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Cited by in F6Publishing
For: Matsubara K, Saito A, Tanaka A, Nakajima N, Akagi R, Mori M, Mizushina Y. Epicatechin conjugated with fatty acid is a potent inhibitor of DNA polymerase and angiogenesis. Life Sci. 2007;80:1578-1585. [PMID: 17328920 DOI: 10.1016/j.lfs.2007.01.049] [Cited by in Crossref: 21] [Cited by in F6Publishing: 16] [Article Influence: 1.5] [Reference Citation Analysis]
Number Citing Articles
1 Qu Z, Liu A, Li P, Liu C, Xiao W, Huang J, Liu Z, Zhang S. Advances in physiological functions and mechanisms of (-)-epicatechin. Crit Rev Food Sci Nutr 2021;61:211-33. [PMID: 32090598 DOI: 10.1080/10408398.2020.1723057] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 6.0] [Reference Citation Analysis]
2 Ueda-Wakagi M, Mukai R, Fuse N, Mizushina Y, Ashida H. 3-O-Acyl-epicatechins Increase Glucose Uptake Activity and GLUT4 Translocation through Activation of PI3K Signaling in Skeletal Muscle Cells. Int J Mol Sci 2015;16:16288-99. [PMID: 26193264 DOI: 10.3390/ijms160716288] [Cited by in Crossref: 19] [Cited by in F6Publishing: 14] [Article Influence: 3.2] [Reference Citation Analysis]
3 Fudouji R, Tanaka T, Taguri T, Matsuo Y, Kouno I. Coupling Reactions of Catechins with Natural Aldehydes and Allyl Alcohols and Radical Scavenging Activities of the Triglyceride-Soluble Products. J Agric Food Chem 2009;57:6417-24. [DOI: 10.1021/jf9010998] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 0.8] [Reference Citation Analysis]
4 Kobori R, Hashimoto S, Koshimizu H, Yakami S, Hirai M, Noro K, Kawasaki T, Saito A. Flavan-3-ols Content in Red Raspberry Leaves Increases under Blue Led-Light Irradiation. Metabolites 2019;9:E56. [PMID: 30901937 DOI: 10.3390/metabo9030056] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
5 Nachtergael A, Lanterbecq D, Spanoghe M, Belayew A, Duez P. Effects of Chemopreventive Natural Compounds on the Accuracy of 8-oxo-7,8-dihydro-2'-deoxyguanosine Translesion Synthesis. Planta Med 2021;87:868-78. [PMID: 34237787 DOI: 10.1055/a-1527-1435] [Reference Citation Analysis]
6 Maruo S, Kuriyama I, Kuramochi K, Tsubaki K, Yoshida H, Mizushina Y. Inhibitory effect of novel 5-O-acyl juglones on mammalian DNA polymerase activity, cancer cell growth and inflammatory response. Bioorg Med Chem 2011;19:5803-12. [PMID: 21903399 DOI: 10.1016/j.bmc.2011.08.023] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 1.0] [Reference Citation Analysis]
7 Kayashima T, Mori M, Yoshida H, Mizushina Y, Matsubara K. 1,4-Naphthoquinone is a potent inhibitor of human cancer cell growth and angiogenesis. Cancer Letters 2009;278:34-40. [DOI: 10.1016/j.canlet.2008.12.020] [Cited by in Crossref: 46] [Cited by in F6Publishing: 30] [Article Influence: 3.8] [Reference Citation Analysis]
8 Liu L, Jin C, Zhang Y. Lipophilic phenolic compounds (Lipo-PCs): emerging antioxidants applied in lipid systems. RSC Adv 2014;4:2879-91. [DOI: 10.1039/c3ra44792h] [Cited by in Crossref: 35] [Article Influence: 5.0] [Reference Citation Analysis]
9 Höltje M, Richartz A, Zdrazil B, Schwanke A, Dugovic B, Murruzzu C, Reißig H, Korting HC, Kleuser B, Höltje H, Schäfer-korting M. Human polymerase α inhibitors for skin tumors. Part 2. Modeling, synthesis and influence on normal and transformed keratinocytes of new thymidine and purine derivatives. Journal of Enzyme Inhibition and Medicinal Chemistry 2010;25:250-65. [DOI: 10.3109/14756360903059579] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
10 Cruz L, Fernandes VC, Araújo P, Mateus N, de Freitas V. Synthesis, characterisation and antioxidant features of procyanidin B4 and malvidin-3-glucoside stearic acid derivatives. Food Chemistry 2015;174:480-6. [DOI: 10.1016/j.foodchem.2014.11.062] [Cited by in Crossref: 25] [Cited by in F6Publishing: 18] [Article Influence: 4.2] [Reference Citation Analysis]
11 Cruz L, Fernandes I, Guimarães M, de Freitas V, Mateus N. Enzymatic synthesis, structural characterization and antioxidant capacity assessment of a new lipophilic malvidin-3-glucoside–oleic acid conjugate. Food Funct 2016;7:2754-62. [DOI: 10.1039/c6fo00466k] [Cited by in Crossref: 27] [Cited by in F6Publishing: 3] [Article Influence: 5.4] [Reference Citation Analysis]
12 Schwanke A, Murruzzu C, Zdrazil B, Zuhse R, Natek M, Höltje M, Korting HC, Reissig H, Höltje H, Schäfer-korting M. Antitumor effects of guanosine-analog phosphonates identified by molecular modelling. International Journal of Pharmaceutics 2010;397:9-18. [DOI: 10.1016/j.ijpharm.2010.06.036] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
13 Mpofu S, Tantoh Ndinteh D, van Vuuren S, Olivier D, Krause R. Interactive efficacies of Elephantorrhiza elephantina and Pentanisia prunelloides extracts and isolated compounds against gastrointestinal bacteria. South African Journal of Botany 2014;94:224-30. [DOI: 10.1016/j.sajb.2014.07.002] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 0.9] [Reference Citation Analysis]
14 Hosseinimehr SJ, Azadbakht M, Abadi AJ. Protective effect of hawthorn extract against genotoxicity induced by cyclophosphamide in mouse bone marrow cells. Environmental Toxicology and Pharmacology 2008;25:51-6. [DOI: 10.1016/j.etap.2007.08.006] [Cited by in Crossref: 21] [Cited by in F6Publishing: 17] [Article Influence: 1.6] [Reference Citation Analysis]
15 Martin MA, Goya L, Ramos S. Potential for preventive effects of cocoa and cocoa polyphenols in cancer. Food and Chemical Toxicology 2013;56:336-51. [DOI: 10.1016/j.fct.2013.02.020] [Cited by in Crossref: 59] [Cited by in F6Publishing: 51] [Article Influence: 7.4] [Reference Citation Analysis]
16 Gazák R, Purchartová K, Marhol P, Zivná L, Sedmera P, Valentová K, Kato N, Matsumura H, Kaihatsu K, Kren V. Antioxidant and antiviral activities of silybin fatty acid conjugates. Eur J Med Chem 2010;45:1059-67. [PMID: 20036447 DOI: 10.1016/j.ejmech.2009.11.056] [Cited by in Crossref: 46] [Cited by in F6Publishing: 40] [Article Influence: 3.8] [Reference Citation Analysis]