Estrogen Receptor/ERR
Estrogen Receptor/ERR(雌激素受体/ERR)
Estrogen receptors are a group of proteins found inside cells. They are receptors that are activated by the hormone estrogen (17β-estradiol). Two classes of estrogen receptor exist: ER, which is a member of the nuclear hormone family of intracellular receptors, and GPER (GPR30), which is a member of the rhodopsin-like family of G protein-coupled receptors. The ER's helix 12 domain plays a crucial role in determining interactions with coactivators and corepressors and, therefore, the respective agonist or antagonist effect of the ligand. Different ligands may differ in their affinity for alpha and beta isoforms of the estrogen receptor: estradiol binds equally well to both receptors, estrone, and raloxifene bind preferentially to the alpha receptor, estriol, and genistein to the beta receptor. Estrogen and its receptors are essential for sexual development and reproductive function, but also play a role in other tissues such as bone. Estrogen receptors are also involved in pathological processes including breast cancer, endometrial cancer, and osteoporosis. Alternative promoter usage and alternative splicing result in dozens of transcript variants, but the full-length nature of many of these variants has not been determined.
Estrogen Receptor/ERR 相关产品(169)
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC10002 | Coumestrol | 479-13-0 | >98.00% | |
A naturally-occurring phytoestrogen | ||||
| GC10139 | Estradiol Cypionate | 313-06-4 | >98.00% | |
A synthetic estrogen | ||||
| GC10389 | ERB 041 | 524684-52-4 | >98.00% | |
An ERβ agonist | ||||
| GC10394 | DY131 | 95167-41-2 | >98.00% | |
An ERRβ/γ agonist | ||||
| GC10558 | GSK 4716 | 101574-65-6 | >98.00% | |
An ERRβ/γ agonist | ||||
| GC10684 | Zearalanone | 5975-78-0 | >99.50% | |
A mycotoxin with estrogen-like effects | ||||
| GC10789 | XCT790 | 725247-18-7 | >98.00% | |
XCT790是一种高效、选择性的ERRα反向激动剂,IC 50 为0.37μM。 | ||||
| GC10852 | Bazedoxifene acetate | 198481-33-3 | >99.50% | |
A selective estrogen receptor modulator | ||||
| GC11215 | Diethylstilbestrol | 56-53-1 | >98.50% / >99.00% | |
A synthetic estrogen receptor agonist | ||||
| GC11282 | β-Estradiol | 50-28-2 | >99.50% | |
The major premenopausal estrogen | ||||
| GC11425 | Lasofoxifene (tartrate) | 190791-29-8 | >99.50% | |
A selective estrogen receptor modulator | ||||
| GC11544 | Toremifene | 89778-26-7 | - | |
托瑞米芬(Z-托瑞米芬)是一种用于预防骨质疏松症的第二代选择性雌激素受体调节剂(SERM)。 | ||||
| GC11669 | Tamoxifen Citrate | 54965-24-1 | >99.50% | |
A selective estrogen receptor modulator | ||||
| GC11734 | α-Zearalenol | 36455-72-8 | >98.00% | |
A major hepatic metabolite of zearalenone | ||||
| GC11796 | Estradiol valerate | 979-32-8 | >99.00% | |
A synthetic estrogen | ||||
| GC11822 | Erteberel (LY500307) | 533884-09-2 | >98.00% | |
A potent and selective agonist of ERβ | ||||
| GC11863 | PHTPP | 805239-56-9 | >99.50% / >98.00% | |
PHTPP是一种选择性ERβ完全拮抗剂,对ERβ的选择性是ERα的36倍。PHTPP可以选择性拮抗ERβ的配体结合和转录功能,阻断其对肿瘤细胞的抑制作用,从而促进细胞增殖。PHTPP被用于验证ERβ的功能。 | ||||
| GC11996 | Ospemifene | 128607-22-7 | >99.50% | |
A selective estrogen receptor modulator | ||||
| GC12140 | Endoxifen | 112093-28-4 | - | |
Endoxifen Z-异构体是最重要的他莫昔芬代谢物,负责在表达雌激素受体-α (ERα) 的乳腺癌细胞中引发该药物的抗雌激素作用。 | ||||
| GC12148 | Ethinyl Estradiol | 57-63-6 | >99.50% | |
A 17β-estradiol analog | ||||
| GC12182 | Estriol | 50-27-1 | >99.00% | |
Estriol是雌激素受体(ERα和ERβ)的激动剂和G蛋白偶联受体30(GPR30)的拮抗剂。 | ||||
| GC12644 | Quinestrol | 152-43-2 | >98.00% | |
A synthetic estrogen | ||||
| GC12766 | G-1 | 881639-98-1 | >99.50% | |
G-1 is a selective and potent agonist of GPR30 with EC50 value about 2 nM. | ||||
| GC13309 | WAY 200070 | 440122-66-7 | >99.00% | |
A potent and selective ERβ agonist | ||||
