30 Results for "

ERα agonist

" in MedChemExpress (MCE) Product Catalog:
Products (30)

30 Results for "ERα 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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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-111226
CAS No.: 877387-37-6
Purity:  99.85%
GSK5182 is a highly selective and orally active inverse agonist of estrogen-related receptor γ (ERRγ) with an IC50 of 79 nM. GSK5182 does not interact with other nuclear receptors, including ERRα or ERα. GSK5182 also induces reactive oxyen species (ROS) generation in hepatocellular carcinoma (HCC) .
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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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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-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-125703
CAS No.: 41743-44-6
Purity:  99.23%
Ferutinin, 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 Ca 2+-ionophore that increases calcium permeability of lipid bilayer membranes, mitochondria. Ferutinin possesses estrogenic, antitumor, antibacterial and antiinflammatory activities .
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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-W1006471
CAS No.: 263717-32-4
Target:  

Estrogen Receptor/ERR

Research Areas:  

Endocrinology

Estrogen receptor-agonist-1 (compound 4e) is a estrogen receptor (ER) agonist that binds to ERα with high affinity .
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Cat. No.: HY-111061
CAS No.: 938067-78-8
Purity:  99.59%
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

GTX-758 is an orally active, nonsteroidal, selective agonist of ERα. GTX-758 plays an important role in castration resistant prostate cancer (CRPC) research .
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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-126932
CAS No.: 1607819-68-0
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

TTC-352 is an orally bioavailable selective human estrogen receptor (ER) α partial agonist (ShERPA). TTC-352 inhibits the growth of three ER+ breast cancer cells. TTC-352 induces tumor regression accompanied by exit of ERα from the nucleus to extranuclear sites .
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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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Cat. No.: HY-B1984S
CAS No.: 93952-20-6
Synonyms: 4,4'-DDD-d8; p,p'-Dichlorodiphenyl dichloroethane-d8
p,p'-DDD-d8 is the deuterium labeled p,p'-DDD[1]. 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-103451
CAS No.: 221368-54-3
Purity:  ≥99.0%
Target:  

Estrogen Receptor/ERR

Research Areas:  

Metabolic Disease

(R,R)-THC is an ERα agonist and an ERβ antagonist, with Kis of 9.0 nM and 3.6 nM for ERα and ERβ, respectively. (R,R)-THC has higher relative binding affinity for ERβ than ERα with the values of 25 and 3.6 .
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Cat. No.: HY-103451A
CAS No.: 138090-06-9
Target:  

Estrogen Receptor/ERR

Research Areas:  

Metabolic Disease

rel-(R,R)-THC is the relative configuration of (R,R)-THC (HY-103451). (R,R)-THC is an ERα agonist and an ERβ antagonist, with Kis of 9.0 nM and 3.6 nM for ERα and ERβ, respectively. (R,R)-THC has higher relative binding affinity for ERβ than ERα with the values of 25 and 3.6 .
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Cat. No.: HY-100689R
CAS No.: 263717-53-9
Synonyms: PPT (Standard)
Research Areas:  

Cancer

Propyl pyrazole triol (Standard) is the analytical standard of Propyl pyrazole triol. This product is intended for research and analytical applications. 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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