8-Hydroxydihydrochelerythrine and 8-hydroxydihydrosanguinarine with a potent acetylcholinesterase inhibitory activity from Chelidonium majus L.

Biological and Pharmaceutical Bulletin

Volumn 29, Issue 11, 2006, Pages 2317-2320

  Cho, Kyung Mi ^a   Yoo, Ick Dong ^a   Kim, Won Gon ^a  

^a Korea Research Institute of Bioscience and Biotechnology (KRIBB)   (South Korea)

Author keywords

8 hydroxydihydrochelerythrine; 8 hydroxydihydrosanguinarine; Acetylcholinesterase; Chelidonium majus L.

Indexed keywords

8 HYDROXYDIHYDROCHELERYTHRINE; 8 HYDROXYDIHYDROSANGUINARINE; ACETYLCHOLINESTERASE; BERBERINE; CHELIDONIUM EXTRACT; CHOLINESTERASE; UNCLASSIFIED DRUG;

ARTICLE; CHELIDONIUM; CONTROLLED STUDY; DRUG EFFECT; DRUG STRUCTURE; IC 50; MASS SPECTROMETRY; NONHUMAN; NUCLEAR MAGNETIC RESONANCE;

ACETYLCHOLINESTERASE; BERBERINE; BUTYRYLCHOLINESTERASE; CHELIDONIUM; CHLOROFORM; CHOLINESTERASE INHIBITORS; CHROMATOGRAPHY; DOSE-RESPONSE RELATIONSHIP, DRUG; ETHANOL; HETEROCYCLIC COMPOUNDS WITH 4 OR MORE RINGS; MEDICINE, HERBAL; METHANOL; MOLECULAR STRUCTURE; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PLANT COMPONENTS, AERIAL; PLANT EXTRACTS; POLYCYCLIC COMPOUNDS;

EID: 33750612044     PISSN: 09186158     EISSN: 13475215     Source Type: Journal    
DOI: 10.1248/bpb.29.2317     Document Type: Article

References (19)

1. Davies P., Maloney A. J. F., Lancet, 2, 1403 (1976).
2. Whitehouse P. J., Price D. L., Struble G. R., Clarke A. W., Coyle J. T., DeLong M. R., Science, 15, 1237-1239 (1982).
3. Davies K. L., Mohs R. C., Am. J. Psychiatry, 139, 1421-1424 (1982).
4. Cummings J. L., Lancet, 356, 2024-2025 (2000).
5. Relman A. S., N. Engl. J. Med., 324, 349-352 (1991).
6. Camps P., Achab R., Morral J., Munoz-Torrero D., Badia A., Banos J. E., Vivas N. M., Barril X., Orozco M., Luque F. J., J. Med. Chem., 43, 4657-4666 (2000).
7. Thomsen T., Zendeh B., Fischer J. P., Kewitz H., Biochem. Pharmacol., 41, 139-141 (1991).
8. Colombo M. L., Bosisio E., Pharmacol. Res., 33, 127-134 (1996).
9. Kosina P., Walterova D., Ulrichova J., Lichnovsky V., Stiborova M., Rydlova H., Vicar J., Krecman V., Brabec M. J., Simanek V., Food Chem. Toxicol., 42, 85-91 (2004).
10. Lenfeld J., Kroutil M., Marsalek E., Slavik J., Preininger V., Simanek V., Planta Med., 43, 161-165 (1981).
11. Ingkaninan K., Phengpa P., Yuenyongsawad S., Khorana N., J. Pharm. Pharmacol., 58, 695-700 (2006).
12. Kim D. K., Lee K. T., Baek N. I., Kim S. H., Park H. W., Lim J. P., Shin T. Y., Eom D. O., Yang J. H., Eun J. S., Arch. Pharm. Res., 27, 1127-1131 (2004).
13. Ellman G. L., Courtney K. D., Andres J. R. V., Featherstone R.-M., Biochem. Pharmacol., 7, 88-95 (1961).
14. Sharma P. N., Shoeg A., Kapil R. S., Popli S. P., Phytochemistry, 21, 252-253 (1982).
15. Zhang G. L., Rucker G., Breitmaier E., Nieger M., Mayer R., Steinbeck C., Phytochemistry, 40, 299-305 (1995).
16. Chattopadhyay S. K., Ray A. B., J. Nat. Prod., 44, 45-49 (1981).
17. Janssen R. H. A. M., Lousberg R. J. J., Wijkens P., Kruk C., Theuns H. G., Phytochemistry, 28, 2833-2839 (1989).
18. Tousek J., Dommisse R., Dostal J., Zak Z., Pieters L., Marek R., J. Mol. Struct., 613, 103-113 (2002).
19. Jones R. R., Harkrader R. J., Southard G. L., J. Nat. Prod., 49, 1109-1111 (1986).