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Signaling Pathways

Signaling Pathways(信号通路)

研究方向

Signaling Pathways 相关产品(35130)

  • GC15311 structure
    GC15311BP 554 maleate
    CAS: 82900-57-0

    Selective 5-HT1A agonist

  • GC15312 structure
    GC15312Chlorprothixene
    CAS: 113-59-7
    纯度: >99.00%

    A dopamine D 2 receptor antagonist

  • GC15315 structure
    GC15315Scriptaid
    CAS: 287383-59-9
    纯度: >98.50%

    HDAC inhibitor

  • GC15317 structure
    GC15317SB408124
    CAS: 288150-92-5
    纯度: >98.50%

    A potent orexin 1 receptor antagonist

  • GC15318 structure
    GC15318GW501516
    CAS: 317318-70-0
    纯度: >99.00%

    GW501516是一种合成PPARδ特异性激动剂，EC 50 值为0.10nM。

  • GC15324 structure
    GC15324Hexestrol
    CAS: 84-16-2
    纯度: >98.00%

    A synthetic non-steroidal estrogen receptor ligand

  • GC15331 structure
    GC15331Prednisolone
    CAS: 50-24-8
    纯度: >98.00%

    The active metabolite of prednisone

  • GC15332 structure
    GC15332Ticagrelor
    CAS: 274693-27-5
    纯度: >99.50%

    A reversible purinergic P2Y 12 receptor antagonist

  • GC15335 structure
    GC15335Saquinavir
    CAS: 127779-20-8
    纯度: >99.00%

    Saquinavir (Ro 31-8959) 是一种 HIV 蛋白酶抑制剂，用于抗逆转录病毒治疗。

  • GC15337 structure
    GC15337Berzosertib (VE-822)
    CAS: 1232416-25-9

    Berzosertib (VE-822)是一种静脉给药的、高度强效且选择性的ATR抑制剂(IC 50 =19nM)。

  • GC15344 structure
    GC15344SP 600125
    CAS: 129-56-6
    纯度: >98.00%

    SP 600125是一种具有口服活性的、可逆的、具有选择性的ATP竞争性JNK 抑制剂，对JNK1、JNK2和JNK3的IC 50 分别为40、40和90nM。SP 600125常用于卵巢癌、肿瘤、帕金森病 (PD)、乳腺癌和哮喘的研究。

  • GC15348 structure
    GC15348Pyridostigmine Bromide
    CAS: 101-26-8
    纯度: >98.00%

    An inhibitor of AChE and BChE

  • GC15353 structure
    GC15353Iniparib (BSI-201)
    CAS: 160003-66-7
    纯度: >99.50%

    A PARP1 inhibitor

  • GC15358 structure
    GC15358PF 750
    CAS: 959151-50-9
    纯度: >98.00%

    A selective, potent FAAH inhibitor

  • GC15359 structure
    GC15359SL-327
    CAS: 305350-87-2
    纯度: >98.00%

    SL-327是MEK1和MEK2的选择性抑制剂，IC 50 值分别为0.18μM和0.22μM。

  • GC15363 structure
    GC15363Felbamate hydrate
    CAS: 1177501-39-1

    An inhibitor of NMDA receptors and a modulator of GABA A receptors

  • GC15366 structure
    GC15366Clomiphene citrate
    CAS: 50-41-9
    纯度: >98.00%

    A selective estrogen receptor modulator

  • GC15371 structure
    GC15371Bardoxolone
    CAS: 218600-44-3
    纯度: >98.00%

    An anti-inflammatory compound that activates Nrf2/ARE signaling

  • GC15373 structure
    GC15373(E)-2-Decenoic acid
    CAS: 334-49-6
    纯度: >98.00%

    An unsaturated fatty acid found in royal jelly

  • GC15374 structure
    GC15374BD 1047 dihydrobromide
    CAS: 138356-21-5
    纯度: >98.00%

    A selective antagonist of σ 1 receptors

  • GC15380 structure
    GC15380PF-562271
    CAS: 717907-75-0
    纯度: >99.50% / >98.00%

    PF-562271是一种针对黏着斑激酶(FAK) 和富含脯氨酸的酪氨酸激酶2(Pyk2)的强效小分子抑制剂，IC 50 分别为1.5nmol/L和14nmol/L。

  • GC15382 structure
    GC15382Isotretinoin
    CAS: 4759-48-2
    纯度: >99.50%

    A retinoid

  • GC15389 structure
    GC15389360A
    CAS: 794458-56-3

    360A 是 G-quadruplex 的选择性稳定剂，也抑制端粒酶活性，在 TRAP-G4 试验中对端粒酶的 IC50 为 300 nM。

  • GC15390 structure
    GC15390Dabigatran etexilate mesylate
    CAS: 872728-81-9
    纯度: >98.00%

    A prodrug form of dabigatran