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171746-21-7

中文名称 4-[2-[5,6-二氢-5,5-二甲基-8-(4-甲基苯基)-2-萘基]乙炔基]苯甲酸
英文名称 4-{[5,5-dimethyl-8-(4-methylphenyl)-5,6-dihydronaphthalen-2-yl]ethynyl}benzoic acid
CAS 171746-21-7
分子式 C28H24O2
分子量 392.49
MOL 文件 171746-21-7.mol
171746-21-7 结构式 171746-21-7 结构式

基本信息

中文别名
4-[2-[5,6-二氢-5,5-二甲基-8-(4-甲基苯基)-2-萘基]乙炔基]苯甲酸
英文别名
CD 3106
AGN 193109
AGN 193109 SodiuM Salt
4-((5,5-Dimethyl-8-p-tolyl-5,6-dihydronaphthalen-2-yl)ethynyl)benzoic acid
4-{[5,5-diMethyl-8-(4-Methylphenyl)-5,6-dihydronaphthalen-2-yl]ethynyl}benzoic acid
4-[2-[5,6-Dihydro-5,5-dimethyl-8-(4-methylphenyl)-2-naphthalenyl]ethynyl]benzoic Acid
Benzoic acid, 4-[2-[5,6-dihydro-5,5-dimethyl-8-(4-methylphenyl)-2-naphthalenyl]ethynyl]-

物理化学性质

熔点246-255?C
沸点564.5±50.0 °C(Predicted)
密度1.21±0.1 g/cm3(Predicted)
储存条件Sealed in dry,Store in freezer, under -20°C
溶解度可溶于氯仿(轻微加热)、DMSO(轻微超声处理)
酸度系数(pKa)4.08±0.10(Predicted)
形态固体
颜色灰白色至淡黄色
稳定性吸湿性

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H302-H315-H319-H335

常见问题列表

生物活性
AGN 193109 是一种视黄酸类似物,是有效的,特异性的视黄酸受体 (RARs) 拮抗剂,可抑制 RARα,RARβ 和 RARγ 的活性,Kd 值分别为 2 nM,2 nM 和 3 nM。
靶点

Kd: 2 nM (RARα), 2 nM (RARβ), 3 nM (RARγ)

体外研究

AGN 193109 is a highly effective antagonist of retinoic acid receptors, with K d s of 2 nM, 2 nM, and 3 nM for RARα, RARβ, and RARγ, respectively. AGN 193109 is completely RAR specific, because it does not bind to or transactivate through any of the RXRs. AGN 193109 (100 nM) inhibits the TTNPB (a retinoic acid receptor agonist)-dependent morphological change in ECE16-1 cells. AGN193109 half-reverses retinoid-dependent growth suppression at 10 nM, and completely shows this effect at 100 nM in ECE16-1 cells. AGN193109 (100 nM) also eliminates TTNPB-induced decrease in levels of K5, K6, K14, K16, and K17 and increase in levels of K7, K8, and K19.

体内研究

AGN 193109 (1.15 μmol/kg) does not causes overt toxicity and has no effect on spleen weight on the mice, but it suppresses TTNPB-induced increase in spleen weight of the mice. AGN 193109 also significantly reduces the cutaneous toxicity induced by ATRA. AGN 193109 (0.30 or 1.20 μmol/kg) by topical treatment significantly reduces both weight loss and cutaneous toxicity caused by oral TTNPB cotreatment.

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