共 71 条
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
收藏
页数:11
相关论文