Trilaciclib Dihydrochloride

CHEMBL4650272 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
519.5 g/mol
LogP
Phase
4

Trilaciclib dihydrochloride is the dihydrochloride salt form of trilaciclib, a CDK4/6 inhibitor that transiently induces G1 cell cycle arrest in hematopoietic progenitor cells to protect bone marrow during chemotherapy. It reduces the need for granulocyte colony-stimulating factor and red blood cell transfusions following myelosuppressive chemotherapy. This salt form is used in the clinical formulation of the intravenous product.

Khối lượng phân tử

519,5000 g/mol

TPSA

91,20 Ų

Lĩnh vực điều trị

Cơ chế tác dụng

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)

Cơ chế

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.

Cấu trúc 2D

SVG PNG

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SMILES

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

InChI

InChI=1S/C24H30N8O.2ClH/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);2*1H

Molecular Formula

C24H32Cl2N8O

HBD / HBA

4 / 7

Liên kết có thể quay

3

Nguyên tử nặng

35

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.

Câu hỏi thường gặp

Trilaciclib dihydrochloride is the dihydrochloride salt form of trilaciclib, a CDK4/6 inhibitor that transiently induces G1 cell cycle arrest in hematopoietic progenitor cells to protect bone marrow during chemotherapy. It reduces the need for granulocyte colony-stimulating factor and red blood cell transfusions following myelosuppressive chemotherapy. This salt form is used in the clinical formulation of the intravenous product.

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 Dihydrochloride 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). CHEMBL4650272. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 124081865. Chemical information database.

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

Tuyên bố miễn trách y tế

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.