Reaction Details |
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Target | Chymotrypsin-C |
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Ligand | BDBM23708 |
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Substrate/Competitor | BDBM23729 |
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Meas. Tech. | Human Neutrophil Elastase Inhibition Assay |
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IC50 | 1800±n/a nM |
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Citation | Schepetkin, IA; Khlebnikov, AI; Quinn, MT N-benzoylpyrazoles are novel small-molecule inhibitors of human neutrophil elastase. J Med Chem50:4928-38 (2007) [PubMed] Article |
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More Info.: | Get all data from this article, Solution Info, Assay Method |
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Chymotrypsin-C |
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Name: | Chymotrypsin-C |
Synonyms: | CLCR | CTRC | CTRC_HUMAN | Caldecrin | Chymotrypsin | Chymotrypsin C | Chymotrypsin-C |
Type: | Enzyme |
Mol. Mass.: | 29487.98 |
Organism: | Homo sapiens (Human) |
Description: | Q99895 |
Residue: | 268 |
Sequence: | MLGITVLAALLACASSCGVPSFPPNLSARVVGGEDARPHSWPWQISLQYLKNDTWRHTCG
GTLIASNFVLTAAHCISNTRTYRVAVGKNNLEVEDEEGSLFVGVDTIHVHKRWNALLLRN
DIALIKLAEHVELSDTIQVACLPEKDSLLPKDYPCYVTGWGRLWTNGPIADKLQQGLQPV
VDHATCSRIDWWGFRVKKTMVCAGGDGVISACNGDSGGPLNCQLENGSWEVFGIVSFGSR
RGCNTRKKPVVYTRVSAYIDWINEKMQL
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BDBM23708 |
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BDBM23729 |
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Name | BDBM23708 |
Synonyms: | 4-bromo-1-[(2,6-difluorophenyl)carbonyl]-1H-pyrazole | N-Benzoylpyrazole deriv., 13 |
Type | Small organic molecule |
Emp. Form. | C10H5BrF2N2O |
Mol. Mass. | 287.06 |
SMILES | Fc1cccc(F)c1C(=O)n1cc(Br)cn1 |
Structure |
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