Synthesis of stilbene derivatives with inhibition of SARS coronavirus replication

European Journal of Medicinal Chemistry

Volumn 41, Issue 9, 2006, Pages 1084-1089

  Li, Yue Qing ^a   Li, Ze Lin ^b   Zhao, Wei Jie ^a   Wen, Rui Xing ^b   Meng, Qing Wei ^a   Zeng, Yi ^b  

^a DALIAN UNIVERSITY OF TECHNOLOGY   (China)

^b BEIJING UNIVERSITY OF TECHNOLOGY   (China)

Author keywords

Coronavirus; Severe acute respiratory syndrome; Stilbene derivatives

Indexed keywords

2',3,5',5 TETRAHYDROXYSTILBENE; 2',3,5,4' TETRAMETHOXYSTILBENE; 2',3,5,5' TETRAMETHOXYSTILBENE; 2',5,4',6 TETRAMETHOXYSTILBENE 2 NITROGEN; 2',5,5',6 TETRAHYDROXYSTILBENE 2 NITROGEN; 2',5,5',6 TETRAMETHOXYSTILBENE 2 NITROGEN; 3',5,5',6 TETRAHYDROXYSTILBENE 2 NITROGEN; 3',5,5',6 TETRAMETHOXYSTILBENE 2 NITROGEN; 3,3',5,5' TETRAHYDROXYSTILBENE; 3,3',5,5' TETRAMETHOXYSTILBENE; 3,4',5 TRIMETHOXYSTILBENE; 4,6 DIMETHYL 2',5,4' TRIMETHOXYSTILBENE 2 NITROGEN; 4,6 DIMETHYL 2',5,5' TRIHYDROXYSTILBENE 2 NITROGEN; 4,6 DIMETHYL 2',5,5' TRIMETHOXYSTILBENE 2 NITROGEN; 4,6 DIMETHYL 3',5,5' TRIHYDROXYSTILBENE 2 NITROGEN; 4,6 DIMETHYL 3',5,5' TRIMETHOXYSTILBENE 2 NITROGEN; RESVERATROL; STILBENE DERIVATIVE; UNCLASSIFIED DRUG;

ANIMAL CELL; ANTIVIRAL ACTIVITY; ARTICLE; CONTROLLED STUDY; CYTOPATHOGENIC EFFECT; DRUG DETERMINATION; DRUG INHIBITION; DRUG SYNTHESIS; IN VITRO STUDY; NONHUMAN; SARS CORONAVIRUS; SEVERE ACUTE RESPIRATORY SYNDROME; VERO CELL; VIRUS INHIBITION; VIRUS REPLICATION; ANIMAL; CERCOPITHECUS; CHEMICAL STRUCTURE; CHEMISTRY; DRUG EFFECT; PHYSIOLOGY; STRUCTURE ACTIVITY RELATION; SYNTHESIS;

ANIMALS; CERCOPITHECUS AETHIOPS; MOLECULAR STRUCTURE; SARS VIRUS; STILBENES; STRUCTURE-ACTIVITY RELATIONSHIP; VERO CELLS; VIRUS REPLICATION;

EID: 33748466674     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2006.03.024     Document Type: Article

References (21)

1. Wieslaw P., and Bogdan K. IL Farmaco 54 (1999) 584-587
2. Ali M.A., Kondo K., and Tsuda Y. Chem. Pharm. Bull. (Tokyo) 40 (1992) 1130-1136
3. Boonlaksiri C., Oonanant W., Kongsaeree P., Kittakoop P., Tanticharoen M., and Thebtaranonth Y. Phytochem. 54 (2000) 415-417
4. Cai Y.J., Fang J.G., Ma L.P., Yang L., and Liu Z.L. Biochim. Biophys. Acta 1637 (2003) 31-38
5. Matsuda H., Morikawa T., Toguchida I., Park J.Y., Harima S., and Yoshikawa M. Bioorg. Med. Chem. 9 (2001) 41-50
6. Zheng J.B., and Ramirez V.D. Biochem. Biophys. Res. Commun. 261 (1999) 499-503
7. Orsini F., Pelizzoni F., Verotta L., and Aburjai T. J. Nat. Prod. 60 (1997) 1082-1087
8. Aburjai T.A. Phytochem. 55 (2000) 407-410
9. Thakkar K., Geahlen R.L., and Cushman M. J. Med. Chem. 36 (1993) 2950-2955
10. G.H. Chen, W. Liu, J.X. Li, W.M. John, P.C.T. Application, 2001 WO 0142231.
11. G.H. Chen, W. Liu, J.X. Li, W.M. John, P.C.T. Application, 2002 WO 02057219.
12. Jiang M.S., Cai L.N., Udeani G.O., Slowing K.V., Thomas C.F., Beecher C.W.W., Fong H.H.S., Farnsworth N.R., Kinghorn A.D., Mehta R.G., Moon R.C., and Pezzuto J.M. Science, 275 (1997) 218-220
13. Yang L.M., Lin S.J., Hsu F.L., and Yang T.H. Bioorg. Med. Chem. Lett. 12 (2002) 1013-1015
14. Wang X., Heredia A., Song H., Zhang Z., Yu B., Davis C., and Redfield R. J. Pharm. Sci. 93 (2004) 2448-2457
15. Likhitwitayawuid K., Sritularak B., Benchanak K., Lipipun V., Mathew J., and Schinazi R.F. Nat. Prod. Res. 19 (2005) 177-182
16. Docherty J.J., Fu M.M.H., Stiffler B.S., Limperos R.J., Pokabla C.M., and DeLucia A.L. Antivir. Res. 43 (1999) 135-145
17. Bhatacharya A.K., and Thyagarajan G. Chem. Rev. 81 (1981) 415-430
18. Piechucki C. Synthesis 3 (1976) 187-188
19. Baker R., and Sims R.J. Synthesis 2 (1981) 117
20. Chen L., Gui C., Luo X., Yang Q., Günther S., Scandella E., Drosten C., Bai D., He X., Ludewig B., Chen J., Luo H., Yang Y., Yang Y., Zou J., Thiel V., Chen K., Shen J., Shen X., and Jiang H. J. Virol. 11 (2005) 7095-7103
21. Murias M., Handler N., Erker T., Pleban K., Ecker G., Saiko P., Szekeres T., and Jäger W. Bioorg. Med. Chem. 12 (2004) 5571-5578