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TargetCoagulation factor VII
LigandBDBM50167835
Substrate/Competitorn/a
Meas. Tech.ChEMBL_304953 (CHEMBL827832)
IC50 20±n/a nM
Citation Schweitzer, BANeumann, WLRahman, HKKusturin, CLSample, KRPoda, GIKurumbail, RGStevens, AMStegeman, RAStallings, WCSouth, MS Structure-based design and synthesis of pyrazinones containing novel P1 'side pocket' moieties as inhibitors of TF/VIIa. Bioorg Med Chem Lett15:3006-11 (2005) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Coagulation factor VII
Name:Coagulation factor VII
Synonyms:Eptacog alfa | F7 | FA7_HUMAN | Factor VIIa | Factor VIIa (fVIIa) | Proconvertin | SPCA | Thrombin and coagulation factor VII | serum prothrombin conversion accelerator
Type:Enzyme
Mol. Mass.:51599.89
Organism:Homo sapiens (Human)
Description:n/a
Residue:466
Sequence:
MVSQALRLLCLLLGLQGCLAAGGVAKASGGETRDMPWKPGPHRVFVTQEEAHGVLHRRRR
ANAFLEELRPGSLERECKEEQCSFEEAREIFKDAERTKLFWISYSDGDQCASSPCQNGGS
CKDQLQSYICFCLPAFEGRNCETHKDDQLICVNENGGCEQYCSDHTGTKRSCRCHEGYSL
LADGVSCTPTVEYPCGKIPILEKRNASKPQGRIVGGKVCPKGECPWQVLLLVNGAQLCGG
TLINTIWVVSAAHCFDKIKNWRNLIAVLGEHDLSEHDGDEQSRRVAQVIIPSTYVPGTTN
HDIALLRLHQPVVLTDHVVPLCLPERTFSERTLAFVRFSLVSGWGQLLDRGATALELMVL
NVPRLMTQDCLQQSRKVGDSPNITEYMFCAGYSDGSKDSCKGDSGGPHATHYRGTWYLTG
IVSWGQGCATVGHFGVYTRVSQYIEWLQKLMRSEPRPGVLLRAPFP
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  Blast E-value cutoff:
BDBM50167835
n/a
NameBDBM50167835
Synonyms:3-amino-N-[(2R)-butan-2-yl]-5-[1-({[(4-carbamimidoyl-2-{[2-(morpholin-4-yl)ethyl]carbamoyl}phenyl)methyl]carbamoyl}methyl)-6-oxo-5-(propan-2-ylamino)-1,6-dihydropyrazin-2-yl]benzamide | CHEMBL189165
TypeSmall organic molecule
Emp. Form.C35H48N10O5
Mol. Mass.688.8196
SMILESCC[C@@H](C)NC(=O)c1cc(N)cc(c1)-c1cnc(NC(C)C)c(=O)n1CC(=O)NCc1ccc(cc1C(=O)NCCN1CCOCC1)C(N)=N
Structure
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