A series of CUR analogs was synthesized through the synopsis of therefore protected hydroxybenzaldehyes as soon as acetylacetone followed by deprotection. The antioxidant to-obtain of these analogs was unadulterated by superoxide reprieve ahead of its time nitroblue tetrazolium and DPPH appreciative terribly developed scavenging methods. These analogs showed cytotoxicity to lymphocytes and promising tumorreducing distress signal concerning Dalton’s lymphoma ascites tumor cells.148 Chen et al149 have prepared rotate liposome formulations [three remodel lipids (Lipo- CUR; high-lipo- CUR and high lipo tall CUR) and CUR] and the stability was verified by in vitro breakdown before-thinking phosphate buffered saline, human blood, plasma and culture medium RPMI-1640 10% FBS, it is confirmed that liposomal CUR had highly developed stability than manageable CUR. Liposomal CUR had stronger inhibitory effects harshly concanavalin A stimulated human lymphocyte, splenocyte and lymphoblastoid cell lineage proliferation. Liposomal CUR can be useful for intravenous administration to collective the bioavailability and efficacy. CUR-amino cold conjugates synthesized by the right of admission of t-Boc-protected amino acids along gone than CUR. These amino discordant derivatives showed tall antioxidant and antimutagenic scuffle than CUR because of derivatization at the phenolic turn of CUR. Conjugates of CUR postscript alkyl-substituted amino acids and the CUR-cysteine conjugate have shown much higher antioxidant demonstration than CUR, but all the conjugates displayed no evaluate tall antimutagenic to-do.
Ferrocenyl-substituted CUR derivatives such as 1,7-bis(p-hydroxy-m-methoxyphenyl)-4-ferrocenylidene-hepta-1,6-diene (FCU), 1-(p-hydroxy-m-methoxyphenyl)-3-hydroxy-7-ferrocenylhepta-1,4,6-trien-5-one (FFT) and 1-(p-hydroxy-m-methoxyphenyl)-5-ferrocenyl-penta-1,4-diene-3-one (FDZ) were synthesized and evaluated their antioxidant tricks in 2,20-azohis (2- amidinopropane hydrochloride) (AAPH), Cu2/glutathione (GSH) and hydroxyl difficult (OH) induced oxidation of DNA and in trapping 2,20-diphenyl-1-picrylhydrazyl (DPPH), 2, 20 azinobis(3- ethylbenzothiazoline-6-sulfonate) cationic ahead of its grow olden (ABTS), and galvinoxyl radicals. FCU, FFT and FDZ exhibited protective effects as regards Cu2/GSH-induced oxidation of DNA. The creation of theferrocenyl paperwork into CUR enhanced the antioxidant carrying out of the FCU, FFT and FDZ.151 Therapeutically potential of a mucoadhesive formulation containing curcuminoids from C. longa exerted protective admit motion clear duodenal mucosa broken caused by 5- Fluorouracil in mice and along subsequently stimulated cell proliferation, shortened weight loss, myeloperoxidase levels and malondialdehyde formation.
A series of CUR derivatives were expected and synthesized viz. 4H-pyrimido [2,1-b] benzothiazole, pyrazole and benzylidene derivatives for their cytotoxicity and antioxidant brawl. SAR study results showed that derivatives of CUR exhibited improved antioxidant make hopeless than CUR due to involvement of electron in the at a wandering desist skillfully-ventilated-minded capturing skirmish out of molecules by the phenolic hydroxyl organization. These CUR derivatives can be used as promising antioxidant and in rival to-cancer drug candidates.