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1-Naphthyl PP1

Cat. No. M5303

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1-Naphthyl PP1 Structure
Synonym:

1-NA-PP 1

Size Price Availability Quantity
5mg USD 90 In stock
10mg USD 125 In stock
25mg USD 250 In stock
50mg USD 400 In stock
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Quality Control & Documentation
Biological Activity

1-NA-PP1 was considerably more potent and showed distinct substituent effects at the pyrazolopyrimidine core. 1-NA-PP1 was cell-active, and potently blocked prostate cancer cell proliferation by inducing G2/M arrest. Overexpression of PKD1 or PKD3 almost completely reversed the growth arrest and the inhibition of tumor cell invasion caused by 1-NA-PP1, indicating that its anti-proliferative and anti-invasive activities were mediated through the inhibition of PKD. Interestingly, a 12-fold increase in sensitivity to 1-NA-PP1 could be achieved by engineering a gatekeeper mutation in the active site of PKD1, suggesting that 1-NA-PP1 could be paired with the analog-sensitive PKD1(M659G) for dissecting PKD-specific functions and signaling pathways in various biological systems.

Chemical Information
Molecular Weight 317.39
Formula C19H19N5
CAS Number 221243-82-9
Solubility (25°C) DMSO ≥ 10 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Tandon M, et al. PLoS One. New pyrazolopyrimidine inhibitors of protein kinase d as potent anticancer agents for prostate cancer cells.

[2] Endo S, et al. Biochem Biophys Res Commun. A single amino-acid change in ERK1/2 makes the enzyme susceptible to PP1 derivatives.

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Keywords: 1-Naphthyl PP1, 1-NA-PP 1 supplier, PKC, inhibitors, activators

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