Trilaciclib

CHEMBL3894860 Phase 4 معتمد Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
446.5 g/mol
LogP
2.6
Phase
4

Trilaciclib is a first-in-class CDK4/6 inhibitor that transiently arrests hematopoietic stem and progenitor cells in G1 phase before chemotherapy administration, thereby protecting bone marrow from chemotherapy-induced damage. It is used to decrease the incidence of chemotherapy-induced myelosuppression in adults receiving certain chemotherapy regimens for small cell lung cancer. Its myeloprotective mechanism distinguishes it from CDK4/6 inhibitors used as antineoplastic agents.

الوزن الجزيئي

446,5000 g/mol

LogP

2,60

TPSA

91,20 Ų

قاعدة ليبينسكي للخمسة

ناجح

المجالات العلاجية

آلية العمل

Selectively inhibits cyclin-dependent kinases 4 and 6 (CDK4/6), blocking the phosphorylation of retinoblastoma protein and arresting the cell cycle at the G1/S transition to prevent cancer cell proliferation.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

الآلية

Selectively inhibits cyclin-dependent kinases 4 and 6 (CDK4/6), blocking the phosphorylation of retinoblastoma protein and arresting the cell cycle at the G1/S transition to prevent cancer cell proliferation.

البنية ثنائية الأبعاد

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SMILES

CN1CCN(c2ccc(Nc3ncc4cc5n(c4n3)C3(CCCCC3)CNC5=O)nc2)CC1

InChI

InChI=1S/C24H30N8O/c1-30-9-11-31(12-10-30)18-5-6-20(25-15-18)28-23-26-14-17-13-19-22(33)27-16-24(7-3-2-4-8-24)32(19)21(17)29-23/h5-6,13-15H,2-4,7-12,16H2,1H3,(H,27,33)(H,25,26,28,29)

Molecular Formula

C24H30N8O

HBD / HBA

2 / 7

الروابط القابلة للدوران

3

الذرات الثقيلة

33

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

Trilaciclib is a first-in-class CDK4/6 inhibitor that transiently arrests hematopoietic stem and progenitor cells in G1 phase before chemotherapy administration, thereby protecting bone marrow from chemotherapy-induced damage. It is used to decrease the incidence of chemotherapy-induced myelosuppression in adults receiving certain chemotherapy regimens for small cell lung cancer. Its myeloprotective mechanism distinguishes it from CDK4/6 inhibitors used as antineoplastic agents.

Selectively inhibits cyclin-dependent kinases 4 and 6 (CDK4/6), blocking the phosphorylation of retinoblastoma protein and arresting the cell cycle at the G1/S transition to prevent cancer cell proliferation.

Yes, Trilaciclib 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). CHEMBL3894860. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 68029831. 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.