Vinorelbine

CAS No:
71486-22-1 Category:
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Product Details:

  • CAS No: 71486-22-1
  • AHFC code: 10:00.0
  • Synonyms: Vinorelbin Vinorelbina [Spanish] Vinorelbine Bitartrate Vinorelbine Ditartarate Vinorelbine Ditartrate Vinorelbine Tartrate Vinorelbinum [Latin]
  • ATC Code: L01CA04
  • Chemical Formula: C10H21NO7
  • Molecular Weight: 778.9323
  • Assay/Purity: Typically NLT 98%
  • DrugBank: DB00361 (APRD00101)
  • SMILES: [H][C,,]12N(C)C3=CC(OC)=C(C=C3[C,,]11CCN3CC=C[C,,](CC)([C,,H](OC(C)=O)[C,,]2(O)C(=O)OC)[C,,]13[H])[C,]1(C[C,,]2([H])CN(CC(CC)=C2)CC2=C1NC1=CC=CC=C21)C(=O)OC
  • InChl: GBABOYUKABKIAF-GHYRFKGUSA-N
  • PubChem: 60780
  • IUPAC:

Additional Details

Indication:
For the treatment of non-small-cell lung carcinoma.
Pharmacodynamics:
Vinorelbine is a vinca alkaloid antineoplastic agent used as a treatment for various cancers including breast cancer, Hodgkin's disease, Kaposi's sarcoma, and testicular cancer. The vinca alkaloids are structurally similar compounds comprised of 2 multiringed units, vindoline and catharanthine. The vinca alkaloids have become clinically useful since the discovery of their antitumour properties in 1959. Initially, extracts of the periwinkle plant (Catharanthus roseus) were investigated because of putative hypoglycemic properties, but were noted to cause marrow suppression in rats and antileukemic effects in vitro. Vinorelbine binds to the microtubular proteins of the mitotic spindle, leading to crystallization of the microtubule and mitotic arrest or cell death. Vinorelbine has some immunosuppressant effect. The vinca alkaloids are considered to be cell cycle phase-specific.
Mode of Action:
The antitumor activity of vinorelbine is thought to be due primarily to inhibition of mitosis at metaphase through its interaction with tubulin. Vinorelbine binds to the microtubular proteins of the mitotic spindle, leading to crystallization of the microtubule and mitotic arrest or cell death. Like other vinca alkaloids, vinorelbine may also interfere with: 1) amino acid, cyclic AMP, and glutathione metabolism, 2) calmodulin-dependent Ca2+-transport ATPase activity, 3) cellular respiration, and 4) nucleic acid and lipid biosynthesis.
Metabolism:
Toxicity:
General Reference:
Marty M, Fumoleau P, Adenis A, Rousseau Y, Merrouche Y, Robinet G, Senac I, Puozzo C: Oral vinorelbine pharmacokinetics and absolute bioavailability study in patients with solid tumors. Ann Oncol. 2001 Nov;12(11):1643-9. Pubmed
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