CC-115 - 98%, high purity , DNA-dependent protein kinase inhibitor, CAS No.1228013-15-7, DNA-dependent protein kinase inhibitor

  • ≥98%
Item Number
C413865
Grouped product items
SKUSizeAvailabilityPrice Qty
C413865-5mg
5mg
2
$39.90
C413865-25mg
25mg
1
$109.90
C413865-50mg
50mg
1
$179.90
C413865-100mg
100mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$324.90

DNA-PK Inhibitors

Basic Description

Synonyms5-ethyl-3-[2-methyl-6-(1H-1,2,4-triazol-5-yl)pyridin-3-yl]-7,8-dihydropyrazino[2,3-b]pyrazin-6-one | AKOS030526334 | AS-74848 | Q27278003 | CC115 | cc-115 | 4-ethyl-6-[2-methyl-6-(1H-1,2,4-triazol-5-yl)-3-pyridyl]-1,2-dihydropyrazino[2,3-b]pyrazin-3-one |
Specifications & Purity≥98%
Biochemical and Physiological MechanismsCC-115 is a dual inhibitor of DNA-dependent protein kinase (DNA-PK) and mammalian target of rapamycin (mTOR) with IC50 values of 0.013 μM and 0.021 μM, respectively. It has potential antineoplastic activity.
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
Action TypeINHIBITOR
Mechanism of actionDNA-dependent protein kinase inhibitor
Product Description

Information

CC-115 CC-115 is a dual inhibitor of DNA-dependent protein kinase (DNA-PK) and mammalian target of rapamycin (mTOR) with IC50 values of 0.013 μM and 0.021 μM, respectively. It has potential antineoplastic activity.


Targets

DNA-PK (Cell-free assay); mTOR (Cell-free assay); PI3Kα (Cell-free assay) 0.013 μM; 0.021 μM; 0.852 μM


In vitro

CC-115 inhibits the DNA damage repair pathway and TORK in CLL cells and induces caspase-dependent cell death in resting CLL cells. It induces cell death with an IC50 of 0.51 µM. CC-115 reverts CD40-induced chemoresistance. CC-115 treatment significantly reduces induction of expression Mcl-1, Bfl-1, and Bcl-XL on CD40 stimulation in CLL cells. It also blocks proliferation of CLL cells. In healthy B cells, CC-115 induces cell death with an IC50 of 0.93 µM. CC-115 and NU7441 completely block the proliferation of CD4+ and CD8+ T cells. Taken together, CC-115 induces direct cytotoxicity and can block signaling pathways that are important for CLL survival, chemo-resistance and proliferation in the in the LN microenvironment.


In vivo

CC-115 decreases lymphadenopathy in CLL patients. CC-115 shows good in vivo PK profiles across multiple species with 53%, 76%, and ∼100% oral bioavailability in mouse, rat, and dog, respectively. CC-115 has favorable physicochemical and pharmacokinetic properties, demonstrates in vivo mTOR pathway inhibition and tumor growth inhibition, as well as a good in vitro and in vivo safety profile, suitable for clinical development.


Cell Research(from reference)

Cell lines:CLL cells 

Concentrations:0.35, 1, 3.5 μM 

Incubation Time:30 min 

AI Insight

Product Properties

ALogP0.664
HBD Count2
Rotatable Bond3

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

Pubchem Sid504771672
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504771672
IUPAC Name 5-ethyl-3-[2-methyl-6-(1H-1,2,4-triazol-5-yl)pyridin-3-yl]-7,8-dihydropyrazino[2,3-b]pyrazin-6-one
INCHI InChI=1S/C16H16N8O/c1-3-24-13(25)7-18-15-16(24)22-12(6-17-15)10-4-5-11(21-9(10)2)14-19-8-20-23-14/h4-6,8H,3,7H2,1-2H3,(H,17,18)(H,19,20,23)
InChi Key GMYLVKUGJMYTFB-UHFFFAOYSA-N
Canonical SMILES CCN1C(=O)CNC2=NC=C(N=C21)C3=C(N=C(C=C3)C4=NC=NN4)C
Isomeric SMILES CCN1C(=O)CNC2=NC=C(N=C21)C3=C(N=C(C=C3)C4=NC=NN4)C
PubChem CID 58298318
Molecular Weight 336.35

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
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7 results found

Lot NumberCertificate TypeDateItem
K2306400Certificate of AnalysisOct 12, 2023 C413865
K2306405Certificate of AnalysisOct 12, 2023 C413865
K2306406Certificate of AnalysisOct 12, 2023 C413865
K2306407Certificate of AnalysisOct 12, 2023 C413865
K2306410Certificate of AnalysisOct 12, 2023 C413865
K2306415Certificate of AnalysisOct 12, 2023 C413865
K2306416Certificate of AnalysisOct 12, 2023 C413865

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