Reaction Details |
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Target | Acrosin |
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Ligand | BDBM50424449 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_967179 (CHEMBL2399923) |
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IC50 | 410000±n/a nM |
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Citation | Tian, W; Han, G; Zhu, J; Qi, J; Chen, Q; Zhao, J; Zheng, C; Zhang, L; Zhou, Y; Lv, J Synthesis and acrosin inhibitory activities of 5-phenyl-1H-pyrazole-3-carboxylic acid amide derivatives. Bioorg Med Chem Lett23:4177-84 (2013) [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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BDBM50424449 |
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n/a |
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Name | BDBM50424449 |
Synonyms: | CHEMBL2316083 |
Type | Small organic molecule |
Emp. Form. | C14H17N3O3 |
Mol. Mass. | 275.3031 |
SMILES | COc1ccc(cc1)-c1cc([nH]n1)C(=O)N(C)CCO |
Structure |
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