Reaction Details |
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Target | Carbonic anhydrase 5B, mitochondrial |
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Ligand | BDBM50513283 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1852928 (CHEMBL4353552) |
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Ki | >10000±n/a nM |
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Citation | Angeli, A; Di Cesare Mannelli, L; Ghelardini, C; Peat, TS; Bartolucci, G; Menicatti, M; Carta, F; Supuran, CT Benzensulfonamides bearing spyrohydantoin moieties act as potent inhibitors of human carbonic anhydrases II and VII and show neuropathic pain attenuating effects. Eur J Med Chem177:188-197 (2019) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Carbonic anhydrase 5B, mitochondrial |
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Name: | Carbonic anhydrase 5B, mitochondrial |
Synonyms: | CA-VB | CA5B | CAH5B_HUMAN | Carbonate dehydratase VB | Carbonic Anhydrase VB | Carbonic anhydrase 5B (CA VB) | Carbonic anhydrase 5B, mitochondrial | Carbonic anhydrase 5B, mitochondrial precursor | Carbonic anhydrase V | Carbonic anhydrase VB (CA VB) |
Type: | Enzyme |
Mol. Mass.: | 36440.83 |
Organism: | Homo sapiens (Human) |
Description: | Human (cloned) isozyme |
Residue: | 317 |
Sequence: | MVVMNSLRVILQASPGKLLWRKFQIPRFMPARPCSLYTCTYKTRNRALHPLWESVDLVPG
GDRQSPINIRWRDSVYDPGLKPLTISYDPATCLHVWNNGYSFLVEFEDSTDKSVIKGGPL
EHNYRLKQFHFHWGAIDAWGSEHTVDSKCFPAELHLVHWNAVRFENFEDAALEENGLAVI
GVFLKLGKHHKELQKLVDTLPSIKHKDALVEFGSFDPSCLMPTCPDYWTYSGSLTTPPLS
ESVTWIIKKQPVEVDHDQLEQFRTLLFTSEGEKEKRMVDNFRPLQPLMNRTVRSSFRHDY
VLNVQAKPKPATSQATP
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BDBM50513283 |
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n/a |
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Name | BDBM50513283 |
Synonyms: | CHEMBL4534829 |
Type | Small organic molecule |
Emp. Form. | C19H26N4O5S |
Mol. Mass. | 422.499 |
SMILES | CC1CCCC2(C1)NC(=O)N(CC(=O)NCCc1ccc(cc1)S(N)(=O)=O)C2=O |
Structure |
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