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5-apdi

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Title: 5-apdi  
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Subject: Apomorphine, Cyproheptadine, Tenocyclidine, Methylenedioxyhydroxyamphetamine, Butylone
Collection: Designer Drugs, Entactogens and Empathogens, Indanes, Serotonin Releasing Agents
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5-apdi

Indanylaminopropane
Systematic (IUPAC) name
(±)-1-(2,3-dihydro-1H-inden-5-yl)propan-2-amine
Clinical data
Legal status
Routes of
administration
Oral
Identifiers
CAS Registry Number  N
ATC code None
PubChem CID:
ChemSpider  Y
ChEMBL  Y
Synonyms 1-(5-indanyl)-2-aminopropane
Chemical data
Formula C12H17N
Molecular mass 175.27 g/mol
 Y   

5-(2-Aminopropyl)-2,3-dihydro-1H-indene (5-APDI), also known as indanylaminopropane (IAP), IAP (psychedelic), 2-API(2-aminopropylindane), indanametamine, and, incorrectly, as indanylamphetamine,[1] is an entactogen and psychedelic drug of the amphetamine family.[2][3] It has been sold by online vendors through the Internet and has been encountered as a designer drug since 2003,[1] but its popularity and availability has diminished in recent years.

5-APDI acts as a potent and weakly selective serotonin releasing agent (SSRA) with IC50 values of 82 nM, 1,848 nM, and 849 nM for inhibiting the reuptake of serotonin, dopamine, and norepinephrine, respectively.[2][3] It fully substitutes for MBDB but not amphetamine in trained animals, though it does produce disruption for the latter at high doses.[2]

5-ADPI has been classified as a class B drug under the Misuse of Drugs Act 1971 since 10 June 2014.

See also

References

  1. ^ a b Casale JF, McKibben TD, Bozenko JS, Hays PA (2005). """Characterization of the "Indanylamphetamines. Microgram Journal 3 (1–2): 3–10. 
  2. ^ a b c Monte AP, Marona-Lewicka D, Cozzi NV, Nichols DE (November 1993). "Synthesis and pharmacological examination of benzofuran, indan, and tetralin analogues of 3,4-(methylenedioxy)amphetamine". Journal of Medicinal Chemistry 36 (23): 3700–6.  
  3. ^ a b Parker MA, Marona-Lewicka D, Kurrasch D, Shulgin AT, Nichols DE (March 1998). "Synthesis and pharmacological evaluation of ring-methylated derivatives of 3,4-(methylenedioxy)amphetamine (MDA)". Journal of Medicinal Chemistry 41 (6): 1001–5.  

External links

  • The Vaults of Erowid - Indanylaminopropane
  • Erowid Experience Vaults - Indanylaminopropane
  • Bluelight Forums - The Big and Dandy Indanylaminopropane (IAP) Thread
  • MadMax - Illustrated Synthesis of Indanylaminopropane
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