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S-(N-PhenethylthiocarbaMoyl)-L-cysteine

更新时间:2024-01-12 06:38:35

S-(N-PhenethylthiocarbaMoyl)-L-cysteine结构式
S-(N-PhenethylthiocarbaMoyl)-L-cysteine结构式
品牌特惠专场
常用名 S-(N-PhenethylthiocarbaMoyl)-L-cysteine 英文名 S-(N-PhenethylthiocarbaMoyl)-L-cysteine
CAS号 53330-02-2 分子量 284.40
密度 N/A 沸点 N/A
分子式 C12H16N2O2S2 熔点 N/A
MSDS N/A 闪点 N/A

 用途


S-(N-苯乙基硫代氨甲酰)-L-半胱氨酸是一种抗癌剂,具有抗白血病活性,GC50值为336nm。S-(N-苯乙基硫代氨甲酰)-L-半胱氨酸抑制HL60细胞中的DNA合成[1]。

 S-(N-PhenethylthiocarbaMoyl)-L-cysteine名称

中文名 S-(N-苯乙硫代氨基甲酰基)-L-半胱氨酸
英文名 phenethyl isothiocyanate cysteine conjugate
英文别名 更多

 S-(N-PhenethylthiocarbaMoyl)-L-cysteine生物活性

描述 S-(N-苯乙基硫代氨甲酰)-L-半胱氨酸是一种抗癌剂,具有抗白血病活性,GC50值为336nm。S-(N-苯乙基硫代氨甲酰)-L-半胱氨酸抑制HL60细胞中的DNA合成[1]。
相关类别
体外研究 S-(N-苯乙基硫代氨甲酰)-L-半胱氨酸抑制HL60细胞的生长,GC50=336 nM[1]。S-(N-苯乙基硫代氨甲酰)-L-半胱氨酸抑制HL60细胞中的DNA合成,IC50=6.47μM[1]。S-(N-苯乙基硫代氨甲酰)-L-半胱氨酸诱导HL 60细胞中的DNA断裂[1]。细胞增殖试验[1]细胞系:HL60细胞浓度:0.1-10μM培养时间:48小时结果:抑制细胞生长,GC50值为336nm。细胞增殖试验[1]细胞系:HL60细胞浓度:4μM培养时间:0,20,40,60,80,100小时结果:抑制细胞生长。
参考文献

[1]. [1] Adesida A, Edwards LG, Thornalley PJ. Inhibition of human leukaemia 60 cell growth by mercapturic acid metabolites of phenylethyl isothiocyanate. Food Chem Toxicol. 1996 Apr;34(4):385-92.

 S-(N-PhenethylthiocarbaMoyl)-L-cysteine物理化学性质

分子式 C12H16N2O2S2
分子量 284.40
精确质量 284.06500
PSA 132.74000
LogP 2.33990
储存条件 -20°C,干燥,密封

 S-(N-PhenethylthiocarbaMoyl)-L-cysteine安全信息

危害码 (欧洲) Xi

 S-(N-PhenethylthiocarbaMoyl)-L-cysteine上下游产品

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 S-(N-PhenethylthiocarbaMoyl)-L-cysteine英文别名

s-(n-methylthiocarbamoyl)-l-cysteine
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S-(N-PhenethylthiocarbaMoyl)-L-cysteine价格

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