15183-37-6

15183-37-6 structure

Name: Estetrol
Chemical Name: (8R,9S,13S,14S,15R,16R,17R)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,15,16,17-tetrol
CAS Number: 15183-37-6
Molecular Formula: C₁₈H₂₄O₄
Molecular Weight: 304.38100
Catalog: Research Areas Cardiovascular Disease
Create Date: 2017-03-20 07:04:11
Modify Date: 2024-01-05 11:50:24
Estetrol, a natural estrogen synthesized exclusively during pregnancy by the human fetal liver, is a selective nuclear estrogen receptor modulator. Estetrol exerts estrogenic actions on the endometrium or the central nervous system but presents antagonistic effects on the breast[1][2].

Name	(8R,9S,13S,14S,15R,16R,17R)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,15,16,17-tetrol
Synonyms	ESTETROL 15\|A-Hydroxyestriol

Description	Estetrol, a natural estrogen synthesized exclusively during pregnancy by the human fetal liver, is a selective nuclear estrogen receptor modulator. Estetrol exerts estrogenic actions on the endometrium or the central nervous system but presents antagonistic effects on the breast[1][2].
Related Catalog	Signaling Pathways >> Others >> Estrogen Receptor/ERR Research Areas >> Cardiovascular Disease
Target	Estrogen receptor[1]
References	[1]. Valéra MC, et al. Effect of estetrol, a selective nuclear estrogen receptor modulator, in mouse models of arterial and venous thrombosis. Mol Cell Endocrinol. 2018 Dec 5;477:132-139. [2]. Montt-Guevara MM, et al. Estetrol Modulates Endothelial Nitric Oxide Synthesis in Human Endothelial Cells. Front Endocrinol (Lausanne). 2015 Jul 22;6:111.

RIDADR	NONH for all modes of transport

16127-99-4

15183-37-6

53-16-7

15183-37-6

Literature: EP2383279 A1, ;

138743-03-0

15183-37-6

Literature: EP2383279 A1, ;

858-98-0

15183-37-6

Literature: EP2383279 A1, ;

213819-19-3

15183-37-6

Literature: EP2383279 A1, ;

16127-98-3

15183-37-6

Literature: Steroids, , vol. 60, # 3 p. 277 - 284