- Signaling Pathways
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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 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 (819)
Related Products (819)
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Recombinant Proteins (2)
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Antibodies (11)
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Estrogen Receptor/ERR Isoform Comparison
- 3-Formylsalicylic acid
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Ferutinin
0 ImagesFerutinin, a natural terpenoid compound, is an estrogen receptor ERα agonist and estrogen ERβ-receptor agonist/antagonist with IC50s of 33.1 nM and 180.5 nM, respectively. Ferutinin acts as an electrogenic Ca2+-ionophore that increases calcium permeability of lipid bilayer membranes, mitochondria. Ferutinin possesses estrogenic, antitumor, antibacterial and antiinflammatory activities. -
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PROTAC ERα Degrader-4
0 ImagesPROTAC ERα Degrader-4 (Compound ZD12) is a highly potent and selectivePROTAC ERα degrader (Ki: 5.08 μM). PROTAC ERα Degrader-4 contains OBHSAs, linker and E3 ligase ligands. PROTAC ERα Degrader-4 shows excellent cell inhibitory and ERα degradation activity against Tamoxifen-sensitive and -resistant ER+ breast cancer (BC) cells and ERα-mutated BC cells. PROTAC ERα Degrader-4 can induce apoptosis and can be used for cancer research. -
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7α-(Thiomethyl)spironolactone
0 ImagesSynonyms: 7α-Thiomethylspironolactone7α-(Thiomethyl)spironolactone is a nuclear steroid receptor antagonist that can be used for the research of coronaviruses. -
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PROTAC ERRα ligand 1
0 ImagesPROTAC ERRα ligand 1 is a PROTAC target protein ligand. PROTAC ERRα ligand 1 is an orally active ERRα inverse agonist with IC50 values of 0.6 μM for ERRα. PROTAC ERRα ligand 1 shows no significant activity against a panel of other nuclear receptors, including ERαc, ERRγ, ERβ, PPARα, PPARγ, PPARδ, and RXRα. PROTAC ERRα ligand 1 can provide enhanced insulin sensitivity in vivo. PROTAC ERRα ligand 1 can be used for metabolic diseases research, such as type 2 diabetes and obesity. -
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- Ethinylestradiol (Standard)
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Tamoxifen-d5
0 ImagesSynonyms: ICI 47699-d5; (Z)-Tamoxifen-d5; trans-Tamoxifen-d5Tamoxifen-d5 is a deuterium labeled Tamoxifen. Tamoxifen (ICI 47699) is an orally active, selective estrogen receptor modulator (SERM). Tamoxifen is a potent Hsp90 activator and enhances the Hsp90 molecular chaperone ATPase activity. -
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Idoxifene
0 ImagesSynonyms: CB7432Idoxifene (CB7432) is a novel tissue-specific selective estrogen receptor modulator (SERM). -
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Taragarestrant meglumine
0 ImagesSynonyms: D-0502 meglumineTaragarestrant (D-0502) meglumine is a potent, orally active and selective estrogen receptor degrader (SERD). Taragarestrant meglumine shows potent activity in various ER+ breast cancer cell lines and xenograft models. -
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H3B-6545 hydrochloride
0 ImagesH3B-6545 hydrochloride is an oral, selective estrogen receptor covalent antagonist (SERCA) for the research of metastatic ER-positive, HER2-negative breast cancer. -
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AZ'6421
0 ImagesAZ'6421 is an orally active ERα PROTAC degrader with a DC50 of 0.4 nM. AZ'6421 recruits the VHL E3 ligase to form a ternary complex, inducing proteasome-mediated polyubiquitination and degradation of ERα. AZ'6421 inhibits the growth of ER+ cancer cells. AZ'6421 can be used in studies related to ER+ breast cancer. -
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Isocurcumenol
0 ImagesIsocurcumenol, an estrogen receptor alpha (ERα) inhibitor isolated from Curcuma zedoaria Rhizomes, possesses anti-tumor acticity, with IC50 values of 99.1μg/mL and 178.2 μg/mL in DLA and KB cells, respectively. -
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Enclomiphene
0 ImagesSynonyms: (E)-Clomiphene; trans-Clomiphene; EnclomifeneEnclomiphene ((E)-Clomiphene) is a potent and orally active non-steroidal estrogen receptor antagonist, with antioestrogenic property. Enclomiphene can be used for the research of ovarian dysfunction, testosterone deficiency, male hypogonadism and type 2 diabetes. -
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Cyproterone
0 ImagesCyproterone is an antiandrogen that suppresses the actions of testosterone via blocking androgen receptors. Cyproterone’s acetate form can be used in the research of hypersexuality and prostate cancer. -
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Estrogen receptor-agonist-1
0 ImagesEstrogen receptor-agonist-1 (compound 4e) is a estrogen receptor (ER) agonist that binds to ERα with high affinity. -
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Zuclomiphene citrate
0 ImagesZuclomiphene citrate is a cis isomer of Clomiphene citrate (HY-B0463). Zuclomiphene citrate is orally active and has an antiestrogenic effect. Zuclomiphene can reduce cholesterol levels. Zuclomiphene citrate can be for the researches of endocrinology and metabolic disease. -
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GPR30 agonist-1
0 ImagesGPR30 agonist-1 is a G protein-coupled receptor 30 (GPR30) agonist. GPR30 agonist-1 exerts vasorelaxant effects. -
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Zeranol
0 ImagesSynonyms: α-ZearalanolZeranol, a metabolite of the mycoestrogen zearalenone, is an estrogen receptor agonist. Zeranol is used as a growth promoter of livestock due to its strong estrogenic activity. -
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Propylparaben-d4
0 ImagesSynonyms: Propyl parahydroxybenzoate-d4; Propyl 4-hydroxybenzoate-d4Propylparaben-d4 (Propyl parahydroxybenzoate-d4) is the deuterium labeled Propylparaben (HY-N2026). Propylparaben (Propyl parahydroxybenzoate) is an antibacterial preservative that can be produced by plants and bacteria. Propylparaben is an orally active weak estrogen receptor agonist. Propylparaben regulates the PI3K-AKT and JNK signaling pathways, and induces oxidative stress. Propylparaben is commonly used in cosmetics, pharmaceuticals and foods, and can be used in studies related to ovarian aging and myocardial ischemia-reperfusion injury. -
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Fulvestrant-d3
0 ImagesCat. No.: HY-13636SSynonyms: ICI 182780-d3; ZD 9238-d3; ZM 182780-d3Fulvestrant-d3 is the deuterium labeled Fulvestrant. Fulvestrant (ICI 182780) is a pure antiestrogen and a potent estrogen receptor (ER) antagonist with an IC50 of 9.4 nM. Fulvestrant is also a GPR30 agonist. Fulvestrant effectively inhibits the growth of ER-positive MCF-7 cells with an IC50 of 0.29 nM. Fulvestrant also induces autophagy and has antitumor efficacy. -
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Your Search Returned No Results.
Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
try each isoform separately.