Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8929 |
BC1618
2-Propanol, 1-[bis(phenylmethyl)amino]-3-[4-(trifluoromethyl)phenoxy]- |
Mitophagy; Others; E1/E2/E3 Enzyme; AMPK | Autophagy; Chromatin/Epigenetic; Others; PI3K/Akt/mTOR signaling; Ubiquitination |
BC1618 (2-Propanol, 1-[bis(phenylmethyl)amino]-3-[4-(trifluoromethyl)phenoxy]-) 是一种具有口服活性的 Fbxo48 抑制剂,可刺激 Ampk 依赖性信号传导。它促进线粒体分裂,促进自噬并提高肝脏胰岛素敏感性。 | |||
T8843 |
APS6-45
|
MAPK; Ras | GPCR/G Protein; MAPK |
APS6-45 是一种可口服的肿瘤校准抑制剂,可抑制 RAS/MAPK 信号传导并表现出抗肿瘤活性。 | |||
T16567 |
PQR530
PQR-530 |
PI3K; mTOR | PI3K/Akt/mTOR signaling |
PQR530 是一具有口服活性,种 ATP 竞争性的,可透过血脑屏障的 PI3K/mTORC1/2双重抑制剂,对于 PI3Kα 和 mTOR (分别为 0.84 和 0.33 nM) 的Kd 为亚摩尔。它具有抗肿瘤作用。 | |||
T40319 |
PIM-IN-1
|
||
PIM-IN-1 is a pan-PIM kinase inhibitor (KG-1, EC 50 = 61 nM; pS6, EC 50 = 71 nM). | |||
T79211 |
mTOR inhibitor-11
|
mTOR | PI3K/Akt/mTOR signaling |
mTORinhibitor-11(Compound 9)是具有穿透血脑屏障能力的mTOR抑制剂,其IC50针对pS6为21 nM。该化合物还可抑制pCHK1及PDE4D,其IC50值分别为17.2 μM和17.0 μM,适用于中枢神经系统疾病的研究。 | |||
T70782 |
PF-05139962
|
||
PF-05139962 is a novel potent mTOR inhibitor with excellent mTOR biochemical inhibition, cellular potency, kinase selectivity and in vitro ADME properties. PF-05139962 has pS473 and pS6 cellular IC50 = 48 and 6 nM respectively. PF-05139962 has great selectivity against other receptors and kinases. No genotoxicity was observed on this compound and no more than 25% inhibiton was observed for major CYP enzymes (3A4, 1A2, 2C9, 2D6) at 3 uM. This compound has LE = 0.35 and LipE up to 6.8 which is in ... | |||
T1961 |
Vistusertib
AZD2014 |
Apoptosis; Akt; PI3K; S6 Kinase; mTOR; Autophagy | Apoptosis; Autophagy; Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling |
Vistusertib (AZD2014) 是一种ATP 竞争性的mTOR 抑制剂,IC50为 2.81 nM。它抑制mTORC1和mTORC2复合物。 |