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125316-60-1

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 125316-60-1
分子式 C27H26O3
分子量 398.49
MOL 文件 125316-60-1.mol
更新日期 2025/05/22 09:46:17
125316-60-1 结构式 125316-60-1 结构式

基本信息

中文别名
阿达帕琳杂质E
O-去甲阿达帕林
邻去甲基阿达帕林
6-[3-(1-金刚烷基)-4-羟基苯基]-2-萘甲酸
6- [3-(1-金刚烷基)-4-羟基苯基]萘-2-羧酸
英文别名
CS-2691
ADAP-IME
CD 437/AHPN
AHPN
CD 437
CD-437
CD437
CD-437
CD 437
Adapalene IMpurity F
O-DesMethyl Adapalene
Apoptosis Activator VI
O-Desmethyl Adapalene-13C6
Apoptosis Activator VI, CD437/AHPN
所属类别
分析化学:药典标准品和杂质标准品

物理化学性质

熔点271.6-276 °C
熔点271.6-276 °C
沸点595.0±50.0 °C(Predicted)
密度1.290
储存条件-20°C
溶解度DMSO: 26 mg/mL
溶解度二甲基亚砜:26 毫克/毫升
酸度系数(pKa)4.17±0.30(Predicted)
形态solid
颜色yellow

安全数据

危险性符号(GHS)GHS hazard pictograms
GHS08
警示词警告
危险性描述H361
安全说明22-24/25
WGK Germany3
WGK Germany3
RTECS号QJ1975900

常见问题列表

生物活性
CD437 是一个选择性视黄酸受体 (Retinoic Acid Receptor γ (RARγ)) 激动剂。
靶点

Retinoic Acid Receptor γ (RARγ)

体外研究

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.

体内研究

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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