Home Other Building Blocks 1168091-68-6
1168091-68-6,MFCD25976760
Catalog No.:AA008TDL

1168091-68-6 | Gdc-0623

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
99+%
in stock  
$36.00   $25.00
- +
2mg
99+%
in stock  
$61.00   $43.00
- +
5mg
99+%
in stock  
$90.00   $63.00
- +
10mg
99+%
in stock  
$134.00   $94.00
- +
50mg
99+%
in stock  
$358.00   $251.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA008TDL
Chemical Name:
Gdc-0623
CAS Number:
1168091-68-6
Molecular Formula:
C16H14FIN4O3
Molecular Weight:
456.2102
MDL Number:
MFCD25976760
SMILES:
OCCONC(=O)c1ccc2n(c1Nc1ccc(cc1F)I)cnc2
Properties
Computed Properties
 
Complexity:
461  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
25  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
6  
XLogP3:
3.7  

Upstream Synthesis Route

[1]Patent:WO2009/85983,2009,A1,.Locationinpatent:Page/Pagecolumn82

[2]Patent:WO2009/85983,2009,A1,.Locationinpatent:Page/Pagecolumn82-83

Downstream Synthesis Route

[1]CurrentPatentAssignee:ROCHEHOLDINGAG-WO2009/85983,2009,A1Locationinpatent:Page/Pagecolumn82

[2]CurrentPatentAssignee:ROCHEHOLDINGAG-WO2009/85983,2009,A1Locationinpatent:Page/Pagecolumn82-83

Literature

Title: Structure based design of novel 6,5 heterobicyclic mitogen-activated protein kinase kinase (MEK) inhibitors leading to the discovery of imidazo[1,5-a] pyrazine G-479.

Journal: Bioorganic & medicinal chemistry letters 20141001

Title: Mechanism of MEK inhibition determines efficacy in mutant KRAS- versus BRAF-driven cancers.

Journal: Nature 20130912

Title: MEK and the inhibitors: from bench to bedside.

Journal: Journal of hematology & oncology 20130101

Title: Hatzivassiliou G, et al. Mechanism of MEK inhibition determines efficacy in mutant KRAS- versus BRAF-driven cancers. Nature. 2013 Sep 12;501(7466):232-6.

Title: Takahashi RH, et al. Elucidating the Mechanisms of Formation for Two Unusual Cytochrome P450-Mediated Fused Ring Metabolites of GDC-0623, a MAPK/ERK Kinase Inhibitor. Drug Metab Dispos. 2015 Dec;43(12):1929-1933.

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SDS
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