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TargetAcrosin
LigandBDBM50354865
Substrate/Competitorn/a
Meas. Tech.ChEMBL_772454 (CHEMBL1839245)
IC50 14000000±n/a nM
Citation Qi, JZhu, JLiu, XDing, LZheng, CHan, GLv, JZhou, 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
More Info.:Get all data from this article,  Assay Method
 
Acrosin
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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  Blast E-value cutoff:
BDBM50354865
n/a
NameBDBM50354865
Synonyms:CHEMBL1834546
TypeSmall organic molecule
Emp. Form.C15H17N3O3
Mol. Mass.287.3138
SMILESCCOC(=O)c1cc(n[nH]1)-c1ccc(NC(=O)CC)cc1
Structure
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