Reaction Details |
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Target | Carbonic anhydrase 5B, mitochondrial |
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Ligand | BDBM50469143 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1803460 (CHEMBL4275752) |
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Ki | 703±n/a nM |
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Citation | Angeli, A; Trallori, E; Ferraroni, M; Di Cesare Mannelli, L; Ghelardini, C; Supuran, CT Discovery of new 2, 5-disubstituted 1,3-selenazoles as selective human carbonic anhydrase IX inhibitors with potent anti-tumor activity. Eur J Med Chem157:1214-1222 (2018) [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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BDBM50469143 |
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n/a |
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Name | BDBM50469143 |
Synonyms: | CHEMBL4293677 |
Type | Small organic molecule |
Emp. Form. | C15H12N2O2SSe |
Mol. Mass. | 363.29 |
SMILES | [#7]S(=O)(=O)c1ccc(cc1)-c1ncc([se;v2]1)-c1ccccc1 |
Structure |
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