Reaction Details |
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Target | Carbonic anhydrase |
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Ligand | BDBM10875 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_515851 (CHEMBL993110) |
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Ki | 565±n/a nM |
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Citation | Isik, S; Kockar, F; Aydin, M; Arslan, O; Guler, OO; Innocenti, A; Scozzafava, A; Supuran, CT Carbonic anhydrase inhibitors: inhibition of the beta-class enzyme from the yeast Saccharomyces cerevisiae with sulfonamides and sulfamates. Bioorg Med Chem17:1158-63 (2009) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Carbonic anhydrase |
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Name: | Carbonic anhydrase |
Synonyms: | CAN_YEAST | NCE103 | NCE3 |
Type: | PROTEIN |
Mol. Mass.: | 24861.97 |
Organism: | Saccharomyces cerevisiae |
Description: | ChEMBL_1507033 |
Residue: | 221 |
Sequence: | MSATESSSIFTLSHNSNLQDILAANAKWASQMNNIQPTLFPDHNAKGQSPHTLFIGCSDS
RYNENCLGVLPGEVFTWKNVANICHSEDLTLKATLEFAIICLKVNKVIICGHTDCGGIKT
CLTNQREALPKVNCSHLYKYLDDIDTMYHEESQNLIHLKTQREKSHYLSHCNVKRQFNRI
IENPTVQTAVQNGELQVYGLLYNVEDGLLQTVSTYTKVTPK
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BDBM10875 |
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n/a |
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Name | BDBM10875 |
Synonyms: | 5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide | CHEMBL360356 | Chlorzolamide, CHL | JMC522226 Compound 19 | JMC523116 Compound 19 | aromatic/heteroaromatic sulfonamide 20 |
Type | Small organic molecule |
Emp. Form. | C8H6ClN3O2S2 |
Mol. Mass. | 275.735 |
SMILES | NS(=O)(=O)c1nnc(s1)-c1ccccc1Cl |
Structure |
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