Acriflavinium chloride
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![]() Pure acriflavinium chloride
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Names | |
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IUPAC name
3,6-Diamino-10-methylacridin-10-ium chloride
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Identifiers | |
65589-70-0 ![]() 10597-46-3 (HCl) ![]() |
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ChEBI | CHEBI:383703 ![]() |
ChEMBL | ChEMBL354349 ![]() |
ChemSpider | 391386 ![]() 21018 (HCl) ![]() |
EC Number | 201-668-8 |
Jmol 3D model | Interactive image Interactive image |
PubChem | 443101 15558347 (HCl) |
UNII | 1S73VW819C ![]() |
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Properties | |
C14H14ClN3 | |
Molar mass | 259.74 g·mol−1 |
Pharmacology | |
ATC code | R02 QG01AC90 (WHO) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references | |
Acriflavine is a topical antiseptic. It has the form of an orange or brown powder. It may be harmful in the eyes or if inhaled. It is a dye and it stains the skin and may irritate. Commercial preparations are often mixtures with proflavine. It is known by a variety of commercial names.
Acriflavine was developed in 1912 by Paul Ehrlich, a German medical researcher, and was used during the First World War against sleeping sickness. It is derived from acridine. The hydrochloride form is more irritating than the neutral form.
Acriflavine is also used as treatment for external fungal infections of aquarium fish.
Acriflavine has been shown to have anti-cancer activity by inhibition of HIF-1 which prevents blood vessels growing to supply tumors with blood and interferes with glucose uptake and use.[1]
Acriflavine is a controlled substance in Australia and dependent on situation, is considered either a Schedule 5 (Caution) or Schedule 7 (Dangerous Poison) substance. The use, storage and preparation of the chemical is subject to strict state and territory laws.
In November 2016 it was suggested that Acrifavinium might be the key to fighting antibiotic-resistant bacteria.[2]
References
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- Encyclopædia Britannica (accessed 2005-08-16)
- ChemExper Chemical Directory (accessed 2005-08-16)
- Houghton Mifflin definition (accessed 2005-08-16)
- Pages with reference errors
- Chemical articles with multiple CAS Registry Numbers
- Articles without KEGG source
- Chembox and Drugbox articles with a broken CheMoBot template
- Articles with changed InChI identifier
- Pages using collapsible list with both background and text-align in titlestyle
- Antiseptics
- Quaternary ammonium compounds
- Acridines
- Chlorides