GlpBio

Signaling Pathways

Signaling Pathways(信号通路)

研究方向

Signaling Pathways 相关产品(35130)

  • GC13673 structure
    GC13673BMS-708163 (Avagacestat)
    CAS: 1146699-66-2
    纯度: >98.00%

    A potent inhibitor of γ-secretase

  • GC13683 structure
    GC13683Rivaroxaban
    CAS: 366789-02-8
    纯度: >99.50%

    A selective inhibitor of Factor Xa

  • GC13694 structure
    GC13694Spermine NONOate
    CAS: 136587-13-8
    纯度: >98.00%

    A nitric oxide donor

  • GC13697 structure
    GC13697AG-1024
    CAS: 65678-07-1
    纯度: >98.50%

    AG-1024是一种可逆的，竞争性和选择性的胰岛素样生长因子-1受体（IGF-1R）抑制剂，IC 50 值为7μM。AG-1024能够抑制胰岛素受体（IR）的磷酸化，IC 50 值为57μM。

  • GC13698 structure
    GC13698Nilvadipine
    CAS: 75530-68-6
    纯度: >99.50%

    An L-type calcium channel blocker

  • GC13705 structure
    GC13705BMS-927711
    CAS: 1289023-67-1
    纯度: >99.00%

    A CGRP receptor antagonist

  • GC13706 structure
    GC13706Droxinostat
    CAS: 99873-43-5
    纯度: >99.50%

    An inhibitor of HDAC3, HDAC6, and HDAC8

  • GC13716 structure
    GC13716Lopinavir
    CAS: 192725-17-0
    纯度: >99.50% / >99.00%

    A potent HIV-1 protease inhibitor

  • GC13723 structure
    GC13723Amitriptyline HCl
    CAS: 549-18-8
    纯度: >99.50%

    A tricyclic antidepressant

  • GC13725 structure
    GC13725NVP-BAG956
    CAS: 853910-02-8

    A dual PDK1 and class I PI3K inhibitor

  • GC13729 structure
    GC13729Cytidine
    CAS: 65-46-3
    纯度: >99.50% / >98.00%

    A pyrimidine nucleoside

  • GC13730 structure
    GC13730Alfuzosin HCl
    CAS: 81403-68-1
    纯度: >98.50%

    α 1 -Adrenergic receptor antagonist

  • GC13733 structure
    GC13733A 438079 hydrochloride
    CAS: 899431-18-6
    纯度: >99.50%

    An antagonist of the nucleotide receptor P2X7

  • GC13747 structure
    GC13747Vilanterol
    CAS: 503068-34-6

    A β 2 -AR agonist

  • GC13750 structure
    GC13750Doxycycline HCl
    CAS: 10592-13-9

    Doxycycline HCl 是一种抗生素，是一种具有口服活性的广谱金属蛋白酶 (MMP) 抑制剂。

  • GC13753 structure
    GC13753Flucytosine
    CAS: 2022-85-7
    纯度: >99.50%

    A prodrug of 5-fluorouracil

  • GC13756 structure
    GC13756Olsalazine Sodium
    CAS: 6054-98-4
    纯度: >99.50%

    A prodrug form of 5-aminosalicylic acid

  • GC13761 structure
    GC13761AZD8931 (Sapitinib)
    CAS: 848942-61-0
    纯度: >99.50%

    A reversible inhibitor of ErbB1/EGFR, ErbB2/HER2, and ErbB3/HER3

  • GC13771 structure
    GC13771Canagliflozin
    CAS: 842133-18-0
    纯度: >99.50% / >98.00%

    Canagliflozin是一种用于治疗2型糖尿病的钠葡萄糖共转运体（SGLT2）抑制剂。

  • GC13779 structure
    GC13779Orphenadrine Citrate
    CAS: 4682-36-4
    纯度: >98.00%

    Orphenadrine citrate 是一种具有口服活性且非竞争性的 NMDA 受体拮抗剂（穿过血脑屏障），Ki 为 6.0 μM。

  • GC13783 structure
    GC13783Phenserine
    CAS: 101246-66-6
    纯度: >98.00%

    An AChE inhibitor

  • GC13792 structure
    GC13792Rufinamide
    CAS: 106308-44-5
    纯度: >99.50%

    An anticonvulsant

  • GC13793 structure
    GC13793NH125
    CAS: 278603-08-0
    纯度: >98.00%

    NH125是一种多靶标的活性物质，是多种组氨酸蛋白激酶家族成员的抑制剂，其中NH125可抑制真核延长因子2激酶（eEF-2K）活性，IC 50 =60nM。

  • GC13799 structure
    GC13799Alfacalcidol
    CAS: 41294-56-8
    纯度: >99.00%

    Prodrug of vitamin D 3