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)

  • GC10002 structure
    GC10002Coumestrol
    CAS: 479-13-0
    纯度: >98.00%

    A naturally-occurring phytoestrogen

  • GC10139 structure
    GC10139Estradiol Cypionate
    CAS: 313-06-4
    纯度: >98.00%

    A synthetic estrogen

  • GC10389 structure
    GC10389ERB 041
    CAS: 524684-52-4
    纯度: >98.00%

    An ERβ agonist

  • GC10394 structure
    GC10394DY131
    CAS: 95167-41-2
    纯度: >98.00%

    An ERRβ/γ agonist

  • GC10558 structure
    GC10558GSK 4716
    CAS: 101574-65-6
    纯度: >98.00%

    An ERRβ/γ agonist

  • GC10684 structure
    GC10684Zearalanone
    CAS: 5975-78-0
    纯度: >99.50%

    A mycotoxin with estrogen-like effects

  • GC10789 structure
    GC10789XCT790
    CAS: 725247-18-7
    纯度: >98.00%

    XCT790是一种高效、选择性的ERRα反向激动剂,IC 50 为0.37μM。

  • GC10852 structure
    GC10852Bazedoxifene acetate
    CAS: 198481-33-3
    纯度: >99.50%

    A selective estrogen receptor modulator

  • GC11215 structure
    GC11215Diethylstilbestrol
    CAS: 56-53-1
    纯度: >98.50% / >99.00%

    A synthetic estrogen receptor agonist

  • GC11282 structure
    GC11282β-Estradiol
    CAS: 50-28-2
    纯度: >99.50%

    The major premenopausal estrogen

  • GC11425 structure
    GC11425Lasofoxifene (tartrate)
    CAS: 190791-29-8
    纯度: >99.50%

    A selective estrogen receptor modulator

  • GC11544 structure
    GC11544Toremifene
    CAS: 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 structure
    GC11669Tamoxifen Citrate
    CAS: 54965-24-1
    纯度: >99.50%

    A selective estrogen receptor modulator

  • GC11734 structure
    GC11734α-Zearalenol
    CAS: 36455-72-8
    纯度: >98.00%

    A major hepatic metabolite of zearalenone

  • GC11796 structure
    GC11796Estradiol valerate
    CAS: 979-32-8
    纯度: >99.00%

    A synthetic estrogen

  • GC11822 structure
    GC11822Erteberel (LY500307)
    CAS: 533884-09-2
    纯度: >98.00%

    A potent and selective agonist of ERβ

  • GC11863 structure
    GC11863PHTPP
    CAS: 805239-56-9
    纯度: >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 structure
    GC11996Ospemifene
    CAS: 128607-22-7
    纯度: >99.50%

    A selective estrogen receptor modulator

  • GC12140 structure
    GC12140Endoxifen
    CAS: 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 structure
    GC12148Ethinyl Estradiol
    CAS: 57-63-6
    纯度: >99.50%

    A 17β-estradiol analog

  • GC12182 structure
    GC12182Estriol
    CAS: 50-27-1
    纯度: >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 structure
    GC12644Quinestrol
    CAS: 152-43-2
    纯度: >98.00%

    A synthetic estrogen

  • GC12766 structure
    GC12766G-1
    CAS: 881639-98-1
    纯度: >99.50%

    G-1 is a selective and potent agonist of GPR30 with EC50 value about 2 nM.

  • GC13309 structure
    GC13309WAY 200070
    CAS: 440122-66-7
    纯度: >99.00%

    A potent and selective ERβ agonist