2017
DOI: 10.17221/584/2015-cjfs
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Curcumin and its allied analogues: epigenetic and health perspectives - a review

Abstract: Curcumin (diferuoyl methane) is a yellow active ingredient present in turmeric. It is a homodimer of feruloylmethane that comprises a hydroxyl and methoxy group (heptadiene with two Michael acceptors), and α-, β-diketone. It contains various metabolites, i.e. hexahydrocurcumin (HHC), tetrahydrocurcumin (THC), octahydrocurcumin (OHC), dihydrocurcumin (DHC), curcumin sulphate, and curcumin glucuronide. Curcumin has been proven the most effective histone deacetylase (HDAC) inhibitor in HeLa nuclear extracts. It h… Show more

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Cited by 8 publications
(4 citation statements)
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References 196 publications
(220 reference statements)
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“…At present, researchers work in the field of bio‐based polymer materials in comparison with conventional polymer‐based materials. But in general, the bio‐based polymer material itself limits its application in the field of packaging due to poor mechanical, thermal, barrier, and antimicrobial properties. To find effective application, the natural biopolymer has been blended with other synthetic polymers or nanomaterials.…”
Section: Introductionmentioning
confidence: 99%
“…At present, researchers work in the field of bio‐based polymer materials in comparison with conventional polymer‐based materials. But in general, the bio‐based polymer material itself limits its application in the field of packaging due to poor mechanical, thermal, barrier, and antimicrobial properties. To find effective application, the natural biopolymer has been blended with other synthetic polymers or nanomaterials.…”
Section: Introductionmentioning
confidence: 99%
“…Curcumin (CUR) and its metabolites are well-researched natural compounds with numerous beneficial biological activities. Curcumin is produced by the plant Curcuma longa, and tetrahydrocurcumin (THC), as one of its primary in vivo metabolites, possesses several CUR-like pharmacological effects [1]. Multiple studies have investigated the protective effects of CUR and its metabolites/analogs on cardiovascular diseases (CVDs).…”
Section: Introductionmentioning
confidence: 99%
“…One of the directions of their modification is the oxyfunctionalization of cycles А, C, and E, leading to new bioactive compounds [3][4][5][6][7][8][9][10][11][12][13][14].…”
mentioning
confidence: 99%
“…13β,28-lactones and 12-oxo-13β,28-lactones [14]. The oxidative lactonization of ursolic acid was effected with H 2 O 2 with the generation of 12β-hydroxy-13β,28-lactone [32].…”
mentioning
confidence: 99%