2,5-二甲氧基-4-碘安非他命
外观
维基百科,自由的百科全书
(R)-DOI, the (R)-enantiomer of DOI | |
| 臨床資料 | |
|---|---|
| 其他名稱 | DOI; 2,5-Dimethoxy-4-iodoamphetamine; 4-Iodo-2,5-dimethoxyamphetamine |
| 给药途径 | Oral[1] |
| 藥物類別 | Serotonergic psychedelic; Hallucinogen; Serotonin 5-HT2 receptor agonist; Anti-inflammatory agent |
| ATC碼 |
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| 法律規範狀態 | |
| 法律規範 | |
| 藥物動力學數據 | |
| 作用時間 | 16–30 hours[1] |
| 识别信息 | |
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| CAS号 | 64584-34-5( 82864-06-0 ((R)-DOI) 99665-04-0 ((S)-DOI) 42203-78-1 (HCl)) |
| PubChem CID | |
| IUPHAR/BPS | |
| ChemSpider |
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| UNII | |
| ChEMBL | |
| CompTox Dashboard (EPA) | |
| 化学信息 | |
| 化学式 | C11H16INO2 |
| 摩尔质量 | 321.16 g·mol−1 |
| 3D模型(JSmol) | |
| 熔点 | 201.5 °C(394.7 °F) (hydrochloride) |
| 水溶性 | 10 mg/mL[3] |
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2,5-二甲氧基-4-碘安非他命(DOI)是一种有机化合物,化学式为C11H16INO2。它是一种精神药品,存在R和S对映异构体。[1]
由于它在美国不属于管制药物,它被广泛用于科学研究。[4]
参考文献
[编辑]- ^ 1.0 1.1 1.2 Shulgin A, Shulgin A (1990). "#67 DOI". PiHKAL: A Chemical Love Story. Transform Press. Archived from the original on 2014-10-27. Retrieved 2014-12-17.
- ^ Anvisa. RDC Nº 804 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial [Collegiate Board Resolution No. 804 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control]. Diário Oficial da União. 2023-07-24 (2023-07-25) [2023-08-27]. (原始内容存档于2023-08-27) (巴西葡萄牙语). 请检查
|publication-date=中的日期值 (帮助) - ^ D101 DOI hydrochloride ≥98% (HPLC), solid. [13 April 2008].
- ^ Glennon RA, Dukat M (June 2024). "1-(2,5-Dimethoxy-4-iodophenyl)-2-aminopropane (DOI): From an Obscure to Pivotal Member of the DOX Family of Serotonergic Psychedelic Agents - A Review". ACS Pharmacology & Translational Science. 7 (6): 1722–1745. doi:10.1021/acsptsci.4c00157. PMC 11184610. PMID 38898956.
外部链接
[编辑]维基共享资源有2,5-二甲氧基-4-碘安非他命相关的多媒体资源
人類痕量胺相关受体配體 | |||||||||||
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| TAAR1(英语:TAAR1) |
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| TAAR2(英语:TAAR2) |
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| TAAR5(英语:TAAR5) |
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†References for all endogenous human TAAR1 ligands are provided at List of trace amines ‡References for synthetic TAAR1 agonists can be found at TAAR1(英语:TAAR1) or in the associated compound articles. For TAAR2 and TAAR5 agonists and inverse agonists, see TAAR for references. 參見: Receptor/signaling modulators | |||||||||||