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PT-262 

Cat. No. M30754

All AbMole products are for research use only, cannot be used for human consumption.

PT-262  Structure

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Quality Control & Documentation
Biological Activity

PT-262 is a potent ROCK inhibitor with an IC50 value of around 5 μM. PT-262 induces the loss of mitochondrial membrane potential and elevates the caspase-3 activation and apoptosis. PT-262 inhibits the ERK and CDC2 phosphorylation via a p53-independent pathway. PT-262 blocks cytoskeleton function and cell migration. PT-262 has anti-cancer activity.

Chemical Information
Molecular Weight 276.72
Formula C14H13ClN2O2
CAS Number 86811-36-1
Form Solid
Solubility (25°C) DMSO 100 mg/mL (ultrasonic)
Storage 4°C, protect from light, dry, sealed
References

[1] Chih-Chien Tsai, et al. Biochem Pharmacol. 7-Chloro-6-piperidin-1-yl-quinoline-5,8-dione (PT-262), a novel ROCK inhibitor blocks cytoskeleton function and cell migration

[2] Tzu-Sheng Hsu, et al. Cancer Chemother Pharmacol. 7-Chloro-6-piperidin-1-yl-quinoline-5,8-dione (PT-262), a novel synthetic compound induces lung carcinoma cell death associated with inhibiting ERK and CDC2 phosphorylation via a p53-independent pathway

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  Catalog
Abmole Inhibitor Catalog




Keywords: PT-262  supplier, ROCK, inhibitors, activators

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