clomiphene

Clomiphene citrate (NSC 35770) is a selective estrogen receptor modulator.

Clomifene is a selective estrogen receptor modulator (SERM), it has both estrogenic and anti-estrogenic activities. This agent causes the release of the pituitary gonadotropins follicle-stimulating hormone (FSH) and luteinizing hormone (LH), leading to ov

EN Clomiphene-D4 Citrate is a deuterated compound of EN Clomiphene Citrate (T7313).

Enclomiphene-D4 hydrochloride is a potent and orally active oestrogen receptor antagonist, with antioestrogenic property. Enclomiphene D4 hydrochloride ( (E)-Clomiphene D4 hydrochloride; trans-Clomiphene D4 hydrochloride; Enclomifene D4 hydrochloride) is a deuterium labeled Enclomiphene hydrochloride (T62572).

Zuclomiphene is a nonsteroidal selective estrogen receptor modulator (SERM) with triphenylethylene group.

Enclomiphene citrate (trans-Clomiphene citrate) is a non-steroidal estrogen receptor antagonist,with antioestrogenic property

Zuclomiphene-D4 Citrate is a deuterated compound of Zuclomiphene Citrate. Zuclomiphene Citrate (T13415) has a CAS number of 14158-66-8.

(Z/E)-Clomiphene-[D5] Citrate (Standard) is a reference standard of (Z/E)-Clomiphene-[D5] Citrate intended for quantitative analysis, quality control, and related biochemical research applications.

Clomifene hydrochloride (Standard) is the standard substance of Clomifene hydrochloride, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Clomifene hydrochloride can induce ovulation and can be used in infertility. hydrochloride is a simple, relatively safe, easy to administer and well tolerated, orally active compound.

Zuclomiphene citrate, a cis isomer of Clomiphene citrate, exhibits an antiestrogenic effect and inhibits the secretion of luteinizing hormone (LH) more effectively than its trans isomer.

Enclomiphene ((E)-Clomiphene) hydrochloride is an orally active, potent non-steroidal estrogen receptor antagonist with anti-estrogenic effects. It is utilized to study ovarian dysfunction, testosterone deficiency, male hypogonadism, and type 2 diabetes mellitus.

Enclomiphene-D4 is the deuterium-labeled analog of Enclomiphene. Enclomiphene (T62017) functions as a potent and orally active estrogen receptor antagonist, exhibiting antiestrogenic properties.

Enclomiphene ((E)-Clomiphene) is a potent and orally active antagonist of non-steroidal estrogen receptor. Enclomiphene has research value in ovarian dysfunction, testosterone deficiency, male hypogonadism and type 2 diabetes.