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TargetChymotrypsinogen A
LigandBDBM222126
Substrate/Competitorn/a
Meas. Tech.α-Chymotrypsin Inhibition Kinetic Assay
Ki 1.619e+5± 1.12e+4 nM
Citation Marasini, BPRahim, FPerveen, SKarim, AMohammed Khan, KAtta-Ur-Rahman, nullChoudhary, MI Synthesis, structure-activity relationships studies of benzoxazinone derivatives as a-chymotrypsin inhibitors. Bioorg Chem70:210-221 (2017) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Chymotrypsinogen A
Name:Chymotrypsinogen A
Synonyms:Alpha-chymotrypsin | CTRA_BOVIN | Chymotrypsin A | Chymotrypsin A chain A | Chymotrypsin A chain B | Chymotrypsin A chain C | Chymotrypsinogen A | alpha-Chymotrypsin (α-Chymotrypsin)
Type:Serine protease
Mol. Mass.:25670.88
Organism:Bos taurus (bovine)
Description:n/a
Residue:245
Sequence:
CGVPAIQPVLSGLSRIVNGEEAVPGSWPWQVSLQDKTGFHFCGGSLINENWVVTAAHCGV
TTSDVVVAGEFDQGSSSEKIQKLKIAKVFKNSKYNSLTINNDITLLKLSTAASFSQTVSA
VCLPSASDDFAAGTTCVTTGWGLTRYTNANTPDRLQQASLPLLSNTNCKKYWGTKIKDAM
ICAGASGVSSCMGDSGGPLVCKKNGAWTLVGIVSWGSSTCSTSTPGVYARVTALVNWVQQ
TLAAN
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  Blast E-value cutoff:
BDBM222126
n/a
NameBDBM222126
Synonyms:2-(3-Methylphenyl)-7-nitro-4H-3,1-benzoxazin-4-one (15)
TypeSmall organic molecule
Emp. Form.C15H10N2O4
Mol. Mass.282.2509
SMILESCc1cccc(c1)-c1nc2cc(ccc2c(=O)o1)[N+]([O-])=O
Structure
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