Home Other Building Blocks 185039-89-8
185039-89-8,MFCD00950060
Catalog No.:AA00ANPX

185039-89-8 | Pd0166285

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Purity
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1mg
98%
in stock  
$8.00   $6.00
- +
5mg
98%
in stock  
$22.00   $15.00
- +
10mg
98%
in stock  
$36.00   $25.00
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25mg
98%
in stock  
$72.00   $50.00
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  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA00ANPX
Chemical Name:
Pd0166285
CAS Number:
185039-89-8
Molecular Formula:
C26H27Cl2N5O2
Molecular Weight:
512.4309
MDL Number:
MFCD00950060
SMILES:
CCN(CCOc1ccc(cc1)Nc1ncc2c(n1)n(C)c(=O)c(c2)c1c(Cl)cccc1Cl)CC
Properties
Computed Properties
 
Complexity:
719  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
35  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
9  
XLogP3:
5.6  

Literature

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

Journal: Bioorganic & medicinal chemistry letters 20130801

Title: In vitro and in silico studies on substrate recognition and acceptance of human PKMYT1, a Cdk1 inhibitory kinase.

Journal: Bioorganic & medicinal chemistry letters 20120115

Title: WEE1 inhibition sensitizes osteosarcoma to radiotherapy.

Journal: BMC cancer 20110101

Title: 2D Autocorrelation, CoMFA, and CoMSIA modeling of protein tyrosine kinases' inhibition by substituted pyrido[2,3-d]pyrimidine derivatives.

Journal: Bioorganic & medicinal chemistry 20080115

Title: Cell cycle regulation by the Wee1 inhibitor PD0166285, pyrido [2,3-d] pyimidine, in the B16 mouse melanoma cell line.

Journal: BMC cancer 20060101

Title: Structure-activity relationships for 2-anilino-6-phenylpyrido[2,3-d]pyrimidin-7(8H)-ones as inhibitors of the cellular checkpoint kinase Wee1.

Journal: Bioorganic & medicinal chemistry letters 20050401

Title: Wild-type TP53 inhibits G(2)-phase checkpoint abrogation and radiosensitization induced by PD0166285, a WEE1 kinase inhibitor.

Journal: Radiation research 20020301

Title: Radiosensitization of p53 mutant cells by PD0166285, a novel G(2) checkpoint abrogator.

Journal: Cancer research 20011115

Title: 2-Substituted aminopyrido[2,3-d]pyrimidin-7(8H)-ones. structure-activity relationships against selected tyrosine kinases and in vitro and in vivo anticancer activity.

Journal: Journal of medicinal chemistry 19980813

Title: Development of a binding model to protein tyrosine kinases for substituted pyrido[2,3-d]pyrimidine inhibitors.

Journal: Journal of medicinal chemistry 19980521

Title: In vitro pharmacological characterization of PD 166285, a new nanomolar potent and broadly active protein tyrosine kinase inhibitor.

Journal: The Journal of pharmacology and experimental therapeutics 19971201

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