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Merck
CN
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主要文件

安全信息

SML1480

Sigma-Aldrich

Alclometasone dipropionate

≥98% (HPLC)

别名:

Alclometasone Dipropanoate, Sch 22219, (7α,11β,16α)-7-Chloro-11-hydroxy-16-methyl-17,21-bis(1-oxopropoxy)pregna-1,4-diene-3,20-dione, 7α-Chloro-11β,17,21-trihydroxy-16α-methylpregna-1,4-diene-3,20-dione 17,21-di(propionate), Alclometasone 17,21-dipropionate

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About This Item

经验公式（希尔记法）:
C28H37ClO7
CAS号:
66734-13-2
分子量:
521.04
EC 号:
266-464-3
UNSPSC代码:
12352200
NACRES:
NA.77

质量水平

100

方案

≥98% (HPLC)

表单

powder

储存条件

desiccated

颜色

white to beige

溶解性

DMSO: 2 mg/mL, clear (warmed)

储存温度

2-8°C

SMILES字符串

Cl[C@H]1[C@@H]2[C@@H]([C@@]4(C(=CC(=O)C=C4)C1)C)[C@H](C[C@]3([C@H]2C[C@H]([C@]3(OC(=O)CC)C(=O)COC(=O)CC)C)C)O

InChI

1S/C28H37ClO7/c1-6-22(33)35-14-21(32)28(36-23(34)7-2)15(3)10-18-24-19(29)12-16-11-17(30)8-9-26(16,4)25(24)20(31)13-27(18,28)5/h8-9,11,15,18-20,24-25,31H,6-7,10,12-14H2,1-5H3/t15-,18+,19-,20+,24-,25+,26+,27+,28+/m1/s1

InChI key

DJHCCTTVDRAMEH-DUUJBDRPSA-N

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生化/生理作用

Alclometasone dipropionate is a glucocorticoid receptor agonist that mimics the metabolic, anti-inflammatory, immunosuppressive, antipruritic, and vasoconstrictive effects of natural glucocorticoids.

象形图

Health hazard
GHS08

警示用语：

Warning

危险声明

H361

危险分类

Repr. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

监管及禁止进口产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000071349
0000071348
046M4734V

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S Aoyama et al.
Drug metabolism and disposition: the biological fate of chemicals, 18(4), 409-417 (1990-07-01)
The metabolic fate of alclometasone dipropionate (ADP or S-3460) has been studied in rats, rabbits, and mice, with consideration of their interspecies differences. Several reference compounds related to ADP were synthesized for the determination and identification of the metabolites. After
Y Nishibe et al.
Japanese journal of pharmacology, 50(4), 435-443 (1989-08-01)
The effect of successive administration of the corticosteroid alclometasone dipropionate (ACM) on the hepatic drug-metabolizing system was examined using male and female rats. Although some pharmacological changes such as increases in plasma enzyme activity, lipid level and protein concentration appeared

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