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Script assisted update of identifiers from ChemSpider, CommonChemistry and FDA for the Chem/Drugbox validation project - Updated: InChI->StdInChI InChI1->InChI InChI1 InChIKey1. |
Script assisted update of identifiers from ChemSpider, CommonChemistry and FDA for the Chem/Drugbox validation project - Updated: InChI1->InChI InChI1 InChIKey1. |
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| StdInChIKey1 = PEJLNXHANOHNSU-UHFFFAOYAC |
| StdInChIKey1 = PEJLNXHANOHNSU-UHFFFAOYAC |
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| SMILES1 = [Cl-].n1c3c(cc2c1cc(N)cc2)ccc(c3)N.Nc3cc2[n+](c1cc(N)ccc1cc2cc3)C |
| SMILES1 = [Cl-].n1c3c(cc2c1cc(N)cc2)ccc(c3)N.Nc3cc2[n+](c1cc(N)ccc1cc2cc3)C |
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| InChI = 1S/C14H13N3.C13H11N3.ClH/c1-17-13-7-11(15)4-2-9(13)6-10-3-5-12(16)8-14(10)17;14-10-3-1-8-5-9-2-4-11(15)7-13(9)16-12(8)6-10;/h2-8H,1H3,(H3,15,16);1-7H,14-15H2;1H |
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| InChIKey = PEJLNXHANOHNSU-UHFFFAOYSA-N |
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| InChI1 = 1S/C14H13N3.C13H11N3.ClH/c1-17-13-7-11(15)4-2-9(13)6-10-3-5-12(16)8-14(10)17;14-10-3-1-8-5-9-2-4-11(15)7-13(9)16-12(8)6-10;/h2-8H,1H3,(H3,15,16);1-7H,14-15H2;1H |
| InChI1 = 1S/C14H13N3.C13H11N3.ClH/c1-17-13-7-11(15)4-2-9(13)6-10-3-5-12(16)8-14(10)17;14-10-3-1-8-5-9-2-4-11(15)7-13(9)16-12(8)6-10;/h2-8H,1H3,(H3,15,16);1-7H,14-15H2;1H |
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| InChIKey1 = PEJLNXHANOHNSU-UHFFFAOYSA-N |
| InChIKey1 = PEJLNXHANOHNSU-UHFFFAOYSA-N |
Revision as of 09:59, 29 November 2010
Names | |
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IUPAC name
3,6-Diamino-10-methylacridin-10-ium chloride
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Identifiers | |
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3D model (JSmol)
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ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.211.047 |
EC Number |
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PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C14H14ClN3 | |
Molar mass | 259.74 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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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.In recent years Acriflavine has been shown to have anti-cancer activity.
References
- Encyclopedia Britannica (accessed 2005-08-16)
- ChemExper Chemical Directory (accessed 2005-08-16)
- Houghton Mifflin definition (accessed 2005-08-16)