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Synthesis of 4-Arylpolyhydroquinoline Derivatives and Evaluation of Their Antitumor Activities

Synthesis of 4-Arylpolyhydroquinoline Derivatives and Evaluation of Their Antitumor Activities
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摘要 Four novel 4-arylpolyhydroquinoline derivatives(1~4) were synthesized and characterized via IR,~1H NMR,H RMS,and single-crystal X-ray crystallography. It crystallizes in triclinic,space group P1 with a = 7.382(5),b = 10.766(7),c = 11.583(8) ?,α = 66.077(10),β = 77.461(10),γ = 82.590(11)o,V = 820.6(10) ?~3,Z = 2,F(000) = 332,Dc = 1.260 Mg/m^3,Mr = 311.37 and μ = 0.085 mm-1. In addition,the antitumor effects of compounds 1~4 were studied on three human tumor cells(NCI-H1688,AGS and 95-D). The results showed that compared with compounds 1 and 2,compounds 3 and 4 displayed efficient antitumor activity. Four novel 4-arylpolyhydroquinoline derivatives(1~4) were synthesized and characterized via IR,~1H NMR,H RMS,and single-crystal X-ray crystallography. It crystallizes in triclinic,space group P1 with a = 7.382(5),b = 10.766(7),c = 11.583(8) ?,α = 66.077(10),β = 77.461(10),γ = 82.590(11)o,V = 820.6(10) ?~3,Z = 2,F(000) = 332,Dc = 1.260 Mg/m^3,Mr = 311.37 and μ = 0.085 mm-1. In addition,the antitumor effects of compounds 1~4 were studied on three human tumor cells(NCI-H1688,AGS and 95-D). The results showed that compared with compounds 1 and 2,compounds 3 and 4 displayed efficient antitumor activity.
出处 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2016年第10期1553-1557,共5页 结构化学(英文)
关键词 4-arylpolyhydroquinoline crystal antitumor 4-arylpolyhydroquinoline crystal antitumor
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