| 去甲二氢骆驼蓬碱 | |
|---|---|
| |
| |
| IUPAC名 1-Methyl-4,9-dihydro-3H-pyrido[4,3-b]indol-7-ol | |
| 别名 | 1-甲基-4,9-二氢-3H-β-咔啉-7-醇 |
| 识别 | |
| CAS号 | 525-57-5  6028-07-5（盐酸盐） 6028-00-8（盐酸盐二水合物） |
| PubChem | 5353656 |
| ChemSpider | 11262879 |
| SMILES |
|
| EINECS | 208-375-4 |
| 性质 | |
| 化学式 | C12H12N2O |
| 摩尔质量 | 200.24 g·mol−1 |
| 熔点 | 100—105 °C（212—221 °F；373—378 K）（三水合物）[1] 212 °C（414 °F；485 K）（自由碱）[2] |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
去甲二氢骆驼蓬碱是一种β-咔啉的衍生物，也是一种骆驼蓬生物碱。[3][4]它存在于骆驼蓬种子中，含量为0.6%[5]—3.90%[6]。它也存在于死藤水中，但含量远少于其它生物碱。[7]
去甲二氢骆驼蓬碱是单胺氧化酶A[5]、乙酰胆碱酯酶、丁酰胆碱酯酶[8]及致癌的CYP1A1的抑制剂。[4]它也用于研究DNA、RNA与生物碱结合的研究。[9][10]对血压正常、麻醉后的狗做的实验显示去甲二氢骆驼蓬碱会降低心率，升高脉压、主动脉血流量、心肌收缩力。[11]
去甲二氢骆驼蓬碱和其它骆驼蓬生物一样，列于澳大利亚出台的药物和毒物的统一调度标准的第9类物质中，即受管制物质，除科学研究外的其它用途都是犯法的。[12]
参见
参考资料
- ^ Thieme Chemistry (Hrsg.): RÖMPP Online – Version 3.37. Georg Thieme Verlag KG, Stuttgart, 27. September 2013.
- ^ The alkaloids: chemistry and physiology. New York: Academic Press. 1965: 49. ISBN 978-0-08-086532-4.
- ^ Sarkar S, Bhadra K. Binding of alkaloid harmalol to DNA: photophysical and calorimetric approach.. J Photochem Photobiol B. 2014, 130: 272–80. PMID 24368411. doi:10.1016/j.jphotobiol.2013.11.021.
- ^ 4.0 4.1 El Gendy MA, Soshilov AA, Denison MS, El-Kadi AO. Harmaline and harmalol inhibit the carcinogen-activating enzyme CYP1A1 via transcriptional and posttranslational mechanisms.. Food Chem Toxicol. 2012, 50 (2): 353–62. PMC 3281145
. PMID 22037238. doi:10.1016/j.fct.2011.10.052.
- ^ 5.0 5.1 Herraiz, T.; González, D.; Ancín-Azpilicueta, C.; Arán, V. J.; Guillén, H. beta-Carboline alkaloids in Peganum harmala and inhibition of human monoamine oxidase (MAO). Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research Association. 2010, 48 (3): 839–845. ISSN 1873-6351. PMID 20036304. doi:10.1016/j.fct.2009.12.019.
- ^ Hemmateenejad, Bahram; Abbaspour, Abdolkarim; Maghami, Homeyra; Miri, Ramin; Panjehshahin, Mohhamad Reza. Partial least squares-based multivariate spectral calibration method for simultaneous determination of beta-carboline derivatives in Peganum harmala seed extracts. Analytica Chimica Acta. 2006-08-11, 575 (2): 290–299. ISSN 1873-4324. PMID 17723604. doi:10.1016/j.aca.2006.05.093.
- ^ McIlhenny, Ethan H.; Pipkin, Kelly E.; Standish, Leanna J.; Wechkin, Hope A.; Strassman, Rick; Barker, Steven A. Direct analysis of psychoactive tryptamine and harmala alkaloids in the Amazonian botanical medicine ayahuasca by liquid chromatography–electrospray ionization-tandem mass spectrometry. Journal of Chromatography A. 2009, 1216 (51): 8960–8968. PMID 19926090. doi:10.1016/j.chroma.2009.10.088.
- ^ Zhao, Ting; Ding, Ke-min; Zhang, Lei; Cheng, Xue-mei; Wang, Chang-hong; Wang, Zheng-tao. Acetylcholinesterase and Butyrylcholinesterase Inhibitory Activities of β ‐Carboline and Quinoline Alkaloids Derivatives from the Plants of Genus Peganum. Journal of Chemistry. 2013, 2013 (1). ISSN 2090-9063. doi:10.1155/2013/717232 .
- ^ Nafisi, Shohreh; Malekabady, Zahra Mokhtari; Khalilzadeh, Mohammad Ali. Interaction of β-carboline alkaloids with RNA. DNA and cell biology. 2010, 29 (12): 753–761. ISSN 1557-7430. PMID 20731607. doi:10.1089/dna.2010.1087.
- ^ Nafisi, Shohreh; Bonsaii, Mahyar; Maali, Pegah; Khalilzadeh, Mohammad Ali; Manouchehri, Firouzeh. Beta-carboline alkaloids bind DNA. Journal of Photochemistry and Photobiology. B, Biology. 2010-08-02, 100 (2): 84–91. ISSN 1873-2682. PMID 20541950. doi:10.1016/j.jphotobiol.2010.05.005.
- ^ Aarons, Darryl H.; Victor Rossi, G.; Orzechowski, Raymond F. Cardiovascular Actions of Three Harmala Alkaloids: Harmine, Harmaline, and Harmalol. Journal of Pharmaceutical Sciences. 1977, 66 (9): 1244–1248. doi:10.1002/jps.2600660910.
- ^ Therapeutic Goods (Poisons Standard—October 2024) Instrument 2024. Federal Register of Legislation. 2024-09-30 [2024-12-02].
