Jump to content

Acriflavine: Difference between revisions

From Wikipedia, the free encyclopedia
Browse history interactively
← Previous editNext edit →
Content deleted Content added
VisualWikitext
→External links: Commonscat-inline template.
MCE-CN (talk | contribs)
41 edits
No edit summary
Line 52: Line 52:
'''Acriflavine''' ([[International nonproprietary name|INN]]: '''acriflavinium chloride''') 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. The [[hydrochloride]] form is more irritating than the neutral form.
'''Acriflavine''' ([[International nonproprietary name|INN]]: '''acriflavinium chloride''') 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. The [[hydrochloride]] form is more irritating than the neutral form.
It is derived from [[acridine]]. Commercial preparations are often mixtures with [[proflavine]].<ref name=Sigma>{{cite web | url = http://www.sigmaaldrich.com/catalog/product/sigma/a8126?lang=en | title = Acriflavine | publisher = [[Sigma-Aldrich]]}}</ref> It is known by a variety of commercial names.
It is derived from [[acridine]]. Commercial preparations are often mixtures with [[proflavine]].<ref name=Sigma>{{cite web | url = http://www.sigmaaldrich.com/catalog/product/sigma/a8126?lang=en | title = Acriflavine | publisher = [[Sigma-Aldrich]]}}</ref> It is known by a variety of commercial names.

== Biological Activity ==
''In Vivo'' Acriflavine treatment inhibits intratumoral expression of VEGF and tumor vascularization. In a murine CML model, acriflavine decreases leukemia development and reduces LSC maintenance. Acriflavine retards tumor growth in a murine model of breast cancer. The combination of sunitinib with acriflavine significantly decreases vascular endothelial growth factor and TGF-β expression and reduces tumor vasculature followed by increased intratumor necrosis and apoptosis.<ref>{{Cite web|url=https://www.medchemexpress.com/Acriflavine.html|title=Acriflavine|last=|first=|date=|website=MedChemExpress|archive-url=|archive-date=|dead-url=|access-date=}}</ref>


==Uses==
==Uses==

Revision as of 02:50, 26 June 2019

Acriflavine
Wireframe of acriflavine
Pure acriflavinium chloride: A brown powder
Sample of pure acriflavine
Names
IUPAC name
3,6-Diamino-10-methylacridin-10-ium chloride
Other names
Acriflavinium chloride (INN)
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.211.047 Edit this at Wikidata
EC Number
  • 201-668-8
UNII
  • InChI=1S/C14H13N3.ClH/c1-17-13-7-11(15)4-2-9(13)6-10-3-5-12(16)8-14(10)17;/h2-8H,1H3,(H3,15,16);1H ☒N
    Key: KKAJSJJFBSOMGS-UHFFFAOYSA-N ☒N
  • 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
    Key: PEJLNXHANOHNSU-UHFFFAOYSA-N
  • Key: PEJLNXHANOHNSU-UHFFFAOYSA-N
  • [Cl-].C[N+]1=C2C=C(N)C=CC2=CC2=C1C=C(N)C=C2
  • [Cl-].n1c3c(cc2c1cc(N)cc2)ccc(c3)N.Nc3cc2[n+](c1cc(N)ccc1cc2cc3)C
Properties
C14H14ClN3
Molar mass 259.74 g·mol−1
Pharmacology
R02AA13 (WHO) QG01AC90 (WHO)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Acriflavine (INN: acriflavinium chloride) 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. The hydrochloride form is more irritating than the neutral form. It is derived from acridine. Commercial preparations are often mixtures with proflavine.[1] It is known by a variety of commercial names.

Biological Activity

In Vivo Acriflavine treatment inhibits intratumoral expression of VEGF and tumor vascularization. In a murine CML model, acriflavine decreases leukemia development and reduces LSC maintenance. Acriflavine retards tumor growth in a murine model of breast cancer. The combination of sunitinib with acriflavine significantly decreases vascular endothelial growth factor and TGF-β expression and reduces tumor vasculature followed by increased intratumor necrosis and apoptosis.[2]

Uses

Medical use

Acriflavine was developed in 1912 by Paul Ehrlich, a German medical researcher, and was used during the First World War against sleeping sickness and as a topical antiseptic.[3]

Other uses

Acriflavine is used in biochemistry for fluorescently labeling high molecular weight RNA.[1]

It is used as treatment for external fungal infections of aquarium fish.[4]

Research

In an animal model, acriflavine has been shown to inhibit HIF-1, which prevents blood vessels growing to supply tumors with blood and interferes with glucose uptake and use.[5]

Acriflavine might be effective in fighting common cold virus, and also aid the fight against increasingly antibiotic resistant bacteria.[6][7][8]

Since 2014, acriflavine has been undergoing testing as an antimalarial drug to treat parasites with resistance to quinine and modern anti-parasitic medicines. [9]

Australia

Acriflavine is a controlled substance in Australia and dependent on situation,[clarification needed] 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.[citation needed]

References

  1. ^ a b "Acriflavine". Sigma-Aldrich.
  2. ^ "Acriflavine". MedChemExpress. {{cite web}}: Cite has empty unknown parameter: |dead-url= (help)
  3. ^ acriflavine Encyclopædia Britannica
  4. ^ Acriflavine use in aquaria
  5. ^ Lee, K.; Zhang, H.; Qian, D. Z.; Rey, S.; Liu, J. O.; Semenza, G. L. (2009). "Acriflavine inhibits HIF-1 dimerization, tumor growth, and vascularization". Proceedings of the National Academy of Sciences. 106 (42): 17910. Bibcode:2009PNAS..10617910L. doi:10.1073/pnas.0909353106. PMC 2764905. PMID 19805192.
  6. ^ "Antiseptic used in WWI could hold key to treating superbugs, viral infections, Melbourne researchers say". ABC. November 28, 2016.
  7. ^ "This forgotten WWI antiseptic could be the key to fighting antibiotic resistance". Science Alert. November 30, 2016.
  8. ^ Pépin, Geneviève; Nejad, Charlotte; Thomas, Belinda J; Ferrand, Jonathan; McArthur, Kate; Bardin, Philip G; Williams, Bryan R.G; Gantier, Michael P (2016). "Activation of cGAS-dependent antiviral responses by DNA intercalating agents". Nucleic Acids Research. 45 (1): 198–205. doi:10.1093/nar/gkw878. PMC 5224509. PMID 27694309.
  9. ^ Dana, Srikanta; Prusty, Dhaneswar; Dhayal, Devender; Gupta, Mohit Kumar; Dar, Ashraf; Sen, Sobhan; Mukhopadhyay, Pritam; Adak, Tridibesh; Dhar, Suman Kumar (2014). "Potent Antimalarial Activity of Acriflavine In Vitroand In Vivo". ACS Chemical Biology. 9 (10): 2366. doi:10.1021/cb500476q. PMC 4201339. PMID 25089658.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Acriflavine&oldid=903506407"