1. Sriramurthy V, Barcan GA, Kwon O. Bisphosphine-catalyzed mixed double-Michael reactions: Asymmetric synthesis of oxazolidines, thiazolidines, and pyrrolidines. J Am Chem Soc 2007; 129:12928-12929.
2. Song ZC, Ma GY, Lv PC, Li HQ, Xiao ZP, Zhu HL. Synthesis, structure and structure-activity relationship analysis of 3-tert-butoxycarbonyl-2-arylthiazolidine-4-carboxylic acid derivatives as potential antibacterial agents. Eur J Med Chem 2009; 44:3903-3908.
3. Moallem SA, Imenshahidi M, Shahini N, Javan AR, Karimi M, Alibolandi M et al. Synthesis, anti-inflammatory and anti-nociceptive activities and cytotoxic effect of novel thiazolidin-4-ones derivatives as selective cyclooxygenase (COX-2) inhibitors. Iran J of Basic Med Sci 2013; 16:1238-1244.
4. Hutt MP, Antibacterial thiazolidine or thiomorpholine substituted quinolones. US Patent 4,473,568 A, 25 Sep. 1984.
5. Onen-Bayram FE, Durmaz I, Scherman D, Herscovici J, Cetin-Atalay R, A novel thiazolidine compound induces caspase-9 dependent apoptosis in cancer cells. Bioorg Med Chem 2012; 20:5094-5102.
6. Li W, Lu Y, Wang Z, Dalton JT, Miller DD, Synthesis and antiproliferative activity of
thiazolidine analogs for melanoma. Bioorg Med Chem Lett 2007; 17:4113-4117.
7. Aiello F, Brizzi A, De Grazia O, Garofalo A, Grande F, Sinicropi, MS et al. An approach to the stereo-controlled synthesis of polycyclic derivatives of l-4-thiazolidinecarboxylic acid active against HIV-1 integrase. Eur J Med Chem 2006; 41:914-917.
8. Ha YM, Park YJ, Lee JY, Park D, Choi YJ, Lee EK et al. Design, synthesis and biological evaluation of 2-(substituted phenyl) thiazolidine-4-carboxylic acid derivatives as novel tyrosinase inhibitors. Biochimie 2012; 94:533-540.
9. Unger L, DeMoss RD. Action of a proline analogue, l-thiazolidine-4-carboxylic acid, in Escherichia coli. J Bacteriol 1966; 91:1556–1563.
10. Anderson RJ, Groundwater PW, Todd A, Worsley AJ. Antibacterial Agents: Chemistry, Mode of Action, Mechanisms of Resistance and Clinical Applications, John Wiley and Sons; 2012.
11. Wise R, Hart T, Cars O, Streulens M, Helmuth R, Huovinen P, Sprenger M. Antimicrobial resistance. Is a major threat to public health. BMJ 1998; 317:609-610.
12. Chauhan R, Abraham J. In vitro antimicrobial potential of the lichen Parmotrema sp. extracts against various pathogens. Iran J of Basic Med Sci 2013; 16: 882-885.
Online Türk Sağlık Bilimleri Dergisi 2017, Cilt 2, Sayı 4, 1-10
Araştırma Makalesi Hayriye GENÇ
7
13. Flaherty JP, Weinstein RA. Nosocomial Infection Caused by Antibiotic-Resistant Organisms in the Intensive-Care Unit. Infect Control Hosp Epidemiol 1996; 17:236-248.
14. Guclu E. Genc H, Zengin M, Karabay O. Effectiveness of menthol and folium menthae piperitae against Acinetobacter baumannii. Afr J Microbiol. Res 2013; 7: 2870-2874.
15. Guclu E, Genc H, Zengin M, Karabay O. Antibacterial Activity of Lythrum salicaria against Multidrug-resistant Acinetobacter baumannii and Pseudomonas aeruginosa. Annu Res Rev Biol 2014; 4:1099-1105.
16. Ogutlu A, Genc H, Dursun T, Zengin M, Karabay O. A new antiseptic - furfurylamine biguanidine derivative synthesis and its effect on multi-drug resistant Acinetobacter baumannii strains. Acta Medica Mediterranea 2014; 30: 133-136.
17. Genç H, Karabay O. The antibacterial activity of 2-aminoindanbiguanide chloride and acetate salts against resistant gram-negative bacilli. Annual Research & Review in Biology 2014; 4:1353-1360.
18. Khan KM, Ullah Z, Lodhi MA, Ali M, Choudhary MI, Rahman A et al. Successful computer guided planned synthesis of (4R)-thiazolidine carboxylic acid and its 2-substituted analogues as urease inhibitors. Molecular Diversity 2006; 10:223-231.
19. Han YK, Park YJ, Ha YM, Park D, Lee JY, Lee N et al. Characterization of a novel tyrosinase inhibitor, (2RS,4R)-2-(2,4-
dihydroxyphenyl)thiazolidine-4-carboxylic acid (MHY384). Biochim Biophys Acta 2012; 20:542-549.
20. Clinical and Laboratory Standards Institute. Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria That Grow Aerobically; Approved Standard- Eighth Edition. CLSI document M07- A8. Clinical and Laboratory Standards Institute, Wayne, Pennsylvania, 2009.
21. Schubert MP. Compounds of thiol acids with aldehydes. J Biol Chem 1936; 114:341-350.
22. Ratner S, Clarke HT, The action of formaldehyde upon cysteine. J Am Chem Soc 1937; 59:200-209.
23. Prabhakar YS, Solomon VR, Gupta MK, Katti SB. QSAR studies on thiazolidines: a biologically privileged scaffold. Top Heterocycl Chem 2006; 4: 161-249.
24. Hahn FE. Thiazolidine-4-carboxylic acid, a selective drug against human cancers. Naturwissenschaften 1980; 67: 307-307.
25. Yang DP, Ji HF, Tang GY, Ren W, Zhang HY. How many drugs are catecholics. Molecules 2007; 12:878-884.
26. Overington JP, Al-Lazikani B, Hopkins AL. How many drug targets are there? Nat Rev Drug Discov 2006; 5:993-996.
27. Dalluge JJ, Nelson BC. Determination of tea catechins. J Chromatogr A 2000; 881:411-424.
Online Türk Sağlık Bilimleri Dergisi 2017, Cilt 2, Sayı 4, 1-10
Araştırma Makalesi Hayriye GENÇ
8
28. Ross AB, Kamal-Eldin A, Aman P. Dietary Alkylresorcinols: Absorption, Bioactivities, and Possible Use as Biomarkers of Whole-grain Wheat–and Rye–rich Foods. Nutr Rev 2004; 62:81-95.
29. Kozubek A, Tyman JH. Resorcinolic lipids, the natural non-isoprenoid phenolic amphiphiles and their biological activity. Chem Rev 1999; 99:1-26.
30. Sanchez PC, Garrido AR, Gallego GG. Lopez, S. V.; Puerto, L. R. M. Methods of use for 2,5-dihydroxybenzene sulfonic acid compounds for the treatment of cancer, rosacea and psoriasis. US Patent 0 149 618 A1, 2007.
Thank you for copying data from http://www.arastirmax.com