Teniposide drug data and news

Teniposide drug data, resources, and news articles (when available). Onconews.org provides news on cancer research. This section, which includes profiles on medicines that may or not be cancer-related is in beta form. If things run smoothly we will be releasing a new format late in the summer of 2006.

Generic name Teniposide
Brand Names/Synonyms CCRIS 2058; EPT; Etoposide; Etoposide Usp26; HSDB 6546; PTG; Teniposide; Teniposide [Usan:Ban:Inn]; Teniposido [Inn-Spanish]; Teniposidum [Inn-Latin]; VM 26; VM-26; Vee M-26; Veham-Sandoz; Vehem; Vumon
Indication Treatment of refractory acute lymphoblastic leukaemia
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Description Not Available
Pharmacology Teniposide is a phase-specific cytotoxic drug, acting in the late S or early G 2 phase of the cell cycle, thus preventing cells from entering mitosis. Teniposide causes dose-dependent single- and double-stranded breaks in DNA and DNA: protein cross-links. The mechanism of action appears to be related to the inhibition of type II topoisomerase activity since teniposide does not intercalate into DNA or bind strongly to DNA.
Mechanism Of Action Binds to and inhibits DNA topoisomerase II. The cytotoxic effects of teniposide are related to the relative number of double-stranded DNA breaks produced in cells, which are a reflection of the stabilization of a topoisomerase II-DNA intermediate.
Teniposide News
(When available)
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Dosage Forms LIQUID
Drug_Category Antineoplastic Agents; ATC:L01CB02
Absorption Not Available
Interactions Interactions for Teniposide:

Drug Interactions:   In a study in which 34 different drugs were tested, therapeutically relevant concentrations of tolbutamide, sodium salicylate and sulfamethizole displaced protein-bound teniposide in fresh human serum to a small but significant extent. Because of the extremely high binding of teniposide to plasma proteins, these small decreases in binding could cause substantial increases in free drug levels in plasma which could result in potentiation of drug toxicity. Therefore, caution should be used in administering VUMON (teniposide injection) to patients receiving these other agents. There was no change in the plasma kinetics of teniposide when coadministered with methotrexate. However, the plasma clearance of methotrexate was slightly increased. An increase in intracellular levels of methotrexate was observed in vitro in the presence of teniposide.

Toxicity Not Available
Organisms Affected Humans and other mammals
Chemical IUPAC Name Not Available
Chemical Formula C32H32O13S
Molecular Weight 656.655 g/mol
Smiles String COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C7C(O6)COC(O7)C8=CC=CS8)O)O
Melting Point Not Available
Water Solubility Not Available
State Solid
LogP/Hphobicity 1.963
Isoelectric Point Not Available
Biotransformation Not Available
Half Life 5 hours
Protein Binding [%] Not Available
RxList Link RXlist
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Drug Reference http://www.drugs.com/cons/Teniposide.html
http://www.rxlist.com/cgi/generic2/teniposide.htm
Drug Type Approved Drug
Accession No APRD00649
CAS Registry Number 29767-20-2
KEGG Compound ID C11153
PubChem ID SID:176397
PharmGKB ID Not Available
SwissProt ID Not Available
GenBank ID Not Available
Drug ID Number [DIN] 588989

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