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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 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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Org 214444-0
0 ImagesCat. No.: HY-182705CAS No.: 914093-78-0Org 214444-0 is an orally active, nanomolar-potent and selective FSHR agonist, with EC50 values of 2.0 nM and 1.2 nM in human and rat (measured in CHO cells). Org 214444-0 activates human granulosa cells in vitro, supports rat follicular development and induces ovulation in vivo. Org 214444-0 can be used for the research of infertility. -
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ER covalent antagonist-1
0 ImagesCat. No.: HY-170382CAS No.: 2757498-74-9ER covalent antagonist-1 (Compound 39D) is the antagonist for estrogen receptor α (ERα). ER covalent antagonist-1 inhibits the proliferation of ERα-positive cell MCF-7 with an IC50 of 0.98 μM, arrests the cell cycle at G0/G1 phase, and induces apoptosis. ER covalent antagonist-1 exhibits antitumor efficacy in mouse model. -
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Toremifene-d6 hydrochloride
0 ImagesCat. No.: HY-B0005S1Synonyms: Z-Toremifene-d6 hydrochloride; NK 622-d6 hydrochloride; FC-1157a-d6 hydrochlorideToremifene-d6 (Z-Toremifene-d6) hydrochloride is deuterium labeled Toremifene. Toremifene is a second-generation selective estrogen-receptor modulator (SERM) in development for the prevention of osteoporosis. Toremifene also potent inhibits infectious EBOV Zaire and Marburg (MARV) with IC50 of 0.07 µM and 2.6 µM, respectively. -
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Estrone acetate
0 ImagesEstrone acetate (Hogival) is an estrogen derivative and an estrogen receptor (ER) activator. It promotes mammary gland development, stimulates pituitary prolactin secretion, and induces the proliferation and activation of lactotrophs (e.g., by reducing prolactin storage granule size while increasing rough endoplasmic reticulum and Golgi apparatus volume density). Estrone acetate holds potential for endocrine research, particularly in studying estrogen's effects on pituitary function, prolactin regulation, and mammary tumor models. -
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ER degrader 1
0 ImagesCat. No.: HY-142925CAS No.: 2667015-33-8ER degrader 1 is a potent degrader of estrogen receptor (ER). The estrogen signaling system plays an important role in regulating cell growth, differentiation and apoptosis. ER degrader 1 has the potential for the research of cancer diseases (extracted from patent WO2021139756A1, compound 11). -
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ER ligand-16
0 ImagesCat. No.: HY-184999ER ligand-16 is a PROTAC target protein ligand that binds specifically to Estrogen Receptor, and it is applicable to research related to PROTAC synthesis, such as serving as the target protein ligand for PROTAC ERα Degrader-4 (HY-149295). -
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CDD-1274
0 ImagesCat. No.: HY-179510CDD-1274 is an ERα (Estrogen receptor α) variant inhibitor. CDD-1274 induces proteasomal degradation of ERα variants in breast cancer cell lines and causes Y537S ERα degradation. CDD-1274 potently blocks ligand-dependent and ligand-independent ER signaling in endocrine-resistant breast cancer cells. CDD-1274 can be used for the study of breast cancer. -
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PROTAC ERα Degrader-7
0 ImagesCat. No.: HY-160562CAS No.: 3025781-93-2PROTAC ERα Degrader-7 (compound i-320) is a potent estrogen receptor alpha(ERα) PROTAC degrader with a DC50 value of 0.000006 µM. PROTAC ERα Degrader-7 comprises a cereblon-binding moiety LBM linked to a ligand ERBM that binds ERα and comprises a benzofused partially saturated 6-membered carbocyclic or heterocyclic ring. -
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Estrogen receptor modulator 12
0 ImagesCat. No.: HY-119088CAS No.: 554431-74-2Estrogen receptor modulator 12 (compound 1a-(R)) is a selective estrogen receptor modulator with estrogen agonist and antagonist activities in in vivo models. Estrogen receptor modulator 12 exhibits antagonist effects on the uterus and estrogen agonist activities on bone, plasma lipids, hot flashes, and vagina in in vivo models, and is a potential compound for suppressing postmenopausal symptoms. -
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- NEP168
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Zeranol-d5 (mixture of diastereomers)
0 ImagesCat. No.: HY-W777284CAS No.: 1217532-71-2 -
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AZD9496 deacrylic acid phenol
0 ImagesCat. No.: HY-46340CAS No.: 2173404-70-9 -
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Diptoindonesin G
0 ImagesCat. No.: HY-125037CAS No.: 1190948-58-3Diptoindonesin G is a 2-arylbenzofuran derivative and a modulator of estrogen receptor and HSP90 middle domain. Diptoindonesin G exhibits strong cytotoxicity against mouse leukemia P-388 cells with an IC50 of 13.2 μM. Diptoindonesin G has antitumor activity and can be used in the research of tumors such as breast cancer. -
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4H-Chromen-4-one-o-carborane
0 ImagesCat. No.: HY-183187CAS No.: 3097646-96-0 -
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LX-039
0 ImagesCat. No.: HY-143439CAS No.: 2135341-09-0LX-039 is a highly potent, selective and orally active estrogen receptor degrader with EC50 value of 2.29 nM. LX-039 has indole C-3 chlorine atom. LX-039 exhibits excellent mouse pharmacokinetics, low clearance, high Cmax and oral exposure. LX-039 has anti-tumor activity. -
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- Arg-TERRα
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Estrogen receptor modulator 11
0 ImagesCat. No.: HY-164726CAS No.: 96719-63-0Estrogen receptor modulator 11 (Compound 27) is a tetrahydroisoquinoline derivative. Estrogen receptor modulator 11 has a certain affinity for estrogen receptors (ER), with IC50 values of 285 nM and 421 nM for ERα and ERβ, respectively. Estrogen receptor modulator 11 lacks antagonist activity in the MCF-7 cellular assay. -
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Gypenoside XVII (Standard)
0 ImagesSynonyms: Gynosaponin S (Standard)Gypenoside XVII (Standard) is the analytical standard of Gypenoside XVII. This product is intended for research and analytical applications. Gypenoside XVII, a novel phytoestrogen belonging to the gypenosides, can activate estrogen receptors. -
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ER degrader 3
0 ImagesCat. No.: HY-142927CAS No.: 2254818-47-6ER degrader 3 is a potent degrader of estrogen receptor (ER). The estrogen signaling system plays an important role in regulating cell growth, differentiation and apoptosis. ER degrader 3 has the potential for the research of cancer diseases (extracted from patent WO2018233591A1, compound 1). -
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RU 45144
0 ImagesCat. No.: HY-118242CAS No.: 119286-92-9RU 45144 is an anti-estrogen compound that has the activity of antagonizing the binding of estrogen receptors to calmodulin. RU 45144 can inhibit the binding of estrogen receptors to calmodulin, and its effect is similar to that of tamoxifen. Its anti-estrogen effect may be related to specific side chains in the molecular structure, and the steroid skeleton may be involved in its anti-proliferative activity. -
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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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