Reaction Details |
| Report a problem with these data |
Target | Carbonic anhydrase 2 |
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Ligand | BDBM50591867 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2202346 (CHEMBL5115054) |
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Ki | 48±n/a nM |
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Citation | Elbadawi, MM; Eldehna, WM; Nocentini, A; Somaa, WR; Al-Rashood, ST; Elkaeed, EB; El Hassab, MA; Abdel-Aziz, HA; Supuran, CT; Fares, M Development of 4-((3-oxo-3-phenylpropyl)amino)benzenesulfonamide derivatives utilizing tail/dual-tail approaches as novel carbonic anhydrase inhibitors. Eur J Med Chem238:0 (2022) [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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BDBM50591867 |
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n/a |
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Name | BDBM50591867 |
Synonyms: | CHEMBL5190695 |
Type | Small organic molecule |
Emp. Form. | C16H17N3O4S |
Mol. Mass. | 347.389 |
SMILES | NS(=O)(=O)c1ccc(cc1)C(=O)NNCCC(=O)c1ccccc1 |
Structure |
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