1314890-29-3,MFCD26522023
Catalog No.:AA009CCC

1314890-29-3 | N-{[4-(4-phenyl-1,3-thiazol-2-yl)oxan-4-yl]methyl}-3-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
≥95%
in stock  
$53.00   $37.00
- +
5mg
98%
in stock  
$100.00   $70.00
- +
50mg
95%
in stock  
$255.00   $179.00
- +
100mg
95%
in stock  
$390.00   $273.00
- +
250mg
95%
in stock  
$601.00   $421.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA009CCC
Chemical Name:
N-{[4-(4-phenyl-1,3-thiazol-2-yl)oxan-4-yl]methyl}-3-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide
CAS Number:
1314890-29-3
Molecular Formula:
C25H21F3N4O3S
Molecular Weight:
514.5194
MDL Number:
MFCD26522023
SMILES:
O=C(c1cccc(c1)c1noc(n1)C(F)(F)F)NCC1(CCOCC1)c1scc(n1)c1ccccc1
Properties
Computed Properties
 
Complexity:
749  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
36  
Hydrogen Bond Acceptor Count:
10  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
6  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
4.8  

Downstream Synthesis Route

[1]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-EP2533783,2015,B1

1092400-82-2    1314886-98-0   
N-((4-(4-phenylthiazol-2-yl)tetrahydro-2H-pyran-4-yl)methyl)-3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzamide 

[1]Patent:EP2533783,2015,B1.Locationinpatent:Paragraph0138-0139

[1]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-EP2533783,2015,B1

Literature

Title: Selective class IIa histone deacetylase inhibition via a nonchelating zinc-binding group.

Journal: Nature chemical biology 20130501

Title: Lobera M, et al. Selective class IIa histone deacetylase inhibition via a nonchelating zinc-binding group. Nat Chem Biol. 2013 May;9(5):319-25.

Title: Sinnett-Smith J, et al. Protein kinase D1 mediates class IIa histone deacetylase phosphorylation and nuclear extrusion in intestinal epithelial cells: role in mitogenic signaling. Am J Physiol Cell Physiol. 2014 May 15;306(10):C961-71.

Title: Kikuchi S, et al. Class IIa HDAC inhibition enhances ER stress-mediated cell death in multiple myeloma. Leukemia. 2015 Sep;29(9):1918-1927.

Title: EricSalgado, et al. Volume 503 HDAC9 overexpression confers invasive and angiogenic potential to triple negative breast cancer cells via modulating microRNA-206. Biochemical and Biophysical Research Communications.

Quotation Request
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Additional Info:
SDS
Related Products of 1314890-29-3
Tags:1314890-29-3 Molecular Formula|1314890-29-3 MDL|1314890-29-3 SMILES|1314890-29-3 N-{[4-(4-phenyl-1,3-thiazol-2-yl)oxan-4-yl]methyl}-3-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide
Catalog No.: AA009CCC
1314890-29-3,MFCD26522023
1314890-29-3 | N-{[4-(4-phenyl-1,3-thiazol-2-yl)oxan-4-yl]methyl}-3-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide
Pack Size: 1mg
Purity: ≥95%
in stock
$53.00 $37.00
Pack Size: 5mg
Purity: 98%
in stock
$100.00 $70.00
Pack Size: 50mg
Purity: 95%
in stock
$255.00 $179.00
Pack Size: 100mg
Purity: 95%
in stock
$390.00 $273.00
Pack Size: 250mg
Purity: 95%
in stock
$601.00 $421.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA009CCC
Chemical Name: N-{[4-(4-phenyl-1,3-thiazol-2-yl)oxan-4-yl]methyl}-3-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide
CAS Number: 1314890-29-3
Molecular Formula: C25H21F3N4O3S
Molecular Weight: 514.5194
MDL Number: MFCD26522023
SMILES: O=C(c1cccc(c1)c1noc(n1)C(F)(F)F)NCC1(CCOCC1)c1scc(n1)c1ccccc1
Properties
Complexity: 749  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 36  
Hydrogen Bond Acceptor Count: 10  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 6  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 4.8  
Downstream Synthesis Route
1314886-95-7    1314890-29-3 

[1]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-EP2533783,2015,B1

1092400-82-2    1314886-98-0   
N-((4-(4-phenylthiazol-2-yl)tetrahydro-2H-pyran-4-yl)methyl)-3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzamide 

[1]Patent:EP2533783,2015,B1.Locationinpatent:Paragraph0138-0139

1877-72-1    1314890-29-3 

[1]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-EP2533783,2015,B1

Literature fold

Title: Selective class IIa histone deacetylase inhibition via a nonchelating zinc-binding group.

Journal: Nature chemical biology20130501

Title: Lobera M, et al. Selective class IIa histone deacetylase inhibition via a nonchelating zinc-binding group. Nat Chem Biol. 2013 May;9(5):319-25.

Title: Sinnett-Smith J, et al. Protein kinase D1 mediates class IIa histone deacetylase phosphorylation and nuclear extrusion in intestinal epithelial cells: role in mitogenic signaling. Am J Physiol Cell Physiol. 2014 May 15;306(10):C961-71.

Title: Kikuchi S, et al. Class IIa HDAC inhibition enhances ER stress-mediated cell death in multiple myeloma. Leukemia. 2015 Sep;29(9):1918-1927.

Title: EricSalgado, et al. Volume 503 HDAC9 overexpression confers invasive and angiogenic potential to triple negative breast cancer cells via modulating microRNA-206. Biochemical and Biophysical Research Communications.

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