- 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 (823)
Related Products (823)
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Recombinant Proteins (2)
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Antibodies (11)
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Estrogen Receptor/ERR Isoform Comparison
- α-Zearalenol
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H3B-5942
0 ImagesH3B-5942 is a selective, irreversible and orally active estrogen receptor covalent antagonist, inactivates both wild-type and mutant ERα by targeting Cys530, with Kis of 1 nM and 0.41 nM, respectively. H3B-5942 reduces ERα target gene GREB1, shows potent antitumor activity both in multiple cell lines or animals bearing ERαWT or ERα mutations. -
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- Regaloside C
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- 2-Hydroxyestrone
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- MC-Val-Cit-PAB-PROTAC ERα Degrader-1
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- BHPI
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- 3-Formylsalicylic acid
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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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PELP1-IN-1
0 ImagesPELP1-IN-1 is a PELP1 inhibitor and an apoptosis inducer with no cytotoxic activity against non-cancer cell lines. PELP1-IN-1 targets wild-type, mutant and drug-resistant ER+ breast cancer, and promotes PELP1 degradation through the proteasome pathway. As an analog of SMIP34 (HY-169903), PELP1-IN-1 is applicable to the research of estrogen receptor α-positive breast cancer. -
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2-Hydroxyestrone-d4
0 ImagesCat. No.: HY-113251SCAS No.: 81586-97-2Synonyms: Catecholestrone-d42-Hydroxyestrone-d4 is the deuterium labeled 2-Hydroxyestrone. 2-Hydroxyestrone (Catecholestrone) is a specific receptor-mediated antiestrogenic agent. 2-Hydroxyestrone is anticarcinogenic. -
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Bexirestrant
0 ImagesBexirestrant is an orally active ER-α degrader. Bexirestrant can be used for the research of antiestrogen, antineoplastic. -
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2-Ethylhexyl diphenyl phosphate
0 ImagesCat. No.: HY-W009066CAS No.: 1241-94-7Synonyms: EHDPP; Octicizer2-Ethylhexyl diphenyl phosphate is an organophosphate flame retardants (OPFRs) and a PPARG agonist (EC20: 2.04 µM). 2-Ethylhexyl diphenyl phosphate also inhibits ERRγ transcriptional activity (IC50: 1.3 µM). 2-Ethylhexyl diphenyl phosphate upregulates 3β-HSD1, human chorionic gonadotropin (hCG) and progesterone secretion. 2-Ethylhexyl diphenyl phosphate can be used in studies of female reproduction and fetal development. -
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- PROTAC ERα Degrader-1
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- PROTAC ERRα Degrader-1
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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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- 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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- (E/Z)-GSK5182
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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.