Tyrosinase inhibitory activities of the compounds isolated from Neolitsea aciculata (Blume) Koidz.

References

• Land EJ, Ramsden CA, Riley PA. Tyrosinase autoactivation and the chemistry of ortho-quinone amines. Acc Chem Res 2003;36:300–308.
   PubMed Web of Science ®Google Scholar
• Uyen LDP, Nguyen DH, Kim EK. Mechanism of skin pigmentation. Biotechnol Bioprocess Eng 2008;13:383–395.
   Web of Science ®Google Scholar
• Chang TS. An updated review of tyrosinase inhibitors. Int J Mol Sci 2009;10:2440–2475.
   PubMed Web of Science ®Google Scholar
• Casañola-Martín GM, Marrero-Ponce Y, Khan MTH, Ather A, Khan KM, Torrens F et al. Dragon method for finding novel tyrosinase inhibitors: biosilico identification and experimental in vitroassays. Eur J Med Chem 2007;42:1370–1381.
   PubMed Web of Science ®Google Scholar
• Khan KM, Maharvi GM, Khan MTH, Jabbar Shaikh A, Perveen S, Begum S et al. Tetraketones: a new class of tyrosinase inhibitors. Bioorg Med Chem 2006;14:344–351.
   PubMed Web of Science ®Google Scholar
• Khan KM, Maharvi GM, Abbas Khan A, Hayat S, Khan MTH, Makhmoor T, Choudhary MI, Shaheen F, Atta-ur-Rahman. Three tyrosinase inhibitors and antioxidant compounds from Salsola foetida. Helvetica Chemica Acta 2003;86:457–469.
   Web of Science ®Google Scholar
• Khan MT, Choudhary MI, Khan KM, Rani M, Atta-ur-Rahman. Structure-activity relationships of tyrosinase inhibitory combinatorial library of 2,5-disubstituted-1,3,4-oxadiazole analogues. Bioorg Med Chem 2005;13:3385–3395.
   PubMed Web of Science ®Google Scholar
• Khan KM, Maharvi GM, Perveen S, Khan MT, Abdel-Jalil RJ, Shah ST et al. Synthesis of methyl ether analogues of sildenafil (Viagra) possessing tyrosinase inhibitory potential. Chem Biodivers 2005;2:470–476.
   PubMed Web of Science ®Google Scholar
• Khan KM, Saify ZS, Khan MT, Butt N, Maharvi GM, Perveen S et al. Tyrosinase inhibition: conformational analysis based studies on molecular dynamics calculations of bipiperidine based inhibitors. J Enzyme Inhib Med Chem 2005;20:401–407.
   PubMed Web of Science ®Google Scholar
• Kim SS, Kim JE, Hyun CG, Lee NH. Neolitsea aciculata essential oil inhibits drug-resistant skin pathogen growth and Propionibacterium acnes-induced inflammatory effects of human monocyte leukemia. Nat Prod Commun 2011;6:1193–1198.
   PubMed Web of Science ®Google Scholar
• Ko RK, Kim GO, Hyun CG, Jung DS, Lee NH. Compounds with tyrosinase inhibition, elastase inhibition and DPPH radical scavenging activities from the branches of Distylium racemosum Sieb. et Zucc. Phytother Res 2011;25:1451–1456.
   PubMed Web of Science ®Google Scholar
• Seo JC. A wild flower in Jeju Island. Il Jin Sa 2004;384–394.
   Google Scholar
• Kim SS, Yoon WJ, Hyun CG, Lee NH. Down-regulation of tyrodinase, TRP-2 and MITF expressions by Neolitsae aciculate extract in Murine B16F10 Melanoma. Int J Pharmacol 2010;6:290–295.
   Google Scholar
• Takeda K, Horibe I, Teraoka M, Minato H. Components of Neolitsea aciculata Kodiz. Structures and absolute configuration of litsealactone, litseaculane, zeylanine, and zeylanane. Chem commun 1968;940–942.
   Web of Science ®Google Scholar
• Yano K, Akihisa T, Tamura T, Matsumoto T. Four 4α-methylsterols and triterpene alcohols from Neolitsea aciculata. Phytochemistry 1992;31:2073–2078.
   Web of Science ®Google Scholar
• Vanni A, Gastaldi D, Giunata G. Kinetic investigation on the double enzymatic activity of the mushroom tyrosinase. Ann Chim 1991;80:35–60.
   Google Scholar
• Frankel EN, Neff WE, Weisleder D. Determination of methyl linoleate hydroperoxides by 13C nuclear magnetic resonance spectroscopy. Meth Enzymol 1990;186:380–387.
   PubMed Web of Science ®Google Scholar
• Parks JS, Cistola DP, Small DM, Hamilton JA. Interactions of the carboxyl group of oleic acid with bovine serum albumin: a 13C NMR study. J Biol Chem 1983;258:9262–9269.
   PubMed Web of Science ®Google Scholar
• Gunstone FD. 13C-NMR spectra of some synthetic glycerol esters alone and as mixtures. Chem Physics Lipids 1990;56:195–199.
   Web of Science ®Google Scholar
• Bang MH, Song JC, Lee SY, Park NK, Beak NI. Isolation and structure determination of antioxidants from the root of Paeonia lactiflora. J Korean Soc Agric Chem Biotechnol 1999;42:170–175.
   Google Scholar
• Kang IH, Cha JH, Lee SW, Kim HJ, Kwon SH, Ham IH, Hwang BS, Whang KA. Isolation and anti-oxidant from domestic Crataegus pinnatifida Bunge leaves. Kor J Pharmacogn 2005;36:121–128.
   Google Scholar
• Kucukislamoglu M, Yayli N, Senturk HB, Genc H. Flavonol glycosides from Consolida armeniaca. Turk J Chem 2000;24: 191–197.
   Web of Science ®Google Scholar
• Fathy MS, Shehata AH, Khaleel AE, Ezzat SM. An acylated kaempferol glycoside from flowers of Foeniculum vulgare and F. dulce. Molecules 2002;7:245–251.
   Web of Science ®Google Scholar
• Nowak R. Separation and quantification of tiliroside from plant extracts by SPE/RP-HPLC. Pharmaceut Biol 2003;41:8.
   Web of Science ®Google Scholar
• Kovganko NV, Kashkan ZN, Borisov EV, Batura EV. 13C NMR spectra of β-sitosterol derivatives with oxidixed rings A and B. Chem Nat Comp 1999;35:646–649.
   Web of Science ®Google Scholar
• Hussain RA, Siddiqui HL, Khan KM, Sharif A. Phytochemical studies on Adiantum incisum. J Chem Soc Pakistan 2008;30:605–608.
   Web of Science ®Google Scholar
• Lee DY, Song MC, Yoo JS, Kim SH, Chung IS, Kim DK, Park MH, Kwon BM, Kim SY, Baek NI. Development of biologically active compounds from edible plant sources-XVII. Isolation of sterols from the fruits of Cornus kousa Burg. J Korean Soc Appl Biol Chem 2006;49:82–85.
   Google Scholar
• Cutillo F, D’Abrosca B, DellaGreca MDi, Marino C, Golino A, Previtera L et al. Cinnamic acid amides from Chenopodium album: effects on seeds germination and plant growth. Phytochemistry 2003;64:1381–1387.
   PubMed Web of Science ®Google Scholar
• Chang TS, Ding HY, Tai SSK, Wu CY. Mushroom tyrosinase inhibitory effects of isoflavones isolated from soygerm koji fermented with Aspergillus oryzae BCRC 32288. Food Chem 2007;105:1430–1438.
   Web of Science ®Google Scholar
• Matoba Y, Kumagai T, Yamamoto A, Yoshitsu H, Sugiyama M. Crystallographic evidence that the dinuclear copper center of tyrosinase is flexible during catalysis. J Biol Chem 2006;281:8981–8990.
   PubMed Web of Science ®Google Scholar
• Nihei K, Kubo I. Identification of oxidation product of arbutin in mushroom tyrosinase assay system. Bioorg Med Chem Lett 2003;13:2409–2412.
   PubMed Web of Science ®Google Scholar