Carbonic anhydrase inhibitors based on sorafenib scaffold: Design, synthesis, crystallographic investigation and effects on primary breast cancer cells

被引:42
作者
Bozdag, Murat [1 ]
Ferraroni, Marta [2 ]
Ward, Carol [3 ,4 ]
Carta, Fabrizio [1 ]
Bua, Silvia [1 ]
Angeli, Andrea [1 ]
Langdon, Simon P. [3 ,4 ]
Kunkler, Ian H. [3 ,4 ]
Al-Tamimi, Abdul-Malek S. [5 ]
Supuran, Claudiu T. [1 ]
机构
[1] Univ Florence, NEUROFARBA Dept, Sez Sci Farmaceut & Nutr, Via Ugo Schiff 6, I-50019 Florence, Italy
[2] Univ Florence, Dept Chem Ugo Schiff, Via Lastruccia 3, I-50019 Florence, Italy
[3] Inst Genet & Mol Med, Breakthrough Breast Unit, Edinburgh EH4 2XU, Midlothian, Scotland
[4] Inst Genet & Mol Med, Div Pathol, Edinburgh EH4 2XU, Midlothian, Scotland
[5] Prince Sattam Bin Abdulaziz Univ, Coll Pharm, Dept Pharmaceut Chem, POB 173, Alkharj 11942, Saudi Arabia
关键词
Carbonic anhydrase; Sorafenib; Enzyme inhibitor; Sulfonamide; Sulfamate; Coumarin; SELECTIVE INHIBITORS; IN-VITRO; IX; SULFOCOUMARINS; POTENT; SERIES; COUMARINS; SHOW; MECHANISM; METASTASIS;
D O I
10.1016/j.ejmech.2019.111600
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Carbonic anhydrase inhibitors (CAIs) of the sulfonamide, sulfamate and coumarin classes bearing the phenylureido tail found in the clinically used drug Sorafenib, a multikinase inhibitor actually used for the management of hepatocellular carcinomas, are reported. All compounds were assayed on human (h) CA isoforms I, II, VII and IX, involved in various pathologies. Among the sulfonamides, several compounds were selective for inhibiting hCA IX, with K-l values in the low nanomolar ranges (i.e. 0.7-30.2 nM). We explored the binding modes of such compounds by means of X-ray crystallographic studies on isoform hCA I in adduct with one sulfonamide and a sulfamate inhibitor. Antiproliferative properties of some sulfamates on breast tumor cell lines were also investigated. (C) 2019 Elsevier Masson SAS. All rights reserved.
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页数:11
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