Talazoparib

CHEMBL3137320 Phase 4 معتمد Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
380.4 g/mol
LogP
2.3
Phase
4

Talazoparib is a potent PARP1/2 inhibitor that traps the PARP-DNA complex on damaged DNA, preventing repair and causing irreparable double-strand breaks and cell death specifically in tumor cells with homologous recombination deficiency (HRD) such as BRCA1/2-mutated cancers. It is approved for the treatment of HER2-negative locally advanced or metastatic breast cancer in patients with germline BRCA mutations, and is under investigation in other BRCA-associated tumors. Its high PARP-trapping potency provides superior cytotoxicity in BRCA-deficient cells compared to earlier PARP inhibitors.

الوزن الجزيئي

380,4000 g/mol

LogP

2,30

TPSA

84,20 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)

الآلية

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

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SMILES

Cn1ncnc1[C@H]1c2n[nH]c(=O)c3cc(F)cc(c23)N[C@@H]1c1ccc(F)cc1

InChI

InChI=1S/C19H14F2N6O/c1-27-18(22-8-23-27)15-16(9-2-4-10(20)5-3-9)24-13-7-11(21)6-12-14(13)17(15)25-26-19(12)28/h2-8,15-16,24H,1H3,(H,26,28)/t15-,16-/m1/s1

Molecular Formula

C19H14F2N6O

HBD / HBA

2 / 7

الروابط القابلة للدوران

2

الذرات الثقيلة

28

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

Talazoparib is a potent PARP1/2 inhibitor that traps the PARP-DNA complex on damaged DNA, preventing repair and causing irreparable double-strand breaks and cell death specifically in tumor cells with homologous recombination deficiency (HRD) such as BRCA1/2-mutated cancers. It is approved for the treatment of HER2-negative locally advanced or metastatic breast cancer in patients with germline BRCA mutations, and is under investigation in other BRCA-associated tumors. Its high PARP-trapping potency provides superior cytotoxicity in BRCA-deficient cells compared to earlier PARP inhibitors.

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, Talazoparib is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL3137320. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 135565082. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

إخلاء المسؤولية الطبية

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.