Reaction Details |
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Target | Carbonic anhydrase 12 |
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Ligand | BDBM50591864 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2202348 (CHEMBL5115056) |
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Ki | 23±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 12 |
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Name: | Carbonic anhydrase 12 |
Synonyms: | CA-XII | CA12 | CAH12_HUMAN | Carbonate dehydratase XII | Carbonic anhydrase | Carbonic anhydrase 12 (CA XII) | Carbonic anhydrase XII | Carbonic anhydrase XII (CA XII) | Carbonic anhydrase XII (CAXII) | Tumor antigen HOM-RCC-3.1.3 |
Type: | Enzyme |
Mol. Mass.: | 39456.00 |
Organism: | Homo sapiens (Human) |
Description: | Catalytic domain of human cloned isozyme was used in the assay |
Residue: | 354 |
Sequence: | MPRRSLHAAAVLLLVILKEQPSSPAPVNGSKWTYFGPDGENSWSKKYPSCGGLLQSPIDL
HSDILQYDASLTPLEFQGYNLSANKQFLLTNNGHSVKLNLPSDMHIQGLQSRYSATQLHL
HWGNPNDPHGSEHTVSGQHFAAELHIVHYNSDLYPDASTASNKSEGLAVLAVLIEMGSFN
PSYDKIFSHLQHVKYKGQEAFVPGFNIEELLPERTAEYYRYRGSLTTPPCNPTVLWTVFR
NPVQISQEQLLALETALYCTHMDDPSPREMINNFRQVQKFDERLVYTSFSQVQVCTAAGL
SLGIILSLALAGILGICIVVVVSIWLFRRKSIKKGDNKGVIYKPATKMETEAHA
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BDBM50591864 |
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n/a |
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Name | BDBM50591864 |
Synonyms: | CHEMBL5183126 |
Type | Small organic molecule |
Emp. Form. | C17H20N2O3S |
Mol. Mass. | 332.417 |
SMILES | NS(=O)(=O)c1ccc(CCNCCC(=O)c2ccccc2)cc1 |
Structure |
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