- Signaling Pathways
- Vitamin D Related/Nuclear Receptor
- Estrogen Receptor/ERR
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 Antagonists
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Estrogen Receptor/ERR Activators
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Estrogen Receptor/ERR Modulators
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Estrogen Receptor/ERR Chemicals
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Estrogen Receptor/ERR Degraders
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Estrogen Receptor/ERR Controls
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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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2-Bromoestradiol
0 Images2-Bromoestradiol is a estrogen 2-hydroxylase inhibitor. 2-Bromoestradiol decreases irreversible binding of radiolabeled estradiol metabolite(s) to microsomal proteins. -
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GTX-758
0 ImagesGTX-758 is an orally active, nonsteroidal, selective agonist of ERα. GTX-758 plays an important role in castration resistant prostate cancer (CRPC) research. -
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Estrogen receptor β antagonist 2
0 ImagesEstrogen receptor β antagonist 2 is a potent and selective estrogen receptor β (ERβ) antagonist with IC50s of 109.10, 0.63 µM for Erα and Erβ, respectively. -
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- Lindleyin
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AC-186
0 ImagesAC-186 is a selective non-steroidal estrogen receptor β (ERβ) agonist with EC50s of 6 nM and 5000 nM for ERβ and ERα, respectively. AC-186 shows gender selective neuroprotective effects in a male rat model of Parkinson's disease. -
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Indazole-Cl
0 ImagesSynonyms: Ind-ClIndazole-Cl (Ind-Cl) is an Estrogen receptor (ER)-β-specific agonist with inflammatory effect. Indazole-Cl inhibits cyclooxygenase-2 exression reduction induced by hypoxia. And Indazole-Cl inhibits ROS production. Indazole-Cl also inhibits cell migration and invasion by hypoxia increased by hypoxia. Indazole-Cl is potent inhibitor of hypoxia-induced inflammation in vascular smooth muscle cells (VSMCs). -
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4,4'-Iminodiphenol
0 Images4-Propionamidophenol (compound 4a) is an inactive estrogen receptor ligand based on the diphenylamine skeleton. -
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- PROTAC ERα Degrader-6
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FSH receptor antagonist 1
0 ImagesCat. No.: HY-149105CAS No.: 487064-35-7FSH receptor antagonist 1 (compound 10) is a potent antagonist of the G(s)-protein-coupled human follicle-stimulating hormone (FSH) receptor. FSH receptor antagonist 1 exhibits an IC50 of 28 nM on a cell line expressing the human FSH receptor. FSH receptor antagonist 1 significantly inhibits follicle growth and ovulation in an ex vivo mouse model. -
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Chlorothalonil (Standard)
0 ImagesChlorothalonil (Standard) is the analytical standard of Chlorothalonil. This product is intended for research and analytical applications. Chlorothalonil is a broad-spectrum foliar fungicide with oral activity. Chlorothalonil can be used to combat fungal diseases in vegetable and crop leaves. Chlorothalonil can alter the microbial community in the soil. Chlorothalonil inhibits spermatogenesis. Chlorothalonil can cause intestinal epithelial barrier dysfunction and fetal toxicity. -
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4'-Hydroxytamoxifen
0 Images4'-Hydroxytamoxifen is a metabolite of Tamoxifen. 4'-Hydroxytamoxifen shows higher affinity for the ER than Tamoxifen. 4'-Hydroxytamoxifen induces a non-apoptotic cytotoxic effect in human endometrial adenocarcinoma cells. -
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- Chrysin (Standard)
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4,7-Dihydroxycoumarin
0 Images4,7-Dihydroxycoumarin is an EGFR inhibitor, estrogen receptor inhibitor, and progesterone receptor inhibitor. 4,7-Dihydroxycoumarin against breast cancer cells with an IC50 velue of 18.36 μg/mL. 4,7-Dihydroxycoumarin can be used for the research of breast cancer. -
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- Fulvestrant-3-boronic acid
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4,4'-Oxydiphenol
0 ImagesCat. No.: HY-W014798CAS No.: 1965-09-9Synonyms: 4,4'-Dihydroxydiphenyl ether4,4'-Oxydiphenol (4,4'-Dihydroxydiphenyl ether) is an inhibitor of estrogen receptor (IC50 = 60 μM ) . -
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(-)-(S)-Equol (Standard)
0 Images(-)-(S)-Equol (Standard) is the analytical standard of (-)-(S)-Equol. This product is intended for research and analytical applications. (-)-(S)-Equol is a high affinity ligand for estrogen receptor β with a Ki of 0.73 nM. -
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Cholesterol-13C5
0 ImagesCholesterol-13C5 is the 13C-labeled Cholesterol. Cholesterol is the major sterol in mammals. It is making up 20-25% of structural component of the plasma membrane. Plasma membranes are highly permeable to water but relatively impermeable to ions and protons. Cholesterol plays an important role in determining the fluidity and permeability characteristics of the membrane as well as the function of both the transporters and signaling proteins. Cholesterol is also an endogenous estrogen-related receptor α (ERRα) agonist. -
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- (E/Z)-GSK5182
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Estrone-d2
0 ImagesSynonyms: E1-d2; Oestrone-d2Estrone-d2 is the deuterium labeled Estrone. Estrone (E1) is a natural estrogenic hormone. Estrone is the main representative of the endogenous estrogens and is produced by several tissues, especially adipose tissue. Estrone is the result of the process of aromatization of androstenedione that occurs in fat cells. -
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Tamoxifen-d3 hydrochloride
0 ImagesCat. No.: HY-13757SPurity: 98.99%Synonyms: ICI 46474-d3 hydrochloride; (Z)-Tamoxifen-d3 hydrochloride; trans-Tamoxifen-d3 hydrochlorideTamoxifen-d3 hydrochloride is deuterated labeled Tamoxifen (Citrate) (HY-13757). Tamoxifen Citrate (ICI 46474) is an orally active, selective estrogen receptor modulator (SERM) which blocks estrogen action in breast cells and can activate estrogen activity in other cells, such as bone, liver, and uterine cells.Tamoxifen Citrate is a potent Hsp90 activator and enhances the Hsp90 molecular chaperone ATPase activity. Tamoxifen Citrate also potent inhibits infectious EBOV Zaire and Marburg (MARV) with IC50 of 0.1 μM and 1.8 μM, respectively. Tamoxifen Citrate activates autophagy and induces apoptosis.Tamoxifen Citrate also can induce gene knockout of CreER(T2) transgenic mouse. -
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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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