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Saruparib

From Wikipedia, the free encyclopedia

Saruparib
Clinical data
Other namesAZD-5305
Identifiers
  • 5-[4-[(7-ethyl-6-oxo-5H-1,5-naphthyridin-3-yl)methyl]piperazin-1-yl]-N-methylpyridine-2-carboxamide
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
Chemical and physical data
FormulaC22H26N6O2
Molar mass406.490 g·mol−1
3D model (JSmol)
  • CCC1=CC2=C(C=C(C=N2)CN3CCN(CC3)C4=CN=C(C=C4)C(=O)NC)NC1=O
  • InChI=InChI=1S/C22H26N6O2/c1-3-16-11-19-20(26-21(16)29)10-15(12-24-19)14-27-6-8-28(9-7-27)17-4-5-18(25-13-17)22(30)23-2/h4-5,10-13H,3,6-9,14H2,1-2H3,(H,23,30)(H,26,29)
  • Key:WQAVGRAETZEADU-UHFFFAOYSA-N

Saruparib is a investigational new drug that is being evaluated for the treatment of cancer.[1] It first-in-class selective inhibitor of poly-ADP ribose polymerase 1 (PARP1), designed to treat cancers with homologous recombination repair (HRR) deficiencies as a result of mutations in BRCA1, BRCA2, PALB2, RAD51C, or RAD51D genes.[2]

References

[edit]
  1. ^ "Saruparib - AstraZeneca". AdisInsight. Springer Nature Switzerland AG.
  2. ^ Herencia-Ropero A, Llop-Guevara A, Staniszewska AD, Domènech-Vivó J, García-Galea E, Moles-Fernández A, et al. (August 2024). "The PARP1 selective inhibitor saruparib (AZD5305) elicits potent and durable antitumor activity in patient-derived BRCA1/2-associated cancer models". Genome Medicine. 16 (1): 107. doi:10.1186/s13073-024-01370-z. PMC 11348616. PMID 39187844.