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Vinflunine

Vinflunine Structure
Vinflunine
  • CAS No.162652-95-1
  • Chemical Name:Vinflunine
  • CBNumber:CB2358406
  • Molecular Formula:C45H54F2N4O8
  • Formula Weight:816.94
  • MOL File:162652-95-1.mol
Vinflunine Property
Hazard and Precautionary Statements (GHS)
  • Symbol(GHS)
  • Signal word
  • Hazard statements
  • Precautionary statements

Vinflunine Chemical Properties,Usage,Production

  • Description Vinflunine (also referred to as PM391) is a semisynthetic analog of the natural vinca alkaloids vinblastine and vincristine that was approved by the European Medicines Agency (EMEA) in 2009 for the treatment of adult patients with advanced or metastatic transitional cell carcinoma of the urothelial tract after failure of a prior platinum-containing regimen. Vinflunine is synthesized from anhydrovinblastine in a superacid media (HF-SbF5) and in the presence of a chlorinated solvent like CHCl3 or CCl4.
  • Originator Pierre Fabre (France)
  • Definition ChEBI: An organic heteropentacyclic compound and an organic heterotetracyclic compound that is vinorelbine in which the tetrahydropyridine moiety of the heterotetracyclic part of the molecule has been redced to the corresponding piperidine, and in which the ethy group attached to this ring has been replaced by a 1,1-difluoroethyl group.
  • brand name Javlor
  • Clinical Use Antineoplastic agent (vinca alkaloid):
    Treatment of advanced or metastatic bladder cancer
  • Drug interactions Potentially hazardous interactions with other drugs
    Antibacterials: possible increased risk of ventricular arrhythmias with delamanid; concentration possibly reduced by rifampicin - avoid.
    Antidepressants: concentration possibly reduced by St Johns wort - avoid.
    Antifungals: concentration increased by ketoconazole and possibly itraconazole (increased risk of neurotoxicity) - avoid.
    Antimalarials: avoid with piperaquine with artenimol.
    Antipsychotics: avoid with clozapine (increased risk of agranulocytosis).
    Antivirals: concentration possibly increased by ritonavir - avoid.
    Grapefruit juice: concentration of vinflunine increased - avoid.
  • Metabolism Metabolised by the cytochrome CYP3A4 isoenzyme, except for 4-O-deacetylvinflunine (DVFL), the only active metabolite and main metabolite in blood which is formed by multiple esterases. Excretion occurs via the faeces (about two-thirds) and the urine (about one-third).
Vinflunine Preparation Products And Raw materials
Raw materials
Preparation Products
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Vinflunine Spectrum
162652-95-1, VinflunineRelated Search:
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  • C45H54F2N4O8
  • 长春氟宁(治疗膀胱癌)
  • 长春氟宁
  • 酒石酸长春氟宁
  • 162652-95-1
  • vinflunine(97%)
  • Aspidospermidine-3-carboxylicacid,4-(acetyloxy)-6,7-didehydro-15-[(2R,4R,6S,8S)-4-(1,1-difluoroethyl)-1,3,4,5,6,7,8,9-octahydro-8-(methoxycarbonyl)-2,6-methano-2H-azecino[4,3-b]indol-8-yl]-3-hydroxy-1
  • Vinflunine (F12158)
  • Vinflunine USP/EP/BP
  • Aspidospermidine-3-carboxylic acid, 4-(acetyloxy)-6,7-didehydro-15-[(2R,4R,6S,8S)-4-(1,1-difluoroethyl)-1,3,4,5,6,7,8,9-octahydro-8-(methoxycarbonyl)-2,6-methano-2H-azecino[4,3-b]indol-8-yl]-3-hydroxy-16-methoxy-1-methyl-, methyl ester, (2β,3β,4β,5α,12R,19α)-
  • Vinflunine 162652-95-1
  • Vinflunine Tartrate
  • 4'-Deoxy-20',20'-difluoro-8'-norvincaleukoblastine
  • 4'-Deoxy-20',20'-difluoro-5'-norvincaleukoblastine
  • 20',20'-Difluoro-3',4'-dihydrovinorelbine
  • VINFLUNINE