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Home > Products >  PF-4708671

PF-4708671 CAS NO.1255517-76-0

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Keywords

  • PF-4708671
  • S6 Kinase inhibitor & Autophagy activator
  • 1255517-76-0

Quick Details

  • ProName: PF-4708671
  • CasNo: 1255517-76-0
  • Molecular Formula: C19H21F3N6
  • ProductionCapacity: Metric Ton/Day
  • Purity: >97%
  • LimitNum: 0 Metric Ton

Superiority

Biological Activity

Description PF-4708671 is a cell-permeable inhibitor of p70 ribosomal S6 kinase (S6K1 isoform) with Ki/IC50 of 20 nM/160 nM in cell-free assays, 400-fold greater selectivity for S6K1 than S6K2, and 4- and >20-fold selectivity for S6K1 than MSK1 and RSK1/2, respectively. PF-4708671 induces autophagy. First S6K1-specific inhibitor to be reported.
Targets
p70 S6K1 [1]
(Cell-free assay)
160 nM
In vitro

PF-4708671 is a piperazinyl-pyrimidine analogue and the first S6K1-specific inhibitor. PF-4708671 does not significantly inhibit the activity of the closely related S6K2 isoform or a number of other AGC kinases (Akt1, Akt2, PKA, PKCα, PKC?, PRK2, ROCK2, RSK1, RSK2 or SGK1) . PF-4708671 prevents the S6K1-mediated phosphorylation of S6 protein in response to IGF-1 (insulin-like growth factor 1), while having no effect upon the PMA-induced phosphorylation of substrates of the highly related RSK (p90 ribosomal S6 kinase) and MSK (mitogen- and stress-activated kinase) kinases. PF-4708671 is also found to induce phosphorylation of the T-loop and hydrophobic motif of S6K1, an effect that is dependent upon mTORC1 (mTOR complex 1). PF-4708671 does not affect activity of mTORC1. [1]

Cell Data
 
Cell Lines Assay Type Concentration Incubation Time Formulation Activity Description PMID
BHT-101 Growth Inhibition Assay       IC50=0.82024 μM SANGER
UACC-893 Growth Inhibition Assay       IC50=5.19886 μM SANGER
A427 Growth Inhibition Assay       IC50=5.72567 μM SANGER

... Click to View More Cell Line Experimental Data

Assay
Methods Test Index PMID
Western blot   28626016 30423811
Growth inhibition assay 30423811

 

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