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Aganodine

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This is an old revision of this page, as edited by JWBE (talk | contribs) at 08:04, 8 July 2015 (removed Category:Organochlorides; added Category:Chloroarenes using HotCat). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Aganodine
Names
IUPAC name
2-(4,7-Dichloro-1,3-dihydroisoindol-2-yl)guanidine
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
  • InChI=1S/C9H10Cl2N4/c10-7-1-2-8(11)6-4-15(3-5(6)7)14-9(12)13/h1-2H,3-4H2,(H4,12,13,14)
    Key: DFKHOVYSCCPSHR-UHFFFAOYSA-N
  • C1C2=C(C=CC(=C2CN1N=C(N)N)Cl)Cl
Properties
C9H10Cl2N4
Molar mass 245.109
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Aganodine is a guanidine that activates presynaptic imidazoline receptors.[1]

References

  1. ^ Molderings, GJ; Likungu, J; Jakschik, J; Göthert, M (1997). "Presynaptic imidazoline receptors and non-adrenoceptor 3H-idazoxan binding sites in human cardiovascular tissues". British Journal of Pharmacology. 122 (1): 43–50. doi:10.1038/sj.bjp.0701343. PMC 1564902. PMID 9298527.


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