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Valrubicin

Catalog No. DB00385 Name DrugBank
CAS Number 56124-62-0 Website http://www.ualberta.ca/
M. F. C34H36F3NO13 Telephone (780) 492-3111
M. W. 723.6437496 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 269

SYNONYMS

IUPAC name
2-oxo-2-[(2S,4S)-2,5,12-trihydroxy-4-{[5-hydroxy-6-methyl-4-(trifluoroacetamido)oxan-2-yl]oxy}-7-methoxy-6,11-dioxo-1,2,3,4,6,11-hexahydrotetracen-2-yl]ethyl pentanoate
IUPAC Traditional name
valtaxin
Brand Name
Valstar
Valstar Preservative Free
Synonyms
Antibiotic Ad 32

DATABASE IDS

PubChem SID 46506642
PubChem CID 41744
CAS Number 56124-62-0

PROPERTIES

Hydrophobicity(logP) 2.2
Solubility insoluble

DETAILS

Description (English)
Item Information
Drug Groups approved
Description Valrubicin (N-trifluoroacetyladriamycin-14-valerate, Valstar®) is a chemotherapy drug used to treat bladder cancer. Valrubicin is a semisynthetic analog of the anthracycline doxorubicin, and is administered by infusion directly into the bladder. [Wikipedia]
Indication For the treatment of cancer of the bladder.
Pharmacology Valrubicin is a semisynthetic analog of the anthracycline doxorubicin, and is administered by infusion directly into the bladder.
Toxicity The primary anticipated complications of overdosage associated with intravesical administration would be consistent with irritable bladder symptoms. Myelosuppression is possible if valrubicin is inadvertently administered systemically or if significant systemic exposure occurs following intravesical administration (e.g., in patients with bladder/rupture perforation). The maximum tolerated dose in humans by either intraperitoneal or intravenous administration is 600 mg/m2.
Affected Organisms
Humans and other mammals
Biotransformation Valrubicin is metabolized to two primary metabolites: N-trifluoroacetyladriamycin and N-trifluoroacetyladriamycinol.
Protein Binding >99%
External Links
Wikipedia
RxList
Drugs.com

REFERENCES