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Onatasertib
Cat. No.:
0225LY-0606
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR, HPLC, and LC-MS.
Size:
Add to basket
Product Overview
Description:
Onatasertib is an oral mTOR kinase inhibitor (IC50: 16 nM) with over 150-fold selectivity over PI3K-alpha; it holds potential as an antitumor treatment by hindering cell proliferation and triggering apoptosis.
Synonym:
CC223; CC 223; 1228013-30-6; 7-(6-(2-hydroxypropan-2-yl)pyridin-3-yl)-1-((1r,4r)-4-methoxycyclohexyl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one; 3-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-5-(4-methoxycyclohexyl)-7,8-dihydropyrazino[2,3-b]pyrazin-6-one; Pyrazino[2,3-b]pyrazin-2(1H)-one, 3,4-dihydro-7-[6-(1-hydroxy-1-methylethyl)-3-pyridinyl]-1-(trans-4-methoxycyclohexyl)-; 7-(6-(2-Hydroxypropan-2-yl)pyridin-3-yl)-1-(trans-4-methoxycyclohexyl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one
CAS No.:
1228013-30-6
Compound CID:
58298316
Formula:
C21H27N5O3
Formula Weight:
397.47
Specification
Targets&IC50:
mTOR: 16 nM
Relative Density:
1.37 g/cm3
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
Onatasertib can be used in clinical pharmacology research to evaluate the impact of dual mTORC1 and mTORC2 blockade in advanced malignancies.
Library Information
Target:
PI3K; FLT; DNA-PK; c-Fms; mTOR
Receptor:
c-Fms; DNA-PK; FLT4; mTOR; PI3K-α
Pathways:
DNA damage/DNA repair; PI3K/Akt/mTOR signaling; Apoptosis; Angiogenesis; Tyrosine kinase/adaptors
Plate Number:
AOCL-8
Plate Location:
g11
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
125 mg/mL; 314.49 mM
Water Max Solubility:
<1 mg/mL (insoluble or slightly soluble)
Ethanol Max Solubility:
73 mg/mL; 183.66 mM
ALogP:
1.66
HBA_Count:
5
HBD_Count:
1
Rotatable Bond:
4





