Reaction Details |
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Target | Carbonic anhydrase |
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Ligand | BDBM10865 |
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Substrate/Competitor | BDBM10856 |
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Meas. Tech. | CA Inhibition Assay |
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Ki | 711±n/a nM |
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Citation | Innocenti, A; Hall, RA; Schlicker, C; Scozzafava, A; Steegborn, C; Mühlschlegel, FA; Supuran, CT Carbonic anhydrase inhibitors. Inhibition and homology modeling studies of the fungal beta-carbonic anhydrase from Candida albicans with sulfonamides. Bioorg Med Chem17:4503-9 (2009) [PubMed] Article |
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More Info.: | Get all data from this article, Solution Info, Assay Method |
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Carbonic anhydrase |
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Name: | Carbonic anhydrase |
Synonyms: | Carbonic Anhydrase 2 (Can2) |
Type: | Enzyme |
Mol. Mass.: | 26594.37 |
Organism: | Cryptococcus neoformans var. grubii (Filobasidiella neoformans var. grubii) |
Description: | n/a |
Residue: | 239 |
Sequence: | MPFHAEPLKPSDEIDMDLGHSVAAQKFKEIREVLEGNRYWARKVTSEEPEFMAEQVKGQA
PNFLWIGCADSRVPEVTIMARKPGDVFVQRNVANQFKPEDDSSQALLNYAIMNVGVTHVM
VVGHTGCGGCIAAFDQPLPTEENPGGTPLVRYLEPIIRLKHSLPEGSDVNDLIKENVKMA
VKNVVNSPTIQGAWEQARKGEFREVFVHGWLYDLSTGNIVDLNVTQGPHPFVDDRVPRA
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BDBM10865 |
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BDBM10856 |
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Name | BDBM10865 |
Synonyms: | 4-Amino-3-iodobenzenesulfonamide | 4-amino-3-iodobenzene-1-sulfonamide | CHEMBL268177 | aromatic/heteroaromatic sulfonamide 10 | halogenosulfanilamide deriv. 5e |
Type | Small organic molecule |
Emp. Form. | C6H7IN2O2S |
Mol. Mass. | 298.101 |
SMILES | Nc1ccc(cc1I)S(N)(=O)=O |
Structure |
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