Enclomifeen

Enclomiphene ((E) -Clomiphene) is a potent and orally active non-steroidal estrogen receptor antagonist, with antioestrogenic property. Enclomiphene can be used for the research of ovarian dysfunction, testosterone deficiency, male hypogonadism and type 2 diabetes[1].

15690-57-0

(E) -Clomiphene; trans-Clomiphene; Enclomifene

12352005

Estrogen Receptor/ERR

Reference compound

Vitamin D Related/Nuclear Receptor

Metabolism-protein/nucleotide metabolism

Endocrinology; Metabolic Disease

https://www.medchemexpress.com/enclomiphene.html

99.79

DMSO : 100 mg/mL (ultrasonic)

Cl/C(C1=CC=CC=C1)=C(C2=CC=C(OCCN(CC)CC)C=C2)\C3=CC=CC=C3

C26H28ClNO

405.96

[1]Rodriguez KM, et al. Enclomiphene citrate for the treatment of secondary male hypogonadism. Expert Opin Pharmacother. 2016 Aug;17 (11) :1561-7. |[2]M S Opsahl, et al. Effects of enclomiphene and zuclomiphene on basal and gonadotrophin-stimulated progesterone secretion by isolated subpopulations of small and large ovine luteal cells. Hum Reprod. 1996 Jun;11 (6) :1250-5.|[3]G E Schmidt, et al. The effects of enclomiphene and zuclomiphene citrates on mouse embryos fertilized in vitro and in vivo. Am J Obstet Gynecol. 1986 Apr;154 (4) :727-36. |[4]E S Huang, et al. Estrogenic and antiestrogenic effects of enclomiphene and zuclomiphene on gonadotropin secretion by ovine pituitary cells in culture. Endocrinology. 1983 Feb;112 (2) :442-8. |[5]R Weissenberg, et al. The effect of clomiphene citrate and its Zu or En isomers on the reproductive system of the immature male rat. Andrologia. 1992 May-Jun;24 (3) :161-5. |[6]R T Turner, et al. Differential responses of estrogen target tissues in rats including bone to clomiphene, enclomiphene, and zuclomiphene. Endocrinology. 1998 Sep;139 (9) :3712-20.

Room Temperature

-20°C, 3 years; 4°C, 2 years (Powder)

http://file.medchemexpress.com/batch_PDF/HY-118861/Enclomiphene-SDS-MedChemExpress.pdf

Reference compound1

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