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Ganesha (psychedelic)

From Wikipedia, the free encyclopedia
Psychedelic drug
For other uses, seeGanesha (disambiguation).
Pharmaceutical compound
Ganesha
Clinical data
Other namesGANESHA; G; G-0; 2,5-Dimethoxy-3,4-dimethylamphetamine; 3,4-Dimethyl-2,5-dimethoxyamphetamine; 3-Methyl-DOM; 3-Me-DOM
Routes of
administration
Oral[1]
Drug classSerotonergic psychedelic;Hallucinogen
ATC code
  • None
Pharmacokinetic data
Onset of actionSlow over 3 hours or rapid[1]
Duration of action18–24 hours[1]
Identifiers
  • 1-(2,5-dimethoxy-3,4-dimethylphenyl)propan-2-amine
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC13H21NO2
Molar mass223.316 g·mol−1
3D model (JSmol)
  • COc1c(C)c(C)c(cc1CC(C)N)OC
  • InChI=1S/C13H21NO2/c1-8(14)6-11-7-12(15-4)9(2)10(3)13(11)16-5/h7-8H,6,14H2,1-5H3 checkY
  • Key:RBZXVDSILZXPDM-UHFFFAOYSA-N checkY
  (verify)

Ganesha (G orG-0), also known as2,5-dimethoxy-3,4-dimethylamphetamine or as3-methyl-DOM, is apsychedelic drug of thephenethylamine,amphetamine, andDOx families.[1] It is the 3-methylderivative ofDOM and the amphetamine (α-methyl) derivative of2C-G.[1] The drug is takenorally.[1]

Use and effects

[edit]

In his bookPiHKAL (Phenethylamines I Have Known and Loved),Alexander Shulgin lists Ganesha's dose range as 24 to 32 mgorally and itsduration as 18 to 24 hours.[1] The drug'sonset was variably described as slow over the course of 3 hours or as rapid.[1] The effects of Ganesha have been reported to include strongclosed-eye visuals, an increased appreciation ofmusic, and powerfulrelaxation andtranquility, among others.[1]

Interactions

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See also:Psychedelic drug § Interactions, andTrip killer § Serotonergic psychedelic antidotes

Chemistry

[edit]

Synthesis

[edit]

Thechemical synthesis of Ganesha has been described.[1]

Homologues

[edit]

G-3

[edit]
G-3 structure.

2,5-Dimethoxy-3,4-(trimethylene)amphetamine:[2]

  • Dose: 12–18 mg
  • Duration: 8-12 hours
  • Effects: Enhancement of reading, no visuals or body load.
  • 2Canalogue:2C-G-3

G-4

[edit]
G-4 structure.

2,5-Dimethoxy-3,4-(tetramethylene)amphetamine:[3]

G-5

[edit]

3,6-Dimethoxy-4-(2-aminopropyl)benzonorbornane:[4]

G-N

[edit]
G-N structure.

1,4-Dimethoxynaphthyl-2-isopropylamine:[5]

G-O

[edit]

1-(5,8-Dimethoxy-3,4-dihydro-1H-isochromen-7-yl)propan-2-amine (CAS # 774538-38-4)[6]

Society and culture

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Names

[edit]

Ganesha was named after theHindu deity,Ganesha.[1] It is one of histen classic ladies.[1][7]

Legal status

[edit]

United Kingdom

[edit]

This substance is a Class A drug in theDrugs controlled by the UK Misuse of Drugs Act.[8]

See also

[edit]

References

[edit]
  1. ^abcdefghijklShulgin, Alexander;Shulgin, Ann (September 1991).PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press.ISBN 0-9630096-0-5.OCLC 25627628.http://www.erowid.org/library/books_online/pihkal/pihkal085.shtml
  2. ^G-3 entry inPiHKAL
  3. ^G-4 entry inPiHKAL
  4. ^G-5 entry inPiHKAL
  5. ^G-N entry inPiHKAL
  6. ^Hellberg MR, Namil A. Benzopyran analogs and their use for the treatment of glaucoma. Patent US 7396856
  7. ^Ger A, Ger D (April 2011)."Triple Goddess of the Night".British Neuroscience Association Bulletin.63:28–30.
  8. ^"UK Misuse of Drugs act 2001 Amendment summary". Isomer Design. Archived fromthe original on 22 October 2017. Retrieved12 March 2014.

External links

[edit]
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