Ribociclib Succinate
The succinate salt formulation of ribociclib used alongside hormonal therapy for advanced breast cancer, blocking key cell cycle proteins to prevent tumor progression. Clinical trials have demonstrated it can significantly extend progression-free survival.
Molecular Weight
552.6000 g/mol
TPSA
166.00 Ų
Therapeutic Areas
Mechanism of Action
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)
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.
2D Structure
Cite this structure
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SMILES
CN(C)C(=O)c1cc2cnc(Nc3ccc(N4CCNCC4)cn3)nc2n1C1CCCC1.O=C(O)CCC(=O)O
InChI
InChI=1S/C23H30N8O.C4H6O4/c1-29(2)22(32)19-13-16-14-26-23(28-21(16)31(19)17-5-3-4-6-17)27-20-8-7-18(15-25-20)30-11-9-24-10-12-30;5-3(6)1-2-4(7)8/h7-8,13-15,17,24H,3-6,9-12H2,1-2H3,(H,25,26,27,28);1-2H2,(H,5,6)(H,7,8)
Molecular Formula
C27H36N8O5
HBD / HBA
4 / 11
Rotatable Bonds
8
Heavy Atoms
40
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.
Frequently Asked Questions
The succinate salt formulation of ribociclib used alongside hormonal therapy for advanced breast cancer, blocking key cell cycle proteins to prevent tumor progression. Clinical trials have demonstrated it can significantly extend progression-free survival.
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, Ribociclib Succinate 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). CHEMBL3707266. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 57334219. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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