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[해외논문] Evaluation of Selective COX-2 Inhibition and In Silico Study of Kuwanon Derivatives Isolated from Morus alba 원문보기

International journal of molecular sciences, v.22 no.7, 2021년, pp.3659 -   

Baek, Seung-Hwa (Department of Predictive Toxicology, Korea Institute of Toxicology, Daejeon 34114, Korea) ,  Hwang, Sungbo (seunghwa.beak@kitox.re.kr (S.-H.B.)) ,  Park, Tamina (sungbo.hwang@kitox.re.kr (S.H.)) ,  Kwon, Yoon-Ju (tamina.park@kitox.re.kr (T.P.)) ,  Cho, Myounglae (Department of Predictive Toxicology, Korea Institute of Toxicology, Daejeon 34114, Korea) ,  Park, Daeui (seunghwa.beak@kitox.re.kr (S.-H.B.))

Abstract AI-Helper 아이콘AI-Helper

Six kuwanon derivatives (A/B/C/E/H/J) extracted from the roots of Morus alba L. were evaluated to determine their cyclooxygenase (COX)-1 and 2 inhibitory effects. Cyclooxygenase (COX) is known as the target enzyme of nonsteroidal anti-inflammatory drugs (NSAIDs), which are the most widely used thera...

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참고문헌 (38)

  1. 1. Alam M.J. Alam O. Khan S.A. Naim M.J. Islamuddin M. Deora G.S. Synthesis, anti-inflammatory, analgesic, COX1/2-inhibitory activity, and molecular docking studies of hybrid pyrazole analogues Drug Des. Devel. Ther. 2016 10 3529 3543 10.2147/DDDT.S118297 

  2. 2. Zidar N. Odar K. Glavac D. Jerse M. Zupanc T. Stajer D. Cyclooxygenase in normal human tissues―Is COX-1 really a constitutive isoform, and COX-2 an inducible isoform? J. Cell. Mol. Med. 2009 13 3753 3763 10.1111/j.1582-4934.2008.00430.x 18657230 

  3. 3. Choi S.-H. Aid S. Bosetti F. The distinct roles of cyclooxygenase-1 and-2 in neuroinflammation: Implications for translational research Trends Pharmacol. Sci. 2009 30 174 181 10.1016/j.tips.2009.01.002 19269697 

  4. 4. Willoughby D.A. Moore A.R. Colville-Nash P.R. COX-1, COX-2, and COX-3 and the future treatment of chronic inflammatory disease Lancet 2000 355 646 648 10.1016/S0140-6736(99)12031-2 10696997 

  5. 5. Pairet M. Van Ryn J. Mauz A. Schierok H. Diederen W. Turck D. Engelhardt G. Differential inhibition of COX-1 and COX-2 by NSAIDs: A summary of results obtained using various test systems Selective COX-2 Inhibitors Springer Berlin/Heidelberg, Germany 1998 27 46 

  6. 6. Cryer B. Feldman M. Cyclooxygenase-1 and cyclooxygenase-2 selectivity of widely used nonsteroidal anti-inflammatory drugs Am. J. Med. 1998 104 413 421 10.1016/S0002-9343(98)00091-6 9626023 

  7. 7. Bagachi A. Semwal A. Bharadwaj A. Traditional uses, phytochemistry and pharmacology of Morus alba Linn.: A review J. Med. Plants Res. 2013 7 461 469 

  8. 8. Ahmad A. Gupta G. Afzal M. Kazmi I. Anwar F. Antiulcer and antioxidant activities of a new steroid from Morus alba Life Sci. 2013 92 202 210 10.1016/j.lfs.2012.11.020 23270943 

  9. 9. Ali A. Ali M. New triterpenoids from Morus alba L. stem bark Nat. Prod. Res. 2013 27 524 531 10.1080/14786419.2012.676547 22480349 

  10. 10. Asano N. Yamashita T. Yasuda K. Ikeda K. Kizu H. Kameda Y. Kato A. Nash R.J. Lee H.S. Ryu K.S. Polyhydroxylated alkaloids isolated from mulberry trees ( Morus alba L.) and silkworms ( Bombyx mori L.) J. Agric. Food Chem. 2001 49 4208 4213 10.1021/jf010567e 11559112 

  11. 11. Qiu F. Komatsu K. Kawasaki K. Saito K. Yao X. Kano Y. A novel stilbene glucoside, oxyresveratrol 3′-O-β-glucopyranoside, from the root bark of Morus alba Planta Med. 1996 62 559 561 10.1055/s-2006-957972 17252500 

  12. 12. Oh H. Ko E.-K. Jun J.-Y. Oh M.-H. Park S.-U. Kang K.-H. Lee H.-S. Kim Y.-C. Hepatoprotective and free radical scavenging activities of prenylflavonoids, coumarin, and stilbene from Morus alba Planta Med. 2002 68 932 934 10.1055/s-2002-34930 12391560 

  13. 13. Nomura T. Fukal T. Katayanagi M. Studies on the constituents of the cultivated mulberry tree. III. Isolation of four new flavones, kuwanon A, B, C and oxydihydromorusin from the root bark of Morus alba L. Chem. Pharm. Bull. 1978 26 1453 1458 10.1248/cpb.26.1453 

  14. 14. Nomura T. Hypotensive constituent, kuwanon H, a new flavone derivative from the root bark of the cultivated mulberry tree ( Morus alba L.) Heterocycles 1980 14 1943 4951 10.3987/R-1980-12-1943 

  15. 15. Nomura T. Fukai T. Kuwanon G, a new flavone derivative from the root barks of the cultivated mulberry tree ( Morus alba L.) Chem. Pharm. Bull. 1980 28 2548 2552 10.1248/cpb.28.2548 

  16. 16. Woo H. Lee J. Park D. Jung E. Protective effect of mulberry ( Morus alba L.) extract against benzo [a] pyrene induced skin damage through inhibition of aryl hydrocarbon receptor signaling J. Agric. Food Chem. 2017 65 10925 10932 10.1021/acs.jafc.7b04044 29231728 

  17. 17. Rayam S. Kudagi B.L. Buchineni M. Pathapati R.M. Immidisetty M.R. Assessment of Morus alba (mulberry) leaves extract for anti-psychotic effect in rats Int. J. Basic Clin. Pharmacol. 2019 8 2130 2133 10.18203/2319-2003.ijbcp20194126 

  18. 18. Wei H. Zhu J.-J. Liu X.-Q. Feng W.-H. Wang Z.-M. Yan L.-H. Review of bioactive compounds from root barks of Morus plants (Sang-Bai-Pi) and their pharmacological effects Cogent Chem. 2016 2 1212320 10.1080/23312009.2016.1212320 

  19. 19. Kim J.-M. Baek J.-M. Kim H.-S. Choe M. Antioxidative and anti-asthma effect of Morus bark water extracts J. Korean Soc. Food Sci. Nutr. 2010 39 1263 1269 10.3746/jkfn.2010.39.9.1263 

  20. 20. ulenova M. Sychrova A. Hassan S.T.S. Berchova-Bimova K. Svobodova P. Helclova A. Michnova H. Ho?ek J. Vasilev H. Suchy P. Multiple In vitro biological effects of phenolic compounds from Morus alba root bark J. Ethnopharmacol. 2020 248 112296 10.1016/j.jep.2019.112296 31610262 

  21. 21. Blobaum A.L. Xu S. Rowlinson S.W. Duggan K.C. Banerjee S. Kudalkar S.N. Birmingham W.R. Ghebreselasie K. Marnett L.J. Action at a Distance: Action at a Distance: Mutations of Peripheral Residues Transform Rapid Reversible Inhibitors to Slow, Tight Binders of Cyclooxygenase-2 J. Biol. Chem. 2015 290 12793 12803 10.1074/jbc.M114.635987 25825493 

  22. 22. Knights K.M. Mangoni A.A. Miners J.O. Defining the COX inhibitor selectivity of NSAIDs: Implications for understanding toxicity Expert Rev. Clin. Pharmacol. 2010 3 769 776 10.1586/ecp.10.120 22111779 

  23. 23. Simmons D.L. Botting R.M. Hla T. Cyclooxygenase Isozymes: The Biology of Prostaglandin Synthesis and Inhibition Pharmacol. Rev. 2004 56 387 437 10.1124/pr.56.3.3 15317910 

  24. 24. Uddin M.J. Crews B.C. Xu S. Ghebreselasie K. Daniel C.K. Kingsley P.J. Banerjee S. Marnett L.J. Antitumor Activity of Cytotoxic Cyclooxygenase-2 Inhibitors ACS Chem. Biol. 2016 11 3052 3060 10.1021/acschembio.6b00560 27588346 

  25. 25. Kitaura K. Ikeo E. Asada T. Nakano T. Uebayasi M. Fragment molecular orbital method: An approximate computational method for large molecules Chem. Phys. Lett. 1999 313 701 706 10.1016/S0009-2614(99)00874-X 

  26. 26. Fedorov D.G. Kitaura K. Pair interaction energy decomposition analysis J. Comput. Chem. 2007 28 222 237 10.1002/jcc.20496 17109433 

  27. 27. Gaus M. Cui Q. Elstner M. DFTB3: Extension of the Self-Consistent-Charge Density-Functional Tight-Binding Method (SCC-DFTB) J. Chem. Theory Comput. 2011 7 931 948 10.1021/ct100684s 23204947 

  28. 28. Ryu T.-B. Ha T.-J. Curtis-Long M.-J. Ryu H.-W. Gap S.-W. Park K.-H. Inhibitory effects on mushroom tyrosinase by flavones from the stem barks of Morus lhou (S.) Koidz J. Enz. Inhibi. Medici. Chem. 2008 23 922 930 10.1080/14756360701810207 

  29. 29. Nomura T. Fukai T. Katayanagi M. Kuwanon A, B, C and oxydihydromorusin, four new flavones from the root bark of the cultivated mulberry tree ( Morus alba L.) Chem. Pharm. Bull. 1977 25 529 532 10.1248/cpb.25.529 

  30. 30. Tang F. Wang Y. Hou A.-J. Total syntheses of Nigrasin I and Kuwanon C Tetrahedron 2014 70 3963 3970 10.1016/j.tet.2014.04.089 

  31. 31. Nomura T. Fukai T. Hano Y. Nemoto K. Terada S. Kuramochi T. Constituents of cultivated mulberry tree Planta Med. 1983 47 151 156 10.1055/s-2007-969975 17404904 

  32. 32. Nomura T. Fukai T. Narita T. Terada S. Uzawa J. Iitaka Y. Takasugi M. Ishikawa S. Nagao S. Masamune T. Confirmation of the structures of kuwanons G and H (albanins F and G) by partial synthesis Tetrahedron Lett. 1981 22 2195 2198 10.1016/S0040-4039(01)90496-4 

  33. 33. Al-Saeed A. Gastrointestinal and cardiovascular risk of nonsteroidal anti-inflammatory drugs Oman Med. J. 2011 26 385 391 10.5001/omj.2011.101 22253945 

  34. 34. Furse K.E. Pratt D.A. Porter N.A. Lybrand T.P. Molecular Dynamics Simulations of Arachidonic Acid Complexes with COX-1 and COX-2: Insights into Equilibrium Behavior Biochemistry 2006 45 3189 3205 10.1021/bi052337p 16519514 

  35. 35. Trott O. Olson A.J. AutoDock Vina: Improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading J. Comput. Chem. 2010 31 455 461 10.1002/jcc.21334 19499576 

  36. 36. Pettersen E.F. Goddard T.D. Huang C.C. Couch G.S. Greenblatt D.M. Meng E.C. Ferrin T.E. UCSF Chimera―A visualization system for exploratory research and analysis J. Comput. Chem. 2004 25 1605 1612 10.1002/jcc.20084 15264254 

  37. 37. Landrum G. RDKit: Open-Source Cheminformatics 2006 Available online: https://www.bibsonomy.org/bibtex/28d01fceeccd6bf2486e47d7c4207b108/salotz (accessed on 15 August 2020) 

  38. 38. Barca G.M.J. Bertoni C. Carrington L. Datta D. De Silva N. Deustua J.E. Fedorov D.G. Gour J.R. Gunina A.O. Guidez E. Recent developments in the general atomic and molecular electronic structure system J. Chem. Phys. 2020 152 154102 10.1063/5.0005188 32321259 

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