Reaction Details |
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Target | Chymotrypsin-C |
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Ligand | BDBM50083959 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_197806 |
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Ki | 13700±n/a nM |
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Citation | Soll, RM; Lu, T; Tomczuk, B; Illig, CR; Fedde, C; Eisennagel, S; Bone, R; Murphy, L; Spurlino, J; Salemme, FR Amidinohydrazones as guanidine bioisosteres: application to a new class of potent, selective and orally bioavailable, non-amide-based small-molecule thrombin inhibitors. Bioorg Med Chem Lett10:1-4 (2000) [PubMed] |
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More Info.: | Get all data from this article, 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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BDBM50083959 |
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n/a |
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Name | BDBM50083959 |
Synonyms: | 3-((4E)-4-{[(E)-amino(imino)methyl]hydrazono}butyl)-5-methoxyphenyl 2-chlorobenzenesulfonate | CHEMBL338396 |
Type | Small organic molecule |
Emp. Form. | C18H21ClN4O4S |
Mol. Mass. | 424.902 |
SMILES | COc1cc(CCCC=NNC(N)=N)cc(OS(=O)(=O)c2ccccc2Cl)c1 |w:9.9| |
Structure |
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