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Axon Ligands (TM) - alphabetic: [A] [B] [C] [D] [E] [F] [G] [H] [I] [J] [K] [L] [M] [N] [O] [P] [Q] [R] [S] [T] [U] [V] [W] [X] [Y] [Z]
 

 

 

  

D-106669

 

 

CAS 938444-93-0

C17H18N6O MW 322.36

Purity: 99%

Soluble in DMSO

 

 

 

 

 

Ordering Information:

 

Cat. No. Axon 1719   Prime Source

 

Qty1:  2 mg (research sample) / €99  $129 

Qty2:  5 mg (research sample) / €145  $189

Qty3:  25 mg (research sample) / €580  $754

 

Qty4: on request contract research synthesis

 

Send enquiry to: order@axonmedchem.com

or by fax to: +31-50-3600390.

 

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Biological Activity:

 

Highly potent and selective PI3K inhibitor, selectively inhibiting class I PI3K (PI3Kα IC50 <10 nM, >3 log selectivity against tyrosine or serine/threonine kinases, except ERK1 and 2) and showed some activity in A549 (lung cancer) xenografts mouse model at oral dose of 30 mg/kg twice daily.

 

References:

 

SM Maira et al. Discovery of novel anticancer therapeutics targeting the PI3K/Akt/mTOR pathway. Future Med. Chem. 2009, 1(1), 137-155. [online]

 

 

 

Chemical Name: 1-Ethyl-3-(3-(p-tolylamino)-3,4-dihydropyrido[2,3-b]pyrazin-6-yl)urea

 

D-106669 | PI3K inhibitor | Axon Medchem | Axon 1719 | D106669

Axon Ligands TM - Research chemicals for biological study. Some high-profile samples could be provided under terms of contract research synthesis.

axon medchem.com © 2012

 

Axon PI3K and PIKK Inhibitors:

 

AS 252424 | PI3K p110γ inhibitor

BAG 956 | PI3K/PDK1 inhibitor

BBD 130 | PI3K/mTOR inhibitor

BEZ 235 | PI3K/mTOR inhibitor

BKM 120 | PI3K inhibitor

D-106669 | PI3K inhibitor

GDC 0941 | PI3K inhibitor

GDC 0980 | PI3K/mTOR inhibitor

GSK 2126458 | PI3K/mTOR inh.

LY 294002 | PI3K inhibitor

PI 103 | PI3K inhibitor

PIK 75 | PI3K p110α inhibitor

PIK 90 | PI3K p110α inhibitor

TGX 221 | PI3K p110β inhibitor

 

AZD 8055 | mTOR inhibitor

KU 0063794 | mTOR inhibitor

Palomid 529 | Akt/mTOR inhibitor

Temsirolimus | mTOR inhibitor

KU 0060648 | DNA-PK inhibitor

NU 7441 | DNA-PK inhibitor

CP 466722 | ATM inhibitor

 

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