Dithiazanine iodide

Dithiazanine iodide
Names
IUPAC name
3-Ethyl-2-[5-(3-ethyl-2-benzothiazolinylidene)-1,3-pentadienyl]-benzothiazolium iodide
Systematic IUPAC name
3-Ethyl-2-[(1E,3E,5Z)-5-(3-ethyl-1,3-benzothiazol-2(3H)-ylidene)penta-1,3-dien-1-yl]-1,3-benzothiazol-3-ium iodide
Identifiers
CAS Number
3D model (JSmol)
  • Interactive image
Beilstein Reference
3838938
ChEBI
  • CHEBI:228275
ChEMBL
  • ChEMBL421701
ChemSpider
  • 4642986
ECHA InfoCard 100.007.443 Edit this at Wikidata
EC Number
  • 208-186-7
KEGG
  • C18391
PubChem CID
  • 5702697
UNII
  • 8OEC3RA07X checkY
UN number 2811
CompTox Dashboard (EPA)
  • DTXSID8022955 Edit this at Wikidata
InChI
  • InChI=1S/C23H23N2S2.HI/c1-3-24-18-12-8-10-14-20(18)26-22(24)16-6-5-7-17-23-25(4-2)19-13-9-11-15-21(19)27-23;/h5-17H,3-4H2,1-2H3;1H/q+1;/p-1[2]
    Key: MNQDKWZEUULFPX-UHFFFAOYSA-M[2]
  • [I-].S\1c4ccccc4N(C/1=C\C=C\C=C\c3sc2ccccc2[n+]3CC)CC
Properties
Chemical formula
C23H23IN2S2
Molar mass 518.48 g·mol−1
Appearance Green crystals
Melting point Decomposes at 478.4 °F (248.0 °C)
Hazards
GHS labelling:
Pictograms
GHS06: ToxicGHS07: Exclamation mark
Danger
H300, H315, H319, H335
P261, P264, P270, P271, P280, P301+P310, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound

Dithiazanine iodide is a chemical compound belonging to the group of polymethine dyes.[1] It is used as a veterinary anthelmintic for dogs.[3] It is a highly toxic chemical, with a lethal dose for humans of about 4–16 mg/kg by oral ingestion. The mechanism of toxicity is not well known but it is believed that this chemical interferes with cells' absorption of glucose, which is essential to obtain energy through cell respiration. [citation needed]

References

  1. ^ a b Cameo Chemicals. "Chemical data". NOAA. Retrieved September 19, 2011.
  2. ^ a b "Chemspider data". Chemspider. Retrieved September 19, 2011.
  3. ^ "Law about use". Justia. Retrieved September 19, 2011.
  • v
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Antiplatyhelmintic agents
Antitrematodals
(schistosomicides)
Binds tubulin
AChE inhibitor
Other/unknown
Anticestodals
(taeniacides)
Binds tubulin
Other/unknown
Antinematodal agents
(including
macrofilaricides)
Binds tubulin
Glutamate-gated chloride channel, GABA receptor
NMDA
Other/unknown