5ULN
Synthesis of novel seleno ureido containing compounds as SLC-0111 analogs. Investigations on carbonic anhydrases activity, glutathione peroxidase and X-ray crystallography
5ULN の概要
| エントリーDOI | 10.2210/pdb5uln/pdb |
| 分子名称 | Carbonic anhydrase 2, ZINC ION, GLYCEROL, ... (6 entities in total) |
| 機能のキーワード | carbonic anhydrase inhibitors, metalloenzymes, glutathione peroxidase, lyase |
| 由来する生物種 | Homo sapiens (Human) |
| 細胞内の位置 | Cytoplasm : P00918 |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 29817.93 |
| 構造登録者 | Peat, T.S.,Angeli, A.,Tanini, D.,Bartolucci, G.,Capperucci, A.,Supuran, C.T.,Carta, F. (登録日: 2017-01-25, 公開日: 2017-10-11, 最終更新日: 2023-10-04) |
| 主引用文献 | Angeli, A.,Tanini, D.,Peat, T.S.,Di Cesare Mannelli, L.,Bartolucci, G.,Capperucci, A.,Ghelardini, C.,Supuran, C.T.,Carta, F. Discovery of New Selenoureido Analogues of 4-(4-Fluorophenylureido)benzenesulfonamide as Carbonic Anhydrase Inhibitors. ACS Med Chem Lett, 8:963-968, 2017 Cited by PubMed Abstract: A series of benzenesulfonamides bearing selenourea moieties was obtained considering the ureido-sulfonamide , in Phase I clinical trials as antitumor agent, as a lead molecule. All compounds showed interesting inhibition potencies against the physiologically relevant human (h) carbonic anhydrase (hCAs, EC 4.2.1.1) isoforms I, II, IV, and IX. The most flexible analogues in the series - showed low nanomolar inhibition constants against hCA I, II, and IX. We assessed selected compounds on the antioxidant properties and binding modes and evaluated human prostate (PC3), breast (MDA-MB-231), and colon-rectal (HT-29) cancer cell lines both in normoxic and hypoxic conditions. PubMed: 28947945DOI: 10.1021/acsmedchemlett.7b00280 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.35 Å) |
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