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)
- GC1388725(R)-27-hydroxy CholesterolCAS: 20380-11-4纯度: >98.00%
25(R)-27-hydroxy Cholesterol是肝脏X受体(LXR)α和LXRβ的激动剂,EC 50 值分别为0.085μM和0.071μM。
- GC14370Propyl pyrazole triol (PPT)CAS: 263717-53-9纯度: >98.00%
Propyl pyrazole triol (PPT)是一种选择性雌激素受体α(ERα)激动剂,可通过在神经系统激活ERα,保护神经元免受氧化应激与炎症损伤。
- GC14883BazedoxifeneCAS: 198481-32-2
Bazedoxifene (TSE-424) 是一种口服的、可渗透 BBB 的非甾体选择性雌激素受体调节剂 (SERM),对 ERα 和 ERβ 的 IC50 分别为 23 nM 和 99 nM。巴多昔芬可用于骨质疏松症的研究。 Bazedoxifene 还作为 IL-6/GP130 蛋白-蛋白相互作用的抑制剂,可用于胰腺癌的研究。
- GC15245Estradiol BenzoateCAS: 50-50-0纯度: >99.50%
Estradiol Benzoate是一种HBx蛋白抑制剂,可抑制雄激素和乙型肝炎病毒(HBV)的转录和复制。Estradiol Benzoate具有抗生育作用、抗弓形虫活性,并能改善卵巢切除(Ovx)雌性小鼠的记忆行为。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC13350 | Raloxifene HCl | 82640-04-8 | >99.50% | |
A selective estrogen receptor modulator | ||||
| GC13477 | Mestranol | 72-33-3 | >99.50% | |
A prodrug of ethynyl estradiol | ||||
| GC13835 | Toremifene Citrate | 89778-27-8 | >99.50% | |
A selective estrogen receptor modulator | ||||
| GC13887 | 25(R)-27-hydroxy Cholesterol | 20380-11-4 | >98.00% | |
25(R)-27-hydroxy Cholesterol是肝脏X受体(LXR)α和LXRβ的激动剂,EC 50 值分别为0.085μM和0.071μM。 | ||||
| GC14370 | Propyl pyrazole triol (PPT) | 263717-53-9 | >98.00% | |
Propyl pyrazole triol (PPT)是一种选择性雌激素受体α(ERα)激动剂,可通过在神经系统激活ERα,保护神经元免受氧化应激与炎症损伤。 | ||||
| GC14385 | Estrone | 53-16-7 | >98.00% | |
Estrone是三种主要的内源性雌激素之一,其他是雌二醇和雌三醇。 | ||||
| GC14405 | AZD9496 | 1639042-08-2 | >99.00% | |
A SERD | ||||
| GC14883 | Bazedoxifene | 198481-32-2 | - | |
Bazedoxifene (TSE-424) 是一种口服的、可渗透 BBB 的非甾体选择性雌激素受体调节剂 (SERM),对 ERα 和 ERβ 的 IC50 分别为 23 nM 和 99 nM。巴多昔芬可用于骨质疏松症的研究。 Bazedoxifene 还作为 IL-6/GP130 蛋白-蛋白相互作用的抑制剂,可用于胰腺癌的研究。 | ||||
| GC15245 | Estradiol Benzoate | 50-50-0 | >99.50% | |
Estradiol Benzoate是一种HBx蛋白抑制剂,可抑制雄激素和乙型肝炎病毒(HBV)的转录和复制。Estradiol Benzoate具有抗生育作用、抗弓形虫活性,并能改善卵巢切除(Ovx)雌性小鼠的记忆行为。 | ||||
| GC15366 | Clomiphene citrate | 50-41-9 | >98.00% | |
A selective estrogen receptor modulator | ||||
| GC15730 | Kaempferide | 491-54-3 | >98.00% | |
A flavonoid with diverse biological activities | ||||
| GC16292 | Equol | 94105-90-5 | >98.00% | |
An estrogen receptor agonist | ||||
| GC16618 | G-15 | 1161002-05-6 | >99.00% | |
G-15是一种高亲和力、选择性的G蛋白偶联雌激素受体(GPER/ GPR30)拮抗剂(K i = 20nM) 。 | ||||
| GC16852 | Estropipate | 7280-37-7 | >98.00% | |
A piperazine salt form of estrone 3-sulfate | ||||
| GC17398 | Cholesterol | 57-88-5 | >99.00% | |
A sterol | ||||
| GC17588 | Bavachin | 19879-32-4 | >98.00% | |
A phytoestrogen | ||||
| GC17688 | Diarylpropionitrile(DPN) | 1428-67-7 | >99.50% | |
An estrogen receptor β agonist | ||||
| GC17803 | 4-Hydroxytamoxifen | 68392-35-8 | >98.00% | |
4-hydroxytamoxifen 是他莫昔芬和选择性雌激素受体拮抗剂的主要代谢产物。 | ||||
| GC17901 | Tamoxifen | 10540-29-1 | >98.00% / >99.00% | |
Tamoxifen(他莫西芬)是一种选择性雌激素受体调节剂 (SERM),可阻断乳腺细胞中的雌激素作用,并可激活不同组织细胞中的雌激素活性;Tamoxifen 还可以作为 Hsp90 激活剂,增强 Hsp90 分子伴侣 ATPase 的活性;Tamoxifen 还可以诱导 CreER(T2) 小鼠的基因敲除。 | ||||
| GC18000 | Fulvestrant (ICI 182,780) | 129453-61-8 | >99.50% / >98.00% | |
Fulvestrant是一种选择性雌激素受体(ER)拮抗剂。 | ||||
| GC18362 | Acolbifene | 182167-02-8 | >98.50% | |
A selective estrogen receptor modulator | ||||
| GC19478 | Estetrol | 15183-37-6 | - | |
A naturally occurring estrogen | ||||
| GC19498 | β-Estradiol 17-acetate | 1743-60-8 | >99.00% | |
β-Estradiol 17-acetate 是雌二醇的代谢物。 | ||||
| GC30650 | ERB-196 (WAY-202196) | 550997-55-2 | - | |
ERB-196 (WAY-202196) 是一种非甾体选择性雌激素受体-β; (ERβ) 激动剂。 | ||||
