Reaction Details |
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Target | Carbonic anhydrase 2 |
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Ligand | BDBM50167410 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_302531 (CHEMBL827383) |
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Ki | >1000±n/a nM |
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Citation | Puccetti, L; Fasolis, G; Vullo, D; Chohan, ZH; Scozzafava, A; Supuran, CT Carbonic anhydrase inhibitors. Inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, IX, and XII with Schiff's bases incorporating chromone and aromatic sulfonamide moieties, and their zinc complexes. Bioorg Med Chem Lett15:3096-101 (2005) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Carbonic anhydrase 2 |
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Name: | Carbonic anhydrase 2 |
Synonyms: | CA-II | CA2 | CAC | CAH2_HUMAN | Carbonate dehydratase II | Carbonic anhydrase 2 (CA II) | Carbonic anhydrase 2 (CA-II) | Carbonic anhydrase 2 (Recombinant CA II) | Carbonic anhydrase C | Carbonic anhydrase II (CA II) | Carbonic anhydrase II (CA-II) | Carbonic anhydrase II (CAII) | Carbonic anhydrase II (hCA II) | Carbonic anhydrase isoenzyme II (hCA II) |
Type: | Enzyme |
Mol. Mass.: | 29250.71 |
Organism: | Homo sapiens (Human) |
Description: | P00918 |
Residue: | 260 |
Sequence: | MSHHWGYGKHNGPEHWHKDFPIAKGERQSPVDIDTHTAKYDPSLKPLSVSYDQATSLRIL
NNGHAFNVEFDDSQDKAVLKGGPLDGTYRLIQFHFHWGSLDGQGSEHTVDKKKYAAELHL
VHWNTKYGDFGKAVQQPDGLAVLGIFLKVGSAKPGLQKVVDVLDSIKTKGKSADFTNFDP
RGLLPESLDYWTYPGSLTTPPLLECVTWIVLKEPISVSSEQVLKFRKLNFNGEGEPEELM
VDNWRPAQPLKNRQIKASFK
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BDBM50167410 |
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n/a |
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Name | BDBM50167410 |
Synonyms: | 1N-amino(imino)methyl-4-[1-(6-methyl-4-oxo-4H-3-chromenyl)-(E)-methylideneamino]-1-benzenesulfonamide | CHEMBL193593 |
Type | Small organic molecule |
Emp. Form. | C18H16N4O4S |
Mol. Mass. | 384.409 |
SMILES | Cc1ccc2occ(C=Nc3ccc(cc3)S(=O)(=O)NC(N)=N)c(=O)c2c1 |w:8.7| |
Structure |
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