Chemical constituents from the bark of Juglans mandshurica Maxim. and their phenol oxidase inhibitory effects

References

• Aloui S, Raboudi F, Ghazouani T, Salghi R, Hamdaoui MH, Fattouch S. 2014. Use of molecular and In Silico bioinformatic tools to investigate pesticide binding to insect (Lepidoptera) phenoloxidases (PO): insights to toxicological aspects. J Environ Sci Health, Part B. 49:654–660.10.1080/03601234.2014.922765
   PubMed Web of Science ®Google Scholar
• Andersen SO. 2010. Insect cuticular sclerotization: a review. Insect Biochem Mol Biol. 40:166–178.10.1016/j.ibmb.2009.10.007
   PubMed Web of Science ®Google Scholar
• Bai PP, Chen EH, Shen GM, Wei D, Wei DD, Wang JJ. 2014. Inhibition of phenoloxidase activity delays development in Bactrocera dorsalis (Diptera: Tephritidae). Florida Entomolo. 97:477–485.10.1653/024.097.0218
   Web of Science ®Google Scholar
• Gao XH, Xie N, Feng F. 2008. Studies on chemical constituents of Salacia prinoides. J Chin Med Mater. 31:1348–1351.
   Google Scholar
• Gholami T, Ghadamyari M, Oliaee AO, Ajamhasani M. 2013. Effects of inhibitors on haemolymph phenoloxidase from rosaceous branch borer, Osphernteria coerulescens (Coleoptera: Cerambycidae). J Plant Prot Res. 53:324–332.
   Google Scholar
• Guerrero A, Rosell G. 2005. Biorational approaches for insect control by enzymatic inhibition. Curr Med Chem. 12:461–469.10.2174/0929867053363126
   PubMed Web of Science ®Google Scholar
• Hirakawa K, Ogiue E, Motoyoshiya J, Yajima M. 1986. Naphthoquinones from juglandaceae. Phytochemistry. 25:1494–1495.10.1016/S0031-9422(00)81321-7
   Web of Science ®Google Scholar
• Hsu CH, Nguyen AD, Chen YW, Wang SL. 2014. Tyrosinase inhibitors and insecticidal materials produced by Burkholderia cepacia using squid pen as the sole carbon and nitrogen source. Res Chem Intermediat. 40:2249–2258.10.1007/s11164-014-1602-0
   Web of Science ®Google Scholar
• Jiang ZH, Tanaka T, Hirata H, Fukuoka R, Kouno I. 1996. Three diarylheptanoids from Rhoiptelea chiliantha. Phytochemistry. 43:1049–1054.10.1016/S0031-9422(96)00390-1
   Web of Science ®Google Scholar
• Kubo I, Kinst HI, Nihei K, Soria F, Takasaki M, Caldern JS, Cspedes CL. 2003. Tyrosinase inhibitors from galls of Rhus javanica leaves and their effects on insects. Zeitschrift fur Naturforschung. C. 58:719–725.
   PubMed Web of Science ®Google Scholar
• Li G, Xu ML, Choi HG, Lee SH, Jahng YD, Lee CS, Moon DC, Woo MH, Son JK. 2003. Four new diarylheptanoids from the roots of Juglans mandshurica. Cheminform. 51:262–264.
   Google Scholar
• Liang C, Lim JH, Kim SH, Kim DS. 2012. Dioscin: a synergistic tyrosinase inhibitor from the roots of Smilax china. Food Chem. 134:1146–1148.10.1016/j.foodchem.2012.03.003
   PubMed Web of Science ®Google Scholar
• Lin H, Zhang YW, Zheng LH, Meng XY, Bao YL, Wu Y. 2011. Anthracene and Anthraquinone derivatives from the stem bark of Juglans mandshurica Maxim. Helv Chim Acta. 94:1488–1495.10.1002/hlca.v94.8
   Web of Science ®Google Scholar
• Liu JX, Di DL, Wei XN, Han Y. 2008. Cytotoxic diarylheptanoids from the pericarps of walnuts (Juglans regia). Planta Med. 74:754–759.10.1055/s-2008-1074536
   PubMed Web of Science ®Google Scholar
• Maeda K, Fukuda M. 1996. Arbutin: mechanism of its depigmenting action in human melanocyte culture. J Pharmacol Exp Ther. 276:765–769.
   PubMed Web of Science ®Google Scholar
• Muñoz E, Avila JG, Alarcón J, Kubo I, Werner E, Céspedes CL. 2013. Tyrosinase Inhibitors from Calceolaria integrifolia s-l.: Calceolaria talcana aerial parts. J Agric Food Chem. 61:4336–4343.
   PubMed Web of Science ®Google Scholar
• Prasad KN, Yang B, Yang S, Chen YL, Zhao M, Ashraf M, Jiang YM. 2009. Identification of phenolic compounds and appraisal of antioxidant and antityrosinase activities from litchi (Litchi sinensis Sonn.) seeds. Food Chem. 116:1–7.10.1016/j.foodchem.2009.01.079
   Web of Science ®Google Scholar
• Rajashekar Y, Ravindra KV, Bakthavatsalam N. 2014. Leaves of Lantana camara Linn. (Verbenaceae) as a potential insecticide for the management of three species of stored grain insect pests. J Food Sci Tech. 51:3494–3499.
   PubMed Web of Science ®Google Scholar
• Ren XW. 1997. Dendrological (North). Beijing: Chinese Forestry Press; p. 48.
   Google Scholar
• Sata T. 1987. Spectral differentiation of 3, 3′-di-O-methylellagic acid from 4, 4′-di-O-methylellagic acid. Phytochemistry. 26:2124–2125.10.1016/S0031-9422(00)81778-1
   Web of Science ®Google Scholar
• Shen Y, Wang QH, Lin HW, Shu W, Zhou JB, Li ZY. 2006. Study on chemical constituents of Potentilla chinensis Ser. J Chin Med Mater. 29:237–239.
   Google Scholar
• Shi XH, Du XL, Kong LY. 2006. Studies on chemical constituents in roots of Euphorbia soongarica. J Chin Mater Med. 31:1503–1506.
   Google Scholar
• Shirai Y. 2000. Temperature tolerance of the diamondback moth, plutella xylostella (lepidoptera: yponomeutidae) in tropical and temperate regions of Asia. Bull Entomol Res. 90:357–364.
   PubMed Web of Science ®Google Scholar
• Terwilliger NB. 1999. Hemolymph proteins and molting in crustaceans and insects. Integr Comp Biol. 39:589–599.
   Google Scholar
• Xie GY, Luo WC, Ma C. 2003. Effect of kojic acid on phenolosidase activity in Diamondback moth. Chinese J Pestic Sci. 5:68–72.
   Google Scholar
• Xu W, Huang FS, Hao HX, Duan JH, Qiu ZW. 2006. Two serine proteases from anopheles dirus haemocytes exhibit changes in transcript abundance after infection of an incompatible rodent malaria parasite. Vet Parasitol. 139:93.10.1016/j.vetpar.2006.02.017
   PubMed Web of Science ®Google Scholar
• Yu DQ, Yang JS. 1999. Handbook of analytical chemistry. Beijing: Chemical Industry Press. Nuclear Magnetic Resonance Spectroscopy. 7:872.
   Google Scholar
• Zhai MZ, Yang XP, Liu L. 2001. The contact effect of extracts from walnut leaves on aphid. J Northwest Forestry Coll. 16:55–56.
   Google Scholar
• Zhang QG, Tan, WJ, Chen KL. 2003. Studies on the chemical constituents of Ampelopsis humulifolia var. heterophylla (Thunb.) K Koch. J Chin Med Mater. 26:636–637.
   Google Scholar
• Zhang Z, Zhang W, Ji YP, Zhao Y, Wang CG, Hu JF. 2010. Gynostemosides A-E, megastigmane glycosides from Gynostemma pentaphyllum. Phytochemistry. 71:693–700.10.1016/j.phytochem.2009.12.017
   PubMed Web of Science ®Google Scholar