15 Results for "

endometrium

" in MedChemExpress (MCE) Product Catalog:
Products (15)

15 Results for "endometrium" in MCE Product Catalog:

20
20 Publications Verification
Cat. No.: HY-13738A
CAS No.: 82640-04-8
Purity:  99.78%
Synonyms: Keoxifene hydrochloride; LY156758; LY139481 hydrochloride
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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1 Cited Publications
Cat. No.: HY-P74551
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: SFRP4; Frizzled Protein, Human endometrium; Secreted Frizzled Related Protein 4; SFRP-4; FrpHE; Secreted Frizzled-Related Protein 4; Secreted Frizzled-Related Protein 4; Secreted Frizzled-Related Protein 4; FRPHE; FRZB-2; PYL; FRP-4
Species:  
Human
Source:  
HEK293
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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-106389
CAS No.: 96346-61-1
Synonyms: ZK 98299
Target:  

Progesterone Receptor

Research Areas:  

Cancer

Onapristone is a progesterone receptor antagonist, with Kds of 11.6 nM and 11.90 nM for human endometrium and myometrium progesterone receptor in saturation analysis. Onapristone has antitumor activity .
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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-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-106299
CAS No.: 97747-88-1
Synonyms: ZK98734
Target:  

Progesterone Receptor

Research Areas:  

Metabolic Disease

Lilopristone (ZK98734) is a progesterone antagonist with a potential to induce menstruation, inhibit nidation, and terminate pregnancy. Lilopristone blocks progesterone action at the endometrium as well as decreases progesterone bioavailability, and can be utilized in antifertility research .
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Cat. No.: HY-105177
CAS No.: 155768-17-5
Target:  

Progesterone Receptor

Research Areas:  

Endocrinology Cancer

ORG 33628 is a potent and selective progesterone receptor modulator. ORG 33628 shows anti-progestational and anti-glucocorticoid activity. ORG 33628 shows ovulation-inhibitory activity. ORG 33628 has the potential for the research of breast and endometrium .
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Cat. No.: HY-15731S
Purity:  97.50%
Estetrol-d4 is the deuterium labeled Estetrol. Estetrol, a natural estrogen synthesized exclusively during pregnancy by the human fetal liver, is a selective nuclear estrogen receptor modulator. Estetrol exerts estrogenic actions on the endometrium or the central nervous system but presents antagonistic effects on the breast .
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Cat. No.: HY-15731S1
CAS No.: 2734920-42-2
Estetrol-d4 (Major) is the deuterium labeled Estetrol (HY-15731). 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-K6128

MCE Human Endometrium Organoid Kit includes a basic culture medium for human endometrium organoids, as well as culture supplements, and is designed for the effective construction of human endometrium organoids.

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Cat. No.: HY-W744272
Estetrol-d3 is the deuterium labeled Estetrol (HY-15731). 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-E72103
Target:  

Cytochrome P450

Research Areas:  

Others

Human CYP1A1, Reductase+b5 refers to a near-physiological recombinant microsomal system co-expressed in insect cells, consisting of human cytochrome P450 1A1, NADPH-P450 oxidoreductase (CPR) and cytochrome b5. Human CYP1A1 is a human cytochrome P450 subtype belonging to the CYP1 family, as well as a major metabolic enzyme. Its expression is concentrated in tissues such as lung, breast, placenta and endometrium, and it can metabolize polycyclic aromatic hydrocarbons and estrogens into carcinogenic intermediates with DNA-damaging activity .
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Cat. No.: HY-P74552
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: SFRP4; Frizzled Protein, Human endometrium; Secreted Frizzled Related Protein 4; SFRP-4; FrpHE; Secreted Frizzled-Related Protein 4; Secreted Frizzled-Related Protein 4; Secreted Frizzled-Related Protein 4; FRPHE; FRZB-2; PYL; FRP-4
Species:  
Human
Source:  
CHO
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Cat. No.: HY-P74550
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: SFRP4; Frizzled Protein, Human endometrium; Secreted Frizzled Related Protein 4; SFRP-4; FrpHE; Secreted Frizzled-Related Protein 4; Secreted Frizzled-Related Protein 4; Secreted Frizzled-Related Protein 4; FRPHE; FRZB-2; PYL; FRP-4
Species:  
Mouse
Source:  
HEK293
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