5-APDI

Indanylaminopropane
臨床資料
其他名稱	5-APDI; 1-(5-Indanyl)-2-aminopropane; Indanylaminopropane; IAP; Indanametamine; 2-Aminopropylindane; 2-API; Indanylamphetamine
给药途径	Oral
ATC碼	未分配;
法律規範狀態
法律規範	加：Schedule III; 德：NpSG; 英：Class B;
识别信息
	IUPAC命名法 (±)-1-(2,3-dihydro-1H-inden-5-yl)propan-2-amine; ;
CAS号	13396-94-6
PubChem CID	192600;
ChemSpider	167142 ;
UNII	4PH68L63R9;
ChEMBL	ChEMBL6842 ;
CompTox Dashboard（英语：CompTox Chemicals Dashboard） (EPA)	DTXSID00896945 ;
化学信息
化学式	C12H17N
摩尔质量	175.28 g·mol−1
3D模型（JSmol（英语：JSmol））	交互式图像;
手性	Racemic mixture
	SMILES c1cc(cc2c1CCC2)CC(N)C;
	InChI InChI=1S/C12H17N/c1-9(13)7-10-5-6-11-3-2-4-12(11)8-10/h5-6,8-9H,2-4,7,13H2,1H3 ; Key:QYVNZHBQYJRLEX-UHFFFAOYSA-N ;

5-APDI（化学名：5-(2-氨丙基)-2,3-二氢-1H-茚，英語：5-(2-Aminopropyl)-2,3-dihydro-1H-indene，别名有indanylaminopropane、2-aminopropylindane、indanametamine等）是一种含氮有机化合物^[1]，化学式C
12H
17N，属于安非他命衍生物^[2]，能作为迷幻药物^[3]。

参考文献

^ Casale JF, McKibben TD, Bozenko JS, Hays PA. Characterization of the "Indanylamphetamines". Microgram Journal. 2005, 3 (1–2): 3–10 [2009-08-06]. （原始内容存档于2009-03-17）.
^ Monte AP, Marona-Lewicka D, Cozzi NV, Nichols DE. Synthesis and pharmacological examination of benzofuran, indan, and tetralin analogues of 3,4-(methylenedioxy)amphetamine. Journal of Medicinal Chemistry. November 1993, 36 (23): 3700–6. PMID 8246240. doi:10.1021/jm00075a027.
^ Parker MA, Marona-Lewicka D, Kurrasch D, Shulgin AT, Nichols DE. Synthesis and pharmacological evaluation of ring-methylated derivatives of 3,4-(methylenedioxy)amphetamine (MDA). Journal of Medicinal Chemistry. March 1998, 41 (6): 1001–5. CiteSeerX 10.1.1.688.9559 . PMID 9526575. doi:10.1021/jm9705925.

外部链接

[journalCharacterization_of_the_“Indanylamphetamines”-1] Casale JF, McKibben TD, Bozenko JS, Hays PA. Characterization of the "Indanylamphetamines". Microgram Journal. 2005, 3 (1–2): 3–10 [2009-08-06]. （原始内容存档于2009-03-17）.

[pmid8246240-2] Monte AP, Marona-Lewicka D, Cozzi NV, Nichols DE. Synthesis and pharmacological examination of benzofuran, indan, and tetralin analogues of 3,4-(methylenedioxy)amphetamine. Journal of Medicinal Chemistry. November 1993, 36 (23): 3700–6. PMID 8246240. doi:10.1021/jm00075a027.

[pmid9526575-3] Parker MA, Marona-Lewicka D, Kurrasch D, Shulgin AT, Nichols DE. Synthesis and pharmacological evaluation of ring-methylated derivatives of 3,4-(methylenedioxy)amphetamine (MDA). Journal of Medicinal Chemistry. March 1998, 41 (6): 1001–5. CiteSeerX 10.1.1.688.9559 . PMID 9526575. doi:10.1021/jm9705925.

[1]

[2]

[3]