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Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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A414215-5mg | 5mg | In stock | $98.90 | |
A414215-10mg | 10mg | In stock | $147.90 | |
A414215-25mg | 25mg | In stock | $246.90 | |
A414215-50mg | 50mg | In stock | $395.90 | |
A414215-100mg | 100mg | In stock | $593.90 | |
A414215-250mg | 250mg | In stock | $1,038.90 |
DNA-PK Inhibitors
Synonyms | 7-methyl-2-[(7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)amino]-9-(oxan-4-yl)purin-8-one | SB23233 | A930641 | BCP30676 | AC-31586 | 7,9-Dihydro-7-methyl-2-[(7-methyl[1,2,4]triazolo[1,5-a]pyridin-6-yl)amino]-9-(tetrahydro-2H-pyran-4-yl)-8H-purin-8-one | S |
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Specifications & Purity | Moligand™, ≥98% |
Biochemical and Physiological Mechanisms | AZD7648 is a potent inhibitor of DNA-PK with an IC50 of 0.6 nM in biochemical assay and more than 100-fold selective against 396 other kinases. |
Storage Temp | Store at -20°C |
Shipped In | Ice chest + Ice pads |
Grade | Moligand™ |
Action Type | INHIBITOR |
Mechanism of action | Inhibitor of phosphatidylinositol-4;5-bisphosphate 3-kinase catalytic subunit alpha;Inhibitor of phosphatidylinositol-4;5-bisphosphate 3-kinase catalytic subunit gamma;Inhibitor of protein kinase; DNA-activated; catalytic subunit |
ALogP | 1.059 |
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hba_count | 6 |
HBD Count | 1 |
Rotatable Bond | 3 |
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IUPAC Name | 7-methyl-2-[(7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)amino]-9-(oxan-4-yl)purin-8-one |
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INCHI | InChI=1S/C18H20N8O2/c1-11-7-15-20-10-21-25(15)9-13(11)22-17-19-8-14-16(23-17)26(18(27)24(14)2)12-3-5-28-6-4-12/h7-10,12H,3-6H2,1-2H3,(H,19,22,23) |
InChi Key | XISVSTPEXYIKJL-UHFFFAOYSA-N |
Canonical SMILES | CC1=CC2=NC=NN2C=C1NC3=NC=C4C(=N3)N(C(=O)N4C)C5CCOCC5 |
Isomeric SMILES | CC1=CC2=NC=NN2C=C1NC3=NC=C4C(=N3)N(C(=O)N4C)C5CCOCC5 |
PubChem CID | 135151360 |
Molecular Weight | 380.4 |
PubChem CID | 135151360 |
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CAS Registry No. | 2230820-11-6 |
RCSB PDB Ligand | MBW |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
---|---|---|---|
I2410055 | Certificate of Analysis | Oct 13, 2022 | A414215 |
K2229245 | Certificate of Analysis | Oct 13, 2022 | A414215 |
K2229254 | Certificate of Analysis | Oct 13, 2022 | A414215 |
K2229267 | Certificate of Analysis | Oct 13, 2022 | A414215 |
K2229269 | Certificate of Analysis | Oct 13, 2022 | A414215 |
K2229270 | Certificate of Analysis | Oct 13, 2022 | A414215 |
K2229271 | Certificate of Analysis | Oct 13, 2022 | A414215 |
Solubility | Solubility (25°C) In vitro DMSO: 6 mg/mL (15.77 mM); Water: Insoluble; Ethanol: Insoluble; |
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DMSO(mg / mL) Max Solubility | 6 |
DMSO(mM) Max Solubility | 15.7728706624606 |
Water(mg / mL) Max Solubility | <1 |
Pictogram(s) | GHS07 |
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Signal | Warning |
Hazard Statements | H315:Causes skin irritation H319:Causes serious eye irritation H335:May cause respiratory irritation |
Precautionary Statements | P261:Avoid breathing dust/fume/gas/mist/vapors/spray. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing. |
Starting at $241.90
1. Goldberg FW, Finlay MRV, Ting AKT, Beattie D, Lamont GM, Fallan C, Wrigley GL, Schimpl M, Howard MR, Williamson B et al.. (2020) The Discovery of 7-Methyl-2-[(7-methyl[1,2,4]triazolo[1,5-a]pyridin-6-yl)amino]-9-(tetrahydro-2H-pyran-4-yl)-7,9-dihydro-8H-purin-8-one (AZD7648), a Potent and Selective DNA-Dependent Protein Kinase (DNA-PK) Inhibitor.. J Med Chem, 63 (7): (3461-3471). [PMID:31851518] [10.1021/op500134e] |