Olaparib 4μM R08 exp512

Inhibits PARP1 and PARP2, blocks ssDNA break repair, selectively toxic to BRCA1/2 negative cancers

  • Class / Subclass 1: DNA Damage, Repair and Replication / PARP Inhibitor

Compound References

  • PubChem Name: Olaparib
  • Synonyms: AZD2281; KU0059436
  • CAS #: 763113-22-0
  • PubChem CID: 23725625
  • IUPAC: 4-[[3-[4-(cyclopropanecarbonyl)piperazine-1-carbonyl]-4-fluorophenyl]methyl]-2H-phthalazin-1-one
  • INCHI Name: InChI=1S/C24H23FN4O3/c25-20-8-5-15(14-21-17-3-1-2-4-18(17)22(30)27-26-21)13-19(20)24(32)29-11-9-28(10-12-29)23(31)16-6-7-16/h1-5,8,13,16H,6-7,9-12,14H2,(H,27,30)
  • INCHI Key: FDLYAMZZIXQODN-UHFFFAOYSA-N
  • Molecular Weight: 434.5
  • Canonical SMILES: C1CC1C(=O)N2CCN(CC2)C(=O)C3=C(C=CC(=C3)CC4=NNC(=O)C5=CC=CC=C54)F
  • Isomeric SMILES: N/A
  • Molecular Formula: C24H23FN4O3

Compound Supplier

  • Supplier Name: Med Chem Express
  • Catalog #: HY-10162
  • Lot #: 24830

Compound Characterization

  • HRMS (ESI-TOF) m/z: (M+H)+ Calcd for C24H23FN4O3 435.1827; found 435.18457

Dose Response Curve

  • Platform ID: Olaparib
  • Min: -6.7026; Max: 94.1282





IC Concentration (µM)
IC10 2.5010
IC20 3.3100
IC30 3.9880
IC40 4.6460
IC50 5.3450
IC60 6.1490
IC70 7.1640
IC80 8.6310
IC90 11.4200


  • Round: 08
  • Dose: 4µM
  • Days of incubation: 8
  • Doublings: 2.2
  • Numbers of reads: 17298761
Sensitive/Resistant hits (FDR<0.05)CRANKSScore PlotTop 30 GenesScreen SimilarityTop 30 Sensitive GO termsTop 30 Resistant GO terms
42/114ScoresViewViewViewViewView

  • Last modified: 2026/01/15 21:36
  • by 127.0.0.1