Tham khảo Glaucine

  1. ↑ G.B. Lapa; O.P. Sheichenko; A.G. Serezhechkin; O.N. Tolkachev (tháng 8 năm 2004). “HPLC Determination of Glaucine in Yellow Horn Poppy Grass (Glaucium flavum Crantz)”. Pharmaceutical Chemistry Journal. 38 (1): 441–442. doi:10.1023/B:PHAC.0000048907.58847.c6. ISSN 0091-150X. S-(+)-Glaucine (C21H25NO4) is the main alkaloid component in the grass of yellow horn poppy (Glaucium luteum L., syn. Glaucium flavum Crantz) of the Papaveraceae family
  2. ↑ Xu, XH; Yu, GD; Wang, ZT (2004). “Resource investigation and quality evaluation on wild Corydalis yanhusuo”. Zhongguo Zhong Yao Za Zhi = Zhongguo Zhongyao Zazhi = China Journal of Chinese Materia Medica. 29 (5): 399–401. PMID 15706885.
  3. ↑ Morteza-Semnani, K; Amin, G; Shidfar, MR; Hadizadeh, H; Shafiee, A (2003). “Antifungal activity of the methanolic extract and alkaloids of Glaucium oxylobum”. Fitoterapia. 74 (5): 493–6. doi:10.1016/s0367-326x(03)00113-8. PMID 12837370.
  4. ↑ Milanowski, DJ; Winter, RE; Elvin-Lewis, MP; Lewis, WH (2002). “Geographic distribution of three alkaloid chemotypes of Croton lechleri”. Journal of Natural Products. 65 (6): 814–9. doi:10.1021/np000270v. PMID 12088421.
  5. 1 2 3 4 5 Cortijo, J; Villagrasa, V; Pons, R; Berto, L; Martí-Cabrera, M; Martinez-Losa, M; Domenech, T; Beleta, J; Morcillo, EJ (1999). “Bronchodilator and anti-inflammatory activities of glaucine: In vitro studies in human airway smooth muscle and polymorphonuclear leukocytes”. British Journal of Pharmacology. 127 (7): 1641–51. doi:10.1038/sj.bjp.0702702. PMC 1566148. PMID 10455321.
  6. ↑ Rühle, KH; Criscuolo, D; Dieterich, HA; Köhler, D; Riedel, G (1984). “Objective evaluation of dextromethorphan and glaucine as antitussive agents”. British Journal of Clinical Pharmacology. 17 (5): 521–4. doi:10.1111/j.1365-2125.1984.tb02384.x. PMC 1463443. PMID 6375709.
  7. ↑ Rovinskiĭ, VI (1989). “A case of hallucinogen-like action of glaucine”. Klinicheskaia Meditsina. 67 (9): 107–8. PMID 2586025.
  8. 1 2 3 Rovinskiĭ, VI (2006). “Acute glaucine syndrome in the physician's practice: The clinical picture and potential danger”. Klinicheskaia Meditsina. 84 (11): 68–70. PMID 17243616.
  9. 1 2 3 4 5 Dargan, PI; Button, J; Hawkins, L; Archer, JR; Ovaska, H; Lidder, S; Ramsey, J; Holt, DW; Wood, DM (2008). “Detection of the pharmaceutical agent glaucine as a recreational drug”. European Journal of Clinical Pharmacology. 64 (5): 553–4. doi:10.1007/s00228-007-0451-9. PMID 18204834.
  10. 1 2 Heng, HL, Chee, CF, Thy, CK, et al. In vitro functional evaluation of isolaureline, dicentrine and glaucine enantiomers at 5‐HT2 and α1 receptors. Chem Biol Drug Des. 2019; 93: 132– 138. https://doi.org/10.1111/cbdd.13390
  11. ↑ Nestler E, Hyman S & Malenka R. Molecular Neuropharmacology: A Foundation for Clinical Neuroscience (2nd ed.). China: McGraw-Hill Companies.
  12. ↑ Asencio, M; Hurtado-Guzmán, C; López, JJ; Cassels, BK; Protais, P; Chagraoui, A (2005). “Structure-affinity relationships of halogenated predicentrine and glaucine derivatives at D1 and D2 dopaminergic receptors: Halogenation and D1 receptor selectivity”. Bioorganic & Medicinal Chemistry. 13 (11): 3699–704. doi:10.1016/j.bmc.2005.03.022. PMID 15862999.
  13. ↑ Orallo, F; Fernández Alzueta, A; Campos-Toimil, M; Calleja, JM (1995). “Study of the in vivo and in vitro cardiovascular effects of (+)-glaucine and N-carbethoxysecoglaucine in rats”. British Journal of Pharmacology. 114 (7): 1419–27. doi:10.1111/j.1476-5381.1995.tb13364.x. PMC 1510273. PMID 7606346.
  14. ↑ Zetler, G (1988). “Neuroleptic-like, anticonvulsant and antinociceptive effects of aporphine alkaloids: Bulbocapnine, corytuberine, boldine and glaucine”. Archives Internationales de Pharmacodynamie et de Thérapie. 296: 255–81. PMID 2907279.

Liên quan