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Estrogen Receptor/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 (79):

Cat. No. Product Name Effect Purity
  • HY-13757A
    Tamoxifen Modulator 99.76%
    Tamoxifen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,并可激活其他细胞,如骨骼,肝脏和子宫细胞中的雌激素活性。
  • HY-13636
    Fulvestrant Inhibitor 99.89%
    Fulvestrant是有效的雌激素受体 (Estrogen Receptor) 拮抗剂,IC50值为 9.4 nM。
  • HY-B0141
    Estradiol Agonist 98.45%
    Estradiol 是一种类固醇性激素,对维持女性的生育能力和第二性征至关重要。
  • HY-16950
    4-Hydroxytamoxifen Modulator 99.27%
    4-Hydroxytamoxifen是一种选择性的雌激素受体调节剂 (SERM)。
  • HY-19822A
    Elacestrant dihydrochloride Inhibitor 98.93%
    Elacestrant dihydrochloride (RAD1901 dihydrochloride) 是有选择性和口服活性的雌激素受体 (ER)的降解剂,对ERα和ERβ的IC50值分别为48和870 nM.
  • HY-112596
    H3B-6545 Antagonist
    H3B-6545 是一种口服有效的选择性雌激素受体共价拮抗剂 (SERCA)。
  • HY-16023A
    Acolbifene Antagonist
    Acolbifene (EM652) 是第四代选择性的estrogen receptor拮抗剂,LC50 值为 22±3 nM。
  • HY-112596A
    H3B-6545 Hydrochloride Antagonist
    H3B-6545 Hydrochloride 是一种口服有效的选择性雌激素受体共价拮抗剂 (SERCA)。
  • HY-13757
    Tamoxifen Citrate Inhibitor >99.0%
    Tamoxifen Citrate 是一种抗雌激素,抑制雌激素结合到雌激素受体 (estrogen receptors)。
  • HY-12870
    AZD9496 Antagonist 99.15%
    AZD9496 是有效,选择性的雌激素受体 (ERα) 拮抗剂,IC50 为 0.28 nM。
  • HY-14590
    Kaempferol Inhibitor 99.47%
    Kaempferol 在乳腺癌细胞中抑制雌激素受体 (estrogen receptor α) 表达,在胶质母细胞瘤细胞和肺癌细胞中,通过激活 MEK-MAPK 诱导细胞凋亡。
  • HY-10426
    XCT790 Antagonist 98.01%
    XCT-790是雌激素相关受体(ERR)α反向激动剂,能诱导化疗抗性的癌细胞死亡。
  • HY-A0036
    Bazedoxifene acetate Modulator 99.93%
    Bazedoxifene acetate是第三代选择性雌激素受体调节剂 (SERM)IC50分别为26和99 nM。
  • HY-12864
    GDC-0810 Inhibitor 99.87%
    GDC-0810 是一种可口服的,选择性的雌激素降能器 (selective estrogen receptor degrader),IC50 值为 0.7 nM。
  • HY-B0234
    Estrone Agonist 99.86%
    Estrone为雌激素。
  • HY-13738A
    Raloxifene hydrochloride Antagonist 99.64%
    Raloxifene(LY156758)盐酸盐是第二代雌激素受体拮抗剂。
  • HY-103456
    PHTPP Antagonist 99.07%
    PHTPP 是一种选择性的 ERβ 拮抗剂。
  • HY-N0835
    (20S)-Protopanaxatriol Agonist >98.0%
    (20S)-Protopanaxatriol 是人参皂苷的代谢物,通过 glucocorticoid receptoroestrogen receptor 起作用,同时为 LXRα 的抑制剂。
  • HY-B0463
    Clomiphene citrate Antagonist >98.0%
    Clomifene柠檬酸盐是雌激素受体调节剂。
  • HY-B0005
    Toremifene Citrate Modulator 99.99%
    Toremifene(NK 622; FC 1157a)柠檬酸盐是第二代选择性雌激素受体调节剂,对雌激素受体的IC50为1μM。
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