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019315 PF-3644022 CAS: 1276121-88-0

Specifications
References
CAS Number
1276121-88-0
Grade
Highly Purified
Molecular Formula
C₂₁H₁₈N₄OS•1/4H2O
Molecular Weight
378.96
EU Commodity Code
38220090
Shipping Temp
RT
Storage Temp
4°C
(10R)-9,10,11,12-Tetrahydro-10-methyl-3-(6-methyl-3-pyridinyl)-8H-[1,4]diazepino[5',6':4,5]thieno[3,2-f]quinolin-8-one

PF-3644022 is a potent freely reversible ATP-competitive compound that inhibits MK2 activity (Ki = 3 nM) with good selectivity when profiled against 200 human kinases. PF-3644022 is a benzothiophene inhibitor of mitogen-activated protein kinase-activated protein kinase 2 inhibits tumor necrosis factor α production and has oral anti-inflammatory efficacy in acute and chronic models of inflammation.

Synonyms
(10R)-9,10,11,12-Tetrahydro-10-methyl-3-(6-methyl-3-pyridinyl)-8H-[1,4]diazepino[5',6':4,5]thieno[3,2-f]quinolin-8-one
CAS No
1276121-88-0
Molecular Formula
C₂₁H₁₈N₄OS
Molecular Weight
374.46
Purity (HPLC)
≥98%
Appearance
White to yellow solid
Melting Point
>180°C (dec.) (lit)
Solubility
DMSO to 40nM
Method for Determining Identity
Proton NMR Spectroscopic and Mass Spectrometric Analysis
TLC Conditions
Rf=0.41 (5% 7M methanolic ammonia/DCM)
Elemental Analysis
Calculated: %C: 66.56, %H: 4.92, %N: 14.78
Storage and Stability
Long-term storage is recommended at 4°C. Stable for 6 months after receipt.
Important Note
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.
Toxicity and Hazards
 All products should be handled by qualified personnel only, trained in laboratory procedures.
References
1. Hegen, M., et al.: J. Immunol., 177, 1913 (2006), Anderson, D., et al.. 2. J. Med. Chem., 50, 2647 (2007), Goldberg, D., et al.. 3. Bioorg. Med. Chem. Lett., 18, 938 (2008). 4. Burnette, B., et al.: Pharmacology, 84, 42 (2009). 5. Mourey, et al.: J. Pharmacol. Exp. Ther., 333, 797 (2010)
USBio References
No references available
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