143
Views
8
CrossRef citations to date
0
Altmetric
Articles

Quinoline based polymeric drug for biological applications: synthesis, characterization, antimicrobial, and drug releasing studies

, , , &
Pages 128-142 | Received 20 Jul 2014, Accepted 04 Nov 2014, Published online: 27 Nov 2014

References

  • Vogl O, Tirrell D. Functional polymers with biologically active group. J. Macromol. Sci. Chem. 1979;13:415–439.10.1080/00222337908068110
  • Mokle SS, Sayeed MA, Chopde K. Synthesis and antimicrobial activity of some chalcone derivatives. Int. J. Chem. Sci. 2004;2:96–100.
  • Ballesteros JF, Sanz MJ, Ubeda A, Miranda MA, Iborra S. Synthesis and pharmacological evaluation of 2′-hydroxychalcones and flavones as inhibitors of inflammatory mediators generation. J. Med. Chem. 1995;38:2794–2797.10.1021/jm00014a032
  • Viana GS, Bandeira MA, Matos F. Analgesic and anti-inflammatory effects of chalcones isolated from myracrodruon urundeuva allemão. J. Phytomedicine. 2003;10:189–195.10.1078/094471103321659924
  • Mukarami S, Muramatsu M, Aihara H, Otomo S. Inhibition of gastric H+, K(+) ATPase by the anti-ulcer agent, sofalcone. Biochem. Pharmacol. 1991;42:1447–1551.
  • Barfod L, Kemp K, Hansen M, Kharazmi A. Synthesis and antimicrobial activity of some chalcone derivatives. Int. J. Immunopharmacol. 2002;2:545–555.10.1016/S1567-5769(01)00202-8
  • Liu M, Wilairat P, Go ML. Antimalarial alkoxylated and hydroxylated chalcone. J. Med. Chem. 2001;44:4443–4452.10.1021/jm0101747
  • Nielsen SF, Chen M, Theander TG, Kharazmi A, Brøgger Christensen SB. Synthesis of antiparasitic licorice chalcones. Bioorg. Med. Chem. Lett. 1995;5:449–452.10.1016/0960-894X(95)00053-V
  • Vogel S, Barbic M, Jürgenliemk G, Heilmann J. Synthesis, cytotoxicity, anti-inflammantory activity of chalcones and influence of A-ring modifications on the pharmacological effect. Eur. J. Med. Chem. 2010;45:2206–2213.10.1016/j.ejmech.2010.01.060
  • Zhao LM, Jin HS, Sun LP, Piao HR, Quan ZS. Synthesis and evaluation of antiplatelet activity of trihydroxychalcone derivatives. Bioorg. Med. Chem. Lett. 2005;15:5027–5029.10.1016/j.bmcl.2005.08.039
  • Satyanarayana M, Tiwari P, Tripathi BK, Srivastava AK, Pratap R. Synthesis and antihyperglycemic activity of chalcone based aryloxypropanolamines. Bioorg. Med. Chem. 2004;12:883–889.10.1016/j.bmc.2003.12.026
  • Nowakowska Z, Kędzia B, Schroeder G. Synthesis, physicochemical properties and antimicrobial evaluation of new (E)-chalcones. Eur. J. Med. Chem. 2008;43:707–713.10.1016/j.ejmech.2007.05.006
  • Mayekar AN. Synthesis, characterization and antimicrobial study of some new cyclohexenone derivatives. Int. J. Chem. 2010;2:114–123.
  • Larsen RD, Corley EG, King AO, Carroll JD, Davis P. Practical route to a new class of LTD4 receptor antagonists. J. Org. Chem. 1996;61:3398–3405.10.1021/jo952103j
  • Chen YL, Fang KC, Sheu JY, Hsu SL, Tzeng CC. Synthesis and antibacterial evaluation of certain quinolone derivatives. J. Med. Chem. 2004;44:2374–2377.
  • Billker O, Lindo V, Panico M, Etiene AE, Paxton T. Identification of xanthurenic acids the putative inducer of malaria development in the mosquito. Nature. 1998;392:289–292.
  • Rezig R, Chebah M, Rhouati S, Ducki S, Lawrence NJ. Synthesis of some quinolinyl aryl unsaturated ketones. J. Soc. Alg. Chim. 2000;10:111–120.
  • Ducki S, Hadfield JA, Lawerence NJ, Liu CY. Isolation of E-1-(4-hydroxyphenyl)-but-1-en-3-one from scutellaria barbata. Planta Med. 1996;62:185–186.10.1055/s-2006-957853
  • Domínguez JN, Charris JE, Lobo G, Dominguez NG, Moreno MM. Synthesis of quinolinyl chalcones and their evaluation of their antimalarial activity. Eur. J. Med. Chem. 2001;36:555–560.10.1016/S0223-5234(01)01245-4
  • Moussaoui F, Belfaitah A, Debache A, Rhouati S. Synthesis and characterization of some new aryl quinolinyl α, β unsaturated ketones. J. Soc. Alg. Chim. 2002;12:71–78.
  • Ruiz C, Haddad M, Alban J, Bourdy G, Reategui R, Castillo D, Sauvain M, Deharo E, Estevez Y, Arevalo J, Rojas R. Activity guided isolation of antileishmanial compounds from piper hispidum. Phytochem. Lett. 2011;4:363–366.10.1016/j.phytol.2011.08.001
  • Ahmed MR, Sasttry VG, Bano N, Ravichantra S, Raghavendra M. Synthesis and cytotoxic, anti oxidant activities of new chalcone derivatives. Russ. J. Chem. 2011;4:289–294.
  • Arun A, Reddy BSR. Polymeric drug for antimicrobial activity studies: synthesis and characterization. J. Bioact. Compat. Polym. 2003;18:219–228.10.1177/0883911503035385
  • Nagaini Z, Siti M, Fadzillah H, Hussain H, Kamaruddin K. Synthesis and antimicrobial studies of (E)-3-(4-Alkyloxyphenyl)1-(2-hydroxyphenyl)prop-2-ene-1-one, (E)-3-(4Alkyloxyphenyl)-1-(4-hydroxyphenyl)prop-2-ene-1-one and their analogues. World J. Chem. 2009;4:09–14.
  • Bolard J, Legrand P, Heitz F, Cybulska B. One sided action of amphotericin boncholestrol-containing membrane is determined by its self-association in the medium. Biochemistry. 1991;30:5707–5715.10.1021/bi00237a011
  • Davaran S, Hanaee J, Khosravi A. Release of 5-amino salicylic acid from acrylic type polymeric prodrugs designed for colon-specific drug delivery. J. Controlled Release. 1999;58:279–287.10.1016/S0168-3659(98)00167-9

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.