CAS 7599-79-3

Enclomiphene citrate

Description:

Enclomiphene citrate is a selective estrogen receptor modulator (SERM) primarily used in the treatment of male hypogonadism and infertility. It is a stereoisomer of clomiphene citrate, which is commonly used for ovulation induction in women. Enclomiphene functions by blocking estrogen receptors in the hypothalamus, leading to an increase in the secretion of gonadotropins, which in turn stimulates the testes to produce more testosterone. This compound is characterized by its ability to selectively modulate estrogen activity, making it effective in promoting endogenous testosterone production without the adverse effects associated with exogenous testosterone therapy. Enclomiphene citrate is typically administered orally and has a favorable pharmacokinetic profile, with a relatively long half-life, allowing for once-daily dosing. Its safety profile is generally well-tolerated, although potential side effects may include hot flashes, mood swings, and gastrointestinal disturbances. As research continues, enclomiphene citrate is being explored for its broader applications in reproductive health and hormone regulation.

Formula: C₃₂H₃₆ClNO₈

InChI: InChI=1S/C26H28ClNO.C6H8O7/c1-3-28(4-2)19-20-29-24-17-15-22(16-18-24)25(21-11-7-5-8-12-21)26(27)23-13-9-6-10-14-23;7-3(8)1-6(13,5(11)12)2-4(9)10/h5-18H,3-4,19-20H2,1-2H3;13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)/b26-25+;

InChI key: InChIKey=PYTMYKVIJXPNBD-BTKVJIOYSA-N

SMILES: C(=C(/Cl)\C1=CC=CC=C1)(\C2=CC=C(OCCN(CC)CC)C=C2)/C3=CC=CC=C3.C(CC(O)=O)(CC(O)=O)(C(O)=O)O

Synonyms:

• trans-Clomiphene citrate
• Clomiphene B citrate
• Ethanamine, 2-[4-[(1E)-2-chloro-1,2-diphenylethenyl]phenoxy]-N,N-diethyl-, 2-hydroxy-1,2,3-propanetricarboxylate (1:1)
• Triethylamine, 2-[p-(2-chloro-1,2-diphenylvinyl)phenoxy]-, citrate (1:1), (E)-
• Ethanamine, 2-[4-(2-chloro-1,2-diphenylethenyl)phenoxy]-N,N-diethyl-, (E)-, 2-hydroxy-1,2,3-propanetricarboxylate (1:1)
• Unii-J303A6U9Y6
• (E)-Clomiphene citrate
• Enclomiphene Citrate /trans-Clomiphene
• Enclomiphene citrate
• Enclomid
• trans-clomifene citrate
• Enclomifene citrate
• Triethylamine, 2-(p-(2-chloro-1,2-diphenylvinyl)phenoxy)-, citrate, (E)-

Enclomiphene citrate

CAS: 7599-79-3

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

Formula: C₃₂H₃₆ClNO₈

Purity: 99.95%

Color and Shape: Solid

Molecular weight: 598.08

Ref: TM-T7313

trans-Clomiphene Citrate

Controlled Product

CAS: 7599-79-3

Applications trans-Clomiphene Citrate, stereoisomer of Clomiphene Citrate (C587025), a synthetic estrogen agonist-antagonist. Gonad-stimulating principle.
References Palopoli, F.P., J. Med. Chem., 10, 84 (1967), Ernst., et al.: J. Pharm. Sci., 65, 148 (1976), Baustian, C.L., et al.: Pharm. Biomed. Anal., 4, 237 (1986),

Formula: C₃₂H₃₆ClNO₈

Color and Shape: Neat

Molecular weight: 598.08

Ref: TR-C587045

Enclomiphene citrate

Controlled Product

CAS: 7599-79-3

Enclomiphene citrate is an active isomer of clomiphene citrate. It is a selective estrogen receptor modulator, that increases serum testosterone levels by raising luteinizing hormone (LH) and follicle stimulating hormone (FSH) levels. This indicates a use for treating secondary hypogonadism in men seeking to preserve fertility.

Formula: C₃₂H₃₆ClNO₈

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 598.08 g/mol

Ref: 3D-HAA59979

Enclomiphene citrate - Bio-X ™

Controlled Product

CAS: 7599-79-3

Enclomiphene citrate is part of our Bio-X ™ Range. These products are aimed at life science researchers who need high quality ready-to-use products for assay development, screening or other R&D work. With a solubility datasheet and convenient vials, all of our Bio-X ™ products are in stock across our global warehouses for rapid delivery and ease of use.

Formula: C₂₆H₂₈ClNO•C₆H₈O₇

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 598.08 g/mol

Ref: 3D-BE184055

Trans-Clomiphene Citrate

CAS: 7599-79-3

Formula: C₂₆H₂₈ClNOC₆H₈O₇

Molecular weight: 406 : 192.12

Ref: ST-EA-CP-C29038