diethylstilbestrol

Diethylstilbestrol (DES) is used in the treatment of menopausal and postmenopausal disorders.

Diethylstilbestrol diphosphate (Fosfestrol) is a diphosphate salt of diethylstilbestrol and acts as an estrogen receptor agonist. Serving as a prodrug to diethylstilbestrol, it exhibits potent anti-gonadotropic effects. Diethylstilbestrol diphosphate is utilized in research related to prostate cancer.

Diethylstilbestrol dipropionate can be used in estrogen therapy of relapsed prostate cancer.

Diethylstilbestrol (Standard) is the standard substance of Diethylstilbestrol, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Diethylstilbestrol (DES) is used in the treatment of menopausal and postmenopausal disorders.

Diethylstilbestrol monoglucuronide is a reagent used in biochemical reactions.

Diethylstilbestrol-BSA is a hapten-carrier protein conjugate formed by coupling Diethylstilbestrol to bovine serum albumin (BSA). As a hapten, Diethylstilbestrol alone cannot induce an immune response and must be conjugated to a large molecular protein to become a complete antigen with immunogenicity. Diethylstilbestrol-BSA may be supplied as a lyophilized powder or as a solution. The solution is prepared in 0.01 M TBS (pH 7.4) buffer at a typical concentration of 1 mg/mL.

Diethylstilbestrol-KLH is a hapten-carrier protein conjugate formed by coupling Diethylstilbestrol to keyhole limpet hemocyanin (KLH). As a hapten, Diethylstilbestrol alone cannot induce an immune response and must be conjugated to a large molecular protein to become a complete antigen with immunogenicity. Diethylstilbestrol-KLH may be supplied as a lyophilized powder or as a solution. The solution is prepared in 0.01 M TBS (pH 7.4) buffer at a typical concentration of 1 mg/mL.

(Rac)-Hexestrol, the racemic mixture of Hexestrol, is a synthetic non-steroidal estrogen. It is commonly available in its deuterated form, serving as an internal standard for precise quantification in analytical chemistry.

Amino-PEG10-amine is a PEG-based PROTAC linker employed for the conjugation of two mono diethylstilbestrol (DES)-based ligands. This compound offers an alternative approach to the synthesis of highly selective and active ER antagonists, which are crucial for the advancement of endocrine therapy in breast cancer treatment[1].

Amino-PEG11-amine, a polyethylene glycol (PEG)-based linker with 12 units, facilitates the conjugation of two mono diethylstilbestrol (DES)-based ligands. This strategy enhances the preparation of selective and potent estrogen receptor (ER) antagonists, offering an innovative approach for endocrine therapy in breast cancer treatment.

Dihydrotestosterone-KLH is a hapten-carrier protein conjugate formed by coupling Dihydrotestosterone (DHT) to keyhole limpet hemocyanin (KLH). As a hapten, Diethylstilbestrol alone cannot induce an immune response and must be conjugated to a large molecular protein to become a complete antigen with immunogenicity. Dihydrotestosterone-KLH may be supplied as a lyophilized powder or as a solution. The solution is prepared in 0.01 M TBS (pH 7.4) buffer at a typical concentration of 1 mg/mL.

Isodienestrol, a derivative of Diethylstilbestrol, acts as a microtubule (Microtubule) inhibitor. It is utilized in cancer research.

Trans-Diethyl-1,1,1',1'-Stilbestrol-3,3',5,5'-D8 is a deuterated compound of Trans-Diethyl-Stilbestrol. Trans-Diethyl-Stilbestrol has a CAS number of 56-53-1. Diethylstilbestrol is used in the treatment of menopausal and postmenopausal disorders.