Product Description
PF 4708671 is a cell-permeable inhibitor of p70 ribosomal S6 kinase (S6K1 isoform) (Ki = 20 nM; IC50 = 160 nM). Suppresses the S6K1-mediated phosphorylation of S6, Rictor and mTOR in response to IGF1; displays no effect on the activity of RSK and MSK in vivo. Exhibits no significant inhibition of S6K2 or other AGC kinases (e.g. Akt, PKA and ROCK) in vitro.Licensing Information
Sold for research purposes under agreement from Pfizer Inc.
Product Specifications for PF 4708671
Molecular Weight
Formula
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Chemical Name
CAS Number
PubChem ID
InChI Key
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The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| DMSO | 19.52 | 50 | |
| Ethanol | 19.52 | 50 |
Preparing Stock Solutions for PF 4708671
The following data is based on the product molecular weight 390.41.
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 0.5 mM | 5.12 mL | 25.61 mL | 51.23 mL |
| 2.5 mM | 1.02 mL | 5.12 mL | 10.25 mL |
| 5 mM | 0.51 mL | 2.56 mL | 5.12 mL |
| 25 mM | 0.10 mL | 0.51 mL | 1.02 mL |
Calculators
Background References
References are publications that support the biological activity of the product. See our Citations tab to view 46 publications citing the usage of this product.
- Pearce Characterisation of PF-4708671 a novel and highly specific inhibitor of p70 ribosomal S6 kinase (S6K1). Biochem.J. 2010 PMID: 20704563
Product Documents for PF 4708671
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Product Specific Notices for PF 4708671
For research use only
Related Research Areas
Citations for PF 4708671
Customer Reviews for PF 4708671 (1)
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Species: HumanAssay Type: In VitroCell Line/Tissue: Du145 and HepG2, Huh&Verified Customer | Posted 08/19/2025We found that 5 um for 24 to 48 hours was effective.This compound can reduce tumour cell growth by inhibiting S6K phosphorylation.
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