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Cat. No. | Product Name | Target | Signaling Pathways |
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T14327 |
AS1949490
|
Phosphatase | Metabolism |
AS1949490 是选择性SHIP-2抑制剂,其IC50=620 nM。它能够通过上调L6肌管GLUT1基因激活葡萄糖代谢。 | |||
T67893 |
PTP1B-IN-22
|
Phosphatase | Metabolism |
PTP1B-IN-22是一种蛋白酪氨酸磷酸酶1B (PTP1B)抑制剂,可抑制骨骼肌 L6肌管的葡萄糖摄取。 | |||
T25111 |
AS1938909
AS 1938909,AS-1938909 |
||
AS1938909 is a SHIP2 inhibitor that works by increasing Akt phosphorylation, glucose consumption, and glucose uptake in L6 myotubes, specifically upregulating the GLUT1 gene. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T74199 |
Beauverolide Ka
|
||
Beauverolide Ka 是一种环四缩酚肽,是 Beauveria bassiana 真菌的代谢产物。Beauverolide Ka 浓度为 50 μM 时可刺激培养的大鼠 L6 成肌细胞的葡萄糖摄取。Beauverolide Ka 在 10 μM 时表现出对 HEI-OC1 细胞的保护作用,并且在 L6 成肌细胞和肌管中表现出剂量依赖性活性。 | |||
T35532 |
Galegine hydrochloride
|
||
Galegine hydrochloride, a guanidine derivative derived from G. officinalis, plays a role in inducing weight loss in mice and has contributed to the development of biguanides, including metformin and phenformin. This compound stimulates AMPK activation in 3T3-L1 adipocytes, L6 myotubes, H4IIE rat hepatoma, and HEK293 human kidney cell lines. Additionally, galegine hydrochloride exhibits antibacterial properties, particularly demonstrating a minimum inhibitory concentration of 4 mg/L against Staph... |