Reaction Details |
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Target | Carbonic anhydrase 13 |
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Ligand | BDBM50329832 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_675715 (CHEMBL1272349) |
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Kd | 700±n/a nM |
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Citation | Capkauskaite, E; Baranauskiene, L; Golovenko, D; Manakova, E; Gražulis, S; Tumkevičius, S; Matulis, D Indapamide-like benzenesulfonamides as inhibitors of carbonic anhydrases I, II, VII, and XIII. Bioorg Med Chem18:7357-64 (2010) [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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BDBM50329832 |
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n/a |
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Name | BDBM50329832 |
Synonyms: | 5-(1H-Benzimidazol-1-ylacetyl)-2-chlorobenzenesulfonamide | CHEMBL1272187 | N-alkylated benzimidazole derivative, 4a | carbonic anhydrase (CA) inhibitors, benzenesulphonamide ligand, 4 |
Type | Small organic molecule |
Emp. Form. | C15H12ClN3O3S |
Mol. Mass. | 349.792 |
SMILES | NS(=O)(=O)c1cc(ccc1Cl)C(=O)Cn1cnc2ccccc12 |
Structure |
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