Identification | |||||||||||||||||||||||||
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Name | Altretamine | ||||||||||||||||||||||||
Accession Number | DB00488 (APRD00652) | ||||||||||||||||||||||||
Type | small molecule | ||||||||||||||||||||||||
Description | An alkylating agent proposed as an antineoplastic. It also acts as a chemosterilant for male houseflies and other insects. [PubChem] | ||||||||||||||||||||||||
Structure |
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Categories (*) | |||||||||||||||||||||||||
Molecular Weight | 210.2794 | ||||||||||||||||||||||||
Groups | approved | ||||||||||||||||||||||||
Monoisotopic Weight | 210.159294606 | ||||||||||||||||||||||||
Pharmacology | |||||||||||||||||||||||||
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. | ||||||||||||||||||||||||
Mechanism of action | The precise mechanism by which altretamine exerts its cytotoxic effect is unknown although it is classified as an alkylating anti-neoplastic agent. Through this mechanism, the drug is metabolized into alkylating agents by N-demethylation. These alkylating species consequently damage tumor cells. | ||||||||||||||||||||||||
Absorption | Not Available | ||||||||||||||||||||||||
Protein binding | 94% | ||||||||||||||||||||||||
Biotransformation | Not Available | ||||||||||||||||||||||||
Route of elimination | Human urinary metabolites were Ndemethylated homologues of altretamine with <1% unmetabolized altretamine excreted at 24 hours. | ||||||||||||||||||||||||
Toxicity | Not Available | ||||||||||||||||||||||||
Affected organisms |
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Interactions | |||||||||||||||||||||||||
Drug Interactions |
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Food Interactions | Not Available |
DNA | |
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Name | DNA |
Gene Name | Not Available |
Pharmacological action | yes |
Actions | other/unknown |
References |
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DTHybrid score | Not Available |
Id | Partner name | Gene Name | Score |
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