Home Other Building Blocks 928037-13-2
928037-13-2,MFCD22124462
Catalog No.:AA00GU0D

928037-13-2 | Golvatinib

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
99+%
in stock  
$18.00   $13.00
- +
5mg
99+%
in stock  
$44.00   $31.00
- +
10mg
99+%
in stock  
$65.00   $46.00
- +
25mg
99+%
in stock  
$110.00   $77.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00GU0D
Chemical Name:
Golvatinib
CAS Number:
928037-13-2
Molecular Formula:
C33H37F2N7O4
Molecular Weight:
633.6882
MDL Number:
MFCD22124462
SMILES:
CN1CCN(CC1)C1CCN(CC1)C(=O)Nc1nccc(c1)Oc1ccc(c(c1)F)NC(=O)C1(CC1)C(=O)Nc1ccc(cc1)F
Properties
Computed Properties
 
Complexity:
1060  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
46  
Hydrogen Bond Acceptor Count:
9  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
8  
XLogP3:
4.1  

Downstream Synthesis Route

[1]CurrentPatentAssignee:EISAICOLTD-EP1889836,2008,A1Locationinpatent:Page/Pagecolumn59

928038-31-7    53617-36-0   
N-(2-fluoro-4-2-(4-(4-methylpiperazin-1-yl)piperidin-1-ylcarbonyl}amino)pyridin-4-yloxy}phenyl)-N'-(4-fluorophenyl)cyclopropane-1,1-dicarboxyamide 

[1]Patent:EP1889836,2008,A1.Locationinpatent:Page/Pagecolumn59;60

[1]CurrentPatentAssignee:EISAICOLTD-US2008/214815,2008,A1Locationinpatent:Page/Pagecolumn24-25

[1]CurrentPatentAssignee:EISAICOLTD-US2008/214815,2008,A1Locationinpatent:Page/Pagecolumn25

Literature

Title: Combined therapy with mutant-selective EGFR inhibitor and Met kinase inhibitor for overcoming erlotinib resistance in EGFR-mutant lung cancer.

Journal: Molecular cancer therapeutics 20121001

Title: Dual inhibition of Met kinase and angiogenesis to overcome HGF-induced EGFR-TKI resistance in EGFR mutant lung cancer.

Journal: The American journal of pathology 20120901

Title: Paracrine receptor activation by microenvironment triggers bypass survival signals and ALK inhibitor resistance in EML4-ALK lung cancer cells.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research 20120701

Title: Met kinase inhibitor E7050 reverses three different mechanisms of hepatocyte growth factor-induced tyrosine kinase inhibitor resistance in EGFR mutant lung cancer.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research 20120315

Title: E7050: a dual c-Met and VEGFR-2 tyrosine kinase inhibitor promotes tumor regression and prolongs survival in mouse xenograft models.

Journal: Cancer science 20100101

Title: Nakagawa T et al. E7050: a dual c-Met and VEGFR-2 tyrosine kinase inhibitor promotes tumor regression and prolongs survival in mouse xenograft models. Cancer Sci, 2010, 101(1), 210-215.

Title: Wang W et al. Met kinase inhibitor E7050 reverses three different mechanisms of hepatocyte growth factor-induced tyrosine kinase inhibitor resistance in EGFR mutant lung cancer. Clin Cancer Res, 2012, 18(6), 1663-1671.

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SDS
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