Cannabis Ruderalis

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'''PTI-2''' is an [[indole]]-based [[synthetic cannabinoid]].<ref>{{cite web | url=https://www.caymanchem.com/app/template/Product.vm/catalog/9001950 | title=PTI-2 | publisher=Cayman Chemical | accessdate=8 July 2015}}</ref> It is one of few [[synthetic cannabinoid|synthetic cannabinoids]] containing a [[thiazole]] group and is closely related to [[PTI-1]]. These compounds may be viewed as simplified analogues of indole-3-heterocycle compounds originally developed by [[Organon International|Organon]] and subsequently further researched by [[Merck & Co.|Merck]].<ref>[http://www.google.com/patents/US7700634 Julia Adam-Worrall, et al. (Indol-3-yl) heterocycle derivatives as agonists of the cannabinoid CB1 receptor. Patent US 7700634, priority date 5 March 2004]</ref><ref>[http://www.google.com/patents/US7763732 Paul David Ratcliffe, et al. Indole Derivatives. Patent US 7763732, priority date 24 August 2005]</ref><ref>[https://patentscope.wipo.int/search/en/detail.jsf?docId=WO2008101995 Julia Adam, et al. Indole Derivatives. Patent WO 2008/101995, priority date 22 February 2007]</ref><ref>Takao Kiyoi, et al. Discovery of potent and orally bioavailable heterocycle-based cannabinoid CB1 receptor agonists. ''Bioorganic and Medicinal Chemistry Letters'' 2011; 21(6):1748-1753. doi: 10.1016/j.bmcl.2011.01.082</ref>
'''PTI-2''' is an [[indole]]-based [[synthetic cannabinoid]].<ref>{{cite web | url=https://www.caymanchem.com/app/template/Product.vm/catalog/9001950 | title=PTI-2 | publisher=Cayman Chemical | accessdate=8 July 2015}}</ref> It is one of few [[synthetic cannabinoid]]s containing a [[thiazole]] group and is closely related to [[PTI-1]]. These compounds may be viewed as simplified analogues of indole-3-heterocycle compounds originally developed by [[Organon International|Organon]] and subsequently further researched by [[Merck & Co.|Merck]].<ref>[http://www.google.com/patents/US7700634 Julia Adam-Worrall, et al. (Indol-3-yl) heterocycle derivatives as agonists of the cannabinoid CB1 receptor. Patent US 7700634, priority date 5 March 2004]</ref><ref>[http://www.google.com/patents/US7763732 Paul David Ratcliffe, et al. Indole Derivatives. Patent US 7763732, priority date 24 August 2005]</ref><ref>[https://patentscope.wipo.int/search/en/detail.jsf?docId=WO2008101995 Julia Adam, et al. Indole Derivatives. Patent WO 2008/101995, priority date 22 February 2007]</ref><ref>Takao Kiyoi, et al. Discovery of potent and orally bioavailable heterocycle-based cannabinoid CB1 receptor agonists. ''Bioorganic & Medicinal Chemistry Letters'' 2011; 21(6):1748-1753. doi: 10.1016/j.bmcl.2011.01.082</ref>


==See also==
==See also==
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[[Category:Cannabinoids]]
[[Category:Cannabinoids]]
[[Category:Designer drugs]]
[[Category:Designer drugs]]



{{cannabinoid-stub}}
{{cannabinoid-stub}}

Revision as of 01:56, 14 November 2017

PTI-2
Legal status
Legal status
Identifiers
  • N-(2-methoxyethyl)-N-((2-(1-pentyl-1H-indol-3-yl)thiazol-4-yl)methyl)propan-2-amine
CAS Number
ChemSpider
UNII
Chemical and physical data
FormulaC23H33N3OS
Molar mass399.60 g/mol g·mol−1
3D model (JSmol)
  • CCCCCN1C=C(C2=CC=CC=C21)C3=NC(CN(C(C)C)CCOC)=CS3
  • InChI=1S/C23H33N3OS/c1-5-6-9-12-26-16-21(20-10-7-8-11-22(20)26)23-24-19(17-28-23)15-25(18(2)3)13-14-27-4/h7-8,10-11,16-18H,5-6,9,12-15H2,1-4H3
  • Key:PSAKYYVEVVAWJL-UHFFFAOYSA-N

PTI-2 is an indole-based synthetic cannabinoid.[1] It is one of few synthetic cannabinoids containing a thiazole group and is closely related to PTI-1. These compounds may be viewed as simplified analogues of indole-3-heterocycle compounds originally developed by Organon and subsequently further researched by Merck.[2][3][4][5]

See also

References

  1. ^ "PTI-2". Cayman Chemical. Retrieved 8 July 2015.
  2. ^ Julia Adam-Worrall, et al. (Indol-3-yl) heterocycle derivatives as agonists of the cannabinoid CB1 receptor. Patent US 7700634, priority date 5 March 2004
  3. ^ Paul David Ratcliffe, et al. Indole Derivatives. Patent US 7763732, priority date 24 August 2005
  4. ^ Julia Adam, et al. Indole Derivatives. Patent WO 2008/101995, priority date 22 February 2007
  5. ^ Takao Kiyoi, et al. Discovery of potent and orally bioavailable heterocycle-based cannabinoid CB1 receptor agonists. Bioorganic & Medicinal Chemistry Letters 2011; 21(6):1748-1753. doi: 10.1016/j.bmcl.2011.01.082


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