Bortezomib D-Mannitol

CHEMBL5315122 Phase 4 Onaylandı Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
530.4 g/mol
LogP
Phase
4

A formulation of bortezomib, a proteasome inhibitor used to treat multiple myeloma and certain types of mantle cell lymphoma, lyophilized with d-mannitol for stability. It disrupts protein degradation pathways in cancer cells, triggering cell death. Side effects include peripheral neuropathy, low blood counts, and fatigue.

Moleküler Ağırlık

530,4000 g/mol

TPSA

183,00 Ų

Etki Mekanizması

Inhibits the 26S proteasome, blocking the ubiquitin-proteasome pathway of intracellular protein degradation. This leads to accumulation of pro-apoptotic proteins and induces cell death in rapidly dividing cancer cells.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mekanizma

Inhibits the 26S proteasome, blocking the ubiquitin-proteasome pathway of intracellular protein degradation. This leads to accumulation of pro-apoptotic proteins and induces cell death in rapidly dividing cancer cells.

2D Yapı

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SMILES

CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)c1cnccn1)B1O[C@H]([C@H](O)CO)[C@@H]([C@H](O)CO)O1

InChI

InChI=1S/C25H35BN4O8/c1-15(2)10-21(26-37-22(19(33)13-31)23(38-26)20(34)14-32)30-24(35)17(11-16-6-4-3-5-7-16)29-25(36)18-12-27-8-9-28-18/h3-9,12,15,17,19-23,31-34H,10-11,13-14H2,1-2H3,(H,29,36)(H,30,35)/t17-,19+,20+,21-,22+,23+/m0/s1

Molecular Formula

C25H35BN4O8

HBD / HBA

6 / 10

Döndürülebilir Bağlar

13

Ağır Atomlar

38

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.

Sıkça Sorulan Sorular

A formulation of bortezomib, a proteasome inhibitor used to treat multiple myeloma and certain types of mantle cell lymphoma, lyophilized with d-mannitol for stability. It disrupts protein degradation pathways in cancer cells, triggering cell death. Side effects include peripheral neuropathy, low blood counts, and fatigue.

Inhibits the 26S proteasome, blocking the ubiquitin-proteasome pathway of intracellular protein degradation. This leads to accumulation of pro-apoptotic proteins and induces cell death in rapidly dividing cancer cells.

Yes, Bortezomib D-Mannitol 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). CHEMBL5315122. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 12990536. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

Tıbbi Sorumluluk Reddi

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.