124 Results for "

Estrogen Receptor Modulator

" in MedChemExpress (MCE) Product Catalog:
Products (124)

124 Results for "Estrogen Receptor Modulator" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-13556A
CAS No.: 182133-27-3
Purity:  98.00%
Synonyms: LY353381 hydrochloride; SERM III hydrochloride
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

Arzoxifene (LY353381) hydrocloride is a selective estrogen receptor modulator that is a potent estrogen antagonist in mammary and uterine tissue while acting as an estrogen agonist to maintain bone density and lower serum cholesterol.
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1
1 Cited Publications
Cat. No.: HY-121149
CAS No.: 82413-20-5
Purity:  99.89%
Synonyms: 3-Hydroxytamoxifen
Research Areas:  

Cancer

Droloxifene, a Tamoxifen derivative, is an orally active and selective estrogen receptor modulator. Droloxifene shows antiestrogenic and anti-implantation effects. Droloxifene induces p53 expression and apoptosis in MCF-7 cells. Droloxifene prevents bone loss in ovariectomized rats .
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Cat. No.: HY-13757AR
CAS No.: 10540-29-1
Purity:  99.76%
Synonyms: ICI 47699(Standard); (Z)-Tamoxifen(Standard); trans-Tamoxifen (Standard)
Tamoxifen (Standard) is the analytical standard of Tamoxifen (HY-13757A). This product is intended for research and analytical applications. Tamoxifen (ICI 47699) is an orally active, selective estrogen receptor modulator (SERM) which blocks estrogen action in breast cells and can activate estrogen activity in other cells, such as bone, liver, and uterine cells . Tamoxifen is a potent Hsp90 activator and enhances the Hsp90 molecular chaperone ATPase activity. Tamoxifen also potent inhibits infectious EBOV Zaire and Marburg (MARV) with IC50 of 0.1 μM and 1.8 μM, respectively . Tamoxifen activates autophagy and induces apoptosis . Tamoxifen also can induce gene knockout of CreER(T2) transgenic mouse .
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Cat. No.: HY-15731
CAS No.: 15183-37-6
Purity:  99.76%
Estetrol, an orally active estrogen synthesized exclusively during pregnancy by the human fetal liver, is a selective nuclear estrogen receptor modulator. Estetrol binds ERα as well as ERβ (with a fourfold lower affinity). Estetrol increases eNOS expression/activity and NO synthesis in endothelial cells. Estetrol exerts estrogenic actions on the endometrium or the central nervous system but presents antagonistic effects on the breast. Estetrol can be used in contraception and menopausal hormone research .
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Cat. No.: HY-13724B
CAS No.: 245124-69-0
Purity:  99.83%
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

Pipendoxifene hydrochloride is a selective estrogen receptor modulator (SERM) that can be used for the research of breast cancer .
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Cat. No.: HY-W011100
CAS No.: 2624-43-3
Cyclofenil is a selective estrogen receptor modulator and an ovulation-inducing agent. Cyclofenil shows an inhibitory effect on dengue virus replication in Vero cells with an EC50 of 1.62 μM. Cyclofenil has anti-dengue-virus activity .
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Cat. No.: HY-16950B
CAS No.: 174592-47-3
Synonyms: (E)-Afimoxifene
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

(E)-4-Hydroxytamoxifen ((E)-Afimoxifene), the less active isomer of (Z)-4-hydroxytamoxifen, is an estrogen receptor modulator.
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Cat. No.: HY-126109
CAS No.: 68682-02-0
(±)-8-Prenylnaringenin, a natural prenylated flavonoid, is a potent phytoestrogen. (±)-8-Prenylnaringenin is an orally active selective estrogen receptor modulator (SERM) (Estrogen Receptor/ERR) that inhibits ERα and ERβ with IC50s of 57 nM and 68 nM, respectively. (±)-8-Prenylnaringenin has anticancer effects, and can be used for osteoporosis research .
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Cat. No.: HY-135582
CAS No.: 182507-22-8
Target:  

Estrogen Receptor/ERR

Research Areas:  

Endocrinology

Raloxifene 4'-glucuronide is a primary metabolite of Raloxifene. Raloxifene 4'-glucuronide formation is mediated mostly by UGT1A10 and UGT1A8. Raloxifene 4'-glucuronide binds to estrogen receptor with an IC50 of 370 μM. . Raloxifene is a selective estrogen receptor modulator. Raloxifene activates TGFβ3 promoter as a full agonist at nanomolar concentrations, and inhibits the estrogen response element-containing vitellogenin promoter expression .
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Cat. No.: HY-110201
CAS No.: 63676-22-2
Purity:  99.91%
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

Estrogen receptor modulator 1 (compound 18) is an orally active and selective estrogen receptor modulator (SERM), with a pIC50 of 0.46. Estrogen receptor modulator 1 induces regression of Tamoxifen-resistant, hormone independent xenograft tumors .
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Cat. No.: HY-B2158
CAS No.: 569-57-3
Chlorotrianisene is a long-acting non-steroidal estrogen and an orally active estrogen receptor modulator. Chlorotrianisene exhibits antiestrogenic activity. Chlorotrianisene potently inhibits the enzyme COX-1 and inhibits platelet aggregation in whole blood .
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Cat. No.: HY-13757AS
CAS No.: 157698-32-3
Purity:  99.99%
Synonyms: ICI 47699-​d5; (Z)-Tamoxifen-d5; trans-Tamoxifen-d5
Tamoxifen-d5 is a deuterium labeled Tamoxifen. Tamoxifen (ICI 47699) is an orally active, selective estrogen receptor modulator (SERM). Tamoxifen is a potent Hsp90 activator and enhances the Hsp90 molecular chaperone ATPase activity .
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Cat. No.: HY-A0036D
CAS No.: 198481-33-3
Synonyms: TSE-424 acetate-D
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

Bazedoxifene (acetate)-D (TSE-424 (acetate)-D) is the D-crystal form compound of Bazedoxifene acetate (HY-A0036). Bazedoxifene acetate is an orally active, nonsteroidal selective estrogen receptor modulator (SERM), with IC50s of 23 nM and 99 nM for ERα and ERβ, respectively .
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Cat. No.: HY-13724
CAS No.: 198480-55-6
Purity:  99.93%
Synonyms: ERA-923
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

Pipendoxifene is a selective estrogen receptor modulator (SERM).
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Cat. No.: HY-U00178
CAS No.: 116057-75-1
Synonyms: CB7432
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

Idoxifene (CB7432) is a novel tissue-specific selective estrogen receptor modulator (SERM).
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Cat. No.: HY-13738AR
CAS No.: 82640-04-8
Purity:  99.84%
Synonyms: Keoxifene hydrochloride(Standard); LY156758(Standard); LY139481 hydrochloride (Standard)
Raloxifene (hydrochloride) (Standard) is the analytical standard of Raloxifene (hydrochloride). This product is intended for research and analytical applications. Raloxifene hydrochloride (Keoxifene hydrochloride) is a second generation selective and orally active estrogen receptor modulator. Raloxifene hydrochloride produces estrogen-agonistic effects on bone and lipid metabolism and estrogen-antagonistic effects on uterine endometrium and breast tissue .
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Cat. No.: HY-164764
CAS No.: 1067189-44-9
Target:  

Estrogen Receptor/ERR

Research Areas:  

Endocrinology

ADX61623 is a potent follicle stimulating hormone (FSH) receptor (FSHR) negative allosteric modulator (NAM). ADX61623 shows luteinizing hormone receptor (LH-R) activity and is not active on thyroid-stimulating hormone (TSH) receptors. ADX61623 can be used for the study of estrogen dependent disease .
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Cat. No.: HY-N2371R
CAS No.: 20380-11-4
Synonyms: 27-OHC (Standard)
27-Hydroxycholesterol (27-OHC) is a selective estrogen receptor modulator and an agonist of the liver X receptor.
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Cat. No.: HY-13556
CAS No.: 182133-25-1
Synonyms: LY353381; SERM III
Target:  

Estrogen Receptor/ERR

Research Areas:  

Metabolic Disease Cancer

Arzoxifene (LY353381) is an orally active selective estrogen receptor modulator with a fixed ring structure similar to raloxifene. Arzoxifene has minimal side effects with powerful antiestrogenic effects on breast cancer and endometrium, with equally strong favorable estrogenic effects on bone and lipid profile .
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Cat. No.: HY-79576
CAS No.: 1624-62-0
Synonyms: Oestrone methyl ether; 3-O-Methylestrone
Target:  

Drug Intermediate

Research Areas:  

Cancer

Estrone 3-methyl ether (Oestrone methyl ether; 3-O-Methylestrone) is a synthetic intermediate useful for synthesis of estrogen receptor modulator .
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