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Cat. No. | Product Name | Target | Signaling Pathways |
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T12148 |
N-Desmethyltamoxifen hydrochloride
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Estrogen Receptor/ERR; Endogenous Metabolite; PKC | Chromatin/Epigenetic; Cytoskeletal Signaling; Endocrinology/Hormones; Metabolism |
N-Desmethyltamoxifen hydrochloride 是 Tamoxifen 在人体内主要的三苯氧胺代谢物。它是蛋白激酶 C 抑制剂,也是人体 AML 细胞神经酰胺代谢的有效调节因子,可限制神经酰胺糖基化、水解和鞘氨醇磷酸化。 | |||
T60115 |
EM-651
2H-1-Benzopyran-7-ol, 3-(4-hydroxyphenyl)-4-methyl-2-[4-[2-(1-piperidinyl)ethoxy]phenyl]-, (2R)- |
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EM-651 (2H-1-Benzopyran-7-ol, 3-(4-hydroxyphenyl)-4-methyl-2-[4-[2-(1-piperidinyl)ethoxy]phenyl]-, (2R)-)是EM-652的一种活性较低的对映体,IC50=20.0 nM。EM-652是一种口服有效的、选择性的雌激素受体拮抗剂,IC50=0.44nM。 | |||
T26295 |
Trioxifene mesylate
LY 133314,LY-133314,LY133314 |
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Trioxifene mesylate is an antiestrogen that suppresses growth hormone secretion. | |||
T25262 |
Clometherone
Lilly 38000,Lilly38000,Clometeron,Lilly-38000 |
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Clometherone is a synthetic pregnane steroid and derivative of progesterone which is used as an antiestrogen and antiandrogen. | |||
T15452 |
GW7604
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Others | Others |
GW7604 is an antiestrogen and it also is the metabolite of GW5638. GW5638 is an antagonist of high-affinity estrogen receptor (ER). | |||
T23737 |
Anordiol
H 241,H241,AF-45,AF 45,AF45 |
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Anordiol is an antiestrogen with estrogenic activity. It also is known to inhibit fertility. | |||
T40166 |
Bexirestrant
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Bexirestrant is an orally active ER-α degrader commonly employed in the research of antiestrogen and antineoplastic therapies. | |||
T23273 | RU 58668 | Others | Others |
Pure antiestrogen that downregulates estrogen receptor expression | |||
T12312 | OP-1074 | Estrogen/progestogen Receptor | Endocrinology/Hormones |
OP-1074 is a pure antiestrogen and a selective degrader of ER, shows specific antiestrogenic activity for ERα and ERβ. | |||
T72945 |
Palazestrant
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Palazestrant为一抗雌激素及抗肿瘤试剂,与HER2抑制剂联合应用,有效抑制ER+/HER2+癌症。 | |||
T70013 |
Pipendoxifene
|
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Pipendoxifene, also known as ERA-923, is a new antiestrogen with potential anticancer activity. ERA-923 potently inhibits estrogen binding to ER-alpha (IC50 = 14 nM). In ER-alpha-positive human MCF-7 breast carcinoma cells, ERA-923 inhibits estrogen-stimulated growth (IC50 = 0.2 nM) associated with cytostasis. In vitro, a MCF-7 variant with inherent resistance to tamoxifen (10-fold) or 4-OH tamoxifen (>1000-fold) retains complete sensitivity to ERA-923 . In preclinical models, ERA-923 has an imp... |
Cat. No. | Product Name | Target | Signaling Pathways |
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TN4731 |
Pachyaximine A
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Antifection | Microbiology/Virology |
Pachyaximine A possesses significant antibacterial activity against Escherichia coli, Staphylococcus aureus, Corynebacterium diphtheriae and Corynebacterium pyrogenes. (-)-Pachyaximine A demonstrates significant activity as antiestrogen binding site (AEBS | |||
TN3472 | Axillaridine A | Others | Others |
Axillaridine A is a new cholinesterase inhibitors, it may act as potential leads in the discovery of clinically useful inhibitors for nervous-system disorders, particularly by reducing memory deficiency in Alzheimer's disease patients by potentiating and |