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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10404 |
ATP synthase inhibitor 1
|
ATPase | Membrane transporter/Ion channel |
ATP synthase inhibitor 1 是 F1/FO-ATP 合酶复合物 c 亚基的有效抑制剂,抑制线粒体通透性转换孔的开放。 | |||
T60877 |
Mtb ATP synthase-IN-1
|
ATPase | Membrane transporter/Ion channel |
Mtb ATP synthase-IN-1 是一种可口服的结核分枝杆菌 (Mtb) ATP 合成抑制剂,可用于研究结核分枝杆菌感染。 | |||
T61649 |
ATP synthase inhibitor 2
|
Others | Others |
ATP synthase inhibitor2 是一个铜绿假单胞菌 (PA)ATP synthase 抑制剂 (IC50=10 μg/mL),在 128 μg/mL 时可完全抑制铜绿假单胞菌 (PA) 的 ATP 合成活性。 | |||
T79004 |
ATP synthase inhibitor 2 TFA
|
Others | Others |
ATP synthase inhibitor2 (Compound 22) TFA 为针对铜绿假单胞菌 (PA) ATP synthase 的抑制剂,具IC50值为10 μg/mL,在浓度达到128 μg/mL 时能够全面阻断铜绿假单胞菌 (PA) ATP的合成活性。 | |||
T35560 |
SAR502250
|
Others | Others |
SAR502250 is a potent, selective, ATP competitive, orally active and brain-penetrant inhibitor of GSK3, with an IC50 of 12 nM for human GSK-3β. SAR502250 displays antidepressant-like activity. SAR502250 can be used for the research of Alzheimer’s disease (AD)[1][2]. SAR502250 (0.01-1 μM; 36 h) attenuates the Aβ25-35-induced cell death in rat embryonic hippocampal neurons[2]. SAR502250 (1-100 mg/kg; a single p.o,) attenuates tau hyperphosphorylation in the cortex and spinal cord of transgenic mic... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6323 |
Oligomycin A
MCH 32,寡霉素A |
ATPase; Antibiotic; Antifungal | Membrane transporter/Ion channel; Microbiology/Virology |
Oligomycin A (MCH 32) 属于天然产物,是一种线粒体 F0F1-ATPase 抑制剂 (Ki=1 μM)。Oligomycin A 可以抑制线粒体氧化磷酸化,诱导细胞凋亡。Oligomycin A 具有抗真菌活性。 |