Synthesis and antimicrobial activity of brominated resorcinol dimers

Bioorganic and Medicinal Chemistry Letters

Volumn 21, Issue 23, 2011, Pages 7142-7145

  Bouthenet, Elise ^a   Oh, Ki Bong ^b   Park, Seungil ^c   Nagi, Navjeet K ^a   Lee, Hyi Seung ^c   Matthews, Susan E ^a  

^a UNIVERSITY OF EAST ANGLIA   (United Kingdom)

^b Seoul National University   (South Korea)

^c Korea Research Institute of Ships and Ocean Engineering   (South Korea)

Author keywords

Antibacterial activity; Antifungal activity; Bromophenol; Red alga; Resorcinol

Indexed keywords

3 NITROPROPIONIC ACID; 4 BROMORESORCINOL; 6,6' [(4 HYDROXYPHENYL)ETHYLENE]BIS(4 BROMOBENZENE 1,3 DIOL); ALCOHOL; ALDEHYDE; AMPICILLIN; ANTIINFECTIVE AGENT; DIMER; HYDROCHLORIC ACID; RESORCINOL DERIVATIVE; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ANTIFUNGAL ACTIVITY; ANTIMICROBIAL ACTIVITY; ARTICLE; BROMINATION; CANDIDA ALBICANS; CHEMICAL REACTION; CONTROLLED STUDY; DEHALOGENATION; DRUG POTENCY; DRUG SYNTHESIS; GRAM NEGATIVE BACTERIUM; GRAM POSITIVE BACTERIUM; MINIMUM INHIBITORY CONCENTRATION; NONHUMAN;

ANTI-BACTERIAL AGENTS; ANTIFUNGAL AGENTS; CANDIDA ALBICANS; DIMERIZATION; HALOGENATION; INHIBITORY CONCENTRATION 50; ISOCITRATE LYASE; MICROBIAL SENSITIVITY TESTS; MOLECULAR STRUCTURE; RESORCINOLS;

CANDIDA ALBICANS; RHODOPHYTA;

EID: 80255126252     PISSN: 0960894X     EISSN: 14643405     Source Type: Journal    
DOI: 10.1016/j.bmcl.2011.09.072     Document Type: Article

References (30)

1. H.-S. Lee, T.-H. Lee, J.H. Lee, C.-S. Chae, S.-C. Chung, D.-S. Shin, J. Shin, and K.-B. Oh J. Agric. Food. Chem. 55 2007 6923
2. K. Kurata, K. Taniguchi, K. Takashima, I. Hyashi, and M. Suzuki Phytochemistry 45 1997 485
3. W. Wang, Y. Okada, H. Shi, Y. Wang, and T. Okuyama J. Nat. Prod. 68 2005 620
4. X.-Y. Duan, X.-M. Li, and B.-G. Wang J. Nat. Prod. 70 2007 1210
5. X. Fan, N.-J. Xu, and J.-G. Shi J. Nat. Prod. 66 2003 455
6. M. Pedersen Phytochemistry 17 1978 291
7. N. Xu, X. Fan, X. Yan, X. Li, R. Niu, and C.K. Tseng Phytochemistry 62 2003 1221
8. M. Suzuki, N. Kowata, and E. Kurosawa Bull. Chem. Soc. Jpn. 53 1980 2099
9. K. Kurata, and T. Amiya Chem. Lett. 1977 1435
10. L. Lundgren, K. Olsson, and O. Theander Acta Chem. Scand. B 333 1979 105
11. X. Xu, F. Song, S. Wang, S. Li, F. Xiao, J. Zhao, Y. Yang, S. Shang, L. Yang, and J. Shi J. Nat. Prod. 67 2004 1661
12. K.-B. Oh, J.H. Lee, S.-C. Chung, J. Shin, H.J. Shin, H.-K. Kim, and H.-S. Lee Bioorg. Med. Chem. Lett. 18 2008 104
13. K.-B. Oh, J.H. Lee, J.W. Lee, K.-M. Yoon, S.-C. Chung, H.B. Jeon, J. Shin, and H.-S. Lee Bioorg. Med. Chem. Lett. 19 2009 945
14. K.-B. Oh, H.B. Jeon, Y.-R. Han, Y.-J. Lee, J. Park, S.H. Lee, D. Yang, M. Kwon, J. Shin, and H.-S. Lee Bioorg. Med. Chem. Lett. 20 2010 6644
15. W. Zhao, X. Feng, S. Ban, W. Lin, and Q. Li Bioorg. Med. Chem. Lett. 20 2010 4132
16. E. Klarmann J. Am. Chem. Soc. 48 1926 791
17. W.C. Harden, and E.E. Reid J. Am. Chem. Soc. 54 1932 4325
18. E. Klarmann, and J. Von Wowern J. Am. Chem. Soc. 51 1929 605
19. F. Weinelt, and H.-J. Schneider J. Org. Chem. 56 1991 5527
20. P. Timmermann, W. Verboom, and D.N. Reinhoudt Tetrahedron 52 1996 2633
21. D. Moore, and S.E. Matthews J. Incl. Phenom. Macrocyl. Chem. 65 2009 137
22. P. Sakhaii, L. Verdier, T. Ikegami, and C. Greisinger Helv. Chim. Acta 85 2002 3895
23. L.M. Tunstad, J.A. Tucker, E. Dalcanale, J. Weiser, J.A. Bryant, J.C. Sherman, R.C. Helgeson, C.B. Knobler, and D.J. Cram J. Org. Chem. 54 1989 1305
24. M. Tabatabai, W. Vogt, and V. Böhmer Tetrahedron Lett. 31 1990 3295
25. G. Rumboldt, V. Böhmer, B. Botta, and E.F. Paulus J. Org. Chem. 63 1998 9618
26. Q. He, E.W. Miller, A.P. Wong, and C.J. Chang J. Am. Chem. Soc. 128 2006 9316
27. Y. Fujikawa, Y. Urano, T. Komatsu, K. Hanaoka, H. Kojima, T. Terai, H. Inoue, and T. Nagano J. Am. Chem. Soc. 130 2008 14533
28. P.T. Lewis, C.J. Davis, L.A. Cabell, M. He, M.W. Read, M.E. McCarroll, and R.M. Strongin Org. Lett. 2 2000 589
29. R.B. Sandin, and R.A. McKee Org. Synth. 17 1937 23
30. D.S. Shin, S. Kim, H.C. Yang, and K.-B. Oh J. Microbiol. Biotecnol. 15 2005 652