Reaction Details |
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Target | Acrosin |
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Ligand | BDBM50018977 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1365286 (CHEMBL3292380) |
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IC50 | 10100±n/a nM |
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Citation | 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 Lett24:2802-6 (2014) [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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BDBM50018977 |
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n/a |
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Name | BDBM50018977 |
Synonyms: | CHEMBL3287449 |
Type | Small organic molecule |
Emp. Form. | C18H18ClN5O2 |
Mol. Mass. | 371.821 |
SMILES | Cl.Cc1ccc(NC(=O)c2cc(on2)-c2ccc(NC(N)=N)cc2)cc1 |
Structure |
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