Chemistry:Ditolylguanidine

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Short description: Experimental drug
Ditolylguanidine
1,3-Ditolylguanidine.svg
Ditolylguanidine 3D BS.png
Clinical data
ATC code
  • none
Identifiers
CAS Number
PubChem CID
IUPHAR/BPS
ChemSpider
UNII
ChEMBL
Chemical and physical data
FormulaC15H17N3
Molar mass239.322 g·mol−1
3D model (JSmol)
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Ditolylguanidine is a sigma receptor agonist.[1] It is somewhat[2] selective for sigma receptors, but non-selective between the two sigma receptor subtypes, binding to both σ1 and σ2 with equal affinity.[3] It has neuroprotective[4] and antidepressant effects,[5] and potentiates the effects of NMDA antagonists.[6]

See also

References

  1. "1,3-Di(2-[5-3Htolyl)guanidine: a selective ligand that labels sigma-type receptors for psychotomimetic opiates and antipsychotic drugs"]. Proceedings of the National Academy of Sciences of the United States of America 83 (22): 8784–8788. November 1986. doi:10.1073/pnas.83.22.8784. PMID 2877462. Bibcode1986PNAS...83.8784W. 
  2. "1,3-Di-o-tolylguanidine | C15H17N3" (in en). PubChem. U.S. National Library of Medicine. https://pubchem.ncbi.nlm.nih.gov/compound/7333#section=BioAssay-Results. 
  3. "Pharmacophore identification for sigma-1 (sigma1) receptor binding: application of the "deconstruction-reconstruction-elaboration" approach". Mini Reviews in Medicinal Chemistry 5 (10): 927–940. October 2005. doi:10.2174/138955705774329519. PMID 16250835. 
  4. "Sigma-1 receptor activation prevents intracellular calcium dysregulation in cortical neurons during in vitro ischemia". The Journal of Pharmacology and Experimental Therapeutics 319 (3): 1355–1365. December 2006. doi:10.1124/jpet.106.107557. PMID 16988055. 
  5. "Sigma1 receptor antagonists attenuate antidepressant-like effect induced by co-administration of 1,3 di-o-tolylguanidine (DTG) and memantine in the forced swimming test in rats". Polish Journal of Pharmacology 55 (6): 1149–1152. 2003. PMID 14730114. 
  6. "Protein kinase C-dependent potentiation of intracellular calcium influx by sigma1 receptor agonists in rat hippocampal neurons". The Journal of Pharmacology and Experimental Therapeutics 307 (2): 705–712. November 2003. doi:10.1124/jpet.103.053447. PMID 12975497.