Olaparib
A PARP inhibitor causing cancer cells with BRCA mutations to accumulate DNA damage and die.
الوزن الجزيئي
434,5000 g/mol
LogP
1,90
TPSA
82,10 Ų
قاعدة ليبينسكي للخمسة
ناجح
المجالات العلاجية
آلية العمل
Inhibits poly(ADP-ribose) polymerase (PARP) enzymes involved in DNA single-strand break repair, exploiting homologous recombination deficiency in cancer cells to cause synthetic lethality.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Inhibits poly(ADP-ribose) polymerase (PARP) enzymes involved in DNA single-strand break repair, exploiting homologous recombination deficiency in cancer cells to cause synthetic lethality.
البنية ثنائية الأبعاد
Cite this structure
Embed this structure
SMILES
O=C(c1cc(Cc2n[nH]c(=O)c3ccccc23)ccc1F)N1CCN(C(=O)C2CC2)CC1
InChI
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)
Molecular Formula
C24H23FN4O3
HBD / HBA
1 / 5
الروابط القابلة للدوران
4
الذرات الثقيلة
32
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
الأسئلة الشائعة
A PARP inhibitor causing cancer cells with BRCA mutations to accumulate DNA damage and die.
Inhibits poly(ADP-ribose) polymerase (PARP) enzymes involved in DNA single-strand break repair, exploiting homologous recombination deficiency in cancer cells to cause synthetic lethality.
Yes, Olaparib is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL521686. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 23725625. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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