Altretamine drug data and news

Altretamine 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 Altretamine
Brand Names/Synonyms Altretamine; Altretaminum [Inn-Latin]; HEXAMETHYLMELAMINE; HMM; HTM; HXM; Hemel; Hexalen; Hexamethylmelamine; Hexastat; Melamine, Hexamethyl-; NC 195
Indication For use as a single agent in the palliative treatment of patients with persistent or recurrent ovarian cancer following first-line therapy with a cisplatin and/or alkylating agent-based combination
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Description Not Available
Pharmacology Altretamine is a novel antineoplastic agent. The precise mechanism by which altretamine exerts its cytotoxic effect is unknown, although a number of theoretical possibilities have been studied. Structurally, altretamine resembles the alkylating agent triethylenemelamine, yet in vitro tests for alkylating activity of altretamine and its metabolitics have been negative. Altretamine has been demonstrated to be efficacious for certain ovarian tumors resistant to classical alkylating agents. Metabolism of altretamine is a requirement of cytotoxicity. Synthetic monohydroxymethylmelamines, and products of altretamine metabolism, in vitro and in vivo, can form covalent adducts with tissue macromolecules including DNA, but the relevance of these reactions to antitumor activity is unknown.
Mechanism Of Action The precise mechanism by which altretamine exerts its cytotoxic effect is unknown.
Altretamine News
(When available)
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Dosage Forms CAPSULE
Drug_Category Antineoplastic Agents; ATC:L01XX03
Absorption Not Available
Interactions Interactions for Altretamine:

Concurrent administration of HEXALEN and antidepressants of the MAO inhibitor class may cause severe orthostatic hypotension.Cimetidine, an inhibitor of microsomal drug metabolism, increased altretamine's half-life and toxicity in a rat model.

Data from a randomized trial of HEXALEN and cisplatin plus or minus pyridoxine in ovarian cancer indicated that pyridoxine significantly reduced neurotoxicity; however, it adversely affected response duration suggesting that pyridoxine should not be administered with HEXALEN and/or cisplatin.1

Toxicity Not Available
Organisms Affected Humans and other mammals
Chemical IUPAC Name N2,N2,N4,N4,N6,N6-hexamethyl-1,3,5-triazine-2,4,6-triamine
Chemical Formula C9H18N6
Molecular Weight 210.28 g/mol
Smiles String CN(C)C1=NC(=NC(=N1)N(C)C)N(C)C
Melting Point 172-174 °C
Water Solubility 91 mg/L
State Solid
LogP/Hphobicity 1.566
Isoelectric Point Not Available
Biotransformation Not Available
Half Life 4.7-10.2 hours
Protein Binding [%] 94%
RxList Link RXlist
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Drug Reference http://www.drugs.com/cons/Altretamine.html
http://www.rxlist.com/cgi/generic/altretamine.htm
Drug Type Approved Drug
Accession No APRD00652
CAS Registry Number 645-05-6
KEGG Compound ID Not Available
PubChem ID SID:155900
PharmGKB ID PA448337
SwissProt ID Not Available
GenBank ID Not Available
Drug ID Number [DIN] 2126230

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