Reaction Details |
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Target | Chymotrypsinogen A |
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Ligand | BDBM50070010 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_49922 |
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IC50 | 1600±n/a nM |
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Citation | Borthwick, AD; Weingarten, G; Haley, TM; Tomaszewski, M; Wang, W; Hu, Z; Bedard, J; Jin, H; Yuen, L; Mansour, TS Design and synthesis of monocyclic beta-lactams as mechanism-based inhibitors of human cytomegalovirus protease. Bioorg Med Chem Lett8:365-70 (1999) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Chymotrypsinogen A |
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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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BDBM50070010 |
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n/a |
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Name | BDBM50070010 |
Synonyms: | 4-((2R,3R)-1-Benzylcarbamoyl-3-methyl-4-oxo-azetidin-2-yloxy)-benzoic acid | CHEMBL122575 |
Type | Small organic molecule |
Emp. Form. | C19H18N2O5 |
Mol. Mass. | 354.3566 |
SMILES | C[C@@H]1[C@@H](Oc2ccc(cc2)C(O)=O)N(C(=O)NCc2ccccc2)C1=O |
Structure |
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