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(Redirecting to Amines)
 
 
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#redirect[[Amines]]
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{{BioPsy}}
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{{Main|Amines}}
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{{Chembox new
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| ImageFile = Chlorisondamine.png
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| ImageSize = 200px
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| IUPACName = 4,5,6,7-Tetrachloro-2,3-dihydro-2-methyl-2-(2-(trimethylammonio)ethyl)-1''H''-isoindolium dichloride
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| OtherNames =
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| Section1 = {{Chembox Identifiers
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| CASNo = 7701-62-4
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| PubChem = 6243
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| SMILES = ClC1=C2C(C[N](C)(CC[N](C)(C)C)C2)=C(Cl)C(Cl)=C1Cl.[Cl-].[Cl-]
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}}
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| Section2 = {{Chembox Properties
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| C=14 | H=20 | Cl=6 | N=2
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| MolarMass = 429.04 g/mol
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| Appearance =
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| Density =
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| MeltingPt =
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| BoilingPt =
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| Solubility = }}
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| Section3 = {{Chembox Hazards
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| MainHazards =
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| FlashPt =
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| Autoignition = }}
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}}
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'''Chlorisondamine''' is a [[nicotinic antagonist]] that produces both ganglionic and central blockades. Chlorisondamine has been shown to form noncovalent complexes with various biomolecules including [[sphingomyelin]] and other associated [[glycolipid]]s.<ref>Woods, A. S.; Moyer, S. C.; Wang, H. Y. J.; Wise, R. A., Interaction of chlorisondamine with the neuronal nicotinic acetylcholine receptor. Journal of Proteome Research 2003, 2 (2), 207-212.</ref><ref>Jackson, S. N.; Wang, H. Y. J.; Woods, A. S., Direct tissue analysis of phospholipids in rat brain using MALDI-TOFMS and MALDI-ion mobility-TOFMS. Journal of the American Society for Mass Spectrometry 2005, 16 (2), 133-138.</ref><ref>Woods, A. S.; Ugarov, M.; Egan, T.; Koomen, J.; Gillig, K. J.; Fuhrer, K.; Gonin, M.; Schultz, J. A., Lipid/peptide/nucleotide separation with MALDI-ion mobility-TOF MS. Analytical Chemistry 2004, 76 (8), 2187-2195.</ref>
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==References==
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<references/>
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[[Category:Amines]]
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{{enWP|Chlorisondamine}}

Latest revision as of 21:06, December 22, 2008

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Main article: Amines


style="background: #F8EABA; text-align: center;" colspan="2" Chlorisondamine
200px
Identifiers
CAS number 7701-62-4
PubChem 6243
SMILES ClC1=C2C(C[N](C)(CC[N](C)(C)C)C2)=C(Cl)C(Cl)=C1Cl.[Cl-].[Cl-]
Properties
Molecular formula C14H20Cl6N2
Molar mass 429.04 g mol-1
Hazards
style="background: #F8EABA; text-align: center;" colspan="2" Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox disclaimer and references


Chlorisondamine is a nicotinic antagonist that produces both ganglionic and central blockades. Chlorisondamine has been shown to form noncovalent complexes with various biomolecules including sphingomyelin and other associated glycolipids.[1][2][3]

ReferencesEdit

  1. Woods, A. S.; Moyer, S. C.; Wang, H. Y. J.; Wise, R. A., Interaction of chlorisondamine with the neuronal nicotinic acetylcholine receptor. Journal of Proteome Research 2003, 2 (2), 207-212.
  2. Jackson, S. N.; Wang, H. Y. J.; Woods, A. S., Direct tissue analysis of phospholipids in rat brain using MALDI-TOFMS and MALDI-ion mobility-TOFMS. Journal of the American Society for Mass Spectrometry 2005, 16 (2), 133-138.
  3. Woods, A. S.; Ugarov, M.; Egan, T.; Koomen, J.; Gillig, K. J.; Fuhrer, K.; Gonin, M.; Schultz, J. A., Lipid/peptide/nucleotide separation with MALDI-ion mobility-TOF MS. Analytical Chemistry 2004, 76 (8), 2187-2195.
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