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PF-562271 - ≥98%, high purity , CAS No.717907-75-0, Inhibitor of aurora kinase A;Inhibitor of fms related receptor tyrosine kinase 3;Inhibitor of protein tyrosine kinase 2;Inhibitor of protein tyrosine kinase 2 beta

  • Moligand™
  • ≥98%
Item Number
P126147
Grouped product items
SKUSizeAvailabilityPrice Qty
P126147-5mg
5mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$155.90
P126147-10mg
10mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$195.90
P126147-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$489.90
P126147-100mg
100mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$882.90

Potent, selective ATP-competitive, reversible FAK Inhibitor

Basic Description

SynonymsPF-562271|717907-75-0|PF-00562271 free base|PF-562271 free base|PF562271|PF 562271|CHEMBL1084546|N-METHYL-N-[3-[[[2-[(2-OXO-2,3-DIHYDRO-1H-INDOL-5-YL)AMINO]-5-TRIFLUOROMETHYLPYRIMIDIN-4-YL]AMINO]METHYL]PYRIDIN-2-YL]METHANESULFONAMIDE|717907-75-0 (free bas
Specifications & PurityMoligand™, ≥98%
Biochemical and Physiological MechanismsPF-562271 is a potent, ATP-competitive, reversible inhibitor of FAK and Pyk2 catalytic activity with a IC50 of 1.5 and 14 nmol/L, respectively.Potent, selective ATP-competitive, reversible FAK Inhibitor (IC 50 values are 1.5, 13, 30, 47 and 58 nM for FAK,
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
GradeMoligand™
Action TypeINHIBITOR
Mechanism of actionInhibitor of aurora kinase A;Inhibitor of fms related receptor tyrosine kinase 3;Inhibitor of protein tyrosine kinase 2;Inhibitor of protein tyrosine kinase 2 beta
NoteWherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

PF-562271 is a potent, ATP-competitive, reversible inhibitor of FAK with IC50 of 1.5 nM, ~10-fold less potent for Pyk2 than FAK and >100-fold selectivity against other protein kinases, except for some CDKs

Product Properties

ALogP2

Names and Identifiers

IUPAC Name N-methyl-N-[3-[[[2-[(2-oxo-1,3-dihydroindol-5-yl)amino]-5-(trifluoromethyl)pyrimidin-4-yl]amino]methyl]pyridin-2-yl]methanesulfonamide
INCHI InChI=1S/C21H20F3N7O3S/c1-31(35(2,33)34)19-12(4-3-7-25-19)10-26-18-15(21(22,23)24)11-27-20(30-18)28-14-5-6-16-13(8-14)9-17(32)29-16/h3-8,11H,9-10H2,1-2H3,(H,29,32)(H2,26,27,28,30)
InChi Key MZDKLVOWGIOKTN-UHFFFAOYSA-N
Canonical SMILES CN(C1=C(C=CC=N1)CNC2=NC(=NC=C2C(F)(F)F)NC3=CC4=C(C=C3)NC(=O)C4)S(=O)(=O)C
Isomeric SMILES CN(C1=C(C=CC=N1)CNC2=NC(=NC=C2C(F)(F)F)NC3=CC4=C(C=C3)NC(=O)C4)S(=O)(=O)C
Alternate CAS 717907-75-0
PubChem CID 11713159
MeSH Entry Terms N-methyl-N-(3-(((2-((2-oxo-1,3-dihydroindol-5-yl)amino)-5-(trifluoromethyl)pyrimidin-4-yl)amino)methyl)pyridin-2-yl)methanesulfonamide;PF-562271;PF562271
Molecular Weight 507.49

Certificates

Certificate of Analysis(COA)

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Lot NumberCertificate TypeDateItem
G1521059Certificate of AnalysisFeb 03, 2023 P126147

Chemical and Physical Properties

SolubilityDMSO 101 mg/mL Water <1 mg/mL Ethanol <1 mg/mL

Related Documents

References

1. Roberts WG, Ung E, Whalen P, Cooper B, Hulford C, Autry C, Richter D, Emerson E, Lin J, Kath J et al..  (2008)  Antitumor activity and pharmacology of a selective focal adhesion kinase inhibitor, PF-562,271..  Cancer Res,  68  (6): (1935-44).  [PMID:18339875]

Solution Calculators