Cabazitaxel

CHEMBL1201748 Phase 4 Zugelassen Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
835.9 g/mol
LogP
2.7
Phase
4

A taxane chemotherapy agent used to treat metastatic castration-resistant prostate cancer in patients who have previously received docetaxel-based treatment. It stabilizes microtubules to prevent cancer cells from dividing and is notable for activity in tumors that have become resistant to docetaxel. Severe neutropenia is its most serious side effect.

Molekularmasse

835,9000 g/mol

LogP

2,70

TPSA

202,00 Ų

Lipinski-Regel der Fünf

Nicht bestanden

Therapeutische Bereiche

Wirkmechanismus

Disrupts microtubule dynamics by binding to tubulin, preventing the formation of the mitotic spindle and arresting cell division at metaphase. This induces apoptosis in rapidly dividing cells.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mechanismus

Disrupts microtubule dynamics by binding to tubulin, preventing the formation of the mitotic spindle and arresting cell division at metaphase. This induces apoptosis in rapidly dividing cells.

2D-Struktur

SVG PNG

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SMILES

CO[C@H]1C(=O)[C@]2(C)[C@@H](OC)C[C@H]3OC[C@@]3(OC(C)=O)[C@H]2[C@H](OC(=O)c2ccccc2)[C@]2(O)C[C@H](OC(=O)[C@H](O)[C@@H](NC(=O)OC(C)(C)C)c3ccccc3)C(C)=C1C2(C)C

InChI

InChI=1S/C45H57NO14/c1-24-28(57-39(51)33(48)32(26-17-13-11-14-18-26)46-40(52)60-41(3,4)5)22-45(53)37(58-38(50)27-19-15-12-16-20-27)35-43(8,36(49)34(55-10)31(24)42(45,6)7)29(54-9)21-30-44(35,23-56-30)59-25(2)47/h11-20,28-30,32-35,37,48,53H,21-23H2,1-10H3,(H,46,52)/t28-,29-,30+,32-,33+,34+,35-,37-,43+,44-,45+/m0/s1

Molecular Formula

C45H57NO14

HBD / HBA

3 / 14

Rotierbare Bindungen

15

Schwere Atome

60

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.

Häufig gestellte Fragen

A taxane chemotherapy agent used to treat metastatic castration-resistant prostate cancer in patients who have previously received docetaxel-based treatment. It stabilizes microtubules to prevent cancer cells from dividing and is notable for activity in tumors that have become resistant to docetaxel. Severe neutropenia is its most serious side effect.

Disrupts microtubule dynamics by binding to tubulin, preventing the formation of the mitotic spindle and arresting cell division at metaphase. This induces apoptosis in rapidly dividing cells.

Yes, Cabazitaxel 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). CHEMBL1201748. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 9854073. Chemical information database.

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

Medizinischer Haftungsausschluss

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.