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1228013-15-7

1228013-15-7 Structure

1228013-15-7 Structure
IdentificationBack Directory
[Name]

CC-115
[CAS]

1228013-15-7
[Synonyms]

CC-115
CS-2038
CC115;CC 115
CC-115, >95%
CC-115(free base)
1-Ethyl-7-(2-methyl-6-(4h-1,2,4-triazol-3-yl)pyridin-3-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1h)-one
1-ethyl-7-(2-methyl-6-(1H-1,2,4-triazol-5-yl)pyridin-3-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one
Pyrazino[2,3-b]pyrazin-2(1H)-one, 1-ethyl-3,4-dihydro-7-[2-methyl-6-(1H-1,2,4-triazol-5-yl)-3-pyridinyl]-
[Molecular Formula]

C16H16N8O
[MDL Number]

MFCD29036965
[MOL File]

1228013-15-7.mol
[Molecular Weight]

336.35
Chemical PropertiesBack Directory
[Boiling point ]

587.3±60.0 °C(Predicted)
[density ]

1.56±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

≥50 mg/mL in DMSO; insoluble in EtOH; insoluble in H2O
[form ]

solid
[pka]

5.94±0.20(Predicted)
[color ]

Pink to red
Hazard InformationBack Directory
[Uses]

CC-115 is a potent and dual DNA-PK and mTOR kinase inhibitor with IC50s of 13 nM and 21 nM, respectively. CC-115 blocks both mTORC1 and mTORC2 signaling.
[Biological Activity]

cc-115 is a inhibitor of mtor/dna-pk.the mammalian target of rapamycin (mtor) kinase is a key mediator of the phosphoinositide 3-kinase /protein kinase b (akt pathway). the dna-dependent protein kinase (dna-pk) is a critical component of the dna repair machinery governings the response to dna damage, which serves to maintain genome integrity.
[in vitro]

previous study found that the proliferation induced by cd40(+) interleukin-21 stimulation could be completely blocked by cc-115, and cd40-mediated resistance to fludarabine and venetoclax could also be reverted by cc-115. moreover, bcr-mediated signaling was blocked by cc-115 and in cll samples from patients with acquired resistance to idelalisib treatment [1].
[in vivo]

preclinical studies showed that cc-115 had good in vivo pk profiles across multiple species with 53%, 76%, and around100% oral bioavailability in mouse, rat, and dog, respectively [2].
[target]

TargetValue
DNA-PK
(Cell-free assay)
0.013 μM
mTOR
(Cell-free assay)
0.021 μM
PI3Kα
(Cell-free assay)
0.852 μM
[IC 50]

21/ 13 nm for mtor/dna-pk
[storage]

Store at -20°C
[References]

[1] thijssen r,et al. dual tork/dna-pk inhibition blocks critical signaling pathways in chronic lymphocytic leukemia. blood.2016 jul 28;128(4):574-83.
[2] mortensen ds, et al. optimization of a series of triazole containing mammalian target of rapamycin (mtor) kinase inhibitors and the discovery of cc-115. j med chem. 2015 jul 23;58(14):5599-5608.
Spectrum DetailBack Directory
[Spectrum Detail]

CC-115(1228013-15-7)1HNMR
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