References
- Aga H, Shibuya T, Sugimoto T, et al. Isolation and identification of antimicrobial compounds in Brazilian Propolis. Biosci Biotechnol Biochem. 1994;58(5):945–946.10.1271/bbb.58.945
- Kujumgieva A, Tsvetkovaa I, Serkedjievaa Y, et al. Antibacterial, antifungal and antiviral activity of propolis of different geographic origin. J Ethnopharmacol. 1999;64(3):235–240.10.1016/S0378-8741(98)00131-7
- Isla MI, Dantur Y, Salas A, et al. Effect of seasonality on chemical composition and antibacterial and anticandida activities of Argentine propolis. Design of a topical formulation. Nat Prod Commun. 2012;7(10):1315–1318.
- Takemura T, Urushisaki T, Fukuoka M, et al. 3,4-Dicaffeoylquinic acid, a major constituent of Brazilian Propolis, increases TRAIL expression and extends the lifetimes of mice infected with the influenza a virus. Evid Based Complement Alternat Med. 2012;2012:946867.
- Paulino N, Abreu SR, Uto Y, et al. Anti-inflammatory effects of a bioavailable compound, Artepillin C Brazilian propolis. Eur J Pharmacol. 2008;587(1–3):296–301.10.1016/j.ejphar.2008.02.067
- Scheller S, Krol W, Swiacik J, et al. Antitumoral property of ethanolic extract of propolis in mice-bearing Ehrlich carcinoma, as compared to bleomycin. Z Naturforsch C. 1989;44(11–12):1063–1065.
- Kimoto T, Aga M, Hino K, et al. Apoptosis of human leukemia cells induced by Artepillin C, an active ingredient of Brazilian propolis. Anticancer Res. 2001;21(1a):221–228.
- Mishima S, Ono Y, Araki Y, et al. Two related cinnamic acid derivatives from Brazilian honey bee propolis, baccharin and drupanin, induce growth inhibition in allografted sarcoma S-180 in mice. Biol Pharm Bull. 2005;28(6):1025–1030.10.1248/bpb.28.1025
- Akao Y, Maruyama H, Matsumoto K, et al. Cell growth inhibitory effect of cinnamic acid derivatives from propolis on human tumor cell lines. Biol Pharm Bull. 2003;26(7):1057–1059.10.1248/bpb.26.1057
- Popolo A, Piccinelli LA, Morello S, et al. Antiproliferative activity of brown Cuban propolis extract on human breast cancer cells. Nat Prod Commun. 2009;4(12):1711–1716.
- Li F, Awale S, Tezuka Y, et al. Cytotoxicity of constituents from Mexican propolis against a panel of six different cancer cell lines. Nat Prod Commun. 2010;5(10):1601–1606.
- Park SI, Ohta T, Kumazawa S, et al. Korean propolis suppresses angiogenesis through inhibition of tube formation and endothelial cell proliferation. Nat Prod Commun. 2014;9(4):555–560.
- Tazawa S, Arai Y, Hotta S, et al. Discovery of a novel Diterpene in Brown Propolis from the State of Parana, Brazil. Nat Prod Commun. 2016;11(2):201–205.
- Park YK, Alencar SM, Aguiar CL. Botanical origin and chemical composition of Brazilian Propolis. J Agric Food Chem. 2002;50(9):2502–2506.10.1021/jf011432b
- Hata T, Tazawa S, Ohta S, et al. Artepillin C, a major ingredient of Brazilian Propolis, induces a pungent taste by activating TRPA1 channels. PLoS One. 2012;7(11):e48072.10.1371/journal.pone.0048072
- Naramoto K, Kato M, Ichihara K. Effects of an ethanol extract of Brazilian green propolis on human cytochrome P450 enzyme activities in vitro. J Agric Food Chem. 2014;62(46):11296–11302.10.1021/jf504034u
- Intekhab J, Aslam M. Isolation of a flavone glucoside from Glycosmis mauritiana (Rutaceae). Arab J Chem. 2011;4(1):79–81.10.1016/j.arabjc.2010.06.023
- Lin LC, Pai YF, Tsai TH. Isolation of Luteolin and Luteolin-7-O-glucoside from Dendranthema morifolium Ramat Tzvel and Their Pharmacokinetics in Rats. J Agric Food Chem. 2015;63(35):7700–7706.10.1021/jf505848z
- Sharon A, Ghirlando R, Gressel J. Isolation, purification, and identification of 2-(p-Hydroxyphenoxy)-5, 7-Dihydroxychromone: a fungal-induced Phytoalexin from Cassia obtusifolia. Plant Physiol. 1992;98(1):303–308.10.1104/pp.98.1.303
- Hong SS, Choi Y-H, Suh H-J, et al. Flavonoid constituents of Acacia catechu. J Appl Biol Chem. 2015;58(2):189–194.10.3839/jabc.2015.030
- Williams CA, Harborne JB, Geiger H, et al. The flavonoids of Tanacetum parthenium and T. vulgare and their anti-inflammatory properties. Phytochemistry. 1999;51(3):417–423.10.1016/S0031-9422(99)00021-7
- Hòrie T, Ohtsuru Y, Shibata K, et al. 13C NMR spectral assignment of the A-ring of polyoxygenated flavones. Phytochemistry. 1998;47(5):865–874.10.1016/S0031-9422(97)00629-8
- van Heerden FR, Viljoen AM, van Wyk BE. The major flavonoid of Dodonaea angustifolia. Fitoterapia. 2000;71(5):602–604.10.1016/S0367-326X(00)00201-X
- Hajime A, Shigeyuki A, Shigeharu F, et al. Physiologically active extract obtained from indigo plant polygonum tinctorium. United States patent US 6,524,625 B2. 2003 Feb. 25.
- Xia H, Qiu F, Zhu S, et al. Isolation and identification of ten metabolites of breviscapine in rat urine. Biol Pharm Bull. 2007;30(7):1308–1316.10.1248/bpb.30.1308
- Komiya T, Tsukui M, Oshio H. Studies on “Inchinko”. I. Capillarisin, a new choleretic substance (author’s transl). Yakugaku Zasshi. 1976;96(7):841–854.10.1248/yakushi1947.96.7_841
- Kijjoa A, Vieira LM, Pereira JA, et al. Further constituents of Achillea ageratum. Phytochemistry. 1999;51(4):555–558.10.1016/S0031-9422(99)00054-0
- Babajide OJ, Babajide OO, Daramola AO, et al. Flavonols and an oxychromonol from Piliostigma reticulatum. Phytochemistry. 2008;69(11):2245–2250.10.1016/j.phytochem.2008.05.003
- Polasek J, Queiroz EF, Marcourt L, et al. Peltogynoids and 2-phenoxychromones from Peltophorum pterocarpum and evaluation of their estrogenic activity. Planta Med. 2013;79(6):480–486.
- Rubio S, Quintana J, Eiroa JL, et al. Betuletol 3-methyl ether induces G(2)-M phase arrest and activates the sphingomyelin and MAPK pathways in human leukemia cells. Mol Carcinog. 2010;49(1):32–43.
- Rubio S, Quintana J, López M, et al. Phenylbenzopyrones structure-activity studies identify betuletol derivatives as potential antitumoral agents. Eur J Pharmacol. 2006;548(1–3):9–20.10.1016/j.ejphar.2006.07.020
- Li J, Zhu F, Lubet RA, et al. Quercetin-3-methyl ether inhibits lapatinib-sensitive and -resistant breast cancer cell growth by inducing G2/M arrest and apoptosis. Mol Carcinog. 2013;52(2):134–143.10.1002/mc.v52.2