Reaction Details |
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Target | Carbonic anhydrase 1 |
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Ligand | BDBM50330336 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_685537 (CHEMBL1285704) |
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Ki | 1630±n/a nM |
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Citation | Kasimogullari, R; Bülbül, M; Arslan, BS; Gökçe, B Synthesis, characterization and antiglaucoma activity of some novel pyrazole derivatives of 5-amino-1,3,4-thiadiazole-2-sulfonamide. Eur J Med Chem45:4769-73 (2010) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Carbonic anhydrase 1 |
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Name: | Carbonic anhydrase 1 |
Synonyms: | CA-I | CA1 | CAB | CAH1_HUMAN | Carbonate dehydratase I | Carbonic anhydrase | Carbonic anhydrase 1 (CA I) | Carbonic anhydrase 1 (CA-I) | Carbonic anhydrase 1 (Recombinant CA I) | Carbonic anhydrase 2 (CA II) | Carbonic anhydrase B | Carbonic anhydrase I | Carbonic anhydrase I (CA I) | Carbonic anhydrase I (CA-I) | Carbonic anhydrase I (CAI) | Carbonic anhydrase I (hCA I) | Carbonic anhydrase isoenzyme I (hCA I) | hCA |
Type: | Enzyme |
Mol. Mass.: | 28873.37 |
Organism: | Homo sapiens (Human) |
Description: | P00915 |
Residue: | 261 |
Sequence: | MASPDWGYDDKNGPEQWSKLYPIANGNNQSPVDIKTSETKHDTSLKPISVSYNPATAKEI
INVGHSFHVNFEDNDNRSVLKGGPFSDSYRLFQFHFHWGSTNEHGSEHTVDGVKYSAELH
VAHWNSAKYSSLAEAASKADGLAVIGVLMKVGEANPKLQKVLDALQAIKTKGKRAPFTNF
DPSTLLPSSLDFWTYPGSLTHPPLYESVTWIICKESISVSSEQLAQFRSLLSNVEGDNAV
PMQHNNRPTQPLKGRTVRASF
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BDBM50330336 |
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n/a |
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Name | BDBM50330336 |
Synonyms: | CHEMBL1276016 | Ethyl1-(3-((4-hydroxyphenyl)diazenyl)phenyl)-5-phenyl-3-(5-sulfamoyl-1,3,4-thiadiazol-2-ylcarbamoyl)-1H-pyrazole-4-carboxylate |
Type | Small organic molecule |
Emp. Form. | C27H22N8O6S2 |
Mol. Mass. | 618.644 |
SMILES | CCOC(=O)c1c(nn(c1-c1ccccc1)-c1cccc(c1)N=Nc1ccc(O)cc1)C(=O)Nc1nnc(s1)S(N)(=O)=O |w:22.24| |
Structure |
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