Description
An ER modulator; acts as an ER antagonist in humans, sheep, and rabbits and an ER agonist in rats; inhibits E2 binding in isolated rabbit uterus at 0.34 µM; decreases E2-induced inhibition of FSH secretion in primary sheep pituitary cells in a concentration-dependent manner; inhibits spermatogenesis and decreases serum LH and testosterone levels in intact or castrated rats at 0.25 and 0.5 mg/animal
Formal name: 2-[4-[(1E)-2-chloro-1,2-diphenylethenyl]phenoxy]-N,N-diethyl-ethanamine, 2-hydroxy-1,2,3-propanetricarboxylate
Synonyms: trans-Clomiphene
Molecular weight: 598.1
CAS: 7599-79-3
Purity: ≥95%
Formulation: A crystalline solid