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1-(2,4-dichlorobenzoyl)-N-methyl-1H-indazole-3-carboxamide
-
-
2,4-dichloro-N-[4-[(diaminomethylidene)sulfamoyl]phenyl]benzamide
-
-
2,6-dichloro-N-[4-[(diaminomethylidene)sulfamoyl]phenyl]benzamide
-
-
2-(3-(2-hydroxyethyl)ureido)-N-(2-methoxybenzyl)-1H-benzo[d]imidazole-5-sulfonamide
-
-
2-(3-(2-hydroxyethyl)ureido)-N-(2-methylbenzyl)-1H-benzo[d]imidazole-5-sulfonamide
-
-
2-(4-chlorophenoxy)-N-[4-[(diaminomethylidene)sulfamoyl]phenyl]acetamide
-
-
2-bromo-N-[4-[(diaminomethylidene)sulfamoyl]phenyl]benzamide
-
-
2-chloro-N-[4-[(diaminomethylidene)sulfamoyl]phenyl]benzamide
-
-
2-{[(2-hydroxyethyl)carbamoyl]amino}-N-[(2-methoxyphenyl)methyl]-1H-benzimidazole-5-sulfonamide
-
-
3,4-dichloro-N-[4-[(diaminomethylidene)sulfamoyl]phenyl]benzamide
-
-
3-(2,4-dichlorophenyl)isoxazole-5-carbaldehyde
-
50% inhibition at 5.8 mM, weak antifungal activity against Candida albicans
3-(2-bromophenyl)isoxazole-5-carbaldehyde
-
50% inhibition at 1.25 mM, weak antifungal activity against Candida albicans
3-(2-chlorophenyl)isoxazole-5-carbaldehyde
-
50% inhibition at 1.1 mM, weak antifungal activity against Candida albicans
3-(3-bromophenyl)isoxazole-5-carbaldehyde
-
50% inhibition at 4.8 mM, weak antifungal activity against Candida albicans
3-(3-chlorophenyl)isoxazole-5-carbaldehyde
-
50% inhibition at 0.625 mM, weak antifungal activity against Candida albicans
3-(4-chlorophenyl)isoxazole-5-carbaldehyde
-
50% inhibition at 1.8 mM, weak antifungal activity against Candida albicans
3-(4-fluorophenyl)isoxazole-5-carbaldehyde
-
50% inhibition at 4.0 mM, weak antifungal activity against Candida albicans
3-(4-nitrophenyl)-1,2-oxazole-5-carbaldehyde
-
-
3-(4-nitrophenyl)isoxazole-5-carbaldehyde
-
50% inhibition at 0.42 mM, weak antifungal activity against Candida albicans
3-chloro-N-[4-[(diaminomethylidene)sulfamoyl]phenyl]benzamide
-
-
3-methylbutyl 1-[2-([4-[(diaminomethylidene)sulfamoyl]phenyl]amino)-2-oxoethyl]piperidine-4-carboxylate
-
-
3-[4-([[4-(aminomethyl)cyclohexyl]carbonyl]oxy)phenyl]propanoic acid
-
-
4-(acetylamino)phenyl 4-carbamimidamidobenzoate
-
-
4-(chloromethyl)-N-[4-[(diaminomethylidene)sulfamoyl]phenyl]benzamide
-
-
4-([4-[3-(ethoxycarbonyl)-1H-pyrazol-5-yl]phenyl]amino)-4-oxobutanoic acid
-
-
4-carbomethoxyphenyl 4-guanidinobenzoate mesylate
-
4'-CMGB, a sperm acrosin inhibitor and candidate for an vaginal contraceptive drug. Method development and evaluation of 4'-CMGB identification and activity determination involving HPLC and LC-tandem mass spectrometry, overview
4-[(2-methylbenzyl)(methylsulfonyl)amino]-N-(pyridin-4-ylmethyl)benzamide
-
-
5-(2,4-dichlorophenyl)-1,2-oxazole-3-carbaldehyde
-
-
5-(2,4-dichlorophenyl)isoxazole-3-carbaldehyde
-
50% inhibition at 0.39 mM, weak antifungal activity against Candida albicans
5-(2-chlorophenyl)isoxazole-3-carbaldehyde
-
50% inhibition at 1.0 mM, weak antifungal activity against Candida albicans
5-(3-bromophenyl)isoxazole-3-carbaldehyde
-
50% inhibition at 1.1 mM, weak antifungal activity against Candida albicans
5-(4-carbamimidamidophenyl)-N-(1-hydroxypropan-2-yl)-1,2-oxazole-3-carboxamide
-
-
5-(4-carbamimidamidophenyl)-N-(2,3-dimethylphenyl)-1,2-oxazole-3-carboxamide
-
-
5-(4-carbamimidamidophenyl)-N-(2,4-dimethoxyphenyl)-1,2-oxazole-3-carboxamide
-
-
5-(4-carbamimidamidophenyl)-N-(2,5-dimethoxyphenyl)-1,2-oxazole-3-carboxamide
-
-
5-(4-carbamimidamidophenyl)-N-(2,6-dimethylphenyl)-1,2-oxazole-3-carboxamide
-
-
5-(4-carbamimidamidophenyl)-N-(2-methoxyphenyl)-1,2-oxazole-3-carboxamide
-
-
5-(4-carbamimidamidophenyl)-N-(2-methylphenyl)-1,2-oxazole-3-carboxamide
-
-
5-(4-carbamimidamidophenyl)-N-(3,5-dimethylphenyl)-1,2-oxazole-3-carboxamide
-
-
5-(4-carbamimidamidophenyl)-N-(3-chlorophenyl)-1,2-oxazole-3-carboxamide
-
-
5-(4-carbamimidamidophenyl)-N-(3-methoxyphenyl)-1,2-oxazole-3-carboxamide
-
-
5-(4-carbamimidamidophenyl)-N-(3-methylphenyl)-1,2-oxazole-3-carboxamide
-
-
5-(4-carbamimidamidophenyl)-N-(4-chlorophenyl)-1,2-oxazole-3-carboxamide
-
-
5-(4-carbamimidamidophenyl)-N-(4-cyanophenyl)-1,2-oxazole-3-carboxamide
-
-
5-(4-carbamimidamidophenyl)-N-(4-ethoxyphenyl)-1,2-oxazole-3-carboxamide
-
-
5-(4-carbamimidamidophenyl)-N-(4-fluorophenyl)-1,2-oxazole-3-carboxamide
-
-
5-(4-carbamimidamidophenyl)-N-(4-methylphenyl)-1,2-oxazole-3-carboxamide
-
-
5-(4-carbamimidamidophenyl)-N-(4-methylpyridin-2-yl)-1,2-oxazole-3-carboxamide
-
-
5-(4-carbamimidamidophenyl)-N-(naphthalen-1-yl)-1,2-oxazole-3-carboxamide
-
-
5-(4-carbamimidamidophenyl)-N-(propan-2-yl)-1,2-oxazole-3-carboxamide
-
-
5-(4-carbamimidamidophenyl)-N-phenyl-1,2-oxazole-3-carboxamide
-
-
5-(4-carbamimidamidophenyl)-N-[4-(trifluoromethyl)phenyl]-1,2-oxazole-3-carboxamide hydrochloride
-
-
5-(4-methylphenyl)isoxazole-3-carbaldehyde
-
50% inhibition at 2.4 mM, weak antifungal activity against Candida albicans
5-([4-[3-(ethoxycarbonyl)-1H-pyrazol-5-yl]phenyl]amino)-5-oxopentanoic acid
-
-
5-phenylisoxazole-3-carbaldehyde
-
50% inhibition at 2.4 mM, weak antifungal activity against Candida albicans
7-amino-1-chloro-3-L-tosylamidoheptan-2-one
-
weak
Benzamidine hydrochloride
-
50% inhibition at 2.2 mM, weak antifungal activity against Candida albicans
butyl 1-[2-([4-[(diaminomethylidene)sulfamoyl]phenyl]amino)-2-oxoethyl]piperidine-4-carboxylate
-
-
diisopropylfluorophosphate
ethyl 1-(2,4-dichlorobenzoyl)-1H-indazole-3-carboxylate
-
-
ethyl 1-(phenylcarbonyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
-
-
ethyl 1-(thiophen-2-ylcarbonyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
-
-
ethyl 1-[(2,4-dichlorophenyl)acetyl]-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
-
-
ethyl 1-[(2,4-dichlorophenyl)carbonyl]-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
-
-
ethyl 1-[(2,4-dimethoxyphenyl)carbonyl]-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
-
-
ethyl 1-[(2,6-dichlorophenyl)carbonyl]-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
-
-
ethyl 1-[(2-bromo-4-fluorophenyl)carbonyl]-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
-
-
ethyl 1-[(2-chloro-4-fluorophenyl)carbonyl]-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
-
most potent inhibitor
ethyl 1-[(2-chlorophenyl)carbonyl]-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
-
-
ethyl 1-[(2-fluorophenyl)carbonyl]-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
-
-
ethyl 1-[(2-methoxyphenyl)carbonyl]-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
-
-
ethyl 1-[(2-methylphenyl)carbonyl]-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
-
-
ethyl 1-[(3,4-dichlorophenyl)carbonyl]-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
-
-
ethyl 1-[(3-fluorophenyl)carbonyl]-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
-
-
ethyl 1-[2-([4-[(diaminomethylidene)sulfamoyl]phenyl]amino)-2-oxoethyl]piperidine-4-carboxylate
-
-
ethyl 4-([[5-(4-carbamimidamidophenyl)-1,2-oxazol-3-yl]carbonyl]amino)benzoate hydrochloride
-
-
ethyl 5-(4-[[(2,4-dichlorophenyl)carbonyl]amino]phenyl)-1H-pyrazole-3-carboxylate
-
-
ethyl 5-(4-[[(2,6-dichlorophenyl)carbonyl]amino]phenyl)-1H-pyrazole-3-carboxylate
-
-
ethyl 5-(4-[[(2,6-difluorophenyl)carbonyl]amino]phenyl)-1H-pyrazole-3-carboxylate
-
-
ethyl 5-(4-[[(2-bromophenyl)carbonyl]amino]phenyl)-1H-pyrazole-3-carboxylate
-
-
ethyl 5-(4-[[(2-chlorophenyl)carbonyl]amino]phenyl)-1H-pyrazole-3-carboxylate
-
-
ethyl 5-(4-[[(4-chlorophenyl)carbonyl]amino]phenyl)-1H-pyrazole-3-carboxylate
-
-
ethyl 5-(4-[[(4-fluorophenyl)carbonyl]amino]phenyl)-1H-pyrazole-3-carboxylate
-
-
ethyl 5-(4-[[(4-methoxyphenyl)carbonyl]amino]phenyl)-1H-pyrazole-3-carboxylate
-
-
ethyl 5-(4-[[(4-methylphenyl)carbonyl]amino]phenyl)-1H-pyrazole-3-carboxylate
-
-
ethyl 5-(4-[[4-(1-phenylpropyl)benzoyl]amino]phenyl)-1H-pyrazole-3-carboxylate
-
-
ethyl 5-[4-(acetylamino)phenyl]-1H-pyrazole-3-carboxylate
-
-
ethyl 5-[4-(benzoylamino)phenyl]-1,2-oxazole-3-carboxylate
-
-
ethyl 5-[4-(butanoylamino)phenyl]-1H-pyrazole-3-carboxylate
-
-
ethyl 5-[4-(pentanoylamino)phenyl]-1H-pyrazole-3-carboxylate
-
-
ethyl 5-[4-(propanoylamino)phenyl]-1H-pyrazole-3-carboxylate
-
-
ethyl 5-[4-([4-[(4-methylphenyl)sulfonyl]benzoyl]amino)phenyl]-1H-pyrazole-3-carboxylate
-
-
ethyl 5-[4-([[4-(chloromethyl)phenyl]carbonyl]amino)phenyl]-1H-pyrazole-3-carboxylate
-
-
ethyl 5-[4-[(2-chlorobenzoyl)amino]phenyl]-1,2-oxazole-3-carboxylate
-
-
ethyl 5-[4-[(3,4-dichlorobenzoyl)amino]phenyl]-1,2-oxazole-3-carboxylate
-
-
ethyl 5-[4-[(3-chloropropanoyl)amino]phenyl]-1H-pyrazole-3-carboxylate
-
-
ethyl 5-[4-[(4-benzylbenzoyl)amino]phenyl]-1H-pyrazole-3-carboxylate
-
-
ethyl 5-[4-[(4-chlorobenzoyl)amino]phenyl]1,2-oxazole-3-carboxylate
-
-
ethyl 5-[4-[(4-fluorobenzoyl)amino]phenyl]-1,2-oxazole-3-carboxylate
-
-
ethyl 5-[4-[(phenylcarbonyl)amino]phenyl]-1H-pyrazole-3-carboxylate
-
-
ethyl 5-[4-[(trifluoroacetyl)amino]phenyl]-1H-pyrazole-3-carboxylate
-
-
guanidinobenzoate
-
KF950
L-1-chloro-3-[4-tosylamido]-7-amino-2-heptanone
-
-
methyl (6-[[4-(trifluoromethyl)phenyl]sulfamoyl]-1H-benzimidazol-2-yl)carbamate
-
-
methyl 1-[2-([4-[(diaminomethylidene)sulfamoyl]phenyl]amino)-2-oxoethyl]piperidine-4-carboxylate
-
-
methyl 4-methyl-3-([4-[(2-methylbenzyl)(methylsulfonyl)amino]benzoyl]amino)benzoate
-
-
methyl [6-(butylsulfamoyl)-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-(hexylsulfamoyl)-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-(phenylsulfamoyl)-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-(propan-2-ylsulfamoyl)-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-[(2,4-dichlorophenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-[(2,4-difluorophenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-[(2,5-dimethylphenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-[(2-chlorophenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-[(2-fluorophenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-[(2-methoxyphenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-[(3,4-dichlorophenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-[(3,4-difluorophenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-[(3,4-dimethoxyphenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-[(3-fluorophenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-[(3-methoxyphenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-[(3-methylphenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-[(4-bromophenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-[(4-chlorophenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-[(4-fluorophenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-[(4-methoxyphenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-[(4-methylphenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-[benzyl(methyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
-
-
methyl [6-[bis(3-methylbutyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
-
-
N,N-bis(2-hydroxyethyl)-5-(4-methoxyphenyl)-1H-pyrazole-3-carboxamide
-
-
N,N-dibenzyl-2-[4-(propan-2-ylsulfamoyl)phenoxy]acetamide
-
-
N-(2-bromophenyl)-5-(4-carbamimidamidophenyl)-1,2-oxazole-3-carboxamide
-
-
N-(2-chlorobenzyl)-2-(3-(2-hydroxyethyl)ureido)-1H-benzo[d]imidazole-5-sulfonamide
-
-
N-(2-fluorobenzyl)-2-(3-(2-hydroxyethyl)ureido)-1H-benzo[d]imidazole-5-sulfonamide
-
-
N-(2-hydroxyethyl)-5-(4-methoxyphenyl)-N-methyl-1H-pyrazole-3-carboxamide
-
-
N-(2-hydroxypropyl)-5-(4-methoxyphenyl)-1H-pyrazole-3-carboxamide
-
-
N-(3, 5-difluorobenzyl)-2-(3-(2-hydroxyethyl)ureido)-1H-benzo[d]imidazole-5-sulfonamide
-
-
N-(3,5-dichlorobenzyl)-2-(3-(2-hydroxyethyl)ureido)-1H-benzo[d]imidazole-5-sulfonamide
-
-
N-(3-bromophenyl)-5-(4-carbamimidamidophenyl)-1,2-oxazole-3-carboxamide hydrochloride
-
-
N-(3-hydroxypropyl)-5-(4-methoxyphenyl)-1H-pyrazole-3-carboxamide
-
-
N-(4-chlorophenyl)-N-[2-[(2E)-2-(3-methoxy-4-methylbenzylidene)hydrazinyl]-2-oxoethyl]benzenesulfonamide (non-preferred name)
-
-
N-(4-tert-butylphenyl)-5-(4-carbamimidamidophenyl)-1,2-oxazole-3-carboxamide hydrochloride
-
-
N-(5-bromobenzo[d]thiazol-2-yl)-2-(4-pentylpiperazin-1-yl)acetamide
-
-
N-(5-bromobenzo[d]thiazol-2-yl)-2-(diisopentylamino)acetamide
-
-
N-(5-bromobenzo[d]thiazol-2-yl)-2-(dipentylamino)acetamide
-
-
N-(6-bromobenzo[d]thiazol-2-yl)-2-(dibutylamino)acetamide
-
-
N-(diaminomethylidene)-4-(4-methylanilino)benzene-1-sulfonamide
-
-
N-alpha-tosyl-L-lysyl-chloromethyl-ketone
-
-
N-alpha-tosyl-L-lysyl-chloromethylketone
-
-
N-benzyl-2-(3-(2-hydroxyethyl)ureido)-1H-benzo[d]imidazole-5-sulfonamide
-
-
N-cyclohexyl-2-[(4,6-diphenylpyrimidin-2-yl)sulfanyl]acetamide
-
-
N-hexyl-2-(3-(2-hydroxyethyl)ureido)-1H-benzo[d]imidazole-5-sulfonamide
-
-
N-tosyl-L-lysine chloromethylketone
-
-
N-[4-(dipropylsulfamoyl)phenyl]-3,4-diethoxybenzamide
-
-
N-[4-[(4-benzylpiperazin-1-yl)carbonyl]phenyl]-2,3,5,6-tetramethylbenzenesulfonamide
-
-
N-[4-[(4-benzylpiperazin-1-yl)carbonyl]phenyl]-4-tert-butylbenzenesulfonamide
-
-
N-[4-[(4-fluorophenyl)sulfamoyl]phenyl]-3,4,5-trimethoxybenzamide
-
-
N-[4-[(4-methoxyphenyl)sulfamoyl]phenyl]-2-(naphthalen-1-yloxy)acetamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2,4,6-trimethylbenzamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2,6-difluorobenzamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2-(2-methylphenoxy)acetamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2-(2-methylpiperidin-1-yl)acetamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2-(3-methylphenoxy)acetamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2-(4-methoxyphenoxy)acetamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2-(4-methylphenoxy)acetamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2-(4-methylpiperidin-1-yl)acetamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2-(4-nitrophenoxy)acetamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2-(piperidin-1-yl)acetamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2-phenoxyacetamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-3,5-dinitrobenzamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-3-(trifluoromethyl)benzamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-4-ethoxybenzamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-4-ethylbenzamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-4-fluorobenzamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-4-methoxybenzamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-4-methylbenzamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]butanamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]pentanamide
-
-
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]propanamide
-
-
Nalpha-tosyl-L-lysine chloromethyl ketone
-
-
propan-2-yl 1-[2-([4-[(diaminomethylidene)sulfamoyl]phenyl]amino)-2-oxoethyl]piperidine-4-carboxylate
-
-
propyl 1-[2-([4-[(diaminomethylidene)sulfamoyl]phenyl]amino)-2-oxoethyl]piperidine-4-carboxylate
-
-
Trypsin inhibitor II
-
-
-
Trypsin-plasmin inhibitor
-
bdellin B-3
-
diisopropylfluorophosphate
-
-
diisopropylfluorophosphate
-
weak
Trypsin inhibitor
-
lima-bean
-
Trypsin inhibitor
-
soybean
-
Trypsin inhibitor
-
bovine pancreatic
-
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Asthenozoospermia
Acrosin activity of human spermatozoa by means of a simple gelatinolytic technique: a method useful for IVF.
Asthenozoospermia
[L-carnitine improves sperm acrosin activity in male infertility patients].
Breast Neoplasms
Upregulation of RHOXF2 and ODF4 Expression in Breast Cancer Tissues.
Carcinoma, Ductal
Upregulation of RHOXF2 and ODF4 Expression in Breast Cancer Tissues.
Fibroadenoma
Upregulation of RHOXF2 and ODF4 Expression in Breast Cancer Tissues.
Herpes Zoster
A delayed sperm penetration of cumulus layers by disruption of acrosin gene in rats.
Herpes Zoster
A mouse serine protease TESP5 is selectively included into lipid rafts of sperm membrane presumably as a glycosylphosphatidylinositol-anchored protein.
Herpes Zoster
Acrosin accelerates the dispersal of sperm acrosomal proteins during acrosome reaction.
Herpes Zoster
Acrosin activity in patients with idiopathic infertility.
Herpes Zoster
Acrosin Activity Regulation by Protein Kinase C and Tyrosine Kinase in Bovine Sperm Acrosome Exocytosis Induced by Lysophosphatidylcholine.
Herpes Zoster
Acrosin is essential for sperm penetration through the zona pellucida in hamsters.
Herpes Zoster
Acrosin shows zona and fucose binding, novel properties for a serine proteinase.
Herpes Zoster
Activation and subsequent degradation of proacrosin is mediated by zona pellucida glycoproteins, negatively charged polysaccharides, and DNA.
Herpes Zoster
Antifertility effects of tetradecyl sodium sulphate in rabbits.
Herpes Zoster
Appropriate timing of the acrosome reaction is a major requirement for the fertilizing spermatozoon.
Herpes Zoster
Boar acrosin digestion of the porcine egg coat, zona pellucida, and rearrangement of the zona proteins.
Herpes Zoster
Caprine acrosin. Purification, characterization and proteolysis of the porcine zona pellucida.
Herpes Zoster
Cell biology of acrosomal proteins.
Herpes Zoster
Changes in composition of the porcine zona pellucida during development of the oocyte to the 2- to 4-cell embryo.
Herpes Zoster
Characterization of the functional domains of boar acrosin involved in nonenzymatic binding to homologous zona pellucida glycoproteins.
Herpes Zoster
Correction for Hirose et al., Acrosin is essential for sperm penetration through the zona pellucida in hamsters.
Herpes Zoster
Diploid expression and translational regulation of rat acrosin gene.
Herpes Zoster
Dissolution of rabbit zona by sperm acrosomal extract: effect of calcium (1).
Herpes Zoster
Distinctive features of the gametes and reproductive tracts of the Asian musk shrew, Suncus murinus.
Herpes Zoster
Early steps of sperm-egg interactions during mammalian fertilization.
Herpes Zoster
Effect of recombinant boar beta-acrosin on sperm binding to intact zona pellucida during in vitro fertilization.
Herpes Zoster
Effector sites in the three-dimensional structure of mammalian sperm beta-acrosin.
Herpes Zoster
Effects of acrosin inhibitors on the soluble and membrane-bound forms of ram acrosin, and a reappraisal of the role of the enzyme in fertilization.
Herpes Zoster
Effects of ram sperm acrosin on the investments of sheep, pig, mouse and gerbil eggs.
Herpes Zoster
Functional interactions between sulphated polysaccharides and proacrosin: implications in sperm binding and digestion of zona pellucida.
Herpes Zoster
Golden hamster perivitelline spermatozoa do not show proacrosin/acrosin at the inner acrosomal membrane.
Herpes Zoster
Histochemical subcellular localization of the acrosomal proteinase effecting dissolution of the zona pellucida using fluorescein-labeled inhibitors.
Herpes Zoster
Identification of a zona-binding protein from boar spermatozoa as proacrosin.
Herpes Zoster
Immunocytochemical localization of acrosin on both acrosomal membranes and in the acrosomal matrix of porcine spermatozoa.
Herpes Zoster
Immunodetection of acrosin during the acrosome reaction of hamster, guinea-pig and human spermatozoa.
Herpes Zoster
Immunolocalization of proacrosin/acrosin in rabbit sperm during acrosome reaction and in spermatozoa recovered from the perivitelline space.
Herpes Zoster
Inhibition of acrosin activity with a trypsin inhibitor blocks human sperm penetration of the zona pellucida.
Herpes Zoster
Inhibition of the vacuolar H(+)-pump with bafilomycin A1 does not induce acrosome reaction or activate proacrosin in mouse spermatozoa.
Herpes Zoster
Limited and specific proteolysis of the zona pellucida by acrosin.
Herpes Zoster
Limited proteolysis by acrosin affects sperm-binding and mechanical resilience of the mouse zona pellucida.
Herpes Zoster
Limited proteolysis of the porcine zona pellucida by homologous sperm acrosin.
Herpes Zoster
Localization of rabbit sperm acrosin during the acrosome reaction induced by immobilized zona matrix.
Herpes Zoster
Mammalian sperm interaction with extracellular matrices of the egg.
Herpes Zoster
Matrix degrading properties of sperm serine proteinase, acrosin.
Herpes Zoster
Mechanical hypothesis of sperm penetration.
Herpes Zoster
Methods to evaluate reproductive health of the human male.
Herpes Zoster
MMP2 and acrosin are major proteinases associated with the inner acrosomal membrane and may cooperate in sperm penetration of the zona pellucida during fertilization.
Herpes Zoster
Molecular mechanisms of the interaction between sperm and the zona pellucida in mammals: studies on the pig.
Herpes Zoster
Monoclonal antibodies to bovine and human acrosin.
Herpes Zoster
Normal penetration of rabbit spermatozoa through a trypsin- and acrosin-resistant zona pellucida.
Herpes Zoster
On the interaction of bull and boar acrosins with the zona pellucida of different mammalian species in vitro.
Herpes Zoster
p-Aminobenzamidine, an acrosin inhibitor, inhibits mouse sperm penetration of the zona pellucida but not the acrosome reaction.
Herpes Zoster
p-Aminobenzamidine-sensitive acrosomal protease(s) other than acrosin serve the sperm penetration of the egg zona pellucida in mouse.
Herpes Zoster
PH-20 but not acrosin is involved in sperm penetration of the macaque zona pellucida.
Herpes Zoster
Predominance of beta-structure in solubilized zona pellucida from porcine ova.
Herpes Zoster
Proacrosin-deficient mice and zona pellucida modifications in an experimental model of multifactorial infertility.
Herpes Zoster
Protease activity involvement in the passage of mammalian sperm through the zona pellucida.
Herpes Zoster
Proteolysis of specific porcine zona pellucida glycoproteins by boar acrosin.
Herpes Zoster
Proteolysis of the zona pellucida by acrosin: the nature of the hydrolysis products.
Herpes Zoster
Proteolytic activity of rabbit perivitelline spermatozoa.
Herpes Zoster
Purification of mouse sperm acrosin, its activation from proacrosin and effect on homologous egg investments.
Herpes Zoster
Randomized trial of partial zona dissection for male infertility.
Herpes Zoster
Role of acrosomal matrix proteases in sperm-zona pellucida interactions.
Herpes Zoster
Site-directed mutagenesis of rabbit proacrosin. Identification of residues involved in zona pellucida binding.
Herpes Zoster
Some effects of zona pellucida glycoproteins and sulfated polymers on the autoactivation of boar sperm proacrosin and activity of beta-acrosin.
Herpes Zoster
Sperm from mice carrying a targeted mutation of the acrosin gene can penetrate the oocyte zona pellucida and effect fertilization.
Herpes Zoster
Spermatozoa lacking acrosin protein show delayed fertilization.
Herpes Zoster
Subcellular immunochemical localization of acrosin in human spermatozoa during the acrosome reaction and zona pellucida penetration.
Herpes Zoster
The action of acrosin on the zona pellucida.
Herpes Zoster
The complete primary structure of three isoforms of a boar sperm-associated acrosin inhibitor.
Herpes Zoster
The histochemical localization of acrosin in guinea-pig sperm after the acrosome reaction.
Herpes Zoster
The inhibition of boar acrosin amidase activity by sulfated polysaccharides.
Herpes Zoster
The interaction of boar sperm proacrosin with its natural substrate, the zona pellucida, and with polysulfated polysaccharides.
Herpes Zoster
The molecular evolution of acrosin in placental mammals.
Herpes Zoster
The morphological and molecular susceptibility of sheep and mouse zona pellucida to acrosin.
Herpes Zoster
The polysulphate binding domain of human proacrosin/acrosin is involved in both the enzyme activation and spermatozoa-zona pellucida interaction.
Herpes Zoster
The serine protease testisin is present on the surface of capacitated stallion spermatozoa and interacts with key zona pellucida binding proteins.
Herpes Zoster
The sperm acrosome: functional and clinical aspects.
Herpes Zoster
The structures of the bovine and porcine proacrosin genes and their conservation among mammals.
Herpes Zoster
Ultrastructure of opossum oocyte investing coats and their sensitivity to trypsin and hyaluronidase.
Herpes Zoster
Wheat germ agglutinin treatment of follicle cell-free mouse oocytes inhibits fertilization.
Herpes Zoster
Zona pellucida induces conversion of proacrosin to acrosin.
Herpes Zoster
Zona pellucida-binding and fucose-binding of boar sperm acrosin is not correlated with proteolytic activity.
Herpes Zoster
Zona pellucida-binding of boar sperm acrosin is associated with the N-terminal peptide of the acrosin B-chain (heavy chain).
Herpes Zoster
[Significance of proteolytic sperm enzymes for the fertility]
Herpes Zoster
[The significance of acrosin and proteinase-inhibitors in human reproduction]
Infections
Chlamydia trachomatis infection in the genital tract is associated with inflammation and hypospermia in the infertile male of China.
Infections
[Automatic detection and clinical application of semen biochemical markers].
Infertility
A simple, clinical assay to evaluate the acrosin activity of human spermatozoa.
Infertility
A study of sperm acrosin in patients with unexplained infertility.
Infertility
Acrosin activity as a potential marker for sperm membrane characteristics in unexplained male infertility.
Infertility
Acrosin activity in patients with idiopathic infertility.
Infertility
Acrosin antibodies and infertility. I. Detection of antibodies towards proacrosin/acrosin in women consulting for infertility and evaluation of their effects upon the sperm protease activities.
Infertility
Acrosomal proteinase activity of human spermatozoa and relation of results to semen quality.
Infertility
Adenosine 5 triphosphate (ATP) content and acrosin activity in polyzoospermic subjects.
Infertility
Antisperm antibody binding to human acrosin: a study of patients with unexplained infertility.
Infertility
Contribution of the male factor to unexplained infertility: a review.
Infertility
Evidence of proacrosin molecule abnormality as a possible cause of low acrosin activity and unexplained failure of fertilization in vitro.
Infertility
Gelatin-substrate film technique for detection of acrosin in single mammalian sperm.
Infertility
High total acrosin activity in varicocele individuals.
Infertility
Inhibition of hamster sperm acrosomal enzyme by gossypol is closely associated with the decrease in fertilization capacity.
Infertility
Is spermatozoan acrosin a predictor of fertilization and embryo quality in the human?
Infertility
Long-term contraceptive efficacy of vaccine of ovine follicle-stimulating hormone in male bonnet monkeys (Macaca radiata).
Infertility
Low acrosin activity in a subgroup of men with idiopathic infertility dose not correlate with sperm density, percent motility, curvilinear velocity, or linearity.
Infertility
Proacrosin-deficient mice and zona pellucida modifications in an experimental model of multifactorial infertility.
Infertility
Relation of human sperm acrosin activity and fertilization in vitro.
Infertility
Relationship of acrosin activity to sperm function tests.
Infertility
The Change of Semen Superoxide Dismutase and Acrosin Activity in the Sterility of Male Patients with Positive Antisperm Antibody.
Infertility
[Indications for determination of acrosin]
Infertility
[The effect of semen antisperm antibody on human sperm acrosin activity]
Infertility
[Value of sperm acrosin activity detection in selecting the method of assisted reproduction for patients with unexplained infertility].
Infertility, Male
Acrosin activity as a potential marker for sperm membrane characteristics in unexplained male infertility.
Infertility, Male
Acrosin activity in spermatozoa from sterile t6/tw32 and fertile control mice.
Infertility, Male
Gelatin-substrate film technique for detection of acrosin in single mammalian sperm.
Infertility, Male
The Change of Semen Superoxide Dismutase and Acrosin Activity in the Sterility of Male Patients with Positive Antisperm Antibody.
Infertility, Male
[Indications for determination of acrosin]
Infertility, Male
[L-carnitine improves sperm acrosin activity in male infertility patients].
Infertility, Male
[The effect of semen antisperm antibody on human sperm acrosin activity]
Neoplasms
Production, purification, and in vivo evaluation of a novel multiepitope peptide vaccine consisted of immunodominant epitopes of SYCP1 and ACRBP antigens as a prophylactic melanoma vaccine.
Neoplasms
Tumor antigen acrosin binding protein normalizes mitotic spindle function to promote cancer cell proliferation.
Neoplasms
[Effects of interferon-gamma and tumor necrosis factor-alpha on the fertilizing capacity of humam sperm and their mechanisms]
Oligospermia
Acrosin activity of human spermatozoa by means of a simple gelatinolytic technique: a method useful for IVF.
Oligospermia
Determination of active, non-zymogen acrosin, proacrosin and total acrosin in different andrological patients.
Oligospermia
[L-carnitine improves sperm acrosin activity in male infertility patients].
Polycystic Kidney Diseases
Characterization of sperm surface protein patterns of ejaculated and capacitated boar sperm, with the detection of ZP binding candidates.
Spinal Cord Injuries
Hyaluronic acid binding and acrosin activity are decreased in sperm from men with spinal cord injury.
Teratozoospermia
Evidence for effects of testis and epididymis expressed genes on sperm quality and boar fertility traits.
Teratozoospermia
[Etiologic analysis of globozoospermia: a 1-case report]
Teratozoospermia
[Indications for determination of acrosin]
Varicocele
"Human sperm physiology: estrogen receptor alpha (ER?) and estrogen receptor beta (ER?) influence sperm metabolism and may be involved in the pathophysiology of varicocele-associated male infertility."
Varicocele
Assessment of sperm functions in infertile patients with varicoceles.
Varicocele
High total acrosin activity in varicocele individuals.
Varicocele
The effect of smoking and varicocele on human sperm acrosin activity and acrosome reaction.
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3.78
1-(2,4-dichlorobenzoyl)-N-methyl-1H-indazole-3-carboxamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00563
2,4-dichloro-N-[4-[(diaminomethylidene)sulfamoyl]phenyl]benzamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00596
2,6-dichloro-N-[4-[(diaminomethylidene)sulfamoyl]phenyl]benzamide
Homo sapiens
-
pH and temperature not specified in the publication
6.04
2-(3-(2-hydroxyethyl)ureido)-N-(2-methoxybenzyl)-1H-benzo[d]imidazole-5-sulfonamide
Homo sapiens
-
pH and temperature not specified in the publication
5.45
2-(3-(2-hydroxyethyl)ureido)-N-(2-methylbenzyl)-1H-benzo[d]imidazole-5-sulfonamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00935
2-(4-chlorophenoxy)-N-[4-[(diaminomethylidene)sulfamoyl]phenyl]acetamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00763
2-bromo-N-[4-[(diaminomethylidene)sulfamoyl]phenyl]benzamide
Homo sapiens
-
pH and temperature not specified in the publication
0.0063
2-chloro-N-[4-[(diaminomethylidene)sulfamoyl]phenyl]benzamide
Homo sapiens
-
pH and temperature not specified in the publication
7.32
2-{[(2-hydroxyethyl)carbamoyl]amino}-N-[(2-methoxyphenyl)methyl]-1H-benzimidazole-5-sulfonamide
Homo sapiens
-
pH and temperature not specified in the publication
0.0038
3,4-dichloro-N-[4-[(diaminomethylidene)sulfamoyl]phenyl]benzamide
Homo sapiens
-
pH and temperature not specified in the publication
0.42
3-(4-nitrophenyl)-1,2-oxazole-5-carbaldehyde
Homo sapiens
-
in 55 mM HEPES and 55 mM NaCl at pH 8.0 and 37°C
0.007
3-chloro-N-[4-[(diaminomethylidene)sulfamoyl]phenyl]benzamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00251
3-methylbutyl 1-[2-([4-[(diaminomethylidene)sulfamoyl]phenyl]amino)-2-oxoethyl]piperidine-4-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.0033
3-[4-([[4-(aminomethyl)cyclohexyl]carbonyl]oxy)phenyl]propanoic acid
Homo sapiens
-
in 55 mM HEPES and 55 mM NaCl at pH 8.0 and 37°C
0.008
4-(acetylamino)phenyl 4-carbamimidamidobenzoate
Homo sapiens
-
in 55 mM HEPES and 55 mM NaCl at pH 8.0 and 37°C
0.00384
4-(chloromethyl)-N-[4-[(diaminomethylidene)sulfamoyl]phenyl]benzamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00925
4-([4-[3-(ethoxycarbonyl)-1H-pyrazol-5-yl]phenyl]amino)-4-oxobutanoic acid
Homo sapiens
-
pH and temperature not specified in the publication
0.3447
4-[(2-methylbenzyl)(methylsulfonyl)amino]-N-(pyridin-4-ylmethyl)benzamide
Homo sapiens
-
in 55 mM HEPES and 55 mM NaCl at pH 8.0 and 37°C
0.39 - 1.7
5-(2,4-dichlorophenyl)-1,2-oxazole-3-carbaldehyde
0.1
5-(4-carbamimidamidophenyl)-N-(1-hydroxypropan-2-yl)-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
0.0115
5-(4-carbamimidamidophenyl)-N-(2,3-dimethylphenyl)-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
0.0014
5-(4-carbamimidamidophenyl)-N-(2,4-dimethoxyphenyl)-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
0.0023
5-(4-carbamimidamidophenyl)-N-(2,5-dimethoxyphenyl)-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
0.0057
5-(4-carbamimidamidophenyl)-N-(2,6-dimethylphenyl)-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
0.0084
5-(4-carbamimidamidophenyl)-N-(2-methoxyphenyl)-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
0.0144
5-(4-carbamimidamidophenyl)-N-(2-methylphenyl)-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
0.0121
5-(4-carbamimidamidophenyl)-N-(3,5-dimethylphenyl)-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
0.0254
5-(4-carbamimidamidophenyl)-N-(3-chlorophenyl)-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
0.0066
5-(4-carbamimidamidophenyl)-N-(3-methoxyphenyl)-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
0.0094
5-(4-carbamimidamidophenyl)-N-(3-methylphenyl)-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
0.0268
5-(4-carbamimidamidophenyl)-N-(4-chlorophenyl)-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
0.0239
5-(4-carbamimidamidophenyl)-N-(4-cyanophenyl)-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
0.0064
5-(4-carbamimidamidophenyl)-N-(4-ethoxyphenyl)-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
0.0205
5-(4-carbamimidamidophenyl)-N-(4-fluorophenyl)-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
0.0101
5-(4-carbamimidamidophenyl)-N-(4-methylphenyl)-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
0.0214
5-(4-carbamimidamidophenyl)-N-(4-methylpyridin-2-yl)-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
0.0299
5-(4-carbamimidamidophenyl)-N-(naphthalen-1-yl)-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
0.1
5-(4-carbamimidamidophenyl)-N-(propan-2-yl)-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
0.0246
5-(4-carbamimidamidophenyl)-N-phenyl-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
0.0203
5-(4-carbamimidamidophenyl)-N-[4-(trifluoromethyl)phenyl]-1,2-oxazole-3-carboxamide hydrochloride
Homo sapiens
-
pH 7.8, 37.8°C
0.0174
5-([4-[3-(ethoxycarbonyl)-1H-pyrazol-5-yl]phenyl]amino)-5-oxopentanoic acid
Homo sapiens
-
pH and temperature not specified in the publication
0.0095
butyl 1-[2-([4-[(diaminomethylidene)sulfamoyl]phenyl]amino)-2-oxoethyl]piperidine-4-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
3.24
ethyl 1-(2,4-dichlorobenzoyl)-1H-indazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.00221
ethyl 1-(phenylcarbonyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.00029
ethyl 1-[(2,4-dichlorophenyl)carbonyl]-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.00174
ethyl 1-[(2-bromo-4-fluorophenyl)carbonyl]-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.00347
ethyl 1-[(2-chloro-4-fluorophenyl)carbonyl]-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.00299
ethyl 1-[2-([4-[(diaminomethylidene)sulfamoyl]phenyl]amino)-2-oxoethyl]piperidine-4-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.0093
ethyl 4-([[5-(4-carbamimidamidophenyl)-1,2-oxazol-3-yl]carbonyl]amino)benzoate hydrochloride
Homo sapiens
-
pH 7.8, 37.8°C
0.00044
ethyl 5-(4-[[(2,4-dichlorophenyl)carbonyl]amino]phenyl)-1H-pyrazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.0048
ethyl 5-(4-[[(2,6-dichlorophenyl)carbonyl]amino]phenyl)-1H-pyrazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.00398
ethyl 5-(4-[[(2,6-difluorophenyl)carbonyl]amino]phenyl)-1H-pyrazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.0024
ethyl 5-(4-[[(2-bromophenyl)carbonyl]amino]phenyl)-1H-pyrazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.00011
ethyl 5-(4-[[(2-chlorophenyl)carbonyl]amino]phenyl)-1H-pyrazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.00331
ethyl 5-(4-[[(4-chlorophenyl)carbonyl]amino]phenyl)-1H-pyrazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.0024
ethyl 5-(4-[[(4-fluorophenyl)carbonyl]amino]phenyl)-1H-pyrazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.0008
ethyl 5-(4-[[(4-methoxyphenyl)carbonyl]amino]phenyl)-1H-pyrazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.0346
ethyl 5-(4-[[(4-methylphenyl)carbonyl]amino]phenyl)-1H-pyrazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.0033
ethyl 5-(4-[[4-(1-phenylpropyl)benzoyl]amino]phenyl)-1H-pyrazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.023
ethyl 5-[4-(acetylamino)phenyl]-1H-pyrazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.46
ethyl 5-[4-(benzoylamino)phenyl]-1,2-oxazole-3-carboxylate
Homo sapiens
-
pH 7.8, 37.8°C
0.017
ethyl 5-[4-(butanoylamino)phenyl]-1H-pyrazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.072
ethyl 5-[4-(pentanoylamino)phenyl]-1H-pyrazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.014
ethyl 5-[4-(propanoylamino)phenyl]-1H-pyrazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.000032
ethyl 5-[4-([4-[(4-methylphenyl)sulfonyl]benzoyl]amino)phenyl]-1H-pyrazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.00331
ethyl 5-[4-([[4-(chloromethyl)phenyl]carbonyl]amino)phenyl]-1H-pyrazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.06
ethyl 5-[4-[(2-chlorobenzoyl)amino]phenyl]-1,2-oxazole-3-carboxylate
Homo sapiens
-
pH 7.8, 37.8°C
0.24
ethyl 5-[4-[(3,4-dichlorobenzoyl)amino]phenyl]-1,2-oxazole-3-carboxylate
Homo sapiens
-
pH 7.8, 37.8°C
0.00576
ethyl 5-[4-[(3-chloropropanoyl)amino]phenyl]-1H-pyrazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.00047
ethyl 5-[4-[(4-benzylbenzoyl)amino]phenyl]-1H-pyrazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.38
ethyl 5-[4-[(4-chlorobenzoyl)amino]phenyl]1,2-oxazole-3-carboxylate
Homo sapiens
-
pH 7.8, 37.8°C
0.14
ethyl 5-[4-[(4-fluorobenzoyl)amino]phenyl]-1,2-oxazole-3-carboxylate
Homo sapiens
-
pH 7.8, 37.8°C
0.008
ethyl 5-[4-[(phenylcarbonyl)amino]phenyl]-1H-pyrazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.0079
ethyl 5-[4-[(trifluoroacetyl)amino]phenyl]-1H-pyrazole-3-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.000027
KF950
Homo sapiens
-
pH and temperature not specified in the publication
10.7
methyl (6-[[4-(trifluoromethyl)phenyl]sulfamoyl]-1H-benzimidazol-2-yl)carbamate
Homo sapiens
-
pH 8.0, 22°C
0.0093
methyl 1-[2-([4-[(diaminomethylidene)sulfamoyl]phenyl]amino)-2-oxoethyl]piperidine-4-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.1555
methyl 4-methyl-3-([4-[(2-methylbenzyl)(methylsulfonyl)amino]benzoyl]amino)benzoate
Homo sapiens
-
in 55 mM HEPES and 55 mM NaCl at pH 8.0 and 37°C
1.77
methyl [6-(butylsulfamoyl)-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
1.8
methyl [6-(hexylsulfamoyl)-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
1.03
methyl [6-(phenylsulfamoyl)-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
0.47
methyl [6-(propan-2-ylsulfamoyl)-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
1.27
methyl [6-[(2,4-dichlorophenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
1.55
methyl [6-[(2,4-difluorophenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
8.86
methyl [6-[(2,5-dimethylphenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
5.75
methyl [6-[(2-chlorophenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
0.31
methyl [6-[(2-fluorophenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
8.42
methyl [6-[(2-methoxyphenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
4.02
methyl [6-[(3,4-dichlorophenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
1.59
methyl [6-[(3,4-difluorophenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
11.5
methyl [6-[(3,4-dimethoxyphenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
1.81
methyl [6-[(3-fluorophenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
7.5
methyl [6-[(3-methoxyphenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
5.06
methyl [6-[(3-methylphenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
1.64
methyl [6-[(4-bromophenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
7.52
methyl [6-[(4-chlorophenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
2.4
methyl [6-[(4-fluorophenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
3.29
methyl [6-[(4-methoxyphenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
3.18
methyl [6-[(4-methylphenyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
1.25
methyl [6-[benzyl(methyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
0.063
methyl [6-[bis(3-methylbutyl)sulfamoyl]-1H-benzimidazol-2-yl]carbamate
Homo sapiens
-
pH 8.0, 22°C
5.73
N,N-bis(2-hydroxyethyl)-5-(4-methoxyphenyl)-1H-pyrazole-3-carboxamide
Homo sapiens
-
pH and temperature not specified in the publication
0.4267
N,N-dibenzyl-2-[4-(propan-2-ylsulfamoyl)phenoxy]acetamide
Homo sapiens
-
in 55 mM HEPES and 55 mM NaCl at pH 8.0 and 37°C
0.0279
N-(2-bromophenyl)-5-(4-carbamimidamidophenyl)-1,2-oxazole-3-carboxamide
Homo sapiens
-
pH 7.8, 37.8°C
1.06
N-(2-chlorobenzyl)-2-(3-(2-hydroxyethyl)ureido)-1H-benzo[d]imidazole-5-sulfonamide
Homo sapiens
-
pH and temperature not specified in the publication
0.08
N-(2-fluorobenzyl)-2-(3-(2-hydroxyethyl)ureido)-1H-benzo[d]imidazole-5-sulfonamide
Homo sapiens
-
pH and temperature not specified in the publication
6.81
N-(2-hydroxyethyl)-5-(4-methoxyphenyl)-N-methyl-1H-pyrazole-3-carboxamide
Homo sapiens
-
pH and temperature not specified in the publication
8.92
N-(2-hydroxypropyl)-5-(4-methoxyphenyl)-1H-pyrazole-3-carboxamide
Homo sapiens
-
pH and temperature not specified in the publication
0.34
N-(3, 5-difluorobenzyl)-2-(3-(2-hydroxyethyl)ureido)-1H-benzo[d]imidazole-5-sulfonamide
Homo sapiens
-
pH and temperature not specified in the publication
2.45
N-(3,5-dichlorobenzyl)-2-(3-(2-hydroxyethyl)ureido)-1H-benzo[d]imidazole-5-sulfonamide
Homo sapiens
-
pH and temperature not specified in the publication
0.0144
N-(3-bromophenyl)-5-(4-carbamimidamidophenyl)-1,2-oxazole-3-carboxamide hydrochloride
Homo sapiens
-
pH 7.8, 37.8°C
1.43
N-(3-hydroxypropyl)-5-(4-methoxyphenyl)-1H-pyrazole-3-carboxamide
Homo sapiens
-
pH and temperature not specified in the publication
0.014
N-(4-chlorophenyl)-N-[2-[(2E)-2-(3-methoxy-4-methylbenzylidene)hydrazinyl]-2-oxoethyl]benzenesulfonamide (non-preferred name)
Homo sapiens
-
in 55 mM HEPES and 55 mM NaCl at pH 8.0 and 37°C
0.0078
N-(4-tert-butylphenyl)-5-(4-carbamimidamidophenyl)-1,2-oxazole-3-carboxamide hydrochloride
Homo sapiens
-
pH 7.8, 37.8°C
5.08
N-(5-bromobenzo[d]thiazol-2-yl)-2-(4-pentylpiperazin-1-yl)acetamide
Homo sapiens
-
pH and temperature not specified in the publication
1.09
N-(5-bromobenzo[d]thiazol-2-yl)-2-(diisopentylamino)acetamide
Homo sapiens
-
pH and temperature not specified in the publication
0.54
N-(5-bromobenzo[d]thiazol-2-yl)-2-(dipentylamino)acetamide
Homo sapiens
-
pH and temperature not specified in the publication
2.78
N-(6-bromobenzo[d]thiazol-2-yl)-2-(dibutylamino)acetamide
Homo sapiens
-
pH and temperature not specified in the publication
142.6
N-alpha-tosyl-L-lysyl-chloromethyl-ketone
Homo sapiens
-
pH and temperature not specified in the publication
0.1426
N-alpha-tosyl-L-lysyl-chloromethylketone
0.28
N-benzyl-2-(3-(2-hydroxyethyl)ureido)-1H-benzo[d]imidazole-5-sulfonamide
Homo sapiens
-
pH and temperature not specified in the publication
0.3551
N-cyclohexyl-2-[(4,6-diphenylpyrimidin-2-yl)sulfanyl]acetamide
Homo sapiens
-
in 55 mM HEPES and 55 mM NaCl at pH 8.0 and 37°C
1.62
N-hexyl-2-(3-(2-hydroxyethyl)ureido)-1H-benzo[d]imidazole-5-sulfonamide
Homo sapiens
-
pH and temperature not specified in the publication
0.1426
N-tosyl-L-lysine chloromethylketone
Homo sapiens
-
pH and temperature not specified in the publication
0.3018
N-[4-(dipropylsulfamoyl)phenyl]-3,4-diethoxybenzamide
Homo sapiens
-
in 55 mM HEPES and 55 mM NaCl at pH 8.0 and 37°C
0.6248
N-[4-[(4-benzylpiperazin-1-yl)carbonyl]phenyl]-2,3,5,6-tetramethylbenzenesulfonamide
Homo sapiens
-
in 55 mM HEPES and 55 mM NaCl at pH 8.0 and 37°C
3.057
N-[4-[(4-benzylpiperazin-1-yl)carbonyl]phenyl]-4-tert-butylbenzenesulfonamide
Homo sapiens
-
in 55 mM HEPES and 55 mM NaCl at pH 8.0 and 37°C
0.2053
N-[4-[(4-fluorophenyl)sulfamoyl]phenyl]-3,4,5-trimethoxybenzamide
Homo sapiens
-
in 55 mM HEPES and 55 mM NaCl at pH 8.0 and 37°C
0.6678
N-[4-[(4-methoxyphenyl)sulfamoyl]phenyl]-2-(naphthalen-1-yloxy)acetamide
Homo sapiens
-
in 55 mM HEPES and 55 mM NaCl at pH 8.0 and 37°C
0.00245
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2,4,6-trimethylbenzamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00718
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2,6-difluorobenzamide
Homo sapiens
-
pH and temperature not specified in the publication
0.0093
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2-(2-methylphenoxy)acetamide
Homo sapiens
-
pH and temperature not specified in the publication
0.0099
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2-(2-methylpiperidin-1-yl)acetamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00892
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2-(3-methylphenoxy)acetamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00984
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2-(4-methoxyphenoxy)acetamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00898
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2-(4-methylphenoxy)acetamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00498
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2-(4-methylpiperidin-1-yl)acetamide
Homo sapiens
-
pH and temperature not specified in the publication
0.0042
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2-(4-nitrophenoxy)acetamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00741
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2-(piperidin-1-yl)acetamide
Homo sapiens
-
pH and temperature not specified in the publication
0.0023
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-2-phenoxyacetamide
Homo sapiens
-
pH and temperature not specified in the publication
0.0025
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-3,5-dinitrobenzamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00705
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-3-(trifluoromethyl)benzamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00013
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-4-ethoxybenzamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00021
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-4-ethylbenzamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00711
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-4-fluorobenzamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00221
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-4-methoxybenzamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00206
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]-4-methylbenzamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00958
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]butanamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00158
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]pentanamide
Homo sapiens
-
pH and temperature not specified in the publication
0.009
N-[4-[(diaminomethylidene)sulfamoyl]phenyl]propanamide
Homo sapiens
-
pH and temperature not specified in the publication
0.00235
propan-2-yl 1-[2-([4-[(diaminomethylidene)sulfamoyl]phenyl]amino)-2-oxoethyl]piperidine-4-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.00331
propyl 1-[2-([4-[(diaminomethylidene)sulfamoyl]phenyl]amino)-2-oxoethyl]piperidine-4-carboxylate
Homo sapiens
-
pH and temperature not specified in the publication
0.39
5-(2,4-dichlorophenyl)-1,2-oxazole-3-carbaldehyde
Homo sapiens
-
in 55 mM HEPES and 55 mM NaCl at pH 8.0 and 37°C
0.39
5-(2,4-dichlorophenyl)-1,2-oxazole-3-carbaldehyde
Homo sapiens
-
pH 7.8, 37.8°C
1.7
5-(2,4-dichlorophenyl)-1,2-oxazole-3-carbaldehyde
Homo sapiens
-
pH 8.0, 22°C
0.1426
N-alpha-tosyl-L-lysyl-chloromethylketone
Homo sapiens
-
pH and temperature not specified in the publication
0.1426
N-alpha-tosyl-L-lysyl-chloromethylketone
Homo sapiens
-
in 55 mM HEPES and 55 mM NaCl at pH 8.0 and 37°C
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Elce, J.S.; McIntyre, E.J.
Purification of bovine and human acrosin
Can. J. Biochem.
60
8-14
1981
Bos taurus, Homo sapiens
brenda
Anderson, R.A.; Beyler, S.A.; Mack, S.R.; Zaneveld, L.J.D.
Characterization of a high-molecular-weight form of human acrosin. Comparison with human pancreatic trypsin
Biochem. J.
199
307-316
1981
Homo sapiens
brenda
Gilboa, E.; Elkana, Y.; Rigbi, M.
Purification and properties of human acrosin
Eur. J. Biochem.
39
85-92
1973
Homo sapiens
brenda
Fritz, H.; Foerg-Brey, B.; Meier, M.; Arnold, M.; Tschesche, H.
Human acrosin: inhibition by protein-proteinase inhibitors
Hoppe-Seyler's Z. Physiol. Chem.
353
1950-1952
1972
Homo sapiens
brenda
Kobayashi, T.; Matsuda, Y.; Oshio, S.; Kaneko, S.; Nozawa, S; Mhori, H.; Akihama, S.; Fujimoto, Y.
Human acrosin: purification and some properties
Arch. Androl.
27
9-16
1991
Homo sapiens
brenda
Hoshi, K.; Sugano, T.; Yoshimatsu, N.; Yanagida, K.
Correlation of semen characteristics with acrosin, hyaluronidase, tubulin, dynein, and actin of spermatozoa
Arch. Androl.
35
165-172
1995
Homo sapiens
brenda
Suter, L.; Habenicht, U.F.
Characterization of mouse epididymal acrosin: comparative studies with acrosin from boar and human ejaculated spermatozoa
Int. J. Androl.
21
95-104
1998
Homo sapiens, Mus musculus, Sus scrofa
brenda
Langlois, M.R.; Oorlynck, L.; Vandekerckhove, F.; Criel, A.; Bernard, D.; Blaton, V.
Discrepancy between sperm acrosin activity and sperm morphology: significance for fertilization in vitro
Clin. Chim. Acta
351
121-129
2005
Homo sapiens
brenda
Chaudhury, K.; Das, T.; Chakravarty, B.; Bhattacharyya, A.K.
Acrosin activity as a potential marker for sperm membrane characteristics in unexplained male infertility
Fertil. Steril.
83
104-109
2005
Homo sapiens
brenda
Furlong, L.I.; Harris, J.D.; Vazquez-Levin, M.H.
Binding of recombinant human proacrosin/acrosin to zona pellucida (ZP) glycoproteins. I. Studies with recombinant human ZPA, ZPB, and ZPC
Fertil. Steril.
83
1780-1790
2005
Homo sapiens
brenda
Furlong, L.I.; Veaute, C.; Vazquez-Levin, M.H.
Binding of recombinant human proacrosin/acrosin to zona pellucida glycoproteins. II. Participation of mannose residues in the interaction
Fertil. Steril.
83
1791-1796
2005
Homo sapiens
brenda
Gupta, G.; Jain, R.K.; Maikhuri, J.P.; Shukla, P.K.; Kumar, M.; Roy, A.K.; Patra, A.; Singh, V.; Batra, S.
Discovery of substituted isoxazolecarbaldehydes as potent spermicides, acrosin inhibitors and mild anti-fungal agents
Hum. Reprod.
20
2301-2308
2005
Homo sapiens
brenda
Emokpae, M.A.; Uadia, P.O.
Acrosin activity in spermatozoa of infertile Nigerian males
Indian J. Clin. Biochem.
21
199-201
2006
Homo sapiens
brenda
Raterman, D.; Springer, M.S.
The molecular evolution of acrosin in placental mammals
Mol. Reprod. Dev.
75
1196-1207
2008
Amblysomus hottentotus (B0LM06), Bos taurus (P79343), Bradypus tridactylus (B0LM16), Canis lupus familiaris, Cavia porcellus (Q60491), Cynocephalus volans (B0LM30), Diceros bicornis (B0LM26), Dugong dugon (B0LM13), Echinops telfairi (B0LM07), Elephantulus edwardii (B0LM09), Equus caballus (B0LM27), Erethizon dorsatum (B0LM36), Euphractus sexcinctus (B0LM17), Felis catus (B0LM18), Galegeeska rufescens (B0LM10), Homo sapiens (P10323), Homo sapiens, Hystrix brachyura (B0LM35), Lama glama (B0LM21), Loxodonta africana (B0LM12), Macaca mulatta, Macroscelides proboscideus (B0LM11), Manis sp. DMR-2008 (B0LM29), Mus musculus (Q3ZB05), Ochotona princeps (B0LM32), Orycteropus afer (B0LM15), Oryctolagus cuniculus (P48038), Otospermophilus beecheyi (B0LM38), Ovis aries (Q9GL10), Pan troglodytes (B0LM34), Procavia capensis (B0LM08), Puma concolor (B0LM19), Rattus fuscipes (B0LM37), Rattus norvegicus (P29293), Sorex cinereus (B0LM24), Sus scrofa (P08001), Sylvilagus floridanus (B0LM33), Tadarida brasiliensis (B0LM23), Talpa europaea (B0LM25), Tapirus pinchaque (B0LM28), Tragelaphus angasii (B0LM22), Trichechus manatus (B0LM14), Tupaia glis (B0LM31), Tursiops truncatus (B0LM20)
brenda
Veaute, C.; Furlong, L.I.; Bronson, R.; Harris, J.D.; Vazquez-Levin, M.H.
Acrosin antibodies and infertility. I. Detection of antibodies towards proacrosin/acrosin in women consulting for infertility and evaluation of their effects upon the sperm protease activities
Fertil. Steril.
91
1245-1255
2009
Homo sapiens
brenda
Veaute, C.; Furlong, L.I.; Cameo, M.; Harris, J.D.; Vazquez-Levin, M.H.
Antiacrosin antibodies and infertility. II. Gene immunization with human proacrosin to assess the effect of immunity toward proacrosin/acrosin upon protein activities and animal fertility
Fertil. Steril.
91
1256-1268
2009
Homo sapiens
brenda
Aquila, S.; Guido, C.; Santoro, A.; Perrotta, I.; Laezza, C.; Bifulco, M.; Sebastiano, A.
Human sperm anatomy: ultrastructural localization of the cannabinoid1 receptor and a potential role of anandamide in sperm survival and acrosome reaction
Anat. Rec. (Hoboken)
293
298-309
2010
Homo sapiens
brenda
Yin, L.; Hang, T.; Zhang, Z.
Determination of 4-carbomethoxyphenyl 4-guanidinobenzoate mesylate by HPLC and identification of its related substances by LC-MS-MS
J. Chromatogr. Sci.
47
872-876
2009
Homo sapiens
brenda
Qi, J.; Zhu, J.; Liu, X.; Ding, L.; Zheng, C.; Han, G.; Lv, J.; Zhou, Y.
Synthesis and acrosin inhibitory activities of substituted ethyl 5-(4-aminophenyl)-1H-pyrazole-3-carboxylate derivatives
Bioorg. Med. Chem. Lett.
21
5822-5825
2011
Homo sapiens
brenda
Ding, L.; Zhu, J.; Zheng, C.; Sheng, C.; Qi, J.; Liu, X.; Han, G.; Zhao, J.; Lv, J.; Zhou, Y.
Synthesis and acrosin inhibitory activity of substituted 4-amino-N-(diaminomethylene) benzenesulfonamide derivatives
Bioorg. Med. Chem. Lett.
21
6674-6677
2011
Homo sapiens
brenda
Jiang, J.; Liu, X.; Zhen, C.; Zhou, Y.; Zhu, J.; Lv, J.; Sheng, C.
Acrosin structure-based design, synthesis and biological activities of 7-azaindol derivatives as new acrosin inhibitors
Chin. Chem. Lett.
22
272-275
2011
Homo sapiens
-
brenda
Liu, X.; Dong, G.; Zhang, J.; Qi, J.; Zheng, C.; Zhou, Y.; Zhu, J.; Sheng, C.; Lue, J.
Discovery of novel human acrosin inhibitors by virtual screening
J. Comput. Aided Mol. Des.
25
977-985
2011
Homo sapiens
brenda
Liu, X.; Chen, Q.; Zhu, J.; Fan, Y.; Ding, L.; Zhao, J.; Han, G.; Tian, W.; Qi, J.; Zhou, Y.; Lv, J.
Synthesis and acrosin inhibitory activity of methyl 5-substituted-1H-benzo[d]imidazol-2-yl carbamate derivatives
Bioorg. Med. Chem. Lett.
22
3554-3559
2012
Homo sapiens
brenda
Zhao, J.; Tian, W.; Qi, J.; Lv, D.; Liu, Y.; Jiang, Y.; Dong, G.; Chen, Q.; Zhou, Y.; Zhu, J.; Wang, H.; Sheng, C.; Lv, J.
Design and synthesis of phenylisoxazole derivatives as novel human acrosin inhibitors
Bioorg. Med. Chem. Lett.
24
2802-2806
2014
Homo sapiens
brenda
Chen, Q.; Tian, W.; Han, G.; Qi, J.; Zheng, C.; Zhou, Y.; Ding, L.; Zhao, J.; Zhu, J.; Lv, J.; Sheng, C.
Design and synthesis of novel benzoheterocyclic derivatives as human acrosin inhibitors by scaffold hopping
Eur. J. Med. Chem.
59
176-182
2013
Homo sapiens
brenda
Zhang, G.; Yang, W.; Zou, P.; Jiang, F.; Zeng, Y.; Chen, Q.; Sun, L.; Yang, H.; Zhou, N.; Wang, X.; Liu, J.; Cao, J.; Zhou, Z.; Ao, L.
Mitochondrial functionality modifies human sperm acrosin activity, acrosome reaction capability and chromatin integrity
Hum. Reprod.
34
3-11
2019
Homo sapiens
brenda
Xu, F.; Zhu, H.; Zhu, W.; Fan, L.
Human sperm acrosomal status, acrosomal responsiveness, and acrosin are predictive of the outcomes of in vitro fertilization A prospective cohort study
Reprod. Biol.
18
344-354
2018
Homo sapiens
brenda