GlpBio

Signaling Pathways

Signaling Pathways(信号通路)

研究方向

Signaling Pathways 相关产品(35130)

  • GC13802 structure
    GC13802Riluzole
    CAS: 1744-22-5
    纯度: >98.00%

    Riluzole 是一种抗惊厥药，属于使用依赖性 Na+ 通道阻滞剂家族，它也可以抑制 GABA 摄取，IC50 为 43 μM。

  • GC13803 structure
    GC13803Triflurdine (Viroptic)
    CAS: 70-00-8
    纯度: >99.50%

    A thymidine analog that inhibits DNA synthesis

  • GC13805 structure
    GC13805Abacavir
    CAS: 136470-78-5
    纯度: >99.50%

    阿巴卡韦是一种具有口服活性和竞争性的核苷类逆转录酶抑制剂。

  • GC13814 structure
    GC13814Adrenalone HCl
    CAS: 62-13-5
    纯度: >98.00%

    Decoyinine (Angustmycin A), a specific inhibitor of bacterial GMPS, has been isolated from Streptomyces .

  • GC13824 structure
    GC13824Indapamide
    CAS: 26807-65-8
    纯度: >99.50% / >98.00%

    An Analytical Reference Standard

  • GC13826 structure
    GC13826JAK2 Inhibitor V, Z3
    CAS: 195371-52-9

    A selective inhibitor of the autophosphorylation of wild type and V617F mutant forms of JAK

  • GC13830 structure
    GC13830Baricitinib phosphate
    CAS: 1187595-84-1
    纯度: >99.50%

    A JAK1 and JAK2 inhibitor

  • GC13831 structure
    GC13831FT-207 (NSC 148958)
    CAS: 17902-23-7
    纯度: >99.50%

    A prodrug form of 5-fluorouracil

  • GC13835 structure
    GC13835Toremifene Citrate
    CAS: 89778-27-8
    纯度: >99.50%

    A selective estrogen receptor modulator

  • GC13837 structure
    GC13837SNS-314 Mesylate
    CAS: 1146618-41-8
    纯度: >99.50%

    A pan-Aurora kinase inhibitor

  • GC13841 structure
    GC13841JNK-IN-8
    CAS: 1410880-22-6
    纯度: >99.50%

    JNK-IN-8 是第一个不可逆的JNK抑制剂,作用于JNK1,JNK2和JNK3,具有高度特异性,在A375细胞系中IC50分别为4.7 nM,18.7 nM和1 nM。

  • GC13842 structure
    GC13842Ro 20-1724
    CAS: 29925-17-5
    纯度: >98.00% / >95.00%

    Ro 20-1724是一种选择性cAMP特异性磷酸二酯酶（PDE4）抑制剂，IC 50 值为1.930μM。

  • GC13843 structure
    GC13843Pyrazinamide
    CAS: 98-96-4
    纯度: >99.50%

    An antimycobacterial compound

  • GC13846 structure
    GC13846Tenofovir hydrate
    CAS: 206184-49-8
    纯度: >98.00%

    An HIV and HBV antiviral

  • GC13848 structure
    GC13848LY2784544
    CAS: 1229236-86-5
    纯度: >99.50%

    Potent inhibitor of JAK2

  • GC13853 structure
    GC13853GBR 12935 dihydrochloride
    CAS: 67469-81-2
    纯度: >98.00%

    An inhibitor of dopamine uptake

  • GC13854 structure
    GC13854AG-490 (Tyrphostin B42)
    CAS: 133550-30-8
    纯度: >98.00%

    AG-490 (Tyrphostin B42)是EGFR抑制剂,IC50为0.1 µM, AG-490对JAK2也有抑制作用。

  • GC13856 structure
    GC13856Dalcetrapib (JTT-705, RO4607381)
    CAS: 211513-37-0
    纯度: >99.00%

    An inhibitor of cholesteryl ester transfer protein

  • GC13860 structure
    GC13860Gatifloxacin mesylate
    CAS: 316819-28-0

    A fluoroquinolone antibiotic

  • GC13861 structure
    GC13861Levofloxacin
    CAS: 100986-85-4
    纯度: >99.50% / >98.00%

    A fluoroquinolone antibiotic

  • GC13863 structure
    GC1386310Panx
    CAS: 955091-53-9
    纯度: >98.00%

    10Panx是一种强效的Panx1通道抑制剂，靶向Panx1蛋白ECL1结构域中的W74至Y83片段。

  • GC13871 structure
    GC13871Duloxetine HCl
    CAS: 136434-34-9
    纯度: >99.50%

    A serotonin and norepinephrine reuptake inhibitor

  • GC13873 structure
    GC13873BMS-690514
    CAS: 859853-30-8
    纯度: >99.50%

    BMS-690514 是一种有效的、具有口服活性的 EGFR 和 VEGFR 抑制剂；对 EGFR、HER 2 和 HER 4 的 IC50 分别为 5、20 和 60 nM。

  • GC13878 structure
    GC13878EPZ005687
    CAS: 1396772-26-1
    纯度: >99.00%

    A potent, selective inhibitor of EZH2