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371935-79-4,MFCD07368753
Catalog No.:AA00C6EH

371935-79-4 | PI-103 (Hydrochloride)

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
≥98%
in stock  
$63.00   $44.00
- +
5mg
97%
in stock  
$174.00   $122.00
- +
10mg
97%
in stock  
$209.00   $147.00
- +
25mg
97%
in stock  
$400.00   $280.00
- +
50mg
97%
in stock  
$524.00   $367.00
- +
100mg
97%
in stock  
$897.00   $628.00
- +
  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA00C6EH
Chemical Name:
PI-103 (Hydrochloride)
CAS Number:
371935-79-4
Molecular Formula:
C19H17ClN4O3
Molecular Weight:
384.8163
MDL Number:
MFCD07368753
SMILES:
Oc1cccc(c1)c1nc(N2CCOCC2)c2c(n1)c1cccnc1o2.Cl
Properties
Computed Properties
 
Complexity:
489  
Covalently-Bonded Unit Count:
2  
Heavy Atom Count:
27  
Hydrogen Bond Acceptor Count:
7  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
2  

Literature

Title: Synthesis and biological evaluation of sulfonylhydrazone-substituted imidazo[1,2-a]pyridines as novel PI3 kinase p110alpha inhibitors.

Journal: Bioorganic & medicinal chemistry 20070901

Title: Synthesis and biological evaluation of pyrido[3',2':4,5]furo[3,2-d]pyrimidine derivatives as novel PI3 kinase p110alpha inhibitors.

Journal: Bioorganic & medicinal chemistry letters 20070501

Title: Raynaud FI, et al. Biological properties of potent inhibitors of class I phosphatidylinositide 3-kinases: from PI-103through PI-540, PI-620 to the oral agent GDC-0941. Mol Cancer Ther. 2009 Jul;8(7):1725-38.

Title: Knight ZA, et al. A pharmacological map of the PI3-K family defines a role for p110alpha in insulin signaling. Cell. 2006 May 19;125(4):733-47.

Title: Park S, et al. PI-103, a dual inhibitor of Class IA phosphatidylinositide 3-kinase anLeukemia. 2008 Sep;22(9):1698-706.d mTOR, has antileukemicactivity in AmL. Leukemia. 2008 Sep;22(9):1698-706.

Title: López-Fauqued M, et al. The dual PI3K/mTOR inhibitor PI-103 promotes immunosuppression, in vivo tumor growth and increases survival of sorafenib-treated melanoma cells. Int J Cancer. 2010 Apr 1;126(7):1549-61.

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