Diminazen
Structural formula | ||||||||||||||||||||||
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Non-proprietary name | Diminazen | |||||||||||||||||||||
other names |
4,4 '- (Triazene-1,3-diyl) dibenzen carbimidamide |
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Molecular formula | C 14 H 15 N 7 | |||||||||||||||||||||
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Drug information | ||||||||||||||||||||||
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Mechanism of action |
unknown |
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properties | ||||||||||||||||||||||
Molar mass | 281.32 g · mol -1 | |||||||||||||||||||||
safety instructions | ||||||||||||||||||||||
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Diminazen is a drug from the group of aromatic di- amidines . Diminazen is used in veterinary medicine as a diaceturate salt ( N -acetylglycinate) intramuscularly, subcutaneously or cutaneously against pathogenic protozoa such as Babesia , Trypanosoma , Leishmania and Cytauxzoon and against some bacteria ( Brucella and streptococci ). The exact mechanism of action is not yet known exactly diminazene probably inhibits DNA - replication .
Since the active ingredient is not listed in any annex of Regulation (EEC) No. 2377/90 on maximum levels for veterinary drug residues in food , the use of Diminazen in food-producing animals is prohibited in the European Union.
Side effects
Diminazen can cause severe, sometimes fatal, damage to the liver, kidneys and brain. Acute side effects are vomiting, diarrhea, and low blood pressure.
Camels in particular are very sensitive to Diminazen, and fatal incidents can occur even at therapeutic doses.
Trade names
Azidine, Berenil, Ganasag, Pirocide
literature
- Peregrine, AS and Mamman, M. (1993): Pharmacology of diminazene: a review. In: Acta Trop. 54 (3-4); 185-203. PMID 7902657 .
Web links
- Entry to diminazene at Vetpharm
Individual evidence
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
- ^ Lut, Lynen: Local application of diminazene aceturate: An effective treatment for cutaneous leishmaniasis? In: researchgate.net. ResearchGate, April 1, 1992, accessed April 9, 2020 .