43 Results for "

ERβ agonist

" in MedChemExpress (MCE) Product Catalog:
Products (43)

43 Results for "ERβ agonist" in MCE Product Catalog:

19
19 Publications Verification
Cat. No.: HY-100689
CAS No.: 263717-53-9
Purity:  99.11%
Synonyms: PPT
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

Propyl pyrazole triol (PPT) is a selective estrogen receptor alpha (ERα) agonist. The relative binding affinity of Propyl pyrazole triol for ERα (ERα: 49%) around 410 times higher compared with estrogen receptor beta (ERβ: 0.12%) .
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14
14 Cited Publications
Cat. No.: HY-N0377
CAS No.: 578-86-9
Synonyms: 4',7-Dihydroxyflavanone
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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11
11 Cited Publications
Cat. No.: HY-10426
CAS No.: 725247-18-7
Purity:  99.67%
Research Areas:  

Cancer

XCT-790 is a potent and selective inverse agonist for ERRα with an IC50 value of 0.37 μM. XCT-790 induces cell death in chemotherapeutic resistant cancer cells. XCT-790 (Compound 12) is inactive against ERRγ and the estrogen receptors ERα and ERβ .
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7
7 Cited Publications
Cat. No.: HY-B0412
CAS No.: 50-27-1
Synonyms: Oestriol
Estriol (Oestriol), an orally active estrogen, is a ERα and ERβ agonist. Estriol is a potent GPR30 antagonist in estrogen receptor-negative breast cancer cells. Estriol can ameliorate disease severity through immunomodulatory mechanisms that decrease tissue inflammation. Estriol has powerful proconvulsant effects .
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5
5 Cited Publications
Cat. No.: HY-15483
CAS No.: 95167-41-2
Purity:  99.22%
Synonyms: GSK 9089
Research Areas:  

Endocrinology Cancer

DY131 (GSK 9089) is a potent and selective ERRγ and ERRβ agonist. DY131displays inactive against ERRα, ERα and ERβ . DY131 also inhibits Smo signaling .
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4
4 Cited Publications
Cat. No.: HY-14933
CAS No.: 524684-52-4
Purity:  98.05%
Synonyms: ERB-041
Research Areas:  

Cancer

Prinaberel (ERB-041) is a potent and selective estrogen receptor (ER) β agonist with IC50s of 5.4, 3.1 and 3.7 nM for human, rat and mouse ERβ, respectively. Prinaberel displays >200-fold selectivity for ERβ over ERα. Prinaberel is a potent skin cancer chemopreventive agent that acts by dampening the WNT/β-catenin signaling pathway. Prinaberel induces ovarian cancer apoptosis .
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2
2 Cited Publications
Cat. No.: HY-18295
CAS No.: 533884-09-2
Synonyms: LY500307
Target:  

Estrogen Receptor/ERR

Research Areas:  

Neurological Disease Cancer

Erteberel (LY500307) is a potent and selective estrogen receptor beta (ERβ) agonist with Ki and EC50 of 1.54 nM and 3.61 nM, respectively. Erteberel has anti-tumor activities .
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1
1 Cited Publications
Cat. No.: HY-101271
CAS No.: 440122-66-7
Purity:  99.57%
Target:  

Estrogen Receptor/ERR

Research Areas:  

Neurological Disease

WAY-200070 is a selective estrogen receptor β (ERβ) agonist with an IC50 of 2.3 nM.
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1
1 Cited Publications
Cat. No.: HY-N0910
CAS No.: 155683-00-4
Notoginsenoside Ft1 is an orally active bioactive saponin. Notoginsenoside Ft1 inhibits the PI3K/AKT/mTOR signaling pathway, activates the p38 MAPK and ERK1/2 signaling pathways, and increases the proportion of CD8 + T cells, thereby inducing apoptosis and lysosomal cell death in various cancer cells, and promoting angiogenesis. Notoginsenoside Ft1 causes vasodilation by activating glucocorticoid receptors (GR) and estrogen receptor beta (ERβ) in endothelial cells. Notoginsenoside Ft1 increases intracellular Ca 2+ accumulation, reduces cAMP levels by activating a signaling network mediated through P2Y12 receptors, and promotes platelet aggregation, thereby exerting a procoagulant effect. Notoginsenoside Ft1 inhibits ferroptosis (ferroptosis) in renal tubular epithelial cells by activating the TGR5 receptor, thereby demonstrating a renal protective effect. Notoginsenoside Ft1 acts as a TGR5 agonist and an FXR antagonist to combat obesity and insulin resistance .
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1
1 Cited Publications
Cat. No.: HY-B1984
CAS No.: 72-54-8
Synonyms: 4,4'-DDD; p,p'-Dichlorodiphenyl dichloroethane
p,p'-DDD (4,4’-DDD) is an organochlorine insecticide, a major metabolite of p,p'-DDT. p,p'-DDD is an agonist at estrogen receptor α(ERα) and ERβ. p,p'-DDD increases DNA damage, apoptosis and necrosis in peripheral blood. p,p'-DDD stimulates cell proliferation in SKBR3 cells. p,p'-DDD activates the AP-1 transcription factor. p,p'-DDD decreases sleep times of barbiturates and steroids in rats .
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Cat. No.: HY-U00425
CAS No.: 1264754-13-3
PROTAC 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 ERα c, 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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Cat. No.: HY-137004
CAS No.: 848142-62-1
Purity:  98.72%
Synonyms: Ind-Cl
Research Areas:  

Inflammation/Immunology

Indazole-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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Cat. No.: HY-110157
CAS No.: 1421854-16-1
Purity:  99.61%
Target:  

Estrogen Receptor/ERR

Research Areas:  

Neurological Disease

AC-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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Cat. No.: HY-108414
CAS No.: 221054-79-1
Purity:  98.93%
Synonyms: (+)-Equol
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

(R)-Equol is an agonist of both ERα and ERβ with Kis of 27.4 and 15.4 nM, respectively.
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Cat. No.: HY-151230
CAS No.: 533884-08-1
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

(-)-Erteberel is a selective estrogen receptor beta (ERβ) agonist. (-)-Erteberel can be utilized in the study of diseases mediated by estrogen receptor beta (ERβ), such as prostate cancer .
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Cat. No.: HY-149584
CAS No.: 2862784-20-9
Purity:  99.91%
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

CIDD-0149897 is a potent, selective and brain-penetrant ERβ agonist. CIDD-0149897 exert antitumor functions in glioblastoma .
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Cat. No.: HY-W114419
CAS No.: 79-97-0
Bisphenol C is an estrogen receptor-α (ERα) agonist and an ERβ antagonist, with IC50 values of 2.65 nM for ERα and 1.94 nM for ERβ. Bisphenol C is a material of manufacturing polyester polymers like polycarbonate, is widely used in daily items like water bottles, food packaging, textile and so on .
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Cat. No.: HY-173474
CAS No.: 2412715-30-9
Research Areas:  

Cancer

ERβ agonist-1 (Compound 8) is a dual-active selective ERβ agonist (EC50: 46.8 nM) and AR antagonist (IC50: 1555 nM). ERβ agonist-1 activates ERβ signaling by binding to ERβ and inhibits AR activity. ERβ agonist-1 retains selective ERβ agonist activity in mouse models and can be used to study prostate cancer .
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Cat. No.: HY-19468
CAS No.: 550997-55-2
Synonyms: WAY-202196
ERB-196 is a nonsteroidal selective estrogen receptor-β (ERβ) agonist.
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Cat. No.: HY-103446
CAS No.: 1111084-78-6
Target:  

Estrogen Receptor/ERR

Research Areas:  

Endocrinology

FERb 033 is a selective and potent ERβ agonist (Ki=7.1 nM, EC50=4.8 nM). FERb 033 shows 62-fold selectivity over ERα .
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