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医药中间体
无机化工
有机原料
原料药
染料及颜料
表面活性剂
香精与香料
化学试剂
食品添加剂
催化剂及助剂
分析化学
125316-60-1
CD437
产品纠错
CAS号:125316-60-1 | 英文名称:CD437
分子式 C27H26O3
分子量 398
EINECS号 200-258-5
MDL MFCD03106506
Smiles
InChIKey
CD437化学百科
基本信息
中文名称 6-[3-(1-金刚烷基)-4-羟基苯基]-2-萘甲酸
英文名称 CD437
CAS号 125316-60-1
分子式 C27H26O3
分子量 398.49
EINECS号 200-258-5
物化性质
熔点 271.6-276 °C
沸点 595.0±50.0 °C(Predicted)
密度 1.290
溶解度 二甲基亚砜:26 毫克/毫升
形态 固体
酸度系数(pKa) 4.17±0.30(Predicted)
颜色 粘黄色
安全信息
安全说明 22-24/25
WGK Germany 3
RTECS号 QJ1975900
生产及用途
CD437 是一个选择性视黄酸受体 (Retinoic Acid Receptor γ (RARγ)) 激动剂。

Retinoic Acid Receptor γ (RARγ)

CD437 is a selective RARγ agonist. Growth inhibition by CD437 in these lung cancer cell lines is apparent after 2 days of treatment with 10 μM CD437. Dose-response experiments demonstrate that CD437 reduces the numbers of H460, SK-MES-1, A549, and H292 cells with 50% inhibitory values of approximately 0.5, 0.4, 3, and 0.85 μM, respectively. Treatment for 72 h with CD437 causes a strong dose-dependent growth inhibition in all melanoma cell lines. At a concentration of 5 μM CD437, only about 5 to 25% of the cells remain viable after 3 d. The concentrations of CD437 required for 50% growth inhibition (IC50) range from 10 μM for MeWo to 0.1 μM for SK-Mel-23 showing the highest sensitivity.

Tumors in CD437-treated mice stop growing, an effect that becomes already statistically significant (P<0.01) at day 13, 3 d after first administration of CD437, and is maintained for more than 3 wk after discontinuation of treatment. Further histologic analysis demonstrates marked c-fos mRNA levels at the tumor-stroma edge in CD437-treated tumors.

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