Reaction Details |
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Target | Acrosin |
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Ligand | BDBM50354865 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_772454 (CHEMBL1839245) |
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IC50 | 14000000±n/a nM |
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Citation | 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 Lett21:5822-5 (2011) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Acrosin |
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Name: | Acrosin |
Synonyms: | ACR | ACRO_HUMAN | ACRS |
Type: | PROTEIN |
Mol. Mass.: | 45865.48 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_1365286 |
Residue: | 421 |
Sequence: | MVEMLPTAILLVLAVSVVAKDNATCDGPCGLRFRQNPQGGVRIVGGKAAQHGAWPWMVSL
QIFTYNSHRYHTCGGSLLNSRWVLTAAHCFVGKNNVHDWRLVFGAKEITYGNNKPVKAPL
QERYVEKIIIHEKYNSATEGNDIALVEITPPISCGRFIGPGCLPHFKAGLPRGSQSCWVA
GWGYIEEKAPRPSSILMEARVDLIDLDLCNSTQWYNGRVQPTNVCAGYPVGKIDTCQGDS
GGPLMCKDSKESAYVVVGITSWGVGCARAKRPGIYTATWPYLNWIASKIGSNALRMIQSA
TPPPPTTRPPPIRPPFSHPISAHLPWYFQPPPRPLPPRPPAAQPRPPPSPPPPPPPPASP
LPPPPPPPPPTPSSTTKLPQGLSFAKRLQQLIEVLKGKTYSDGKNHYDMETTELPELTST
S
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BDBM50354865 |
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n/a |
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Name | BDBM50354865 |
Synonyms: | CHEMBL1834546 |
Type | Small organic molecule |
Emp. Form. | C15H17N3O3 |
Mol. Mass. | 287.3138 |
SMILES | CCOC(=O)c1cc(n[nH]1)-c1ccc(NC(=O)CC)cc1 |
Structure |
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