Reaction Details |
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Target | Carbonic anhydrase 15 |
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Ligand | BDBM50300203 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_592895 (CHEMBL1048398) |
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Ki | 93100±n/a nM |
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Citation | Temperini, C; Innocenti, A; Scozzafava, A; Parkkila, S; Supuran, CT The coumarin-binding site in carbonic anhydrase accommodates structurally diverse inhibitors: the antiepileptic lacosamide as an example and lead molecule for novel classes of carbonic anhydrase inhibitors. J Med Chem53:850-4 (2010) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Carbonic anhydrase 15 |
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Name: | Carbonic anhydrase 15 |
Synonyms: | CAH15_MOUSE | Ca15 | Car15 |
Type: | PROTEIN |
Mol. Mass.: | 35484.02 |
Organism: | Mus musculus |
Description: | ChEMBL_651955 |
Residue: | 324 |
Sequence: | MWALDFLLSFLLIQLAAQVDSSGTWCYDSQDPKCGPAHWKELAPACGGPTQSPINIDLRL
VQRDYTLKPFIFQGYDSAPQDPWVLENDGHTVLLRVNSCQQNCPAIRGAGLPSPEYRLLQ
LHFHWGSPGHQGSEHSLDEKHGSMEMHMVHMNTKYQSMEDARSQPDGFAILAVLLVEEDR
DNTNFSAIVSGLKNLSSPGVAVNLTSTFALASLLPSALRLLRYYRYSGSLTTPGCEPAVL
WTVFENTVPIGHAQVVQFQAVLQTGPPGLHPRPLTSNFRPQQPLGGRRISASPEASVRSS
VSTLPCLHLALVGLGVGLRLWQGP
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BDBM50300203 |
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n/a |
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Name | BDBM50300203 |
Synonyms: | (S)-6-(1-hydroxy-3-methylbutyl)-7-methoxy-2H-chromen-2-one | 6-(1S-hydroxy-3-methylbutyl)-7-methoxy-2H-chromen-2-one | CHEMBL572366 |
Type | Small organic molecule |
Emp. Form. | C15H18O4 |
Mol. Mass. | 262.301 |
SMILES | COc1cc2oc(=O)ccc2cc1[C@@H](O)CC(C)C |r| |
Structure |
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