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Items: 1 to 20 of 77

1.

Nature identical curcumin.

Jain R.

Int J Appl Basic Med Res. 2013 Jul;3(2):134. doi: 10.4103/2229-516X.117104. No abstract available.

2.

Biological activities of curcumin and its analogues (Congeners) made by man and Mother Nature.

Anand P, Thomas SG, Kunnumakkara AB, Sundaram C, Harikumar KB, Sung B, Tharakan ST, Misra K, Priyadarsini IK, Rajasekharan KN, Aggarwal BB.

Biochem Pharmacol. 2008 Dec 1;76(11):1590-611. doi: 10.1016/j.bcp.2008.08.008. Epub 2008 Aug 19. Review.

PMID:
18775680
3.

In vitro studies on the intestinal absorption of curcumin in rats.

Ravindranath V, Chandrasekhara N.

Toxicology. 1981;20(2-3):251-7.

PMID:
7256789
4.

[Study on stability of curcumine, demethoxycurcumin and bisdemethoxycurcumin].

Han G, Cui JJ, Bi R, Zhao LL, Zhang WG.

Zhongguo Zhong Yao Za Zhi. 2008 Nov;33(22):2611-4. Chinese.

PMID:
19216153
5.

Immunomodulatory and therapeutic activity of curcumin.

Srivastava RM, Singh S, Dubey SK, Misra K, Khar A.

Int Immunopharmacol. 2011 Mar;11(3):331-41. doi: 10.1016/j.intimp.2010.08.014. Epub 2010 Sep 8. Review.

PMID:
20828642
6.

Effect of curcumin on glucose absorption: an experimental study on albino rats.

Dvivedi J, Pandey S, Gupta R.

Indian J Physiol Pharmacol. 2011 Jul-Sep;55(3):207-12.

PMID:
22471226
7.

Fast dissolving eutectic compositions of curcumin.

Goud NR, Suresh K, Sanphui P, Nangia A.

Int J Pharm. 2012 Dec 15;439(1-2):63-72. doi: 10.1016/j.ijpharm.2012.09.045. Epub 2012 Oct 3.

PMID:
23041131
8.

Curcumin: from chemistry to chemistry-based functions.

Jitoe-Masuda A, Fujimoto A, Masuda T.

Curr Pharm Des. 2013;19(11):2084-92. Review.

PMID:
23116314
9.

Discovery of the curcumin metabolic pathway involving a unique enzyme in an intestinal microorganism.

Hassaninasab A, Hashimoto Y, Tomita-Yokotani K, Kobayashi M.

Proc Natl Acad Sci U S A. 2011 Apr 19;108(16):6615-20. doi: 10.1073/pnas.1016217108. Epub 2011 Apr 5.

10.

Dimethoxycurcumin, a Synthetic Curcumin Analogue, Induces Heme Oxygenase-1 Expression through Nrf2 Activation in RAW264.7 Macrophages.

Jeong SO, Oh GS, Ha HY, Soon Koo B, Sung Kim H, Kim YC, Kim EC, Lee KM, Chung HT, Pae HO.

J Clin Biochem Nutr. 2009 Jan;44(1):79-84. doi: 10.3164/jcbn.08-194. Epub 2008 Dec 27.

11.

Production of unnatural glucosides of curcumin with drastically enhanced water solubility by cell suspension cultures of Catharanthus roseus.

Kaminaga Y, Nagatsu A, Akiyama T, Sugimoto N, Yamazaki T, Maitani T, Mizukami H.

FEBS Lett. 2003 Dec 4;555(2):311-6.

12.

Interaction of curcumin with phosphatidylcholine: A spectrofluorometric study.

Began G, Sudharshan E, Udaya Sankar K, Appu Rao AG.

J Agric Food Chem. 1999 Dec;47(12):4992-7.

PMID:
10606563
13.

Enhanced dissolution performance of curcumin with the use of supersaturatable formulations.

Gosangari S, Dyakonov T.

Pharm Dev Technol. 2013 Mar-Apr;18(2):475-80. doi: 10.3109/10837450.2012.710239. Epub 2012 Aug 13.

PMID:
22881446
14.

Binding of curcumin to milk proteins increases after static high pressure treatment of skim milk.

Rahimi Yazdi S, Bonomi F, Iametti S, Miriani M, Brutti A, Corredig M.

J Dairy Res. 2013 May;80(2):152-8. doi: 10.1017/S0022029913000125. Epub 2013 Apr 3.

PMID:
23552051
15.

Biotransformation of curcumin through reduction and glucuronidation in mice.

Pan MH, Huang TM, Lin JK.

Drug Metab Dispos. 1999 Apr;27(4):486-94.

16.

Interaction of alphaS1-casein with curcumin and its biological implications.

Sneharani AH, Singh SA, Appu Rao AG.

J Agric Food Chem. 2009 Nov 11;57(21):10386-91. doi: 10.1021/jf902464p.

PMID:
19831420
17.

Curcumin recognizes a unique binding site of tubulin.

Chakraborti S, Das L, Kapoor N, Das A, Dwivedi V, Poddar A, Chakraborti G, Janik M, Basu G, Panda D, Chakrabarti P, Surolia A, Bhattacharyya B.

J Med Chem. 2011 Sep 22;54(18):6183-96. doi: 10.1021/jm2004046. Epub 2011 Aug 29.

PMID:
21830815
18.

Antitumor, anti-invasion, and antimetastatic effects of curcumin.

Kuttan G, Kumar KB, Guruvayoorappan C, Kuttan R.

Adv Exp Med Biol. 2007;595:173-84. Review.

PMID:
17569210
19.

Curcumin (diferuloylmethane), a singlet oxygen ((1)O(2)) quencher.

Das KC, Das CK.

Biochem Biophys Res Commun. 2002 Jul 5;295(1):62-6.

PMID:
12083767
20.

Cellular effects of curcumin on Plasmodium falciparum include disruption of microtubules.

Chakrabarti R, Rawat PS, Cooke BM, Coppel RL, Patankar S.

PLoS One. 2013;8(3):e57302. doi: 10.1371/journal.pone.0057302. Epub 2013 Mar 7.

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