Exploring isoxazoles and pyrrolidinones decorated with the 4,6-dimethoxy-1,3,5-triazine unit as human farnesyltransferase inhibitors

被引:8
作者
Lucescu, Liliana [1 ]
Ghinet, Alina [1 ,2 ,3 ]
Shova, Sergiu [4 ]
Magnez, Romain [5 ]
Thuru, Xavier [5 ]
Farce, Amaury [2 ,6 ]
Rigo, Benoit [2 ,3 ]
Belei, Dalila [1 ]
Dubois, Joelle [7 ]
Bicu, Elena [1 ]
机构
[1] AI I Cuza Univ Iasi, Fac Chem, Bd Carol I 11, Iasi 700506, Romania
[2] Univ Lille, CHRU Lille, Fac Med Pole Rech, LIRIC,INSERM,U995, Lille, France
[3] UC Lille, Yncrea Hauts De France, Lab Chim Durable & Sante Hautes Etud Ingn HEI, Lille, France
[4] Petru Poni Inst Macromol Chem, Iasi, Romania
[5] Univ Lille, UMR S 1172, JPARC, Ctr Rech Jean Pierre AUBERT Neurosci & Canc, Lille, France
[6] Fac Sci Pharmaceut & Biol Lille, Lille, France
[7] CNRS, UPR2301, Inst Chim Subst Nat, Ctr Rech Gif, Gif Sur Yvette, France
关键词
antitumor compound; cycloaddition; farnesyltransferase; inhibitor; isoxazole; pyrrolidine; triazine; ONE-POT SYNTHESIS; BIOLOGICAL EVALUATION; AEROBIC OXIDATION; PRIMARY AMINES; DERIVATIVES; TRIAZINE; DISCOVERY; ANALOGS; AGENTS; SERIES;
D O I
10.1002/ardp.201800227
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Unprecedented triazinyl-isoxazoles were afforded via an effective cycloaddition reaction between nitrile oxides and the scarcely described 2-ethynyl-4,6-dimethoxy-1,3,5-triazine as dipolarophile. The biological evaluation of the newly synthesized compounds showed that the inhibition of human farnesyltransferase by zinc complexation could be improved with triazine-isoxazole moieties. The replacement of the isoxazole unit by a pyrrolidin-2-one was detrimental to the inhibitory activity while the pyrrolidin-2-thione derivatives conserved the biological potential. The potential of selected compounds to disrupt protein farnesylation in Chinese hamster ovary (CHO) cells transfected with pEGFP-CAAX was also evaluated.
引用
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页数:11
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