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羟基哌啶酮抗肿瘤药物的结构及抗肿瘤活性研究 被引量:1

Structure and Antitumor Activities of Hydroxy-Substituted Piperidone Antitumor Drugs
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摘要 通过X-ray单晶衍射表征药物(3E,5E)-N-苄基-3,5-二(4-羟基苯亚甲基)-4-哌啶酮盐酸盐(A)的结构。A(C_(26)H_(24)ClNO_3,Mr=433.91)结晶在triclinic晶系,P-1空间群,a=9.8813(4),b=11.1292(4),c=12.9552(5)?,α=98.058(3)°,β=108.134(4)°,γ=107.353(3)°,U=1248.93(8)?~3,Z=2。CCK-8法评价其对A549、SGC-7901、HePG2、Hela、K562等肿瘤细胞系的抗肿瘤活性及对正常细胞HUVEC的细胞毒性。结果显示,A对SGC7901、K562和Hela的活性较好,其中对K562的抑制活性最好,IC50=7.86μM。并且对正常细胞HUVEC的细胞毒性较小。 ( 3E,5E)-N-benzyl-3,5-bis( 4-hydroxybenzylidene)-4-Piperidone( A) was characterized by X-ray diffractometer. A( C_(26)H_(24)ClNO_3,Mr = 433. 91) belongs to the triclinic system,space group P-1 with a = 9. 8813( 4),b =11. 1292( 4),c = 12. 9552( 5) ?,α = 98. 058( 3) °,β = 108. 134( 4) °,γ = 107. 353( 3) °,U = 1248. 93( 8) ?~3,Z = 2.The antitumor activities against human neoplastic cell lines A549,HePG2,MCF-7,SGC-7901,OVCA-433 and the cytotoxicity for HUVEC cell lines by CCK-8 method were subsequently evaluated. The antitumor activities against SGC7901,K562 and Hela were better with the lower cytotoxicity against HUVEC cell,while the best one was K562 cells,which IC50= 7. 86μM.
机构地区 滨州医学院
出处 《山东化工》 CAS 2017年第16期1-2,4,共3页 Shandong Chemical Industry
基金 山东省自然科学基金(No.ZR2014BL008) 烟台市科技计划(2015WS010)
关键词 Α Β-不饱和酮 抗肿瘤 单晶结构 α β-unsaturated ketone antitumor single-crystal structure
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