Amoscanate

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Amoscanate
Skeletal formula
Space-filling model
Names
IUPAC name
4-isothiocyanato-N-(4-nitrophenyl)aniline
Other names
4-Isothiocyanato-4′-nitrodiphenylamine
Nithiocyamine
Identifiers
26328-53-0 YesY
ChEBI CHEBI:38944 YesY
ChEMBL ChEMBL93385 YesY
ChemSpider 30904 YesY
Jmol 3D model Interactive image
Interactive image
PubChem 33488
UNII X0MK46CVRB YesY
  • InChI=1S/C13H9N3O2S/c17-16(18)13-7-5-12(6-8-13)15-11-3-1-10(2-4-11)14-9-19/h1-8,15H YesY
    Key: DKVNAGXPRSYHLB-UHFFFAOYSA-N YesY
  • InChI=1/C13H9N3O2S/c17-16(18)13-7-5-12(6-8-13)15-11-3-1-10(2-4-11)14-9-19/h1-8,15H
  • O=N(=O)c1ccc(Nc2ccc(cc2)N=C=S)cc1
  • [O-][N+](=O)c1ccc(cc1)Nc2ccc(N=C=S)cc2
Properties
C13H9N3O2S
Molar mass 271.29 g·mol−1
Melting point 204 to 206 °C (399 to 403 °F; 477 to 479 K)
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Amoscanate (INN), also known as nithiocyamine, is an experimental anthelmintic agent of the arylisothiocyanate class which was found to be highly effective in animals against the four major species of schistosomes which infect humans,[1] and is also highly active against hookworm infection.[2][3] However, significant liver toxicity was seen in lab animals at higher doses. The ether analogue of amoscanate, nitroscanate, is used in veterinary medicine as an anthelmintic.

Amoscanate was developed by Ciba.[4][5]

References

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  5. Lua error in package.lua at line 80: module 'strict' not found. Retrieved on September 10, 2008 through Google Book Search.


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