PDF Publication Title:
Text from PDF Page: 017
Molecules 2014, 19 20107 30. Babu, K.V.; Rajasekharan, K.N. A convenient synthesis of curcumin-I analogues. Org. Prep. Proced. Int. 1994, 26, 674–677. 31. Venkateswarlu, S.; Ramachandra, M.S.; Subbaraju, G.V. Synthesis and biological evaluation of polyhydroxycurcuminoids. Bioorg. Med. Chem. 2005, 13, 6374–6380. 32. Venkata Rao, E.; Sudheer, P. Revisiting curcumin chemistry part I: A new strategy for the synthesis of curcuminoids. Indian J. Pharm. Sci. 2011, 73, 262–270. 33. Priyadarsini, K.I. Photophysics, Photochemistry and Photobiology of Curcumin: Studies from organic solutions, bio-mimetics and living cells. J. Photochem. Photobiol. C 2009, 10, 81–96. 34. Borsari, M.; Ferrari, E.; Grandi, R.; Saladini, M. Curucminoids as potential new iron-chelating agents: Spectroscopic, polarographic and potentiometric study on their Fe(III) complexing ability. Inorg. Chim. Acta 2002, 328, 61–68. 35. Priyadarsini, K.I. Free radical reactions of curcumin in model membranes. Free Radic. Biol. Med. 1997, 23, 838–884. 36. Priyadarsini, K.I.; Maity, D.K.; Naik, G.H.; Kumar, M.S.; Unnikrishnan, M.K.; Satav, J.G.; Mohan, H. Role of phenolic O-H and methylene hydrogen on the free radical reactions and antioxidant activity of curcumin. Free Radic. Biol. Med. 2003, 35, 475–484. 37. Mishra, B.; Priyadarsini, K.I.; Bhide, M.K.; Kadam, R.M.; Mohan, H. Reactions of superoxide radicals with curcumin: Probable mechanisms by optical spectroscopy and EPR. Free Radic. Res. 2004, 38, 355–362. 38. Jovanovic, S.V.; Boone, C.W.; Steenken, S.; Trinoga, M.; Kaskey, R.B. How curcumin works preferentially with water soluble antioxidants. J. Am. Chem. Soc. 2001, 12, 3064–3068. 39. Sun, Y.M.; Zhang, H.Y.; Chen, D.Z.; Liu, C.B. Theoretical Elucidation on the Antioxidant Mechanism of Curcumin: A DFT Study. Org. Lett. 2002, 4, 2909–2911. 40. Kim, J.E.; Kim, A.R.; Chung, H.Y.; Han, S.Y.; Kim, B.S.; Choi, J.S. In vitro peroxynitrite scavenging activity of diarylheptanoids from Curcumia longa. Phytother. Res. 2003, 17, 481–484. 41. Iwunze, M.O.; McEwan, D. Peroxynitrite interaction with curcumin solubilised in ethanol. Cell. Mol. Biol. 2004, 50, 749–752. 42. Shen, L.; Ji, H.F. The pharmacology of curcumin: Is it the degradation products? Trends Mol. Med. 2012, 18, 138–143. 43. Price, L.C.; Buescher, R.W. Kinetics of alkaline degradation of the food pigments curcumin and curcuminoids. J. Food Sci. 1997, 62, 267–269. 44. Wang, Y.J.; Pan, M.H.; Cheng, A.L.; Lin, L.I.; Ho, Y.S.; Hsieh, C.Y.; Lin, J.K. Stability of curcumin in buffer solution and characterization of its degradation products. J. Pharm. Biomed. Anal. 1997, 15, 1867–1876. 45. Canamares, M.V.; Garcia-Ramos, J.V.; Sanchez-Cortes, S. Degradation of curcumin in aqueous solutions and Ag nanoparticle studied by Uv-Vis absorption and surface enhanced Raman spectroscopy. Appl. Spectrosc. 2006, 60, 1386–1391. 46. Khurana, A.; Ho, C.T. High performance liquid chromatographic analysis of curcuminoids and their photo-oxidative decomposition compounds in curcuma longa. J. Liquid Chromatogr. 1988, 11, 2295–2304.PDF Image | Curcumin: From Extraction to Therapeutic Agent
PDF Search Title:
Curcumin: From Extraction to Therapeutic AgentOriginal File Name Searched:
molecules-19-20091.pdfDIY PDF Search: Google It | Yahoo | Bing
CO2 Organic Rankine Cycle Experimenter Platform The supercritical CO2 phase change system is both a heat pump and organic rankine cycle which can be used for those purposes and as a supercritical extractor for advanced subcritical and supercritical extraction technology. Uses include producing nanoparticles, precious metal CO2 extraction, lithium battery recycling, and other applications... More Info
Heat Pumps CO2 ORC Heat Pump System Platform More Info
| CONTACT TEL: 608-238-6001 Email: greg@infinityturbine.com | RSS | AMP |