Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Discovery of Monoamine Oxidase A Inhibitors Derived from in silico Docking

  • Jo, Geunhyeong (Division of Bioscience and Biotechnology, BMIC, Konkuk University) ;
  • Sung, Su Hyun (Division of Bioscience and Biotechnology, BMIC, Konkuk University) ;
  • Lee, Younggiu (Division of Bioscience and Biotechnology, BMIC, Konkuk University) ;
  • Kim, Bong-Gyu (Division of Bioscience and Biotechnology, BMIC, Konkuk University) ;
  • Yoon, JunWie (Division of Bioscience and Biotechnology, BMIC, Konkuk University) ;
  • Lee, Hye Ok (Division of Bioscience and Biotechnology, BMIC, Konkuk University) ;
  • Ji, Sang Yun (National Institute of Animal Science, Rural Development Administration) ;
  • Koh, Dongsoo (Department of Applied Chemistry, Dongduk Women's University) ;
  • Ahn, Joong-Hoon (Division of Bioscience and Biotechnology, BMIC, Konkuk University) ;
  • Lim, Yoongho (Division of Bioscience and Biotechnology, BMIC, Konkuk University)
  • Received : 2012.07.10
  • Accepted : 2012.08.06
  • Published : 2012.11.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Youdim, M. B.; Bakhle, Y. S. Br. J. Pharmacol. 2006, 147, 287.
  2. Bortolato, M.; Chen, K.; Shih, J. C. Adv. Drug Deliv. Rev. 2008, 60, 1527. https://doi.org/10.1016/j.addr.2008.06.002
  3. Lan, N. C.; Heinzmann, C.; Gal, A.; Klisak, I.; Orth, U.; Lai, E.; Grimsby, J.; Sparkes, R. S.; Mohandas, T.; Shih, J. C. Genomics 1989, 4, 552. https://doi.org/10.1016/0888-7543(89)90279-6
  4. Grimsby, J.; Lan, N. C.; Neve, R.; Chen, K.; Shih, J. C. J. Neurochem. 1990, 55, 1166. https://doi.org/10.1111/j.1471-4159.1990.tb03121.x
  5. Westlund, K. N.; Denney, R. M.; Rose, R. M.; Abell, C. W. Neuroscience 1988, 25, 439. https://doi.org/10.1016/0306-4522(88)90250-3
  6. Patkar, A. A.; Pae, C. U.; Masand, P. S. CNS. Spectr. 2006, 11, 363. https://doi.org/10.1017/S1092852900014498
  7. Da Prada, M.; Kettler, R.; Keller, H. H.; Burkard, W. P.; Muggli- Maniglio, D.; Haefely, W. E. J. Pharmacol. Exp. Ther. 1989, 248, 400.
  8. Ma, J.; Yoshimura, M.; Yamashita, E.; Nakagawa, A.; Ito, A.; Tsukihara, T. J. Mol. Biol. 2004, 338, 103. https://doi.org/10.1016/j.jmb.2004.02.032
  9. Dreiseitel, A.; Korte, G.; Schreier, P.; Oehme, A.; Locher, S.; Domani, M.; Hajak, G.; Sand, P. G. Pharmacol. Res. 2009, 59, 306. https://doi.org/10.1016/j.phrs.2009.01.014
  10. Johnson, S.; Stockmeier, C. A.; Meyer, J. H.; Austin, M. C.; Albert, P. R.; Wang, J.; May, W. L.; Rajkowska, G.; Overholser, J. C.; Jurjus, G.; Dieter, L.; Johnson, C.; Sittman, D. B.; Ou, X. M. Neuropsychopharmacology 2011, 36, 2139. https://doi.org/10.1038/npp.2011.105
  11. Cryan, J. F.; Dalvi, A.; Jin, S. H.; Hirsch, B. R.; Lucki, I.; Thomas, S. A. J. Pharmacol. Exp. Ther. 2001, 298, 651.
  12. Cases, O.; Seif, I.; Grimsby, J.; Gaspar, P.; Chen, K.; Pournin, S.; Muller, U.; Aguet, M.; Babinet, C.; Shih, J.; De Maeyer, E. Science 1995, 268, 1763. https://doi.org/10.1126/science.7792602
  13. Gingrich, J. A.; Ansorge, M. S.; Merker, R.; Weisstaub, N.; Zhou, M. CNS Spectr. 2003, 8, 572. https://doi.org/10.1017/S1092852900018848
  14. Amsterdam, J. D.; Chopra, M. Psychiatr. Ann. 2001, 31, 361. https://doi.org/10.3928/0048-5713-20010601-05
  15. Ban, T. A. J. Neural. Transm. 2001, 108, 707. https://doi.org/10.1007/s007020170047
  16. Lopez-Munoz, F.; Alamo, C. Curr. Pharm. Des. 2009, 15, 1563. https://doi.org/10.2174/138161209788168001
  17. Curet, O.; Damoiseau, G.; Aubin, N.; Sontag, N.; Rovei, V.; Jarreau, F. X. J. Pharmacol. Exp. Ther. 1996, 277, 253.
  18. Medvedev, A. E.; Kirkel, A. A.; Kamyshanskaya, N. S.; Moskvitina, T. A.; Axenova, L. N.; Gorkin, V. Z.; Andreeva, N. I.; Golovina, S. M.; Mashkovsky, M. D. Biochem. Pharmacol. 1994, 47, 303. https://doi.org/10.1016/0006-2952(94)90021-3
  19. Binda, C.; Newton-Vinson, P.; Hubalek, F.; Edmondson, D. E.; Mattevi, A. Nat. Struct. Biol. 2002, 9, 22. https://doi.org/10.1038/nsb732
  20. De Colibus, L.; Li, M.; Binda, C.; Lustig, A.; Edmondson, D. E.; Mattevi, A. Proc. Natl. Acad. Sci. USA 2005, 102, 12684. https://doi.org/10.1073/pnas.0505975102
  21. Son, S. Y.; Ma, J.; Kondou, Y.; Yoshimura, M.; Yamashita, E.; Tsukihara, T. Proc. Natl. Acad. Sci. U. S. A. 2008, 105, 5739. https://doi.org/10.1073/pnas.0710626105
  22. Wallace, A. C.; Laskowski, R. A.; Thornton, J. M. Protein Eng. 1995, 8, 127. https://doi.org/10.1093/protein/8.2.127
  23. Gao, G. Y.; Li, D. J.; Keung, W. M. J. Med. Chem. 2001, 44, 3320. https://doi.org/10.1021/jm0101390
  24. Han, X. H.; Hong, S. S.; Hwang, J. S.; Lee, M. K.; Hwang, B. Y.; Ro, J. S. Arch. Pharm. Res. 2007, 30, 13. https://doi.org/10.1007/BF02977772
  25. Pisani, L.; Muncipinto, G.; Miscioscia, T. F.; Nicolotti, O.; Leonetti, F.; Catto, M.; Caccia, C.; Salvati, P.; Soto-Otero, R.; Mendez- Alvarez, E.; Passeleu, C.; Carotti, A. J. Med. Chem. 2009, 52, 6685. https://doi.org/10.1021/jm9010127
  26. Stahl, S. M.; Felker, A. CNS. Spectr. 2008, 13, 855. https://doi.org/10.1017/S1092852900016965
  27. Murphy, D. L.; Karoum, F.; Pickar, D.; Cohen, R. M.; Lipper, S.; Mellow, A. M.; Tariot, P. N.; Sunderland, T. J. Neural. Transm. Suppl. 1998, 52, 39. https://doi.org/10.1007/978-3-7091-6499-0_5
  28. Xu, Y.; Li, S.; Chen, R.; Li, G.; Barish, P. A.; You, W.; Chen, L.; Lin, M.; Ku, B.; Pan, J.; Ogle, W. O. Pharmacol. Biochem. Behav. 2010, 94, 447. https://doi.org/10.1016/j.pbb.2009.10.007
  29. Dixon Clarke, S. E.; Ramsay, R. R. J. Neural. Transm. 2011, 118, 1031. https://doi.org/10.1007/s00702-010-0537-x
  30. Sloley, B. D.; Urichuk, L. J.; Morley, P.; Durkin, J.; Shan, J. J.; Pang, P. K.; Coutts, R. T. J. Pharm. Pharmacol. 2000, 52, 451. https://doi.org/10.1211/0022357001774075
  31. Holmes, A. R.; Keniya, M. V.; Ivnitski-Steele, I.; Monk, B. C.; Lamping, E.; Sklar, L. A.; Cannon, R. D. Antimicrob. Agents Chemother. 2012, 56, 1508. https://doi.org/10.1128/AAC.05706-11

Cited by

  1. )-1-(1-Hydroxynaphthalen-2-yl)-3-(2,4,5-trimethoxyphenyl)prop-2-en-1-one vol.69, pp.4, 2013, https://doi.org/10.1107/S1600536813006843
  2. )-1-(3,5-Dimethoxyphenyl)-3-(3-methoxyphenyl)prop-2-en-1-one vol.69, pp.5, 2013, https://doi.org/10.1107/S1600536813008982
  3. Quercetin and Related Chromenone Derivatives as Monoamine Oxidase Inhibitors: Targeting Neurological and Mental Disorders vol.24, pp.3, 2019, https://doi.org/10.3390/molecules24030418
  4. Recent developments on the structure-activity relationship studies of MAO inhibitors and their role in different neurological disorders vol.6, pp.48, 2012, https://doi.org/10.1039/c6ra00302h
  5. Monoamine Oxidases (MAOs) as Privileged Molecular Targets in Neuroscience: Research Literature Analysis vol.12, pp.None, 2012, https://doi.org/10.3389/fnmol.2019.00143
  6. Monoamine Oxidase (MAO) as a Potential Target for Anticancer Drug Design and Development vol.26, pp.19, 2021, https://doi.org/10.3390/molecules26196019