Reaction Details |
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Target | Carbonic anhydrase 13 |
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Ligand | BDBM50163864 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1673899 (CHEMBL4023928) |
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KOFF | 0.080000 s-1 |
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Citation | Linkuvien?, V; Talibov, VO; Danielson, UH; Matulis, D Introduction of Intrinsic Kinetics of Protein-Ligand Interactions and Their Implications for Drug Design. J Med Chem61:2292-2302 (2018) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Carbonic anhydrase 13 |
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Name: | Carbonic anhydrase 13 |
Synonyms: | CA13 | CAH13_HUMAN | Carbonic anhydrase | Carbonic anhydrase 13 (CA XIII) | Carbonic anhydrase XIII (CA XIII) |
Type: | Enzyme |
Mol. Mass.: | 29445.78 |
Organism: | Homo sapiens (Human) |
Description: | Q8N1Q1 |
Residue: | 262 |
Sequence: | MSRLSWGYREHNGPIHWKEFFPIADGDQQSPIEIKTKEVKYDSSLRPLSIKYDPSSAKII
SNSGHSFNVDFDDTENKSVLRGGPLTGSYRLRQVHLHWGSADDHGSEHIVDGVSYAAELH
VVHWNSDKYPSFVEAAHEPDGLAVLGVFLQIGEPNSQLQKITDTLDSIKEKGKQTRFTNF
DLLSLLPPSWDYWTYPGSLTVPPLLESVTWIVLKQPINISSQQLAKFRSLLCTAEGEAAA
FLVSNHRPPQPLKGRKVRASFH
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BDBM50163864 |
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n/a |
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Name | BDBM50163864 |
Synonyms: | 3-(1H-benzimidazol-1-ylacetyl)benzenesulfonamide (3a) | CHEMBL3799296 | carbonic anhydrase (CA) inhibitors, benzenesulphonamide ligand, 3 |
Type | Small organic molecule |
Emp. Form. | C15H13N3O3S |
Mol. Mass. | 315.347 |
SMILES | NS(=O)(=O)c1cccc(c1)C(=O)Cn1cnc2ccccc12 |
Structure |
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