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
給藥途徑	Oral
ATC碼	未分配;
法律規範狀態
法律規範	加：Schedule III; 德：NpSG; 英：Class B;
識別資訊
	IUPAC命名法 (±)-1-(2,3-dihydro-1H-inden-5-yl)propan-2-amine; ;
CAS號	13396-94-6
PubChem CID	192600;
ChemSpider	167142 ;
UNII	4PH68L63R9;
ChEMBL	ChEMBL6842 ;
CompTox Dashboard（英語：CompTox Chemicals Dashboard） (EPA)	DTXSID00896945 ;
化學資訊
化學式	C12H17N
摩爾質量	175.28 g·mol−1
3D模型（JSmol（英語：JSmol））	交互式圖像;
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（化學名：5-(2-氨丙基)-2,3-二氫-1H-茚，英語：5-(2-Aminopropyl)-2,3-dihydro-1H-indene，別名有indanylaminopropane、2-aminopropylindane、indanametamine等）是一種含氮有機化合物^[1]，化學式C
12H
17N，屬於安非他命衍生物^[2]，能作為迷幻藥物^[3]。

參考文獻

^ Casale JF, McKibben TD, Bozenko JS, Hays PA. Characterization of the "Indanylamphetamines". Microgram Journal. 2005, 3 (1–2): 3–10 [2009-08-06]. （原始內容存檔於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.

外部連結

[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]. （原始內容存檔於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.

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