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Estrogen Receptor/ERR
Estrogen Receptor/ERR Isoform Specific Products
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Estrogen Receptor/ERR Inhibitors
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Estrogen Receptor/ERR Agonists
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Estrogen Receptor/ERR Ligands
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Estrogen Receptor Proteins
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ER-alpha Proteins
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ER-beta Proteins
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Estrogen Receptor/ERR Related Products (831)
Related Products (831)
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Recombinant Proteins (2)
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Antibodies (11)
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Estrogen Receptor/ERR Isoform Comparison
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Diethylstilbestrol diphosphate
0 ImagesCat. No.: HY-W554614CAS No.: 522-40-7Synonyms: FosfestrolDiethylstilbestrol diphosphate (Fosfestrol) is a diphosphate of diethylstilbestrol and an agonist of estrogen receptors. Diethylstilbestrol diphosphate is a prodrug of diethylstilbestrol and has a powerful anti-gonadotropin effect. Diethylstilbestrol diphosphate can be used in the research of prostate cancer. -
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ER degrader 7
0 ImagesCat. No.: HY-155197CAS No.: 2922929-63-1ER degrader 7 is an estrogen receptor α (ERα) degrader and a tubulin (tubulin) inhibitor. ER degrader 7 inhibits the cell viability of various cancer cell lines. ER degrader 7 disrupts the microtubule network in breast cancer cells, induces G2/M phase cell cycle arrest, and exhibits concentration-dependent accumulation in Tamoxifen-resistant LCC2 cells. ER degrader 7 suppresses tumor growth in vivo without causing body weight loss. ER degrader 7 can be applied in studies related to breast cancer. -
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Prolactin-Releasing Peptide (1-31) (rat)
0 ImagesCat. No.: HY-P4689CAS No.: 215510-06-8Prolactin-Releasing Peptide (1-31) (rat) is a UHR-1/GRP10 receptor ligand. Prolactin-Releasing Peptide (1-31) (rat) reduces fasting-induced food intake, increases plasma levels of LH, FSH, and testosterone in rats. -
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Estradiol valerate-d4
0 ImagesCat. No.: HY-B0672S1CAS No.: 2673269-82-2Synonyms: β-Estradiol 17-valerate-d4Estradiol valerate-d4 (β-Estradiol 17-valerate-d4) is the deuterated-labeled Estradiol valerate (HY-B0672). Estradiol valerate (β-Estradiol 17-valerate) is a synthetic estrogen widely used in combination with other steroid hormones in hormone replacement therapy agents. -
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ERα degrader 13
0 ImagesCat. No.: HY-172937CAS No.: 3070968-56-5ERα degrader 13 is an orally active, methylene blue-Raloxifene (HY-13738) conjugated photoactivatable ERα degrader with a Kd value of 27.1 nM. Upon irradiation at 660 nm, ERα degrader 13 generates ROS and heat near the ligand-binding domain of ERα, triggering oxidation, residue unfolding, and ERα degradation via the ubiquitin-proteasome system. ERα degrader 13 inhibits cancer cell proliferation and induces tumor regression in breast cancer xenograft models. ERα degrader 13 can be used in breast cancer-related research. -
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ER degrader 13
0 ImagesCat. No.: HY-176956CAS No.: 2839847-93-5ER degrader 13 (Compound 37) is an estrogen receptor (ER) degrader. ER degrader 13 has a significant inhibitory effect on the proliferation of ER-positive breast cancer MCF-7 cells. -
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(E/Z)-Panomifene hydrochloride
0 ImagesCat. No.: HY-122411ACAS No.: 3026790-25-7Synonyms: (E/Z)-EGIS 5650 hydrochloride; (E/Z)-GYKI-13504 hydrochloride -
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Etacstil
0 ImagesCat. No.: HY-112746CAS No.: 155701-61-4Synonyms: DPC974; GW5638Etacstil (GW5638) is a estrogen receptor antagonist that displays minimal uterotropic activity in ovariectomized rats and inhibits the agonist activity of Estradiol (HY-B0141), Tamoxifen (HY-13757A) and Raloxifene (HY-13738) in the environment. Etacstil is promising for research of breast cancer and bone protection. -
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Raloxifene 4'-glucuronide-d4
0 ImagesCat. No.: HY-135582SCAS No.: 1279033-52-1Raloxifene 4'-glucuronide-d4 is deuterated labeled Raloxifene 4'-glucuronide (HY-135582). Raloxifene 4'-glucuronide is a primary metabolite of Raloxifene. Raloxifene 4'-glucuronide formation is mediated mostly by UGT1A10 and UGT1A8. Raloxifene 4'-glucuronide binds to estrogen receptor with an IC50 of 370 μM. . Raloxifene is a selective estrogen receptor modulator. Raloxifene activates TGFβ3 promoter as a full agonist at nanomolar concentrations, and inhibits the estrogen response element-containing vitellogenin promoter expression. -
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TOP5300
0 ImagesCat. No.: HY-160856CAS No.: 1848981-48-5Synonyms: TOP05300TOP5300 is an orally active follicle-stimulating hormone receptor allosteric agonist. TOP5300 can induce the production of testosterone in stromal cells and promote follicular genesis and superovulation in rats. -
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(20S)-Protopanaxatriol (Standard)
0 ImagesSynonyms: 20(S)-APPT (Standard); g-PPT (Standard)(20S)-Protopanaxatriol (Standard) is the analytical standard of (20S)-Protopanaxatriol. This product is intended for research and analytical applications. (20S)-Protopanaxatriol is a metabolite of ginsenoside. (20S)-Protopanaxatriol works through the glucocorticoid receptor (GR) and estrogen receptor (ER), and is also a LXRα inhibitor. (20S)-Protopanaxatriol shows a broad spectrum of antitumor effects. -
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Estrogen receptor antagonist 3
0 ImagesCat. No.: HY-144139CAS No.: 2730011-50-2Estrogen receptor antagonist 3 is a potent antagonist of estrogen receptor (ER). The estrogen signaling system plays an important role in regulating cell growth, differentiation and apoptosis. Estrogen receptor antagonist 3 has the potential for the research of cancer diseases (extracted from patent WO2021213358A1, compound 7). -
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- CV2a
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AhR modulator-1
0 ImagesCat. No.: HY-135671CAS No.: 118174-38-2AhR modulator-1 (compound 6-MCDF) is a selective and orally active aryl hydrocarbon receptor (AhR) modulator. AhR modulator-1 inhibits metastasis, in part, by inhibiting prostatic VEGF production prior to tumor formation. AhR modulator-1 also possess anti-estrogenic properties in rat uterus. -
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β-Zearalenol (Standard)
0 ImagesCat. No.: HY-N6741RCAS No.: 71030-11-0β-Zearalenol (Standard) is the analytical standard of β-Zearalenol (HY-N6741). This product is intended for research and analytical applications. β-Zearalenol is a zearalenone metabolite and Estrogen receptor binder (Kd = 0.406 nM) that induces apoptosis through activation of p53, JNK, and p38 kinases and the mitochondrial apoptosis pathway, while inhibiting CYP19A1 and inducing autophagy via SIRT1. β-Zearalenol is used in research on cardiotoxicity, mycotoxin-induced reproductive toxicity, and breast cancer. -
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Ethisterone-13C2
0 ImagesCat. No.: HY-W766130Synonyms: Pregneninolone-13C2; 17α-Ethynyltestosterone-13C2Ethisterone-13C2 (Pregneninolone-13C2) is the 13C-labeled Ethisterone (HY-B0487). Ethisterone (Pregneninolone; 17α-Ethynyltestosterone) is a synthetic steroidal estrogen, is an orally active steroidal contraceptive agent. Ethisterone has almost no effect on the phagocytic activity of the reticuloendothelial system in male guinea pigs, while in utero exposure can induce abnormalities in the urogenital system of offspring. -
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ER ligand-14-PEG3-Boc
0 ImagesCat. No.: HY-180852ER ligand-14-PEG3-Boc is a conjugate of a target protein ligand and linker, composed of an estrogen receptor ligand and a corresponding linker. ER ligand-14-PEG3-Boc can be used to synthesize PROTACs such as ERB-2 (HY-180850). ERB-2 exhibits good antiproliferative activity against Osimertinib (HY-15772)-resistant non-small cell lung cancer. -
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ER ligand-15
0 ImagesCat. No.: HY-184091CAS No.: 2847831-50-7 -
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Zearalenone in Acetonitrile (Standard)
0 ImagesCat. No.: HY-103447R1CAS No.: 17924-92-4Synonyms: Mycotoxin F2 in Acetonitrile (Standard); Toxin F2 in Acetonitrile (Standard)Zearalenone in Acetonitrile (Standard) is the solution of Zearalenone (Standard) . This product is intended for research and analytical applications. Zearalenone is a mycotoxin produced mainly by fungi belonging to the genus Fusarium in foods and feeds. Possess oestrogenic activity in pigs, cattle and sheep, with low acute toxicity. Causes precocious development of mammae and other estrogenic effects in young gilts. -
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Estrogen receptor α antagonist 1
0 ImagesCat. No.: HY-150692CAS No.: 2580941-45-1Estrogen receptor α antagonist 1 (compound 35) is a highly selective antagonist of estrogen receptor α, with IC50s of 0.02, 6.55 and 7.73 μM for estrogen receptor α, estrogen receptor β and MCF-7 cells, respectively. Estrogen receptor α antagonist 1 can be used for the research of cancer. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
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