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Cat. No. | Product Name | Target | Signaling Pathways |
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T20759 |
XRP44X
XRP-44-X,XRP 44X,XRP-44X,XRP 44 X |
Ras | GPCR/G Protein; MAPK |
XRP44X (XRP 44X) 是Ras 诱导的转录激活的抑制剂,IC50为 10 nM,通过 FGF-2 抑制 Ras-Erk-1/2 通路激活。它抑制Elk3。它还对微管有影响。 | |||
T69195 |
UC-857993
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UC-857993 是一种选择性SOS1-Ras 抑制剂 (Kd=14.7 μM, His6-SOS1cat),抑制其催化活性。UC-857993 还能抑制ERK 和Ras 激活,抑制小鼠胚胎成纤维细胞 (MEF) 的生长。 | |||
T37422 |
Ras Inhibitory Peptide
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Son of sevenless homolog 1 (Sos1) is a guanine nucleotide exchange factor (GEF) that directs the exchange of Ras-GDP to Ras-GTP by binding to SH3 domains of the growth factor receptor-bound protein 2 (Grb2), leading to the activation of ERK. Ras inhibitory peptide is a synthetic peptide that contains the sequence PVPPR, which corresponds to a region within human Sos1 that interacts with an SH3 domain of Grb2. It specifically blocks the interaction of the GEF with Grb2, preventing an interaction ... | |||
T71163 |
Pimasertib HCl
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Pimasertib HCl is an orally bioavailable small-molecule inhibitor of MEK1 and MEK2 (MEK1/2) with potential antineoplastic activity. Pimasertib selectively binds to and inhibits the activity of MEK1/2, preventing the activation of MEK1/2-dependent effector proteins and transcription factors, which may result in the inhibition of growth factor-mediated cell signaling and tumor cell proliferation. MEK1/2 (MAP2K1/K2) are dual-specificity threonine/tyrosine kinases that play key roles in the activati... |
Cat. No. | Product Name | Target | Signaling Pathways |
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TN2114 |
Pseudoginsenoside Rh2
拟人参皂苷RH2,拟人参皂苷 Rh2 |
ERK; Raf; p53 | Apoptosis; MAPK |
Pseudoginsenoside Rh2 has cytotoxicity, it induces mitochondrial apoptosis in A549 cells and is responsible for excessive activation of the Ras/Raf/ERK/p53 pathway. (20Z) -Pseudoginsenoside Rh2 and (20E)-Pseudoginsenoside Rh2 have antioxidative activity. |