MAPK Signaling

MAPK Signaling(MAPK信号通路)

研究方向

MAPK Signaling 相关产品(575)

  • GC11076 structure
    GC11076XMD8-92
    CAS: 1234480-50-2
    纯度: >98.00%

    XMD8-92是一种BMK1激酶抑制剂,IC 50 为1.5μM,解离常数(Kd)为80nM。

  • GC11157 structure
    GC11157LL-Z 1640-4
    CAS: 66018-41-5

    A negative control for MAPK signaling

  • GC11180 structure
    GC11180CMPD-1
    CAS: 41179-33-3
    纯度: >99.00%

    A substrate-selective p38α MAPK inhibitor

  • GC11277 structure
    GC11277MEK inhibitor
    CAS: 334951-92-7
    纯度: >98.50%

    MEK 抑制剂是一种有效的 MEK 抑制剂,具有抗肿瘤效力。

  • GC11307 structure
    GC11307ML-264
    CAS: 1550008-55-3
    纯度: >99.50%

    A selective KLF5 inhibitor

  • GC11362 structure
    GC11362K 252a
    CAS: 99533-80-9
    纯度: >98.00%

    A non-selective PKC inhibitor

  • GC11422 structure
    GC11422Ulixertinib (hydrochloride)
    CAS: 1956366-10-1
    纯度: >99.50%

    An ERK1/2 inhibitor

  • GC11497 structure
    GC11497BIRB 796 (Doramapimod)
    CAS: 285983-48-4
    纯度: >99.50%

    A potent inhibitor of p38 MAPK

  • GC11542 structure
    GC11542SU 3327
    CAS: 40045-50-9
    纯度: >98.50%

    A JNK1 inhibitor with antidiabetic and antibiotic activity

  • GC11559 structure
    GC11559Anisomycin
    CAS: 22862-76-6
    纯度: >98.50% / >98.00%

    Anisomycin是一种从灰链霉菌中分离出来的抗生素,也是一种JNK激活剂。

  • GC11605 structure
    GC11605C-1
    CAS: 84468-24-6
    纯度: >99.50%

    C-1 是一种有效的蛋白激酶抑制剂,IC50 为 4 μM, 8 μM, 12 μM 和 240 μM 用于 cGMP 依赖性蛋白激酶 (PKG)、cAMP 依赖性蛋白激酶 (PKA) ,分别为蛋白激酶 C (PKC) 和 MLC 激酶。 C-1 也用作 ROCK 抑制剂。

  • GC11635 structure
    GC11635TA 02
    CAS: 1784751-19-4
    纯度: >99.50%

    An inducer of cardiomyocyte differentiation

  • GC11857 structure
    GC11857Pexmetinib (ARRY-614)
    CAS: 945614-12-0
    纯度: >98.00%

    A dual inhibitor of Tie2 and p38 MAPK

  • GC11922 structure
    GC11922SB 706504
    CAS: 911110-38-8

    p38 MAPK inhibitor

  • GC12006 structure
    GC12006GDC-0994
    CAS: 1453848-26-4
    纯度: >99.00%

    A selective ERK1/2 inhibitor

  • GC12089 structure
    GC12089LY2584702
    CAS: 1082949-67-4
    纯度: >98.00%

    A p70S6K inhibitor

  • GC12124 structure
    GC12124Selonsertib (GS-4997)
    CAS: 1448428-04-3
    纯度: >98.50%

    An ASK1 inhibitor

  • GC12201 structure
    GC12201HI TOPK 032
    CAS: 487020-03-1
    纯度: >99.00%

    An inhibitor of TOPK, Chk1, and MEK1 kinases

  • GC12220 structure
    GC12220BIX 02189
    CAS: 1265916-41-3
    纯度: >99.50%

    An inhibitor of MEK5 and ERK5

  • GC12297 structure
    GC12297AT7867
    CAS: 857531-00-1
    纯度: >98.00%

    A potent and orally bioavailable pan-Akt inhibitor

  • GC12304 structure
    GC12304OTS514
    CAS: 1338540-63-8
    纯度: >98.00%

    A TOPK inhibitor

  • GC12406 structure
    GC12406RO5126766(CH5126766)
    CAS: 946128-88-7
    纯度: >98.00%

    A dual inhibitor of MEK1 and Raf kinases

  • GC12486 structure
    GC12486Dabrafenib Mesylate (GSK-2118436)
    CAS: 1195768-06-9
    纯度: >99.50%

    A Raf kinase inhibitor

  • GC12532 structure
    GC12532CHPG
    CAS: 170846-74-9
    纯度: >98.00%

    A potent and selective mGluR5 agonist