GlpBio

Signaling Pathways

Signaling Pathways(信号通路)

研究方向

Signaling Pathways 相关产品(35130)

  • GC10956 structure
    GC10956Imeglimin hydrochloride
    CAS: 775351-61-6
    纯度: >98.00%

    Imeglimin hydrochloride是一种口服降糖药物，可抑制多药及毒素外排蛋白1（MATE1），IC 50 值为19.24μM。

  • GC10959 structure
    GC10959Boceprevir
    CAS: 394730-60-0
    纯度: >98.00%

    An NS3/4A protease inhibitor

  • GC10962 structure
    GC10962Cinaciguat
    CAS: 329773-35-5
    纯度: >99.00%

    An activator of sGC

  • GC10963 structure
    GC10963Bacitracin Zinc
    CAS: 1405-89-6
    纯度: >98.50%

    A cyclic polypeptide antibiotic

  • GC10966 structure
    GC10966Fexofenadine HCl
    CAS: 153439-40-8
    纯度: >99.50%

    Fexofenadine HCl是一种具有口服活性和非镇静作用的组胺H1受体拮抗剂。

  • GC10969 structure
    GC10969INK 128 (MLN0128)
    CAS: 1224844-38-5
    纯度: >99.00% / >99.50%

    Inhibitor of TORC1/2

  • GC10970 structure
    GC10970WP1130
    CAS: 856243-80-6
    纯度: >99.50%

    A deubiquitinase inhibitor

  • GC10972 structure
    GC10972Gallamine Triethiodide
    CAS: 65-29-2
    纯度: >98.00%

    An allosteric modulator of muscarinic acetylcholine receptors

  • GC10973 structure
    GC10973SC 236
    CAS: 170569-86-5
    纯度: >99.00% / >99.50%

    A potent, selective COX-2 inhibitor

  • GC10974 structure
    GC10974AWD 131-138
    CAS: 188116-07-6
    纯度: >99.00%

    A partial agonist of the GABA A receptor

  • GC10975 structure
    GC10975GW4064
    CAS: 278779-30-9
    纯度: >99.50%

    GW4064作为合成的FXR激动剂，用于治疗胆汁淤积性肝病、代谢综合征和酒精性肝病。

  • GC10977 structure
    GC10977Methylcobalamin
    CAS: 13422-55-4
    纯度: >98.00%

    An analog of vitamin B 12

  • GC10978 structure
    GC10978Terfenadine
    CAS: 50679-08-8
    纯度: >98.00%

    A selective histamine H 1 -receptor antagonist

  • GC10982 structure
    GC10982YM201636
    CAS: 371942-69-7
    纯度: >98.00%

    Inhibitor of PIKfyve

  • GC10984 structure
    GC10984Zanamivir
    CAS: 139110-80-8
    纯度: >98.00%

    An inhibitor of influenza neuraminidase

  • GC10985 structure
    GC10985MDL 72832 hydrochloride
    CAS: 113777-40-5

    ligand for 5-HT1A receptor, potent and selective

  • GC10989 structure
    GC109896,2',4'-Trimethoxyflavone
    CAS: 720675-74-1
    纯度: >97.00%

    A flavonoid with diverse biological activities

  • GC10995 structure
    GC10995PJ34
    CAS: 344458-19-1
    纯度: >98.00%

    PJ34是一种有效且特异性的PARP抑制剂，IC 50 值为110nM。

  • GC10997 structure
    GC10997Oxethazaine
    CAS: 126-27-2
    纯度: >99.00% / >98.00% / >95.00%

    Oxethazaine (Oxetacaine) 是芬特明酸性的前体，是一种具有抗酸和口服活性的镇痛剂。

  • GC10999 structure
    GC10999Avasimibe
    CAS: 166518-60-1
    纯度: >99.50% / >98.00%

    Avasimibe是一种选择性口服酰基辅酶A：胆固醇酰基转移酶（ACAT）抑制剂（IC 50 =12μmol/L）。

  • GC11006 structure
    GC11006Montelukast Sodium
    CAS: 151767-02-1

    A CysLT 1 receptor antagonist

  • GC11007 structure
    GC11007VO-Ohpic trihydrate
    CAS: 476310-60-8
    纯度: >98.00%

    A specific inhibitor of PTEN

  • GC11008 structure
    GC11008Necrostatin-1
    CAS: 4311-88-0
    纯度: >98.00% / >99.00%

    Necrostatin-1主要作用于细胞中的RIP1，Necrostatin-1是一种RIP1激酶抑制剂，IC50值为0.32 mM。

  • GC11009 structure
    GC11009Cetirizine DiHCl
    CAS: 83881-52-1
    纯度: >99.00%

    A selective histamine H 1 receptor antagonist