Cannabaceae

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Hexamidine
Skeletal formula of hexamidine
Ball-and-stick model
Names
Preferred IUPAC name
4,4′-[Hexane-1,6-diylbis(oxy)]di(benzene-1-carboximidamide)
Other names
4-[6-(4-carbamimidoylphenoxy)hexoxy]benzamidine
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
DrugBank
UNII
  • InChI=1S/C20H26N4O2/c21-19(22)15-5-9-17(10-6-15)25-13-3-1-2-4-14-26-18-11-7-16(8-12-18)20(23)24/h5-12H,1-4,13-14H2,(H3,21,22)(H3,23,24) checkY
    Key: OQLKNTOKMBVBKV-UHFFFAOYSA-N checkY
  • InChI=1/C20H26N4O2/c21-19(22)15-5-9-17(10-6-15)25-13-3-1-2-4-14-26-18-11-7-16(8-12-18)20(23)24/h5-12H,1-4,13-14H2,(H3,21,22)(H3,23,24)
    Key: OQLKNTOKMBVBKV-UHFFFAOYAW
  • O(c1ccc(cc1)C(=[N@H])N)CCCCCCOc2ccc(C(=[N@H])N)cc2
Properties
C20H26N4O2
Molar mass 354.446
Pharmacology
D08AC04 (WHO) R01AX07 (WHO) R02AA18 (WHO) S01AX08 (WHO) S03AA05 (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 ?)

Hexamidine is an antiseptic and disinfectant. Hexomedine is the trade name of a diisethionate solution (1/1.000) of hexamidine.[1] Hexamidine is used primarily as its diisethionate salt, which is more water-soluble than the dihydrochloride. The dihydrochloride was first synthesized and patented as a trypanocide for May & Baker in 1939. Its amoebicidal properties emerged in the 1990s. The exact mechanism of its biocidal action is unknown, but presumed similar to quaternary ammonium compounds, involving binding to the negatively charged lipid membranes of pathogens. Hexamidine and its shorter congener, propamidine, are used as antiseptics and preservatives in pharmaceuticals and cosmetics. They are particularly used for the topical treatment of acanthamoebiasis (Acanthamoeba keratitis).[2]

References[edit]

  1. ^ "Final Report on the Safety Assessment of Hexamidine and Hexamidine Diisethionate". International Journal of Toxicology. 26 (3_suppl): 79–88. 2007. doi:10.1080/10915810701663168. PMID 18273451. S2CID 2059780.
  2. ^ Parisi, N.; et al. (2017), "Hexamidine salts - applications in skin health and personal care products" (PDF), International Journal of Cosmetic Science, 39 (4): 361–365, doi:10.1111/ics.12392, PMID 28129440, S2CID 3385063


source: https://en.wikipedia.org/wiki/Hexamidine

One thought on “Cannabaceae”

  1. Well, that’s interesting to know that Psilotum nudum are known as whisk ferns. Psilotum nudum is the commoner species of the two. While the P. flaccidum is a rare species and is found in the tropical islands. Both the species are usually epiphytic in habit and grow upon tree ferns. These species may also be terrestrial and grow in humus or in the crevices of the rocks.
    View the detailed Guide of Psilotum nudum: Detailed Study Of Psilotum Nudum (Whisk Fern), Classification, Anatomy, Reproduction

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