Synthesis and anti-bacterial properties of mono-carbonyl analogues of curcumin

Chemical and Pharmaceutical Bulletin

Volumn 56, Issue 2, 2008, Pages 162-167

  Liang, Guang ^a,b   Yang, Shulin ^a   Jiang, Lijuan ^b   Zhao, Yu ^b   Shao, Lili ^b   Xiao, Jian ^b   Ye, Faqing ^b   Li, Yueru ^c   Li, Xiaokun ^a,b,c  

^a NANJING UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^b WENZHOU MEDICAL UNIVERSITY   (China)

^c JILIN AGRICULTURAL UNIVERSITY   (China)

Author keywords

Analogue; Anti bacterial activity; Curcumin; Enterobacter cloacae; Substituent effect

Indexed keywords

AMPICILLIN; CARBONYL DERIVATIVE; CURCUMIN;

ANTIBACTERIAL ACTIVITY; ANTIBIOTIC SENSITIVITY; ARTICLE; COMPARATIVE STUDY; CONTROLLED STUDY; DRUG EFFICACY; DRUG SYNTHESIS; ENTEROBACTER CLOACAE; ENTEROCOCCUS; ESCHERICHIA COLI; GRAM NEGATIVE BACTERIUM; GRAM POSITIVE BACTERIUM; IN VITRO STUDY; MICROCOCCUS LUTEUS; NONHUMAN; STAPHYLOCOCCUS AUREUS; STAPHYLOCOCCUS EPIDERMIDIS; STAPHYLOCOCCUS SAPROPHYTICUS; STRUCTURE ACTIVITY RELATION;

ANTI-BACTERIAL AGENTS; BACTERIA; CURCUMIN; DRUG RESISTANCE, MULTIPLE, BACTERIAL; ENTEROBACTER CLOACAE; GRAM-NEGATIVE BACTERIA; GRAM-POSITIVE BACTERIA; INDICATORS AND REAGENTS; MAGNETIC RESONANCE SPECTROSCOPY; MICROBIAL SENSITIVITY TESTS; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 38849154619     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.56.162     Document Type: Article

References (23)

1. Ammon H. P., Wahl M. A., Plant Med., 57, 1-7 (1991).
2. Thangapazham R. L., Sharma A., Maheshwari R. K., The AAPS Journal, 8, E443-E449 (2006).
3. Negi P. S., Jayaprakasha G. K., Rao J. M., Sakariah K. K., J. Agric. Food Chem., 47, 4297-4300 (1999).
4. Jovanovic S. V., Boone C. W., Steenken S., Trinoga M., Kaskey R. B., J. Am. Chem. Soc., 123, 3064-3068 (2001).
5. Began G., Sudharshan E., Udaya Sankar K., Appu Rao A. G., J. Agric. Food Chem., 47, 4992-4997 (1999).
6. Iqbal M., Sharma S. D., Okazaki Y., Fujisawa M., Okada S., Pharmacol. Toxicol., 92, 33-38 (2003).
7. Yadav V. S., Mishra K. P., Singh D. P., Mehrotra S., Singh V. K., Immunopharmacol. Immunotoxicol., 27, 485-497 (2005).
8. Somparn P., Phisalaphong C., Nakornchai S., Unchern S., Morales N. P., Biol. Pharm. Bull., 30, 74-78 (2007).
9. Kawamori T., Lubet R., Steele V. E., Kelloff G. J., Kaskey R. B., Rao C. V., Reddy B. S., Cancer Res., 59, 597-601 (1999).
10. Feng R., Lu Y., Bowman L. L., Qian Y., Castranova V., Ding M., J. Biol. Chem., 280, 27888-27895 (2005).
11. Sharma R. A., Steward W. P., Gescher A. J., Adv. Exp. Med. Biol., 595, 453-470 (2007).
12. Maheshwari R. K., Singh A. K., Gaddipati J., Srimal R. C., Life Sci., 78, 2081-2087 (2006).
13. Zambre A. P., Kulkarni V. M., Padhye S., Sandur S. K., Aggarwal B. B., Bioorg. Med. Chem., 14, 7196-7204 (2006).
14. Handler N., Jaeger W., Puschacher H., Leisser K., Erker T., Chem. Pharm. Bull., 55, 64-71 (2007).
15. Ohtsu H., Xiao Z., Ishida J., Nagai M., Wang H. K., Itokawa H., Su C. Y., Shih C., Chiang T., Chang E., Lee Y., Tsai M. Y., Chang C., Lee K. H., J. Med. Chem., 45, 5037-5042 (2002).
16. Lin L., Shi Q., Su C. Y., Shih C. C., Lee K. H., Bioorg. Med. Chem., 14, 2527-2534 (2006).
17. Sardjiman S. S., Reksohadiprodjo M. S., Hakim L., Goot H., Timmerman H., Eur. J. Med. Chem., 32, 625-630 (1997).
18. Markaverich B. M., Schauweker T. H., Gregory R. R., Varma M., Kittrell F. S., Medina D., Varma R. S., Cancer Res., 52, 2482-2488 (1992).
19. Artico M., Santo R. D., Costi R., Novellino E., Greco G., Massa S., Tramontano E., Marongiu M. E., Montis A. D., Petal L. C., J. Med. Chem., 41, 3948-3960 (1998).
20. El-Subbagh H. I., Abu-Zaid S. M., Mahran M. A., Badria F. A., Al-Obaid A. M., J. Med. Chem., 43, 2915-2921 (2000).
21. Mishra S., Narain U., Mishra R., Misra K., Bioorg. Med. Chem., 13, 1477-1486 (2005).
22. Weber W. M., Hunsaker L. A., Abcouwer S. F., Deck L. M., Vander Jagt D. L., Bioorg. Med. Chem., 13, 3811-3820 (2005).
23. Tamaki M., Sawa K., Kikuchi S., Shindo M., Uchida Y., J. Antibiot., 59, 370-372 (2006).