938440-64-3,MFCD22666594
Catalog No.:AA00GRS1

938440-64-3 | (5-(2-((2R,6S)-2,6-Dimethylmorpholino)-4-morpholinopyrido[2,3-d]pyrimidin-7-yl)-2-methoxyphenyl)methanol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5mg
≥98%
in stock  
$105.00   $73.00
- +
10mg
≥98%
in stock  
$198.00   $138.00
- +
25mg
in stock  
$325.00   $228.00
- +
50mg
≥98%
in stock  
$566.00   $396.00
- +
100mg
≥98%
in stock  
$822.00   $575.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00GRS1
Chemical Name:
(5-(2-((2R,6S)-2,6-Dimethylmorpholino)-4-morpholinopyrido[2,3-d]pyrimidin-7-yl)-2-methoxyphenyl)methanol
CAS Number:
938440-64-3
Molecular Formula:
C25H31N5O4
Molecular Weight:
465.5447
MDL Number:
MFCD22666594
SMILES:
COc1ccc(cc1CO)c1ccc2c(n1)nc(nc2N1CCOCC1)N1C[C@H](C)O[C@@H](C1)C
Properties
Computed Properties
 
Complexity:
643  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
2  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
34  
Hydrogen Bond Acceptor Count:
9  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
5  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
2.6  

Downstream Synthesis Route
938443-23-3    908142-03-0   
KU-63794 

[1]Patent:WO2007/60404,2007,A1.Locationinpatent:Page/Pagecolumn61-62

[1]Pike,KurtG.;Malagu,Karine;Hummersone,MarcG.;Menear,KeithA.;Duggan,HeatherM.E.;Gomez,Sylvie;Martin,NiallM.B.;Ruston,Linette;Pass,SarahL.;Pass,Martin[BioorganicandMedicinalChemistryLetters,2013,vol.23,#5,p.1212-1216]

[2]CurrentPatentAssignee:ASTRAZENECAPLC-WO2007/60404,2007,A1Locationinpatent:Page/Pagecolumn88-89

[1]Pike,KurtG.;Malagu,Karine;Hummersone,MarcG.;Menear,KeithA.;Duggan,HeatherM.E.;Gomez,Sylvie;Martin,NiallM.B.;Ruston,Linette;Pass,SarahL.;Pass,Martin[BioorganicandMedicinalChemistryLetters,2013,vol.23,#5,p.1212-1216]

64321-24-0   
KU-63794 

[1]BioorganicandMedicinalChemistryLetters,2013,vol.23,p.1212-1216

938443-19-7   
KU-63794 

[1]BioorganicandMedicinalChemistryLetters,2013,vol.23,p.1212-1216

Literature

Title: Identification of potent Yes1 kinase inhibitors using a library screening approach.

Journal: Bioorganic & medicinal chemistry letters 20130801

Title: Optimization of potent and selective dual mTORC1 and mTORC2 inhibitors: the discovery of AZD8055 and AZD2014.

Journal: Bioorganic & medicinal chemistry letters 20130301

Title: Harnessing the PI3K/Akt/mTOR pathway in T-cell acute lymphoblastic leukemia: eliminating activity by targeting at different levels.

Journal: Oncotarget 20120801

Title: Threonine-120 phosphorylation regulated by phosphoinositide-3-kinase/Akt and mammalian target of rapamycin pathway signaling limits the antitumor activity of mammalian sterile 20-like kinase 1.

Journal: The Journal of biological chemistry 20120706

Title: Inhibition of mTORC1 kinase activates Smads 1 and 5 but not Smad8 in human prostate cancer cells, mediating cytostatic response to rapamycin.

Journal: Molecular cancer research : MCR 20120601

Title: The synergistic interaction of MEK and PI3K inhibitors is modulated by mTOR inhibition.

Journal: British journal of cancer 20120410

Title: Quantitative visualization of autophagy induction by mTOR inhibitors.

Journal: Methods in molecular biology (Clifton, N.J.) 20120101

Title: Inhibition of PI3K-Akt-mTOR signaling in glioblastoma by mTORC1/2 inhibitors.

Journal: Methods in molecular biology (Clifton, N.J.) 20120101

Title: Mechanical regulation of glycogen synthase kinase 3β (GSK3β) in mesenchymal stem cells is dependent on Akt protein serine 473 phosphorylation via mTORC2 protein.

Journal: The Journal of biological chemistry 20111111

Title: The inhibition of MAPK potentiates the anti-angiogenic efficacy of mTOR inhibitors.

Journal: Biochemical and biophysical research communications 20110422

Title: Discovery of 9-(6-aminopyridin-3-yl)-1-(3-(trifluoromethyl)phenyl)benzo[h][1,6]naphthyridin-2(1H)-one (Torin2) as a potent, selective, and orally available mammalian target of rapamycin (mTOR) inhibitor for treatment of cancer.

Journal: Journal of medicinal chemistry 20110310

Title: The discovery and optimisation of pyrido[2,3-d]pyrimidine-2,4-diamines as potent and selective inhibitors of mTOR kinase.

Journal: Bioorganic & medicinal chemistry letters 20091015

Title: Ku-0063794 is a specific inhibitor of the mammalian target of rapamycin (mTOR).

Journal: The Biochemical journal 20090701

Title: Garcia-Martinez et al. Ku-0063794 is a specific inhibitor of the mammalian target of rapamycin (mTOR). Biochem.J. (2009)421 29.

Title: Collak FK, et al. Threonine-120 phosphorylation regulated by phosphoinositide-3-kinase/Akt and mammalian target of rapamycin pathway signaling limits the antitumor activity of mammalian sterile 20-like kinase 1.J Biol Chem. 2012 Jul 6;287(28):23698-709. E

Title: Haagensen EJ, et al. The synergistic interaction of MEK and PI3K inhibitors is modulated by mTOR inhibition. Br J Cancer. 2012 Apr 10;106(8):1386-94.

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Additional Info:
SDS
Tags:938440-64-3 Molecular Formula|938440-64-3 MDL|938440-64-3 SMILES|938440-64-3 (5-(2-((2R,6S)-2,6-Dimethylmorpholino)-4-morpholinopyrido[2,3-d]pyrimidin-7-yl)-2-methoxyphenyl)methanol
Catalog No.: AA00GRS1
938440-64-3,MFCD22666594
938440-64-3 | (5-(2-((2R,6S)-2,6-Dimethylmorpholino)-4-morpholinopyrido[2,3-d]pyrimidin-7-yl)-2-methoxyphenyl)methanol
Pack Size: 5mg
Purity: ≥98%
in stock
$105.00 $73.00
Pack Size: 10mg
Purity: ≥98%
in stock
$198.00 $138.00
Pack Size: 25mg
Purity:
in stock
$325.00 $228.00
Pack Size: 50mg
Purity: ≥98%
in stock
$566.00 $396.00
Pack Size: 100mg
Purity: ≥98%
in stock
$822.00 $575.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00GRS1
Chemical Name: (5-(2-((2R,6S)-2,6-Dimethylmorpholino)-4-morpholinopyrido[2,3-d]pyrimidin-7-yl)-2-methoxyphenyl)methanol
CAS Number: 938440-64-3
Molecular Formula: C25H31N5O4
Molecular Weight: 465.5447
MDL Number: MFCD22666594
SMILES: COc1ccc(cc1CO)c1ccc2c(n1)nc(nc2N1CCOCC1)N1C[C@H](C)O[C@@H](C1)C
Properties
Complexity: 643  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 2  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 34  
Hydrogen Bond Acceptor Count: 9  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 5  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 2.6  
Downstream Synthesis Route
938443-23-3    908142-03-0   
KU-63794 

[1]Patent:WO2007/60404,2007,A1.Locationinpatent:Page/Pagecolumn61-62

938440-64-3    938443-29-9 

[1]Pike,KurtG.;Malagu,Karine;Hummersone,MarcG.;Menear,KeithA.;Duggan,HeatherM.E.;Gomez,Sylvie;Martin,NiallM.B.;Ruston,Linette;Pass,SarahL.;Pass,Martin[BioorganicandMedicinalChemistryLetters,2013,vol.23,#5,p.1212-1216]

[2]CurrentPatentAssignee:ASTRAZENECAPLC-WO2007/60404,2007,A1Locationinpatent:Page/Pagecolumn88-89

38496-18-3    938440-64-3 

[1]Pike,KurtG.;Malagu,Karine;Hummersone,MarcG.;Menear,KeithA.;Duggan,HeatherM.E.;Gomez,Sylvie;Martin,NiallM.B.;Ruston,Linette;Pass,SarahL.;Pass,Martin[BioorganicandMedicinalChemistryLetters,2013,vol.23,#5,p.1212-1216]

64321-24-0   
KU-63794 

[1]BioorganicandMedicinalChemistryLetters,2013,vol.23,p.1212-1216

938443-19-7   
KU-63794 

[1]BioorganicandMedicinalChemistryLetters,2013,vol.23,p.1212-1216

Literature fold

Title: Identification of potent Yes1 kinase inhibitors using a library screening approach.

Journal: Bioorganic & medicinal chemistry letters20130801

Title: Optimization of potent and selective dual mTORC1 and mTORC2 inhibitors: the discovery of AZD8055 and AZD2014.

Journal: Bioorganic & medicinal chemistry letters20130301

Title: Harnessing the PI3K/Akt/mTOR pathway in T-cell acute lymphoblastic leukemia: eliminating activity by targeting at different levels.

Journal: Oncotarget20120801

Title: Threonine-120 phosphorylation regulated by phosphoinositide-3-kinase/Akt and mammalian target of rapamycin pathway signaling limits the antitumor activity of mammalian sterile 20-like kinase 1.

Journal: The Journal of biological chemistry20120706

Title: Inhibition of mTORC1 kinase activates Smads 1 and 5 but not Smad8 in human prostate cancer cells, mediating cytostatic response to rapamycin.

Journal: Molecular cancer research : MCR20120601

Title: The synergistic interaction of MEK and PI3K inhibitors is modulated by mTOR inhibition.

Journal: British journal of cancer20120410

Title: Quantitative visualization of autophagy induction by mTOR inhibitors.

Journal: Methods in molecular biology (Clifton, N.J.)20120101

Title: Inhibition of PI3K-Akt-mTOR signaling in glioblastoma by mTORC1/2 inhibitors.

Journal: Methods in molecular biology (Clifton, N.J.)20120101

Title: Mechanical regulation of glycogen synthase kinase 3β (GSK3β) in mesenchymal stem cells is dependent on Akt protein serine 473 phosphorylation via mTORC2 protein.

Journal: The Journal of biological chemistry20111111

Title: The inhibition of MAPK potentiates the anti-angiogenic efficacy of mTOR inhibitors.

Journal: Biochemical and biophysical research communications20110422

Title: Discovery of 9-(6-aminopyridin-3-yl)-1-(3-(trifluoromethyl)phenyl)benzo[h][1,6]naphthyridin-2(1H)-one (Torin2) as a potent, selective, and orally available mammalian target of rapamycin (mTOR) inhibitor for treatment of cancer.

Journal: Journal of medicinal chemistry20110310

Title: The discovery and optimisation of pyrido[2,3-d]pyrimidine-2,4-diamines as potent and selective inhibitors of mTOR kinase.

Journal: Bioorganic & medicinal chemistry letters20091015

Title: Ku-0063794 is a specific inhibitor of the mammalian target of rapamycin (mTOR).

Journal: The Biochemical journal20090701

Title: Garcia-Martinez et al. Ku-0063794 is a specific inhibitor of the mammalian target of rapamycin (mTOR). Biochem.J. (2009)421 29.

Title: Collak FK, et al. Threonine-120 phosphorylation regulated by phosphoinositide-3-kinase/Akt and mammalian target of rapamycin pathway signaling limits the antitumor activity of mammalian sterile 20-like kinase 1.J Biol Chem. 2012 Jul 6;287(28):23698-709. E

Title: Haagensen EJ, et al. The synergistic interaction of MEK and PI3K inhibitors is modulated by mTOR inhibition. Br J Cancer. 2012 Apr 10;106(8):1386-94.

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