Reaction Details |
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Target | Carbonic anhydrase 13 |
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Ligand | BDBM10857 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_592893 (CHEMBL1048396) |
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Ki | 32±n/a nM |
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Citation | Temperini, C; Innocenti, A; Scozzafava, A; Parkkila, S; Supuran, CT The coumarin-binding site in carbonic anhydrase accommodates structurally diverse inhibitors: the antiepileptic lacosamide as an example and lead molecule for novel classes of carbonic anhydrase inhibitors. J Med Chem53:850-4 (2010) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Carbonic anhydrase 13 |
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Name: | Carbonic anhydrase 13 |
Synonyms: | CA13 | CAH13_HUMAN | Carbonic anhydrase | Carbonic anhydrase 13 (CA XIII) | Carbonic anhydrase XIII (CA XIII) |
Type: | Enzyme |
Mol. Mass.: | 29445.78 |
Organism: | Homo sapiens (Human) |
Description: | Q8N1Q1 |
Residue: | 262 |
Sequence: | MSRLSWGYREHNGPIHWKEFFPIADGDQQSPIEIKTKEVKYDSSLRPLSIKYDPSSAKII
SNSGHSFNVDFDDTENKSVLRGGPLTGSYRLRQVHLHWGSADDHGSEHIVDGVSYAAELH
VVHWNSDKYPSFVEAAHEPDGLAVLGVFLQIGEPNSQLQKITDTLDSIKEKGKQTRFTNF
DLLSLLPPSWDYWTYPGSLTVPPLLESVTWIVLKQPINISSQQLAKFRSLLCTAEGEAAA
FLVSNHRPPQPLKGRKVRASFH
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BDBM10857 |
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n/a |
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Name | BDBM10857 |
Synonyms: | 4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanilamide | aromatic sulfonamide compound 5 | aromatic/heteroaromatic sulfonamide 2 | halogenosulfanilamide deriv. 5a |
Type | Small organic molecule |
Emp. Form. | C6H8N2O2S |
Mol. Mass. | 172.205 |
SMILES | Nc1ccc(cc1)S(N)(=O)=O |
Structure |
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