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Estrogenprogestogen Receptor

Estrogenprogestogen Receptor

Estrogenprogestogen Receptor related products

Structure Cat No. Product Name CAS No. Product Description
14-3-3σ/ERα stabilizer-1 V78794 14-3-3σ/ERα stabilizer-1 14-3-3σ/ERα stabler-1 (Compound 181) is a covalent 14-3-3σ/ERα stabilizer.
Amcenestrant (SAR439859) V40395 Amcenestrant (SAR-439859) 2114339-57-8 Amcenestrant (SAR-439859; SAR439859) is a potent, orally available, and nonsteroidalestrogen receptor degrader (SERD)with potential anticancer activity.
Bisphenol AF-d4 (BPAF-d4; 4,4'-(Perfluoropropane-2,2-diyl)diphenol-d4) V77195 Bisphenol AF-d4 (BPAF-d4; 4,4'-(Perfluoropropane-2,2-diyl)diphenol-d4) Bisphenol AF-d4 is an isotopically labeled analog of Bisphenol AF.
BTC (Estrogen receptor modulator 1) V17164 BTC (Estrogen receptor modulator 1) 63676-22-2 BTC, formerly known as RALOXIFENE CORE, is a selective andorally active estrogen receptor modulator (SERM) with apIC50of 0.46.
ERα degrader 6 V79338 ERα degrader 6 ERα degrader 6 (Compound 31q) is an ERα degrader (KI: 75 nM).
ERα degrader 7 V78502 ERα degrader 7 ERα degrader 7 (Compound B1) is a potent ERα degrader with IC50 of 14.6 nM and a DC 50 of 9.7 nM.
ET receptor antagonist 1 V79343 ET receptor antagonist 1 ET receptor antagonist 1 (compound 16h) is an ET receptor antagonist (IC50=0.18 nM) and may be utilized in pulmonary arterial hypertension (PAH) research.
ET receptor antagonist 2 V79391 ET receptor antagonist 2 ET receptor antagonist 2 (compound 16j) is an ET receptor antagonist (IC50=0.22 nM) that may be utilized in pulmonary arterial hypertension (PAH) research.
ET receptor antagonist 3 V78664 ET receptor antagonist 3 ET receptor antagonist 3 (compound 17d) is an ET receptor antagonist (IC50=0.26 nM) that may be utilized in pulmonary arterial hypertension (PAH) research.
Fulvestrant-d3 (ICI 182780-d3; ZD 9238-d3; ZM 182780-d3) V79534 Fulvestrant-d3 (ICI 182780-d3; ZD 9238-d3; ZM 182780-d3) Fulvestrant-d3 is the deuterium labelled form of Fulvestrant.
H3B-5942 V31869 H3B-5942 2052128-15-9 H3B-5942 (H3B5942) is a selective, irreversible (covalent) and orally bioavailable estrogen receptor antagonist with antitumor activity (better than fulvestrant).
hFSH-β-(33-53) (TFA) V76934 hFSH-β-(33-53) (TFA) hFSH-β-(33-53) TFA is a thiol-containing peptide corresponding to the second FSH receptor-binding domain and is an FSHR (follicle-stimulating hormone receptor) antagonist.
Raloxifene-d10 V81275 Raloxifene-d10 Raloxifene-d10 is the deuterated form of Raloxifene.
Yp537 TFA (Anti-estrogen TFA) V73484 Yp537 TFA (Anti-estrogen TFA) Yp537 TFA is an estrogen receptor (ER) inhibitor that prevents dimerization of the human estrogen receptor.
丹参酮 IIA V1755 Sinomenine (Cucoline) 568-72-9 Sinomenine(Coculine; Cucoline; Kukoline) is a naturally occuring alkaloid found in the root of the climbing plant Sinomenium acutum which is native to Japan and China.
乌利司他 V1752 Ulipristal (CDB-2914) 159811-51-5 Ulipristal(CDB-2914;HRP2000, VA2914,RTI 3021-012, RU 44675, EllaOne, Ella, Esmya) is a potent and selective SPRM (selective progesterone receptor modulator) used for emergency contraception after an unprotected intercourse or contraceptive failure.
乙炔雌二醇 V1735 Ethinyl Estradiol (Ethynylestradiol) 57-63-6 Ethinyl Estradiol (17α-Ethynylestradiol; Ginestrene; Ethinyl Estradiol; Ethynylestradiol; Microfollin Forte; Organon; Progynon C) is an orally bioactive and semi-synthetic estrogen used in various formulations of combined oral contraceptive pills.
他立喹达二甲磺酸盐 V1756 Tariquidar dimesylate 625375-84-0 Tariquidar dimesylate (formerly known as XR9576; D06008; XR-9576; D-06008), the dimesylate salt ofTariquidar, is a novel potent and selective noncompetitive inhibitor of P-glycoprotein (P-gp) with potential antitumor activity.
去氢孕酮 V10360 Dydrogesterone 152-62-5 Dydrogesterone is a synthetic progestin.
去氢表雄酮 V1733 Dehydroepiandrosterone (DHEA) 53-43-0 Dehydroepiandrosterone (trans-Dehydroandrosterone; DHEA; Prasterone; Psicosterone; EL-10; GL-701; IP-1001;NSC-9896;PB-007; SH-K-04828; Androstenolone; Diandrone) is an endogenous steroidal hormone acting asan androgen receptor antagonist and an estrogen receptor agonist.
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