跳转至内容
Merck
CN

A9295

4-Androsten-4-ol-3,17-dione acetate

别名:

4-Acetoxy-4-androstene-3,17-dione

登录 查看组织和合同定价。

选择尺寸


关于此项目

经验公式(希尔记法):
C21H28O4
化学文摘社编号:
分子量:
344.44
UNSPSC Code:
12352202
PubChem Substance ID:
MDL number:
Form:
solid
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

InChI

1S/C21H28O4/c1-12(22)25-19-16-5-4-13-14-6-7-18(24)21(14,3)10-8-15(13)20(16,2)11-9-17(19)23/h13-15H,4-11H2,1-3H3/t13-,14-,15-,20+,21-/m0/s1

SMILES string

CC(=O)OC1=C2CC[C@H]3[C@@H]4CCC(=O)[C@@]4(C)CC[C@@H]3[C@@]2(C)CCC1=O

InChI key

LRXSFNGKRCOHRS-VMRCMBGLSA-N

form

solid

shipped in

ambient

storage temp.

2-8°C

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

新产品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Recent advances in studies on estrogen biosynthesis.
A M Brodie
Journal of endocrinological investigation, 2(4), 445-460 (1979-10-01)
A M Brodie et al.
Cancer research, 42(8 Suppl), 3360s-3364s (1982-08-01)
Aromatase inhibitor, 4-hydroxyandrostene-3,17-dione (4-OHA), is a highly effective treatment in rats with 7,12-dimethylbenz(a) anthracene-induced hormone-dependent mammary tumors. Over 90% of tumors regress to less than one-half of their original size, and a high proportion regress completely. Treatment of rats with
Effect of an aromatase inhibitor (4-acetoxy-4-androstene-3,17-dione) on the stimulatory action of luteinizing hormone on estradiol-17 beta synthesis by rat preovulatory follicles in vitro.
G Evans et al.
Biology of reproduction, 25(2), 290-294 (1981-09-01)
S A Daniel et al.
Canadian journal of physiology and pharmacology, 61(5), 507-511 (1983-05-01)
Androgens have been shown to enhance follicle-stimulating hormones (FSH) induced aromatase activity in cultured granulosa cells obtained from the ovaries of immature rats, however, aromatizable androgens are more effective than nonaromatizable androgens. The present study was designed to investigate the
A M Brodie et al.
Steroids, 38(6), 693-702 (1981-12-01)
4-Hydroxy-4-androstene-3,17-dione (4-OHA) and 4-acetoxy-4-androstene-3,17-dione (4-AcA), in addition to being competitive inhibitors of aromatase, cause time-dependent, irreversible, loss of enzyme activity in both human placental and rat ovarian microsomes. In vivo, treatment of rats with 4-OHA also causes loss of ovarian

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持