carboxylic acid, 254

£rans-4-Aminomethylcyclohexanecar- boxylic acid, 254, 256

k-a-Amino-£-methyleneeyclopropane- propionic acid, 316

Aminomethylhexenoic acid, 117 2-Amino-4-methylhex-4-enoic acid, 116 4-Amino-a-methyl-DL-phenylalanine, 66 6-Aminonicotinamide adenine dinucleo­

tide phosphate, 339 Aminooligonucleosides, 166-167 Aminooxyacetate, 338

iY-(5-Aminopentyl)-5-dimethylamino-l- naphthalenesulfonamide, 255

£-Aminophenylpropionic acid, 70 6-Aminopurine, 114

Aminosulfuric groups, 282 Aminotriazines, 190

(3)

3-Amino-L-tyrosine, 67 Ammonia, 112, 186, 188

uncoupling by, 194, 198 Ammonium ion

carbon dioxide reduction and, 204 glutamate dehydrogenase and, 23 Amphetamine, 76, 79, 86, 89 Amphipathic substances, 279 Amphiphilic substances, 279 Anabaena, 197

Aniline, detoxification of, 56 1-Anilinonaphthalene 8-sulfonate, 29 Anion transport, inhibitors of, 334-337 Anisomycin, 161-162, 165

Anomalous order, 2 Anorexogenic agent, 84

A N S , see 1-Anilinonaphthalene 8-sul­

fonate

Anterior pituitary gland, adenyl cyclase in, 408

Anthranilic acid, 18

Antibiotics, see specific types Antibody E F G , 153

Anticoagulant (s), acquired, 267-272 Anticoagulant therapy, oral, 260 Anticonvulsant action, a - M M T and, 75 Antidepressants, tricyclic, 419

Anti-EFG, 153

Antifibrinolytic activity, 285 Antihemophilic factor, 284 Anti-IgM antiserum, 271

Antilipolytic agents, classification of, 313 Antimycin, 190

Antimycin A, 21, 23, 39 Antioxidants, 361 Antisulfhydryls, 118

amino acid activation and, 111-112 Antithrombin(s), 226-229

Antithromboplastins, 276-279 Antitrypsin, 229

Apomorphine, 59, 61, 63, 72 Aquayamycin, 63, 64, 65 Arachidic acid, 278 Argasin, 227, 248-249 Argentaffin cells, 46 Arginine, 20 Arsenate, 196 Arsenite, 204 Arvin, 219, 286

Arvin IRC-50, 286

Ascaris trypsin inhibitor, 234 Ascorbate, 187

photooxidation of, 188 Ascorbic acid, 51, 185

Asialo Tay-Sachs ganglioside, 363 Asparaginase therapy, 117 Asparagine, 113

Asparagine amide, 117

L-Aspartate, pyruvate carboxylase and, 328

Aspartate aminotransferase, 338 Aspartate transcarbamylase, 3, 18, 30-34

bromocytidine triphosphate and, 16 carbamyl phosphate and, 16 p-chloromercuribenzoate and, 14 number of substrate binding units, 7 sodium dodecylsulfate and, 15 succinate and, 16

yeast, 38

Aspartic acid ligase, 117 Asnftr+okinase, 20

feedback control of, 22 Aspartokinase-homoserine dehy­

drogenase complex, 15 Aspirin, 227, 279

Astrocytoma cells, 402 Atebrin, 195

Atherosclerosis, 255

ATP:Citrate oxaloacetate lyase, inhibi­

tors of, 330-331

A T P - P i exchange reaction, 199

A T P l P P i exchange, hydroxylamine and, 124-125

A T P sulfurylase, 21 A T P thiokinases, 315 ATPase, 21

Ca

2 +

-dependent, 196, 199

"light-triggered," 208 Mg

2 +

-dependent, 199

Atractyloside, fatty acyl-CoA synthetase and, 315

Atrazine, 180, 190

Auditory stimulation, habituation to, 78 Aurintricarboxylic acid, 139-141 Autoantibodies, 267

Autoimmune diseases, 267 Autoprothrombin c, 222

Autoprothrombin c inhibitor, 242

(4)

Autoprothrombin I

C

and 1

P

, 243

Avidin, acetyl-CoA carboxylase and, 331

Avoidance active, 78 conditional, 78 Azaserine, 204

Azetidinecarboxylic acid, 116, 117 Azur eosin, 64

B

Bacillus cereus, 355

Bacillus stear other mophilus, 157 Bacillus subtilis, 160

Bacteria, halophilic, 123 Bacterial toxins, 364 Bacteriophage MS2, 149 Bacteriophage T4, 133 B A L , 57

Bases, amino acid activation and, 112-114

monovalent, 112-113 polyvalent, 113-114 Batrachotoxin, 414 Bdellins A and B, 249-250 Bee venom, 354

Benzamidine, 253

Benzamidinosulfonyl fluoride, 288 1,?,3-Benzene tricarboxylate, 336 Benzimidazoles, 191

2-alkyl-, 198 Benzoctamine, 88 p-Benzoquinone, 193

Benzothiadiazine derivatives, 419 Benzyl p-guanidinobenzoate, 253 2-Benzyl malonate, 336

Benzyloxycarbonyl-L-glutaminylglycine, 287

Bethamethason, 86

B G B , see Benzyl p-guanidinobenzoate Bile acids, 223, 277

Bilirubin, 62

Bimolecular associations, 10-11 Binding, nonexclusive, 10

Binding sites, fractional saturation of, 6

Biotin, 328

Bishydroxycoumarin, 261

Bis-3- (4-hydroxycoumarinyl) ethyl ace­

tate, 262

Bitis gabonica, 275, 285 Blasticidin S, 156-157 Blastocladiella, 31 Bleeding time, 230 Blighia sapida, 316 Blocking agents

a-adrenergic, 313 /3-adrenergic, 313 neuromuscular, 21

Blood clotting inhibitors, classification of, 225-226

Blood-clotting mechanisms, inhibitors of, 215-289

Blood coagulation B a S 0

4

and, 227

bentonite and, 227 kaolin and, 227

lipid-protein interactions, 226 mechanisms of, 216-225 M g ( O H )

2

and, 227

role of heparin in, 282-284

Blood coagulation inhibitors, laboratory tests for, 229-231

Blood-sucking insects, 286 B o d y temperature, 78 Borst shuttle, 337

Bovine pancreas trypsin inhibitor, 232 Bovine serum albumin

cooperative binding to, 13 lysophospholipase and, 354 Bradykinin, 219

Brain, adenyl cyclase in, 399 Brain lipids, 83

Brain phospholipid, 273 Breast tumor, 401

Brightness discrimination learning, 78 Bromoacylcarnitine, 317-319

(—)-Bromoacetylcarnitine, 319 2-Bromoacylcarnitine, 319 2-Bromoacyl-CoA, 319

2-(5'-Bromoamyl) malonate, 336 m-Bromobenzoate, 336

Bromocytidine triphosphate, aspartate.

transcarbamylase and, 16, 32 3-Bromo-a-methyl-DL-phenylalanine, 66 3-Bromo-a-methyl-DL-tyrosine, 67 Bromomyristic acid, 321

(5)

2-£-Bromomyristoylthiocarnitihe, 319 Bromopalmitoylcarnitine, 319 2-Bromopalmitoyl-CoA, 319 p-Bromophenylalanine, 56 3-Bromo-DL-phenylalanine, 66 5-Bromotryptophan, 77 5-Bromo-DL-tryptophan, 67, 69 Brucine, 195

sec-Butylamine, 117

n-Butyl-3,5-diiodo-4-hydroxybenzoic acid, 191

a-n-Butyldopacetamide, 60 2-n-Butyl malonate, 334, 335, 336 Butyltin chloride, 200

Butyrylcarnitine, 319 Butyryl-CoA, 21

Butyryl-CoA dehydrogenase, 320

C

Cadaverine, 257 Caffeine

cyclic A M P phosphodiesterase and, 418

lipolysis and, 314 Calcitonin, 396

Calcium deoxycholate, phospholipase C and, 356

Calcium ions, factor X and, 245 California buckeye, 117 Canavalia ensijormis, 117 Canavanine, 116

Carbamates, chlorophenyl, 190 Carbamoyl phosphate :L-aspartate car-

bamoyltransferase, 30 Carbamyl L-aspartate, 31

synthesis of, 17 Carbamyl phosphate, 4

aspartate transcarbamylase and, 16 synthesis of, 17

Carbamyl phosphate synthetase, 19, 34 yeast, 38

Carbobenzoxy-L-asparaginylamide, 255 Carbohydrases, 362

Carbohydrate(s), as allosteric inhibitors, 22

Carbohydrate metabolism, purine nu­

cleotides and, 17 Carbomycin, 160

Carbon dioxide fixation, 192 inhibition of, 201-204

Carbon dioxide reduction, inhibition of, 201-204

Carbon disulfide, 85

Carbonylcyanide phenylhydrazones, 195 Carboxydismutase, 203

Carboxymethylation, 251 Carboxypeptidase B, 234, 250 Carcinoid tumor, 52 Cardiomegaly, 422 Carnitine, 316

Carnitine acetyltransferase, 317 inhibitors of, 317-319

Carnitine octanoyltransferase, 317 Carnitine palmitoyltransferase, 317, 318 Carnitine palmitoyltransferase I, 318 Caseinolytic activity, 285

Catalase, 48, 54, 361 Catalytic activity, 2 Cataractogenic effects, 82 Catatonia, 78

Catecholamine (s)

adenyl cyclase and, 397-399 levels in brain, 77 receptor sites, 88 synthesis

dietary tyrosine and, 50 tyrosine hydroxylase and, 50 tissue receptors and, 396 transport, 88

Catecholinergic system, 72

Catechol O-methyltransferase, 21, 73 Catehols, 61

hydroxylases and, 57-63, 71-73 o-Catechols, 57

Cations

divalent, nucleotide allosteric interac­

tions and, 17 t R N A and, 121-123

C C C P , see Carbonylcyanide 3-chloro- phenylhydrazone

CDP-Diglyceride synthesis, inhibitors of, 367-368

CDP-Ethanolamine, 368 Cells, permeability of, 132 Ceramidase, 369

inhibitors of, 362

(6)

Ceramide, 356

biosynthesis, inhibitors of, 369-370 en/£/iro-Ceramide(s), 371

£/ireo-Ceramide(s), 371

Ceramide aminoethyl phosphonate, 356 Ceramide phosphorylcholine, 356 Ceramide phosphorylethanolamine, 356 Ceramide synthetase, 369

Cerebroside biosynthesis, inhibitors of, 371

Ceruloplasmin, 274 Cetavlon, 358

phospholipase C and, 356 phospholipase D and, 360 Cetyl pyridinium chloride, 416

Cetyltrimethylammonium bromide, 282 Chalcomycin, 160

Chang's liver cells, 401

Chelating agents, blood coagulation and, 227

Chemical probe mechanisms, 14-15 Chicken ovomucoid trypsin inhibitor,

234

Chlamydomonas, 191

Chloramphenicol, 154, 157, 159-160 Chlorella, 203

p-Chloroamphetamine, 79, 83 Chloride ion, 188

glycogen synthetase and, 23 Chloroacylanilides, energy transfer in­

hibition and, 201 4-Chlorobenzylamine, 253

5-Chloro-3-(3-chlorophenyl-2',4',5'-tri- chlorosalicylanilide, 197

a-Chloro-3,4-dihydroxyacetophenone, 59 Chloro K, 288

p-Chloromercuribenzene sulfonate, amino acid activation and, 111 p-Chloromercuribenzoate, 56, 258

adenyl cyclase and, 398 amino acid activation and, 111 aspartate transcarbamylase and, 14 energy transfer inhibition and, 199 pyruvate carboxylase and, 328 pyruvate kinase and, 327

p-Chloro-Af-methylamphetamine, 83, 90 Chloromethyl dihydroxyphenylketone,

€0

Chloromethyl ketones, 252

3-Chloro-a-methyl-DL-phenylalanine, 66 4-Chloro-a-methyl-DL-phenylalanine, 66 5-Chloro-2-methyl-DL-tryptophan, 67 2-Chloro-a-methyl-DL-tyrosine, 67 3-Chloro-a-methyl-DL-tyrosine, 67 Chlorophenyl carbamates, 190 p-Chlorophenylalanine, 56, 78, 80 4-Chloro-DL-phenylalanine, 66 p-Chloro-DL-phenylalanine, 69 p-Chlorophenylpyruvic acid, 64 Chlorophyll, 181

Chlorophyll b , 183

2-Chloro-3-phytyl-l,4-naphthoquinone, 288

Chloroplasts, aging, of, 188

lamellae, light-dependent reactions of, 181-184

phosphorylation, 195

2-Chloro-4-(2-propylamino)-6-ethyl- amino-s-triazine, 190 Chloroquine, 195

L-l-Chloro-3-tosylamido-7-amino-2- heptanone, 220, 252

5-Chloro-DL-tryptophan, 67 6-Chloro-DL-tryptophan, 67 Chlorpromazine, 76, 79, 88, 195

cyclic A M P formation and, 415, 417 Chlortetracycline, 145

Cholate, 39

Chondroitin sulfate, 281 Choriocarcinoma, 83 Chorismate mutase, 20 Chromaffin cells, 46

a-Chymotrypsin, 217

2-Cinnamylidine malonate, 336 Circadian rhythm, 422

Circular dichroism, 235 Cirrhosis of liver, 280 Citrate

transport of, 324 uncoupling and, 198 Citrate lyase, 324, 331 Citrate synthetase, 19 inhibitors of, 329-330 Citrate thrombin, 251

Citric acid cycle dehydrogenases, 17 Clofibrate, 288

Clostridum perfringens, 355, 357

(7)

Clostridium welchii, 356, see Clostridium perfringens

Clot retraction, 280 Clotting time, 230 Clumping methods, 221

CMP-N-Acetylneuraminic acid, 19, 369 C M U , see 3-(4-chlorophenyl)-l,l-di-

methylurea or Monuron

Coagulant protein, biosynthesis, 260-265 Coagulase, 236

Coagulation, see also Biood clotting, Blood coagulation

intravascular, inhibitors of, 280-282 Cobefrin, 61

Cobra venom, 353 Cocaine, 89

cyclic A M P formation and, 414 Cocoonase, 232

Cohn Fraction I V , 245 Colchicine, 279

Cold, amino acid activation and, 114 Colicin E l , 167

Colicin E3, 167-168 Colicin K , 167 Collidine, 112

Compartmentalization, 84

Competitive inhibitors of amino acid activation, 114-123

C O M T , see Catechol o-methyltrans- ferase

"Conflict," 78

Conformational states, 8

Congenital factor I X inhibitors, 266 Cooperative interactions, 3

subunit protomers and, 8

Cooperativity, kinetic analysis and, 5 Copper-chelating agents, 73

Copper protein, 184

Corynebacterium diphtheria, 152 Corynebacterium ovis, 359 Coumadin, 261

Coumarin analogs, 260

Coumarin-indandione compounds, 286

"Coupling factor," 196 antibody against, 200

C P T - I , see Carnitine palmitoyltrans­

ferase I o-Cresol, 201

Cro talus admanteus, 351

Crotonoyl-CoA, 320

pyruvate carboxylase and, 328 Culex pipiens, 354

Cutscum, 368 Cupric ions, 51 Cyanide, 56, 192

carbon dioxide reduction and, 202-203 Cyanoethylation, 121

Cyanuric fluoride, 235 Cyclic A M P , 3, 86

distribution, 390

regulation of cellular concentration, 389-423

formation

inhibitors of, 415-417

regulation in cultured cells, 419-420 levels

lipolysis and, 312 regulation of, 395-419 Cyclic A M P phosphodiesterase

activators of, 417-418

distribution and subcellular location, 393-394

effect of age on, 420-421 inhibitors of, 418-419

purification and properties, 394-395 Cyclic GMP-dependent phosphodiester­

ases, 394

Cyclic photophosphorylation, 185 czs-l,2-Cyclohexane dicarboxylate, 335 Cycloheximide, 87, 88, 162-163, 263, 288

adenyl cyclase and, 406 Cyclopropanecarboxylic acid, 316 Cyclopropene fatty acid, 332 Cysteine, uncoupling and, 195 Cytidine deaminase, 19 Cytidine triphosphate, 3 Cytochrome b reductase, 39 Cytochrome f, 182, 183

inactivation of, 191 photoreduction of, 189

D

D A D , see Diaminodurene, 2,3,5, 6-Tetramethylphenylenediamine Dansyl cadaverine, 257

D C A , see Dichloroacetic acid

D C C D , see Dieyelohexylearbodiimide

(8)

D C I P , see 2,6-Dichlorophenolindophenol D C I P H

2

, see 2,6-Dichlorophenolindo­

phenol, reduced form

D C M U , see Diuron, 3-(3,4-Di-chloro- phenyl) -1,1-dimethylurea Decamethylenediguanidine, 199 3-Decanoyl-iV-acetylcysteamine, 332 (+)-Decanoylcarnitine, 318, 321 Dehydrogenases, citric acid cycle, 17 irans-Dehydrolysine, 116

Dendroaspis angusticeps, 285 Dendroaspis jamesoni, 285 Dendroaspis polylepis, 285 5'-Deoxyadenosine, 114

therapy and, 127

2-Deoxyadenosine triphosphate, 115, 125-126

3-Deoxy-D-arabinoheptulosonate 7-phos- phate synthetase, 20, 22

Deoxycholate, phospholipase A and, 353 Deoxycytidylate deaminase, 19 4-Deoxyphloretin 2

/

-galactoside, 199 4

/

-Deoxyphlorizin, 199 Deoxystreptamine, 148

Depolarizing agents, adenyl cyclase and, 410-414

Desaspidin, 196 Desferal, 361 Desferrioxiamine, 62 Desmethylimipramine, 56 Desulfo-CoA, citrate synthase and,

330

Detergent(s), effects on lipid metabo­

lism, 373-376

Detergent treatment, uncoupling and, 197

D F P , see Diisopropyl phosphorofluori- date

D H A P , see Dihydroxyacetone phosphate Diacyl glycero-3-phosphate, 359

Diamidinophenyl compounds, 253 2,5-Diaminobutyric acid, 256 Diaminodurene, 185, 189 Dianemycin, 198

Diathesis, hemorrhagic, 229, 267 Dibenamine, 313

Dibenzo[/,/i]quinoxaline, 62 iV,./V-Dibenzylarterenone, 60 5,5-Dibromobarbiturate, 416

Dibutyryl cyclic A M P , 420

Dicarboxylate transport, inhibitors of, 335-337

C

4

-Dicarboxylic acid, 181

Dicarboxylic acids, pyruvate carboxylase and, 328

Dichloroacetic acid, 320 Dichloroacetylcarnitine, 320 Dichloroacetyl-CoA, 320

2,6-Dichlorobenzoindophenol, 64, 65 Dichloroisoproterenol, 313, 398 l,3-Dichloro-l,4-naphthoquinone, 64 2,6-Dichlorophenolindophenol, 185

uncoupling and, 197

3-(3,4-Dichlorophenyl) -1,1-dimethylurea, 186

Dicoumarol, 191, 261 uncoupling and, 195 A^A^-Dicyclohexylcarbodiimide

cyclic A M P and, 389

energy transfer inhibition and, 200 Dielectric effects, t R N A and, 121-123 /3-Diethylaminoethyl diphenylpropylace-

tate, 56

Diethyldithiocarbamate, 85 Diethylergosterol, 419

A^,Af-Diethyl-p-phenylenediamine, 64 Diethylstilbestrol, 29

Digitonin, 187, 191, 417 adenyl cyclase and, 405

Dihydroergotamine, lipolysis and, 314 Dihydropteridine reductase, 54 Dihydrosphingosine, 277, 362, 372 Dihydrotestosterone, adenyl cyclase and,

408

Dihydrostreptomycin, 146 Dihydrouridine, 121

3,4-Dihydroxyacetophenone, 61 3,4-Dihydroxybenzaldehyde, 60 3,4-Dihydroxybenzoic acid, 59 3,4-Dihydroxybenzophenone, 60 3,4-Dihydroxybutyrophenone, 71 6,7-Dihydroxycoumarin, 60 3,4-Dihydroxy-a-dimethylaminoaceto-

phenone, 57

l,8-Dihydroxy-4,5-dinitroanthraquinone, 64

3,5-Dihydroxy-4-methoxybenzoate, 21

(9)

3,4-Dihydroxy-6-methyl-a;-methylamino- acetophenone, 71

3',4'-Dihydroxy-2-methylpropiophenone, 73

3,4-Dihydroxyphenylacetamide, 59 3,4-Dihydroxyphenylacetic acid, 59 3,4-Dihydroxyphenylalanine, 45 3,4-Dihydroxyphenylethylamine, 59 Dihydroxyphenyl ethyl ketone, 60 Dihydroxyphenyl ketone, 60 3,4-Dihydroxy phenyl ketone, 59 3,4-Dihydroxyphenyl a-methylamino-

ethyl ketone, 60

2,5-Dihydroxyphenylpyruvic acid, 64, 65 3,4-Dihydroxyphenylserine, 76

3,5-Diiodotyrosine, 65, 77 3,5-Diiodo-L-tyrosine, 67, 69 Diisopropylphosphate, 250

Diisopropyl phosphorofluoridate, 220, 250 2,5-Dimethoxybenzoquinone, 64 Dimethylaminoacetocatechol, 61 Dimethylaminobiphenyl, 419 Dimethylaminoethanol, 281

6-(l,2-Dimethylbutyl)-2,4-dinitrophenol, 195

2,9-Dimethyl-l,10-phenanthroline, 62 A^,iV-Dimethyl-p-phenylenediamine, 64,

65

Dimethyl sulfoxide, 28

5,6-Dimethyltetrahydropteridine, 48 3a-Dimethyltyrosine, 76

2a-Dimethyl-DL-tyrosine, 67

Dinitrophenols, uncoupling and, 195 Dinitrophenylation, 28

Dinucleotide tetraphosphates, 115 Dio-9, 199

Dioleyl phosphate, 356

D I P , see Diisopropylphosphate Diphenylcarbazide, 185 Diphosphoinositide, 357 Diphtheria toxin, 152-153 Dipyridyl, 361

a,a'-Dipyridyl, 52, 55, 62, 63, 73 Direct feedback (product) inhibition,

84-85

Disalicylidenepropanediamine-1,2- disulfonic acid, 193 Disialoganglioside synthesis, 372

2,3-Distearoyloxypropyl (dimethyl)-0- hydroxyethyl ammonium acetate, 356

Disulfiram, 62 5,5

/

-Dithiobis(2-nitrobenzoic acid), 37, 328

Dithiothreitol, 54, 65, 196 adenyl cyclase and, 392 amino acid activation and, 112 Diuron, 189

Divinyl ether, 282

D M P H

4

, see 5,6-Dimethyltetrahydrop- teridine

D O P A , see also 3,4-Dihydroxyphenyl- alanine

L-, 60, 76

D O P A decarboxylase, 47, 50 Dopacetamide, 59

2,3-Dopacetamides, 72 3,4-Dopacetamides, 72 Dopamine, 59, 61

adenyl cyclase and, 397 pineal gland and, 403

Dopamine /3-hydroxylase, 50, 73, 74, 84 Dopamine /3-oxidase, 85

Drugs, t R N A ' s and, 121 Duke bleeding time, 230 Dysproteinemic syndromes, 268

E

E A C A , see e-Aminocaproic acid Edeine, 149-150

E F G , 150

E F G antibody, 153 EFTs, 136 E F T u , 136 E F T u T s , 142 Elastase, 219

Electron acceptor Q, 183 Electron microscopy, 273, 393 Electron transport, inhibitors of, 185,

187-193 Electroosmosis, 281

Electroshock, hormones and, 87 Ellman's reagent, 37

Emphysema, 228, 236 E n o y l - C o A hydrolases, 319 Enterobacteriaceae, 167

(10)

Enzyme (s), see also specific types allosteric

ionic strength and, 14 Lineweaver-Burk plots and, 5 mercurials and, 14

p H and, 14

surface active agents and, 14 copper-containing, 46

multisubstrate, 5 single-site, 8

Enzyme complexes, allosteric inhibition in, 38-40

Enzyme repression, 2 L-Epinephrine, 61

adenyl cyclase and, 397 lipolysis and, 312 Epinine, 60

Erythrocytes, thromboplastic properties of, 278

Erythromycin, 154, 157, 160-161 Escherichia coli, aspartate transcar­

bamylase from, 14 Esculetin, 60

Eserine, inositol phosphatides and, 368 Estradiol, 401

Estrous behavior, 72, 78 Ethanol, 155

Ethanolamine, 278

Ether, phospholipase D and, 359 Ethyl 3-amino-4i/-pyrroloisoxazole-

5(6#)-carboxylate, 62, 63 Ethyl biscoumacetate, 262 Ethyl 2-(p-chlorophenyl) -2-methyl-

propionate, 332 2-Ethyl citrate, 335, 336

Ethyl /3-3,4-dihydroxyphenylpropionate, 59, 61, 71

a-Ethyldopacetamide, 61

Ethylenediaminetetraacetic acid, 62, 63, 114

Ethylenemaleic acid, polymers of, 282 Ethylenemaleic acid-trypsin copolymer,

250

iV-Ethylglycine, 116 N-Ethylmaleimide, 258

amino acid activation and, 112 cyclic A M P formation and, 415 glyceride biosynthesis and, 333 lipolysis and, 314

DL-Af-Ethylnorepinephrine, 61 a-Ethyl-DL-tyrosine, 67 Euthyroid rats, 404

F

Fabry's disease, 363 Factor TT, 288 Factor II, 222 Factor V , 223

inhibition of, 273 inhibitors of, 268 Factor V I I , 224

inhibitors of, 271 Factor V I I time, 264 Factor V I I I

inhibition of, 273 inhibitors of, 227, 268-269 Factor I X

abnormal, 266-267 congenital inhibitor, 266 inhibitors of, 271 Factor X , 222

abnormal, 267

activated, generation of, 224-225 activation of, 274

Factor X Friuli, 267 Factor X a , 223

inhibitors of, 242 Factor X I inhibitors, 271 Factor X I I I , 219

inhibitors of, 271 Factor E F G , 150 Factor F, 8 Factor IF1, 133 Factor IF2, 133 Factor IF3, 133 Factor R F l , 137 Factor R F 2 , 137 Factor R F 3 , 137 Fatty acid(s)

carbon dioxide reduction and, 204 biosynthesis, from glucose, inhibitors

of, 311-341 composition, 277

metabolism, purine nucleotides and, 17

long chain, uncoupling and, 198 oxidation, 311-321

(11)

polyunsaturated, 409 synthesis

inhibition of, 321-339

reducing-power requirements for, 337-339

Fatty acid oxidase complex, 317 Fatty acid salts, nonesterified, 278 Fatty acid synthetase, inhibitors of,

332-333

Fatty acyl-CoA, inhibition o f lipid m e ­ tabolism, 378

Fatty acyl-CoA dehydrogenases, 319 Fatty acyl-CoA derivatives, 311 Fatty acyl-CoA synthetases, inhibitors

of, 315-317

F C C P , see Carbonylcyanide 4-trifluoro- methoxyphenylhydrazone

F D P , see Fibrinogen degradation prod­

ucts F e

2 +

, 54

amino acid hydroxylation and, 46 Fenclonine, 80

Fenfluoramine, 84 Ferredoxin, 182

"Ferredoxin-cyclic" photophosphoryla- tion, 191

Ferredoxin-NADP

+

reductase, 183 Ferredoxin-NADP

+

reductase antibodies, 193

Ferredoxin-reducing substance, 184 antibodies to, 192-193

removal of, 192 Ferricyanide, 185, 191

Ferrocytochrome b , a absorbance band of, 39

Fibrin, degradation b y plasmin, 220 Fibrin clot

formation of, 216-221 ultrastructure of, 273 Fibrin cross-linking, 283

Fibrin polymerization, F D P and, 272-273 Fibrin-stabilizing factor, 219

Fibrinogen

conversion to fibrin clot, 216-221 anticoagulant fraction of incubated,

229

degradation b y plasmin, 220 degradation products, 226, 272-276

anticoagulant effects of, 272-273

antithrombin effect of, 272 procoagulant effeots of, 274 half-life of, 217

Fibrinogenolytic activity, 285 Fibrinoligase, 219

Fibrinolysin, 220 Fibrinopeptides A, 219 Fibrinopeptides B, 219 Flagella formation, 390 Flavins, 184, 192 Fluorescence, 183

Fluorescence spectra, allosteric binding and, 15

Fluoride

acyl-CoA synthetases and, 315 glyceride biosynthesis and, 333 Fluoroacetyl-CoA, citrate synthetase

and, 330

l-Fluoro-2,4-dinitrobenzene, 28 4-Fluoro-a-methyl-DL-phenylalanine, 66 2-Fluoro-a-methyl-DL-tyrosine, 67 Fluorophenylalanine, 116 ra-Fluorophenylalanine, 82 p-Fluorophenylalanine, 82 2-Fluorophenylalanine, 56, 66 3-Fluorophenylalanine, 56 4-Fluorophenylalanine, 56, 66 Fluoropyruvate, 329

p- [m-(m-Fluorosulf onyTphenylureido) - phenoxyethoxy] benzamidine, 288 6-Fluorotryptophan, 81

5-Fluorotryptophan, 67, 69 6-Fluorotryptophan, 67, 69 3-Fluoro tyrosine, 116 3-Fluoro-L-tyrosine, 67

Folic acid antagonist, 57, 83

Follicle-stimulating hormone, adenyl c y ­ clase and, 408

F o r m y l - M e t - t R N A , 135

Fractional binding site saturation, 3 Fragment D , 220

Fragment E, 220 Fragment Y , 220 Fragment X , 220

F R S , see Ferridoxin-reducing substance Fructose diphosphatase, 19

Fructose 1,6-diphosphate, 21 phosphofructokinase and, 37 Fructose phosphate (s), 204, 208

(12)

Fructose 6-phosphate, 322 phosphorylation of, 37 Furanomycin, 116

Fusidic acid, 137, 150-152, 165 G

Gabon viper, 275 7-Galactonolactone, 363 a-Galaetosidase, inhibitors of, 363 /3-Galactosidase, 390

inhibitors of, 363 Galactosylceramide, 362 O-Galactosylsphingosine, 371 Galactosyltransferase, 372

Ganglioside biosynthesis, inhibitors of, 371-372

Garcinia cambozia, 330 Gastrointestinal hormones, 396 G D P C P , see 5-Guanylylmethylenedi-

phosphonate

G E E , see Glycine ethyl ester Gentamycin, 142, 147 Gewebsthrombokinase, 248 Giemsa stain, 64

Gliomas, 401 Globoside, 361, 363

^-Globulin, 238 7-Globulin, 229 Glucagon

adenyl cyclase and, 404 lipolysis and, 312 Glucocorticoids, 399

adenyl cyclase and, 406 Glucocorticosteroid, 86 Glucokinase, 322 Gluconeogenesis

control of, 24

fatty acid oxidation inhibitors and, 321 7-Gluconolactone, 362

Glucosamine, 265 Glucose 1-phosphate

phosphorylase a and, 12 phosphorylase b and, 36 Glucose 6-phosphate, 322

Glucose 6-phosphate dehydrogenase, 18 /3-Glucosidase, inhibitors of, 362 Glucosylceramide, 362

Glucosylsphingosine, a-galactosidase and, 363

Glucosyltransferase, 372

Glutamate dehydrogenase, 8, 18, 20, 31 ammonium ion and, 23

L-Glutamate dehydrogenase, 27-30 Glutamate-pyruvate transaminase, 38 Glutamine synthetase, 19, 34-35 Glutamokinase, 19

Glutaraldehyde, 405 phosphorylase b and, 36 Glutarimide antibiotics, 162 Glutathione, 259

D-Glycerate dehydrogenase, 18

Glyceride biosynthesis, inhibition of, 333 Glycerol, 123

a-Glycerol phosphate, esterification of, 322

L-Glycerol 3-phosphate pathway, 337 Glycerophosphatides, synthesis of,

365-369

Glycerophosphorylethanolamine, 367 Glycine ethyl ester, 255

Glycine methyl ester, 258 Glycinol, 118

Glycodiazine, 312 Glycogen, 12

Glycogen synthetase, 18 chloride ion and, 23 Glycolate, 205 Glycolipases, 362

Glycolipid biosynthesis, inhibitors of, 371-372

iV-Glycolylneuraminic acid, 364 ai-Glycoprotein, 238

Glycosphingolipid(s), 362

Glycosphingolipid hydrolases, inhibitors of, 361-365

Glycosphingolipid synthesis, inhibitors of, 369-372

Glycylglycine, 255

Glycylglycine methyl ester, 258 Glyoxal, 329

Glyoxalate, 113

Glyoxalate cycle intermediates, 27 Gonadal hormones, pineal gland adenyl

cyclase and, 403 Gougerotin, 156-157, 165 Gouy-Chapman model, 279

(13)

Gramicidin D , 198 Gramicidin S, 198 Growth hormone, 396 G T P acyl-CoA synthetase, 315 GTPase, 169

ribosomal-dependent, 150, 154 Guanidine(s)

Afunctional, 253-254

competitive inhibition by, 253 Guanidine salts, pyruvate carboxylase

and, 328

w-Guanidino acid hexyl esters, 254 Guanidinosuccinic -acid, 280 Guanine deaminase, 21 Guanyl nucleotides, 405

5'-Guanylylmethylenediphosphonate, 135, 168-169

Guinea pig hair follicle, 287

H

Halobacterium cutirubrum, 123 6-Halotryptophans, 81

m-Halotryosine, 56 Hansenula ciferri, 370 Heart failure, congestive, 47 Heat, amino acid activation and, 114 Helmholtz-Smoluchowski equation, 281 Hemoglobin, 6

synthesis, 143 Hemophilia A, 268 Hemophilia B, 267

Hemophiliacs, autoimmune, 268 Heparin, role in blood coagulation,

282-284

Heparin cofactor phenomenon, 240 Heparin plasma cofactor, 228 Heparin-prothrombin complex, 284 n-Heptane, 197

2-Heptyl-4-hydroxyquinoline-iV-oxide, 190

Herbicides, 189

H e t e r o t o p i c interactions, 4 synergistic effects, 9

2-Hexadecoxy-3-octadecoxypropyl- phosphonate, 333

Hexadecylphosphate, 358 Hexamethonium, 313

£?Yms-Hexamic acid, 256

Hexamine, 255 Hexanoylcarnitine, 319 Hexokinase, 19, 322 Hexosamines, 364 Hexosaminidase A, 364

Hexose monophosphate shunt, 339 Hexose phosphate aminotransferase, 19 O-Hexosylsphingosines, 362

5-HIAA, see 5-Hydroxindoleacetic acid Hill equation, 6

negative effectors and, 7 Hirudin, 227, 246-248, 286 Histamine, 258

adenyl cyclase and, 396, 408 pineal gland and, 403 Histidine, 360

dye-sensitized photooxidation of, 38 L-isomer, 21

Histones, 282, 372

Homarus americanus, 258 Homoserine, 22

Homoserine dehydrogenase, 20 Homoserine dehydrogenase-as-

partokinase complex, 15

Homotropic cooperativity, positive, 5 Homotropic interactions, 4

Homotropism, negative, 5 Hormones, see also specific types

adenyl cyclase activators, 396-409 hydroxylases and, 86

lipolytic, 312

Howell's theory of blood coagulation, 284

H Q N O , see 2-n-Heptyl-4-hydroxy- quinoline iV-oxide

5-HTP, see 5-Hydroxytryptophan Hunger, 78

Hybrid states, formation of, 9 Hydrazine, 255

Hydrocortisone, 86 Hydrogen peroxide, 48, 259 Hydrogen sulfide, 180

Hydroquinone, 185, 187, 260, 361 Hydroxamates, 110

pyrophosphate and, 125

3-Hydroxyacyl-CoA dehydrogenases, 319 7-Hydroxy-/3-aminobutyramide, 117 5-Hydroxyarterenone, 61

^/ireo-Hydroxyaspartate, 338

(14)

(—)-Hydroxycitrate, 330 4-Hydroxycoumarin, 261 7-Hydroxycoumarin, 261 a-Hydroxydopacetamide, 61 6-Hydroxydopamine, 59, 72-73, 89 Hydroxy fatty acids, cerebroside biosyn­

thesis and, 371 4-Hydroxyglutamate, 338 a-Hy droxy hexadecanal, 361

5-Hydroxyindoleacetic acid, 51, 83-84 3-Hydroxykynurenine, 86

Hydroxylamine, 112, 185, 188, 235, 255 aminoacyl adenylate and, 110 A T P : P P i exchange and, 124-125 Hydroxylase inhibitors, 45-90 Hydroxylases

hormonal influences, 86-88 in vitro inhibitors of, 56-71 in vivo inhibitors of, 71-84

Hydroxylation, molecular oxygen and, 46

2-Hydroxymalonate, 334 p-Hydroxymercuribenzoate, 57

amino acid activation and, 111 p-Hydroxymethylphenylalanine, 56 3-Hydroxy-a-methyl-L-phenylalanine, 66 3-Hydroxy-2-naphthaldehyde, 64 m-Hydroxynorephedrine, 74, 80 2-Hydroxy-DL-phenylalanine, 66 3-Hydroxy-DL-phenylalanine, 66 p-Hydroxyphenylpyruvic acid, 64 aZ/o-4-Hydroxyproline, 116 Hydroxypyridylalanine, 116 8-Hydroxyquinoline, 62 Hydroxystilbamidine, 121 Hydroxy toluene, butylated, 361 5-Hydroxytryptophan, 45, 67 Hypercoagulability, 280 Hypergammaglobulinemia, 268 Hypertension, 76

Hyperthyroid rats, 404 Hypoglycemia, 87, 317 Hypoglycine, 315-317 Hypolipidemic agents, 332 Hypophysectomized animals, 87 Hypophysectomy, pineal gland and, 403 Hypoprothrombinemic rats, 264 Hypothalamic hormones, 396

Hypothalamic releasing hormones, adenyl cyclase and, 408 Hypothyroid rats, 404

I

IF1, 133 IF2, 133 IF3, 133

Imidazole, 124, 191, 360

amino acid activation and, 112 cyclic A M P phosphodiesterase and,

418 Imipramine, 88 Immune diffusion, 221

"Immunity factor," 168 Immunoelectrophoresis, 221 Immunoglobulins, 163, 268

IgC, 268 I g M , 268

Indole-3-pyruvic acid, 64, 65 Indophenols, 65, 185

uncoupling and, 197 Induced-fit hypothesis, 10 Inhibition

allosteric

limiting models for, 3-13 probe mechanisms, 13-16 feedback, 2

indirect, 88-89 interneuronal, 88-89

Inhibitors, see also specific types acquired, 225

allosteric, 1-40 classes of, 17-23

models requiring changes in confor­

mational state, 9-10

multiple reaction pathways, 10-13 time-dependent enzyme activity,

10-13

hereditary, 225, 265-267 hyperbolic response, 5

noncompetitive, of amino acid activa­

tion, 111-114 stoichiometry of, 123-124 Inorganic phosphate, glutamate de­

hydrogenase and, 30 Inorganic pyrophosphatase, 19 Inosine triphosphate, 18

(15)

Inositol phosphatide synthesis, inhibitors of, 368

Insulin

adenyl cyclase and, 404 lipolysis and, 313

serotonin synthesis and, 87 Insulin deficiency, 322

Interstitial-cell-stimulating hormone, adenyl cyclase and, 408

Inter-a-trypsin inhibitor, 236 Intravascular flow rates, 280 Iodoacetamide, 258

photosynthesis and, 203

4-(Iodoacetamido)salicyclic acid, 28, 29 Iodoacetate, 56, 258

amino acid activation and, 112 Iodoacetic acid, photosynthesis and, 203 Iodobenzoates, 335

m-Iodobenzoate, 336 p-Iodobenzoate, 336

2-p-Iodobenzyl malonate, 335, 336, 338 5-Iodo-8-hydroxyquinoline, 62 3-Iodo-5-methoxy-DL-phenylalanine, 66 3-Iodo-a-methyl-DL-phenylalanine, 66 2-Iodo-a-methyl-DL-tyrosine, 77 3-Iodo-a-methyl-DL-tyrosine, 66, 69 p-Iodophenyl acetate, 336

p-Iodophenylalanine, 56 3-Iodo-DL-phenylalanine, 66 4-Iodo-DL-phenylalanine, 66 3-Iodophenylglycine, 70

4-(3-Iodophenyl)-2-methyl-2-aminobu- tanoic acid, 70

iV-Iodosuccinimide, 54 5-Iodotryptophan, 67, 69, 77 3-Iodotyrosine, 69, 77 2-Iodo-L-tyrosine, 77 3-Iodo-L-tyrosine, 69

Ionophores, uncoupling and, 198 Ionophorus antibiotics, adenyl cyclase

and, 416 Ions

adenyl cyclase and, 410-414

inorganic, as allosteric inhibitors, 23 Iron chelators, 361

Iron-complexing agents, hydroxylases and, 63, 73-74

a-Isobutyldopacetamide, 60

Isobutyryl-CoA, pyruvate carboxylase, 328

Isocitrate dehydrogenase, 18, 26-27 NADP-linked, 339

Isocitrate oxidation, 334 Isoleucine, 20

Isoleucine hydroxamate, 115 Isoleucinol, 118

Isoleucinyl adenylate, 118 Isoleucinyl-AMP, 125

Isonicotinic acid hydrazide, 258 4-Isooctyl-2,6-dinitrophenol, 195 Isopropylaminoacetocatechol, 61 a-Isopropyldopacetamide, 61

Isopropyl methylphosphorofluoridate, 250

DL-Isopropylnorepinephrine, 60 4-Isopropyltropolone, 62, 63, 73 Isoproterenol, adenyl cyclase and, 397 Isovaleryl-CoA dehydrogenase, 317 I v y bleeding time, 230

Ixodes ricinus, 249 Ixodin, 249

J

Jack bean, 117

Jamaican ackee tree, 316

K

Kallikrein, 250 Kanamycin, 142, 146 Kaolin, 280

Kasugamycin, 121, 142-143, 146 K D F , see Vitamin K-dependent factor Kethoxal, 121

a-Keto acids, aminooxyacetate and, 338 a-Ketobutyrate, 22, 327

3-Ketodihydrosphingosine, 372 Ketogenesis, 321

a-Ketoglutarate, 20

Ketomalononitrile-3-chlorophenyl- hydrazone, 195

Ketomalononitrile-4-trifluoromethoxy- phenylhydrazone, 195

a-Ketomethylenecyclopropylpropionic acid, 317

Kidney bean trypsin inhibitor, 236

(16)

Kinetic probe mechanisms, 13-14 Krebs cycle intermediates, 27 i£-type system, 3

Kynurenine, 86

L

D-Lactate dehydrogenase, 18 inhibition b y G T P , 6, 24 L-Lactate dehydrogenase, 24 Laki-Lorand factor, 219

Langmuir adsorption isotherm, 228 Laurie acid, phospholipase A and, 352 Laurylcarnitine, 319

"Leakiness," 164

Lecithin synthesis, from CDP-choline and diglyceride, 368

Leeches, 286 Leucinol, 118 Leucoproteases, 237 Leukemia, 83

Leukocytes, basophil, 408 Leupeptins, 232

Lever pressing, 78

Lima bean trypsin inhibitor, 232 Lincomycin, 154, 157-159

Linoleic acid phospholipase A and, 352 Linolenic acid, uncoupling and, 198 Lipase, hormone-sensitive, 313 Lipid (s)

adenyl cyclase activation and, 421 in blood coagulation, 276-280 Lipid metabolism

effects of albumin, 381-382 of detergents, 373-376 of metal ions, 376-378

of substrate and product, 378-379 Lipid-protein interactions, blood coagu­

lation and, 226

Lipid solvents, adenyl cyclase and, 417 Lipolysis, inhibitors of, 312-315 Lipolytic hormones, 312 Lipophilic acceptors, 185, 191 Lipopolysaccharide, 265

Lipoproteins in blood coagulation, 276-280

Liquid crystals, 223 Lithium, 89

adenyl cyclase and, 413

Lithium carbonate, 86

Lobster, blood coagulation in, 258 Locomotor activity, 78

LSD-25, 79 Lubrol P X , 392 Lupus erythematosus

inhibitor, 269-271 systemic, 269

Luteinizing hormone, 396 adenyl cyclase and, 408 Lutidine, 112

Lysinol, 118 Lysolecithin, 352

Lysolecithin acylation, inhibitors of, 367 Lysophosphatidyl-j9-methylcholine, 367 Lysophospholipase, inhibitors of, 353-355 Lysoplasmalogen, 360

Lysozomes, 352 Lys-puromycin, 161 L y s - t R N A - E F l - G T P , 136 L y s - t R N A - E F T u - G T P , 136 Lysyl adenylate, 112

M

«

2

-Macroglobulin, 238

a

2

-Macroglobulin antithrombin, 229 a

2

-Macroglobulin inhibitor, 287 Macroglobulinemia, 268, 280 Macrolide antibiotics, 160 Magnesium hydroxide, 221

Magnesium ion, amino acid activation and, 114

Malate

NADP-linked oxidation of, 25 pyruvate carboxylase and, 329 Malate dehydrogenase, 18, 21, 25, 338

fructose 1,6-diphosphate and, 22 3-phospho-D-glycerate and, 22 Malate pathway, 339

Malayan pit viper, 220 Malic acid, 201

Malic dehydrogenases, NADP-specific, acetyl-CoA and, 26

Malic enzymes, 23, 25-26

Malonate, carbon dioxide reduction and, 204

Malonyl-CoA, 324

Manganese deficiency, 187-188

(17)

M A O , see Monoamine oxidase Maze learning, 78

a-Me-5-HTP, see a-Methyl-5-hydroxy- tryptophan

Melanocyte-stimulating hormone, 396 adenyl cyclase and, 408

Melanoma, melantotic, 90 Melatonin, 396, 398

adenyl cyclase and, 408 hydroxylation of, 56 Melatonin-producing cells, 46

Membrane systems, allosteric inhibition in, 38-40

Menadione, 64, 261 Meperidine, 79

Mercaptide formation, 28 2-Mercaptoethanol, 52, 54, 112 Mercurials, 14

aspartate transcarbamylase and, 32 energy transfer inhibition and, 199-200 Mercurial diuretic meralluride, 416 p-Mercuribenzenesulfonate, energy trans­

fer inhibition and, 200 Mercuric chloride, 56

Mercury ions, lysophosphatides and, 367 Mescaline, 79

Mesoxalate, 329

Metal-chelating agents, 52

Metal ions, effect on lipid metabolism, 376-378

Metamorphosis, viscous, 275 Metaraminol, 74, 80 Methadone, 87 Methioninol, 118

Methioninyl adenylate, 112 Methioninyl-AMP, 125 a-Methoxydopacetamide, 61

3-Methoxy-4-hydroxphenyl catechols, 57 Methylamine, 188, 253

uncoupling, 198

Methylaminoacetocatechol, 60 6-Methylarterenone, 71

2-Me thyl-2- (p-chlorophenylphenoxy) - propionate, 332

/S-Methylcysteine, 64

a-Methyl-2,3-dihydroxyphenylalanine, 72 a-Methyl-DOPA, 61, 72

a-Methyldopacetamide, 61 a-Methyldopamine, 61, 72

N-Methyldopamine, 60

Methylenebis-3-(4-hydroxycoumarin), 262 Methylene blue, 64

Methylenecyclopropaneacetic acid, 316 Methylene diphosphonate, 113

therapy and, 127 Methylene tryptophan, 51 iV-Methylepinephrine, 60 N-Methylglycine, 116 Methylglyoxal synthase, 21

Af-Methyl-iV-3-hydroxyphenylhydrazine, 47

a-Methyl-5-hydroxytryptophan, 67, 79 3-Methylisoxazole-5-carboxylic acid, 314 5-Methylisoxazole-3-carboxylic acid,

314

Methylmalonyl-CoA, 329, 332 Methylmercuric iodide, 28 Methylmercuric nitrate, 259 2-Methyl-a-methyl-DOPA, 59 Methyl-DL-a-methyltyrosinate, 77 2-Methyl-l,4-naphthoquinone, 64 Methyl-p-nitrobenzenesulfonate, 258 a-Methy norepinephrine, 61, 72 6- (1 -Methy lpenty 1) -2,4-dinitrophenol,

195

iV-Methylphenazonium ion, 179, 185 a-Methylphenylalanine, 66, 80 /3-Methylphenylalanine, 66 p-Methylphenylalanine, 56 2-Methyl-2-[p-(l,2,3,4-tetrahydro-l-

naphthyl) phenoxy] propionate, 332 6-Methyltetrahydropteridine, 48 O-Methylthreonine, 116 L-a-Methyltryptophan, 53 a-Methyl-DL-tryptophan, 67 2-Methyl-DL-tryptophan, 67 5-Methyl-DL-tryptophan, 67 6-Methyl-DL-tryptophan, 67 a-Methyl-m-tyramine, 74 m-Methyltyrosine, 56 a-Methyl-L-tyrosine, 66, 69 a-Methyl-ra-tyrosine, 74 a-Methyl-p-tyrosine, 74, 76, 78 fMet-puromycin, 155 f M e t - t R N A , 133

M I C A , see Methylisoxazole-5-carboxylic acid

Minosine, 116

(18)

a - M M T , see a-Methyl-m-tyrosine Monactin, 198

Monensin, 198

Monoacylglycerophosphorylcholine, 353 Monoacylglycerophosphorylethanola-

mine, 353

Monoamine oxidase, 51 Monochloroacetic acid, 219 M o n o d model, 9

Monoglyceride pathway, 325 Monomer-micelle transition, 364 6-Monomethyltetrahydroperidine, 55 Monophosphoinositide, 357

Monosialoganglioside, 364

Monosialoganglioside synthesis, 372 Monuron, 189

Morphine, 75, 89 M o t o r activity, 77 Mounting, 78 Mouse mast cells, 46

tumor, 52

a - M P T , see a-Methyl-p-tyrosine MS2 bacteriophage, 149

Mucopolysaccharide, 282 sulfated, 282

Muscle contraction, 219 adenyl cyclase and, 414 allosteric mechanism, 39 Mutations, nonsense, 164 Mycoplasma laidlawii, 354 Myeloma, 268

Myometrium, 410

Myristic acid, phospholipase A and, 352 N

Nacturus, 391

NADP-linked isocitrate dehydrogenase, 339

N A D (P)-linked oxidoreductases, 17 N A D P

+

, photoreduction of, 189 Naja melanoleuca, 285 Naja nigricollis, 285 Naja naja venom, 353 1,2-Naphthoquinone, 64 1,4-Naphthoquinone, 64 Nectrus, 408

Negative effectors, 2 Hill equation and, 7

N E M , see iV-Ethylmaleimide Neomycin, 142, 146

Nerve cells, dopaminergic, 46 noradenergic, 46

postganglionic, 46 Nervonic acid, 278

Neuraminidase, inhibitors of, 364-365 Neuroblastoma, 47, 391, 402

Neuromodulator synthesis, 47 Neurons, dopaminergic, 47, 52

noradrenergic, 52 serotonergic, 46, 52 Neurospora crassa, 26, 113 Neurotransmitter synthesis, 47

Nicotinamide dinucleotides, as allosteric inhibitors, 17

Nicotinic acid, triglyceride hydrolysis and, 313

Nigericin, 198 N I H shift, 50

Nitrate, reduction of, 180 Nitration, 28

Nitrite, photosynthesis and, 204 Nitrobenzene, detoxification of, 56 5-Nitro-l,2,3-benzene tricarboxylate, 335 Nitrogen, reduction of, 180

3-Nitro-l,8-naphthalate, 335, 336 p-Nitrophenoxide, 253

4-Nitrophenylalanine, 66 o-Nitrophenylgalactoside, 363 p-Nitroj)henylglucoside, 362

p-Nitrophenyl ra-guanidinobenzoate, 253 p-Nitrophenyl p-guanidinobenzoate, 253 p-Nitrophenylphosphorylcholine, 356 a-Nitroso-/3-naphthol, 62

3-Nitro-L-tyrosine, 67 Nitrous acid, 227

carbon dioxide reduction and, 204 Nonactin, 198

adenyl cyclase and, 416 Noncovalent forces, 9 2-Nonyl-4-hydroxyquinoline-A

r

-oxide, 190 Norepinephrine, 59, 61, 76

adenyl cyclase and, 397 lipolysis and, 312 synthesis, 50 Norvaline, 115

p - N P G B , see p-Nitrophenyl p-guani­

dinobenzoate

(19)

N Q N O , see 2-n-Nonyl-4-hydroxy- quinoline N-oxide

Nuclear exoribonuclease, 21

Nucleophiles, amino acid activation and, 112-114

Nucleophilic agents, 167 5'-Nucleotidase, 19 Nucleotides

adenyl cyclase and, 410-414 as allosteric inhibitors, 17-22 inhibitors of cyclic A M P formation,

415-416 O Octadecylamine, 358

2-Octadecyleicosylphosphonate, 333 Octanoylcarnitine, 319

Octylguanidine, 198 Oleandomycin, 160

Oleic acid, phospholipase A and, 352 Oligomeric enzyme, 9

Oligomycin, 200

Oligonucleotides, synthetic, amino­

acyl-tRNA formation and, 120 Ontogenic development, 420 Ophiophagus hannah, 285 Optical rotatory dispersion, 37 Organophosphorus compounds, 250-251 Ornithine, 116

Ornithodorus moubata, 248

Orthophosphate, phosphorylase b and, 35

Osmotic fragility, 275 Ouabain, 21, 23, 85

cyclic A M P formation and, 414 inositol phosphatides and, 368 lipolysis and, 314

Ouchterlony immunodiffusion, 163 Ovariectomy, 87, 403

Oxaloacetate, 27, 201 from pyruvate, 323

phosphorylating decarboxylation of, 22 Oxalysine, 116

Oxamate, 329 /3-Oxidation, 311

enzymes, inhibitors of, 319-320 Oxidoreductases, N A D (P)-linked, 17 Oxoglutarate, 334

Oxotremorine, 416 Oxygen

amino acid hydroxylation and, 46 partial pressure, hydroxylases and, 86 Oxytocin, lipolysis and, 314

P

P700, 182

photoreduction of, 189 Pactamycin, 141-142

"Pactamycin protein," 142 Pain, sensitivity to, 78 (+)-Palmitoylcarnitine, 318 Palmitoyl-CoA, 366

Palmitoyltransferase, 317-318 Palmityl-acyl carrier protein, 365 Palmitylaldehyde, 372

Pancreatic 0 cells, 398 Pancreatic lipase, 353 Papain, 269

Parathyroid hormone, 396 adenyl cyclase and, 407 Parenchymal cells, 46 Parkinson's disease, 63 Parotid gland, 401 Pasteur effect, 204 P C , see Plastocyanin

P C P , see p-Chlorophenylalanine P D S , see Polydextran sulfate Penicillium notatum, 357 Pentachlorophenol, 191

uncoupling and, 195 n-Pentadecanal, 361 Pentamines, 255 Pentanoic acid, 316 2-Pentenoic acid, 316 4-Pentenoic acid, 316

4-Pentenoyl-(—) -carnitine, 316 4-Pentenoyl-CoA, 316

2-n-Pentyl malonate, 335, 336 P E P , see Phosphoenolpyruvate Peptide bond formation, 155-163 Peptide chain elongation, inhibitors of,

144-163

Peptide chain initiation, inhibitors of, 139-144

Peptide chain termination inhibitors of, 163-165

(20)

premature, 165-167 Peptide release, 166

Peptidyltransferase, 136, 162 activity, 158

Peptidyl-tRNA-mRNA-ribosome, 141 Performic acid, 259

Periodate oxidized t R N A , 119 Peroxisome, 205

PF3, see Platelet factor 3 P F K , see Phosphofructokinase P G A , see 3-Phosphoglyceric acid Phagocytosis, 409

o-Phenanthroline, 62, 63, 73, 113, 124, 361

1,10-Phenanthroline, 190 Phenazine methosulfate, 189, 339 Phenindione, 261

Phenol

energy transfer inhibition and, 201 uncoupling and, 195

Phenoxybenzamine, 88, 398 Phentolamine, 314, 398

pineal gland and, 403 Phenylalanine, 19, 20, 22

derivatives, 66 L-isomer, 66

Phenylalanine hydroxylase, 54-56 assay, 54

catechols and, 58 location, 55 properties, 55 Phenylalaninol, 118 Phenylalanylamides, 117 p-Phenylenediamine, 185, 187

photooxidation of, 188 Phenylindandione, 261, 262 Phenylketonuria, 49, 54, 55, 81 2-Phenyl malonate, 336

Phenylmercuric acetate, energy transfer inhibition and, 200

Phenylmethanesulfonyl fluoride, 251 Phenylpyruvate, 329

Phenyl pyruvic acid, 64 2-Phenyl succinate, 335 Phenylureas, 189-190, 191 Pheochromocytoma, 47, 76, 85 Phloretin, 199

Phloretin 2'-/3-glucoside, 199 Phlorizin, 186, 199

Phlorobutyrophenone, 196 Phosphatase, 327

Phosphate

acyl-CoA synthetase and, 315 uncoupling and, 198

analogs, 196

L-a-Phosphatidate phosphohydrolase, 333 inhibitors of, 358-359

Phosphatidic acid phosphohydrolase, 333 Phosphatidic acid synthesis, inhibitors

of, 365-367

Phosphatidic analogs, synthetic, 333 Phosphatidylcholine, 270

Phosphatidyl glycerophosphate, 365 Phosphatidylserines, 227, 270, 276

decarboxylation of, 368 synthesis, inhibitors of, 368 phosphodiesterase, Ca

2 +

-dependent, 395

cyclic A M P and, 313 Phosphoenolpyruvate, 21, 326

Phosphoenolpyruvate carboxylase, 20, 26 Phosphoenolpyruvic acid, carboxylation

of, 201, 205

Phosphofructokinase, 19, 21, 37, 322, 323 inhibitors of, 325-326

6-Phosphogluconate dehydrogenase, 339 3-Phosphoglycerate, 21

Phosphoglyceric acid, 201 Phosphohexoisomerase, 322

Phosphoinositide hydrolases, inhibitors of, 357-358

Phosphokinase, 313 Phospholipase A

adenyl cyclase and, 405, 417 inhibitors of, 351-353

Phospholipase B, from bee venom, 354 Phospholipase C, 287

inhibitors of, 355-356

Phospholipase D , inhibitors of, 359-360 Phospholipid ( s ) , 265

binding to prothrombin and factor X a , 223

factor X and, 245 liquid crystals, 223

Phospholipid hydrolases, 351-361 Phosphonate analogs, 118

Phosphorescence spectra, allosteric bind­

ing and, 15

(21)

Phosphorylase, cooperativity in, 11 Phosphorylase a, 10, 38

kinetic mechaism for, 12 Phosphorylase b , 21, 35-37

Phosphorylating decarboxylation, 22 Phosphorylation, inhibitors of, 185 Phosphoribosyl-ATP pyrophosphorylase,

21

Phosphoribosyl pyrophosphate amido- transf erase, 18

Phosphorylcholine, 356 Phosphorylethanolamine, 372 Phosphoserine, 251

Phosphosphingolipid synthesis, inhibitors of, 369-372

Photooxidation, dye sensitized, 38 Photophosphorylation, cyclic, 185 Photoreduction, 189

reactions, 180

Photorespiration, 204-206 Photosynthesis

inhibition b y oxygen, 204-206 inhibitors of, 179-210 mechanism of, 180-181

physiological control of, 206-209 Photosystem I, 182

oxidizing side, inhibition of, 191-192 reducing side, inhibition of, 192-193 Photosystem II, 182

reducing side, inhibition of, 189-191 Phthalate, 335

Phycobilins, 183 Phylloquinone, 261 Phylloquinone oxide, 288 Physical displacements, 9 Phytoene, 288

Phytohemaglutinin, 401 adenyl cyclase and, 409 Pineal gland, 46, 52

adenyl cyclase in, 403-404 1-Piperidinoacetocatechol, 61 Plants

" C „ " 206

"C«," 206

oxygen-resistant, 205

P M S , see Phenazine methosulfate, iV-Methylphenazonium

P M S F , see p-[m-(m-fluorosulfonyl- phenylureido)phenoxyethoxy] benza­

midine

P M S F , see Phenylmethanesulfonyl fluoride

Polyanionic compounds, 227 Polycyclic compounds, aromatic, 260 Polydextran sulfate, 21

Polygonatum multifiorum, 117 Polylysine, 372

Poly-L-lysine, 197 Polylysyl puromycin, 161 Polymyxin B sulfate, 258

Polypeptide (s), as anticoagulants, 286 Polypeptide hormones, 390

Polypeptide inhibitors, 246-250 Polyphenylalanine synthesis, 143, 158 Polyphosphoinositides, hydrolysis of,

357-358

Polysaccharide storage, 321 Polysome breakdown, 155, 166 Polyuridylic acid, 147

Porcine pancreatic kallikrein, 250 Porcine plasmin, 250

Post-heparin lipase, 353

Potassium ion, cyclic A M P formation and, 413

Plasma recalcification time, 230 Plasmalogen content, 277

Plasmalogen vinyl-ether linkage, cleav­

age of, 360-361 Plasmin, 219

inhibition b y F D P , 274 Plasmin inhibitor, 245-246 tfi-Plasmin inhibitor, 236 Plasminogen, 220

activation, 254 Plastocyanin, 182, 183

photoreduction of, 189 Plastoquinones, 182, 183 Platelets, 224

aggregation F D P and, 275

thrombin induction of, 241 Platelet factor 3, 223, 273

inhibition of, 273

release, inhibitors of, 279-280 PQ, see Plastoquinones Prephenate, 20, 22

(22)

Prethrombin, 260 Probe mechanisms

allosteric inhibition and, 13-16 physical, 15-16

Product I, 222 Proflavin, 121

Prolactin, lipolysis and, 314 Proline amide, 117 Prolinol, 118

Prolyl-tRNA ligase, 123 Pronase, 219

Pronethalol, 398 lipolysis and, 314 Propionylcarnitine, 319

Propionyl-CoA, pyruvate carboxylase and, 328

Propranolol, 314 Propylamine, 117 2-Propyl citrate, 335, 336

a-n-Propyldopacetamide, 57, 59, 60, 71 w-Propyl gallate, 57, 60

Prostaglandin(s), 227, 279 adenyl cyclase and, 409-410 cyclic A M P phosphodiesterase and,

418

lipolysis and, 314

Prostaglandin Ei, lipolysis and, 314 Protamine, 242

Protamine sulfate, 240, 282 Protein(s)

biosynthesis, 132-139 inhibitors of, 170 metal-containing, 183 P10, 146

pseudosubstrates, 231-246 synthesis, inhibitors of, 131-170 Protein kinases, cyclic AMP-dependent,

391

Protein-lipid interactions, blood coagula­

tion and, 226 Prothrombin

activation to thrombin, 221-224 activator, 223

complex, 222 consumption, 274, 280 consumption time, 230 time, 230, 267

one-stage, 285

Prothrombinase, 223, 245, 269, 283

Pseudohypoparathyroidism, 407, 421 Pseudosubstrates, protein, 231 Pseudouridine residues, 121 Psychosines, 362, 371 Pteridine, 46

Pulmonary emphysema, 228

Puromycin, 127, 144, 157, 165-166, 263, 283

blood clotting and, 227 phosphodiesterase and, 419 Pyocyanine, 185

Pyridine, 112

2-Pyridine aldoxime methochloride, 251 2,3-Pyridine dicarboxylate, 335, 336 Pyridoxal phosphate, 28, 372

phosphorylase b and, 36 a-Pyridylaminoacetocatehol, 60 Pyrimethamine, 121

Pyrimidine biosynthesis, 3 purine nucleotides and, 17 Pyrimidine nucleoside antibiotics,

156-157

Pyrimidine nucleotides, halogenated de­

rivatives, 17 Pyrophosphatase, 113 Pyrrolidine, 117 Pyroglutamic acid, 217 Pyrophosphate

aminoacyl-tRNA and, 125 hydroxamate and, 125 1-Pyrrolidinoacetocatechol, 61 Pyrroloisoxazoles, 63

Pyruvate, from glucose, 322-323 Pyruvate carboxylase, 20, 324

inhibitors of, 328-329 inhibition b y G T P , 24 Pyruvate dehydrogenase, 323

inhibitors of, 326 4-pentenoic acid and, 316 Pyruvate kinase, 19, 20, 325

inhibitors of, 326 Pythiam, 6

Q

Quaternary structure, 2

homotropic interactions and, 9 Quercetine, 361

Quinacrin, 121

(23)

Quinoidal antibiotics, 63 Quinones, 185, 260 Quinonediimides, 185, 192 Quinone sulfonates, 184

R

Raphe system, 46

Recalcification time, plasma, 230 a-Receptors, 397

/3-Receptors, 397 Reduviin, 248 Reptilase, 219, 286 Reserpine, 76, 79, 86 Restraint, hormones and, 87 Reticuloendothelial cells, 405 R F l , 137

antibodies to, 163 R F 2 , 137

antibodies to, 163 R F 3 , 137

Rheumatoid arthritis, 229 Rhizopus arhizus, 353 Rhodnius prolexus, 248 Ribosomal A site, 144 Ribosomal P site, 144 Ribulose diphosphate accumulation of, 203 carboxylation of, 201, 205

Ribulose disphosphate carboxylase, 203 Ribulose phosphates, 208

m R N A , polysomal, 160

R N A polymerase, DNA-dependent, 263 RNase, 167

Rotarod performance, 78 Russell's viper venom, 222, 249, 260

factor X Friuli and, 267

S

Saccharomyces, 162 Salicylaldoxime, 192

energy transport inhibition and, 201 Salicylanilide, 197

Salicylates, 126 lipolysis and, 314 Sarcoplasmic reticulum, 405 Salicylic acid, 118

Sarin, 250

Schiff base formation, 28 Sea urchin eggs, 420 Secretin, lipolysis and, 312 Sedative action, a - M M T and, 75 Sedimentation velocities, 15 Sedoheptalose phosphates, 204, 208 Seizure susceptibility, 78

Seizure threshold, 83 Self stimulation, 78 Semiquinone, 260 Serine proteases, 223, 252 Serotonin, 51, 75, 85, 279

adenyl cyclase and, 396, 408 pineal gland and, 403 synthesis of, 54

thyroid hormone and, 87 Serum, inhibitor activity of, 236 Sexual development of females, 78 Sialyllactose, 364

Siomycin, 154-155

SLE, see Systemic lupus erythematosus Sodium borohydride, 57

Sodium deoxycholate, 277

Sodium diethyldithiocarbamate, 62, 63 Sodium dodecyl sulfate

aspartate transcarbamylase and, 32 phosphatidic acid phosphatase, 358 phospholipase D and, 360

pyruvate carboxylase and, 328 Sodium fluoride, 143-144, 162

adenyl cyclase and, 392

sphingosine base metabolism and, 372 Sodium indophenol, 64

Sodium ion, cyclic A M P formation and, 413

Sodium salicylate, lipolysis and, 314 Sodium stearate, 278

Sodium tetraphenyl boron, 416 Solomon's seal, 117

Solvents, effect on adenyl cyclase, 417 Sonication, uncoupling and, 197 Soybean trypsin inhibitor, 227, 231 Sparsomycin, 155-156, 165

Spectinomycin, 147 Spermine, 126

Sphingolipid hydrolases, 369 Sphingomyelin

biosynthesis, inhibitors of, 370-371 phospholipase C and, 356

(24)

Sphingomyelinase, inhibitors of, 356-357 Sphingosine, 277, 362

er?/£/iro-Sphingosine, 371

£/ireo-Sphingosine, 371 Sphingosine bases

metabolism of, 372 phosphorylation of, 372 Sphingosylphosphorylcholine, 370 er^£/iro-Sphingosylphosphorylcholine,

371

£/ireo-Sphingosylphosphorylcholine, 371 Spin-labeled compounds, 16

Spiramycin, 160

Staphylococci, agglutination of, 275 Staphylokinase, 220

Starvation, 322

Stearyl glycerophosphate, 366 Sterculic acid, 332

Steroid hormones, 396 Steroidal antibiotic, 150 Sterols, 278

STI, see Soybean trypsin inhibitor Streaming potentials, 281

Streptamine, 148 Streptokinase, 220, 237

plasminogen activation by, 254 Streptococcus jaecalis, 25 Streptomyces lincolenensis, 157 Streptomycin, 127, 141, 142, 146-149, 164

"Streptomycin protein," 142 Stuart-Prower factor, 222 Stypven tests, 280 Substrate affinity, 2 Substrate availability, 85 Subtilisin, 250

Succinate, aspartate transcarbamylase and, 16

Succinate-cytochrome c reductase, 21 Succinic dehydrogenase, 65

Succinyl-CoA, citrate synthase and, 330 Sucrose phosphate synthetase, 18 Sulfate

phosphorylase b and, 36 reduction of, 180 uncoupling and, 198 Sulfhydryl reagents

blood coagulation and, 258-259 hydroxylases and, 56

Sulfonyl halides, 251-252

Sulfonylation, 251

Sulfur-containing antibiotic, 155 Sympathetic nervous system, 46 Synthalin, 199

Synthetases, ion dependence, 378

T

T4 Bacteriophage, 133 Tabanin, 248

T A M e , see p-Tosyl-L-arginine methyl ester

Taurocholate

ceramidase and, 362 phospholipase A and, 353 Tay-Sachs ganglioside, 363

T C I P , see 2,3',6-Trichlorophenolindo- phenol

TDP-glucose, 20 Telencephalon, 72 Temperature

adaptation, hormones and, 87 multisite allosteric behavior and, 15 Ternary complexes, multisubstrate sys­

tems and, 14 Tertiary structure, 2

Testosterone, adenyl cyclase and, 408 Tetrabenazine, 76

4,5,6,7-Tetrabromo-2-trifluoromethylben- zimidazole, 200

Tetracycline, 144-146, 164 Tetrahydrobiopterin, 48, 55

Tetrahydropteridine, amino acid hy- droxylation and, 46

Tetrahydrofolate, 48, 135 Tetrahymena, 368

Af,Af,Af',Af'-Tetramethyl-p-phenylenedia- mine, 339

Tetranitromethane, 28, 288 Tetraphosphates, 115

T F T B , see 4,5,6,7-Tetrabromo-2- trifluoromethylbenzimidazole Theophylline, 314

adenyl cyclase and, 404 cyclic A M P formation and, 413 cyclic A M P phosphodiesterase and,

418

Therapy, inhibitors in, 108

(25)

T H F A , see Tetrahydrofolate Thiazolidine-4-carboxylic acid, 116 2-(4-Thiazolyl)benzimidazole, 62 /3-2-Thienylalanine, 56

Thiokinases, 315 Thiolases, 319 Thiopeptin, 154 Thiophosphate, 196 Thioproperazine, 88 Thiosine, 116 Thiostrepton, 137, 154 Threonine, 20

X-irradiation protection and, 15 Threonine deaminase, 7, 20

feedback control of, 22 Thrombin

bioactivated, 251 bovine, properties of, 217 inhibition

aluminum hydroxide and, 239 of plasma and serum, 237-242 siliconized vessels and, 274 Thrombin esterase activity, 241, 287 Thrombinogenic potential, 274 Thrombocytasthenias, 280 Thrombocytopathies, 280 Thrombocytopenias, 280 Thromboelastograms, 273 Thrombokinase, 222, 248 Thromboplastin, 265

generation, 280

Thrombosis, inhibitors of, 280-282 Thrombotest procedure, 265 Thylakoids, 182

swelling of, 194 Thymocytes, 412 o-Thymotic acid, 255 Thyrocalcitonin, 401

adenyl cyclase and, 407 Thyroidectomy, 407 Thyroid hormones, 87

biosynthesis of, 77

Thyroid-stimulating hormone, 396 adenyl cyclase and, 407

Thyroxine, 396

adenyl cyclase and, 407 tyrosine hydroxylase and, 70 Tissue coagulase, 258

Tissue thromboplastins, 225

T L C K , see L-l-Chloro-3-tosylamido-7- amino-2-heptanone

T M P D , see A ^ i V y V ' - T e t r a m e t h y l - p - phenylenediamine

Toluidine blue, 282

L-l-Tosylamido-2-phenylethyl chloro­

methyl ketone, 252

p-Tosyl-L-arginine methyl ester, 220

" T o s y l hole," 253

iV-a-p-Tosyl-L-lysine chloromethyl k e ­ tone, 227

T P C K , see L-l-Tosylamido-2-phenyl- ethyl chloromethyl ketone Transamidase, 252

Ca

2 +

-dependent, 219 Transesterification, 158 Transferrin, 274 Transfer R N A

cations and, 121-123 competitive inhibitors of, 118 dielectric effects and, 121-123 drugs and, 121

modified, 119-120 native, 118-119 periodate oxidized, 119 Transglutaminase, 258, 287 Transient forms, 10 Transition metals, 51 Translation factors, 140 Translocation, 150-155, 160

EFG-dependent, 160

ribosomal, allosteric mechanism, 39 Transpeptidase, 219

Transpeptidation, 160

Transport-inducing antibiotics, 198 uncoupling and, 198

Transport, active, allosteric mechanism, 39

Transport processes, control of lipogene­

sis, 333-339

Transport systems, colicins and, 167 Trasylol, 232, 235

Tremor, 78 Tremorine, 79

Triatoma infestans, 248 s-Triazines, 191

Triazinones, 191

Tri-n-butyltin chloride, 200 Tricarballylate, 331

(26)

1,2,3-Tricarboxybenzene, 335

Tricarboxylate transport, inhibitors of, 335

1,2,3-Tricarboxypropane, 331 2,3',6-Trichlorophenolindophenol, 197 Trifluoroperazine, 416

[ra-Trifluoromethylphenyl]-2-ethylami- nopropane, 84

Triglyceride hydrolysis, 311 Triglyceride storage, 321 Triglyceride synthesis, 325 Trihexosylceramide, 363 Triiodothyronine, 400, 407

phosphodiesterase and, 419 a,/3,/3-Trimethyl D O P A , 57, 71, 82 Trimethyloctadecylammonium chloride,

358

Trinitrobenzene sulfonate, 28 Tri-n-octylamine, 358 Triose phosphate, 201

Triose phosphate dehydrogenase, 203, 323

dichloroacetic acid and, 320 Triphenylmethan dyes, 139 Triphosphoinositides, 357 2,4,6-Tripyridyl-s-triazine, 62

Tris, 189

amino acid activation, 112 5-Tritio-DOPA, 46

p-Tritiophenylalanine, 54 5-Tritiotryptophan, 50 3-Tritiotyrosine, 54 3,5-Tritio-L-tyrosine, 46

Triton X-100, phospholipase A and, 353 Trypsin-carboxymethylcellulose, 250 Trypsin-ethylenemaleic acid copolymer,

250

Trypsin inhibitor bovine pancreas, 232 lima bean, 232 Tryptophan, 19, 20, 22

derivatives, 67 L-Tryptophan, 67, 69

Tryptophan hydroxamate, 117 Tryptophan hydroxylase, 50-54

assay, 50-51 biosynthesis, 86 catechols and, 58

location, 51-52 properties, 52-54

Tryptophan pyrrolase, 18, 53, 86 Tylosin, 160

Tyramine, 48, 117

conversion to dopamine, 56 Tyrosinase, 46

Tyrosine, 20, 22 derivatives, 66-67 m-Tyrosine, 48

Tyrosine hydroxylase, 46-50 assay, 46-47

catechols and, 58 location, 47-48 properties of, 48-50 Tyrosinol, 118

Tyrosyl deoxyadenylate, 115

U

UDP-iV-acetylgalactosamine, 369 UDP-AT-Acetyl-D-glucosamine, 19 UDP-Af-Acetylglucosamine 2-epimerase,

19

UDP-Galactose, 369

UDP-Galactose 4-epimerase, 20 UDP-Glucose, 369

Ultracentrifugal analysis, 15 Ultraviolet irradiation, 15 Umbelliferon, 261 Uncoupling, 193-199 Uracils, 191 Urea, 39

adenyl cyclase and, 405

aspartate transcarbamylase and, 34 Uremia, 280

Uridine-cytidine kinase, 20 Urokinase, 220, 237

V

Valine ligase, 113 Valinol, 118

Valinomycin, 194, 198 adenyl cyclase and, 416 Valinyl adenylate, 118 Valinyl-AMP, 125 Vasoconstriction, 219 Vasopressin, 396

(27)

adenyl cyclase and, 407 lipolysis and, 314

Venoms, 285,see alsospecific types Veratridine, 414

Vinyl-ether linkage, cleavage of, 360-361 Viologens, 184, 192

Vitamin K, 64, 260 antagonists, 227

clotting factors, 225, 284

Vitamin K series (K-S) , blood clotting and, 261

"Vomiting sickness," 316 V-type system, 3

w

Warburg effect, 204

Warfarin, 227,261

Water oxidation, inhibition of, 187-189

x

X-Irradiation, 15

aspartate transcarbamylase and, 34 hormones and, 87

y

Yeast, 38, 161

z

Zea mays, 190, 205 Zeta potential, 360 Zinc, 32

Hivatkozások

KAPCSOLÓDÓ DOKUMENTUMOK

[r]

"packing" of carbinol group of, 57 Transferases, role in drug metabolism, 61 Transferrin, in iron transport, 32 Tremorine, antagonists of, 97. Trichloroethanol,

[r]

relative nutritional values of, 158 utilization, effect of heat

[r]

High-temperature phosphorescence, see Ε-Type delayed fluorescence Homologs of aromatic hydrocarbons,. phosphorescence of, 77 Hund's

batatas, 117 Fusarium oxysporum f.. cubense, 72 Fusarium

in Pectinaria and Spisula eggs, 507-512 Mitotic apparatus, 547, 549-597, see also Mitosis, Motile systems with continu- ous filaments, Saltatory movements effect of low