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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 Chemicals
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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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Bazedoxifene-d4
0 ImagesCat. No.: HY-A0031SCAS No.: 1133695-49-4Synonyms: TSE-424-d4Bazedoxifene-d4 is deuterium labeled Bazedoxifene. Bazedoxifene (TSE-424) is an oral, BBB-penetrant nonsteroidal selective estrogen receptor modulator (SERM), with IC50s of 23 nM and 99 nM for ERα and ERβ, respectively. Bazedoxifene can be used for the research of osteoporosis. Bazedoxifene also acts as an inhibitor of IL-6/GP130 protein-protein interactions and can be used for the research of pancreatic cancer[1][2]. -
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Dienestrol-d8
0 ImagesCat. No.: HY-B1403S2Dienestrol-d8 is the deuterated-labeled Dienestrol (HY-B1403). Dienestrol is an orally active nonsteroidal estrogen. Dienestrol prevents the formation of implantation swellings in the uterus by inhibiting ovum discharge. -
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Ethisterone (Standard)
0 ImagesSynonyms: Pregneninolone (Standard); 17α-Ethynyltestosterone (Standard)Ethisterone (Pregneninolone; 17α-Ethynyltestosterone) (Standard) is the analytical standard of Ethisterone (HY-B0487). This product is intended for research and analytical applications. Ethisterone 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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Tracheloside (Standard)
0 ImagesCat. No.: HY-N1507RCAS No.: 33464-71-0Tracheloside (Standard) is the analytical standard of Tracheloside. This product is intended for research and analytical applications. Tracheloside is an antiestrogenic lignin. Tracheloside promotes keratinocyte proliferation through ERK1/2 stimulation. Tracheloside is a good candidate to promote wound healing. -
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E2-CDS
0 ImagesCat. No.: HY-106828CAS No.: 103562-82-9Synonyms: Estradiol 17-DihydrotrigonellineE2-CDS (Estradiol 17-Dihydrotrigonelline) is a redox-based chemical delivery system for estradiol (E2). E2-CDS is capable of sustained and brain-selective delivery of estradiol. -
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Estrone-N-O-C1-amido
0 ImagesCat. No.: HY-111845CAS No.: 138219-84-8Synonyms: ERα ligand 1Estrone-N-O-C1-amido (ERα ligand 1) is an Estrone-based estrogen ligand, which targets estrogen receptor α (ERα). Estrone-N-O-C1-amido (ERα ligand 1) binds to cIAP1 ligand Bestatin via a linker to form SNIPER. -
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ERα ligand 4
0 ImagesCat. No.: HY-W749028CAS No.: 97818-93-4ERα ligand 4 is a ligand of ERα and can be used for the synthesis of PROTACs, such as NEP168 (HY-180959). -
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Estradiol-13C6
0 ImagesCat. No.: HY-B0141S4Synonyms: β-Estradiol-13C6; E2-13C6; 17β-Estradiol-13C6; 17β-Oestradiol-13C6Estradiol-13C6 is the 13C-labeled Estradiol. Estradiol is a steroid sex hormone vital to the maintenance of fertility and secondary sexual characteristics in females. Estradiol upregulates IL-6 expression through the estrogen receptor β (ERβ) pathway. -
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(E/Z)-4-Hydroxytamoxifen (Standard)
0 ImagesSynonyms: Afimoxifene (Standard); 4-OHT (Standard)(E/Z)-4-Hydroxytamoxifen (Standard) is the analytical standard of (E/Z)-4-Hydroxytamoxifen. This product is intended for research and analytical applications. (E/Z)-4-Hydroxytamoxifen (Afimoxifene) is a racemic compound of (Z)-4-Hydroxytamoxifen and (E)-4-Hydroxytamoxifen isomers. (E/Z)-4-Hydroxytamoxifen is a selective estrogen receptor modulator with mixed estrogenic and antiestrogenic activity, which is also an active metabolite of Tamoxifen (HY-13757A). (E/Z)-4-Hydroxytamoxifen is an agonist of the G protein-coupled estrogen receptor (GPER) with relatively low affinity (100-1000 nM). (E/Z)-4-Hydroxytamoxifen is promising for research of cyclical mastalgia, such as breast pain, tenderness, and nodularity. -
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Diethylstilbestrol-d4
0 ImagesCat. No.: HY-W744064CAS No.: 2519535-80-7Diethylstilbestrol-d4 is the deuterium labeled Diethylstilbestrol (HY-14598). Diethylstilbestrol is a non-steroidal female hormone that has oral activity and can act on menopausal and postmenopausal disorders. Diethylstilbestrol can induce DNA oxidation and?Apoptosis?of spermatogonial stem cells. Diethylstilbestrol can induce thymocyte?Autophagy?Diethylstilbestrol is a?11β-hydroxysteroid dehydrogenase 2 (HSD11B2)?inhibitor. -
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rel-Erteberel
0 ImagesCat. No.: HY-18295ACAS No.: 533883-77-1Synonyms: rel-LY500307 -
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Etonogestrel (Standard)
0 ImagesSynonyms: 3-Oxodesogestrel (Standard); 3-keto-Desogestrel (Standard)Etonogestrel (Standard) is the analytical standard of Etonogestrel. This product is intended for research and analytical applications. Etonogestrel (3-Oxodesogestrel), a biologically active metabolite of progestin Desogestrel, binds with high affinity to progesterone receptors and estrogen receptors in the target organs. Etonogestrel induce FKBP51 mRNA and protein expression in cultured human endometrial stromal cells (HESCs). -
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Estradiol enanthate (Standard)
0 ImagesEstradiol enanthate (Standard) is the analytical standard of Estradiol enanthate. Estradiol enanthate (E2EN) is a shorter-acting estrogen. Estradiol enanthate is an injectable contraceptive in combination with Dihydroxyprogesterone acetophenide. Estradiol enanthate promotes withdrawal bleeding, in a pattern similar to menstruation. -
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Liquiritigenin-d4
0 ImagesCat. No.: HY-N0377SSynonyms: 4',7-Dihydroxyflavanone-d4Liquiritigenin-d4 (4',7-Dihydroxyflavanone-d4) is the deuterium labeled Liquiritigenin (HY-N0377). Liquiritigenin, a flavanone isolated from Glycyrrhiza uralensis, is a highly selective estrogen receptor β (ERβ) agonist with an EC50 of 36.5 nM for activation of the ERE tk-Luc. -
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Etonogestrel-d6
0 ImagesCat. No.: HY-B0652S1Synonyms: 3-Oxodesogestrel-d6; 3-keto-Desogestrel-d6Etonogestrel-d6 is deuterium labeled Etonogestrel. Etonogestrel (3-Oxodesogestrel), a biologically active metabolite of progestin Desogestrel, binds with high affinity to progesterone receptors and estrogen receptors in the target organs. Etonogestrel induce FKBP51 mRNA and protein expression in cultured human endometrial stromal cells (HESCs). -
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rel-Vepdegestrant
0 ImagesCat. No.: HY-138642BCAS No.: 2614417-52-4Synonyms: rel-ARV-471; rel-PF-07850327(Rac)-Vepdegestrant is the relative configuration of Vepdegestrant (HY-138642). Vepdegestrant is an orally active PROTAC estrogen receptor degrader against breast cancer. Vepdegestrant is a hetero-bifunctional molecule that facilitates the interactions between estrogen receptor alpha and an intracellular E3 ligase complex. Vepdegestrant leads to the ubiquitylation and subsequent degradation of estrogen receptors via the proteasome. Vepdegestrant robustly degrades ER in ER-positive breast cancer cell lines with a half-maximal degradation concentration (DC50) of about 2 nM. -
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ERRγ-IN-1
0 ImagesCat. No.: HY-177011CAS No.: 2170732-60-0ERRγ-IN-1 is a ERRγ inhibitor with an IC50 of 0.040 μM. ERRγ-IN-1 activates MAPK (p44/p42) and inhibits the activity of ERRγ. ERRγ-IN-1 significantly increases iodine uptake in anaplastic thyroid carcinoma xenografts and suppresses tumor growth in nude mice. ERRγ-IN-1 is applicable for the research of anaplastic thyroid carcinoma. -
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ER degrader 6
0 ImagesCat. No.: HY-155196CAS No.: 2922929-62-0ER degrader 6 (compound 35s) is a potent Estrogen Receptor (ER)α degrader. ER degrader 6 disrupts the microtubule network by restraining tubulin polymerization. ER degrader 6 suppresses tumor growth without noticeable poisonousness. -
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ERβ agonist-2
0 ImagesCat. No.: HY-186074CAS No.: 628321-25-5ERβ agonist-2 (Page 72) is a selective ERβ agonist with an EC50 of 800 nM or lower. ERβ agonist-2 selectively inhibits T cell activation and/or proliferation, thereby reducing circulating T cell levels in subjects, without exerting significant effects on circulating neutrophil, monocyte or B cell levels. ERβ agonist-2 is applicable to studies of chronic heart failure after myocardial infarction, as well as graft-versus-host disease, multiple sclerosis and experimental autoimmune encephalomyelitis. -
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E,E-Dienestrol-d6-1
0 ImagesCat. No.: HY-B1403S1E,E-Dienestrol-d6-1 is a deuterated labeled Dienestrol. -
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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.