E Scientific Research of Guizhou (No.20126006) for the financial assistance. Author information 1 Guizhou Fruit Institute, Guizhou Academy of Agricultural Sciences, Guiyang 550006, P R China. 2Research Institute of Traditional Chinese Medicine, Yangtze River Pharmaceutical Group Beijing Haiyan Pharmaceutical Co., Ltd, Beijing 102206, P R China. 3State key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Important Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of ATGL manufacturer Education, Guizhou University, Guiyang 550025, P R China. Received: 15 December 2013 Accepted: 30 December 2013 Published: 3 January 2014 References 1. Jaafar RA, Rahman ARBA, Mahmod NZC, Vasudevan R: Proximate analysis of dragon fruit (Hylecereus polyhizus). Am J Appl Sci 2009, six:1341?346. 2. Choo WS, Yong WK: Antioxidant properties of two species of Hylocereus fruits. Adv Appl Sci Res 2011, two:418?25. three. De Freitas ST, Mitcham EJ: Top quality of pitaya fruit (Hylocereus undatus) as influenced by storage temperature and packaging. Sci Agric 2013, 70:257?62. 4. Rebecca OPS, Boyce AN, Chandran S: Pigment identification and antioxidant properties of red dragon fruit (Hylocereus polyrhizus). Afr J Biotechnol 2010, 9:1450?454. 5. Esquivel P, Stintzing FC, Carle R: Phenolic compound profiles and their corresponding antioxidant capacity of purple pitaya (Hylocereus sp.) genotypes. Z Naturforsch C 2007, 62:636?44. six. Nurliyana R, Syed Zahir I, Mustapha Suleiman K, Aisyah MR, VEGFR manufacturer Kamarul Rahim K: Antioxidant study of pulps and peels of dragon fruits: a comparative study. Int Meals Res J 2010, 17:367?75. 7. Herbacha KM, Stintzinga FC, Elssb S, Prestonb C, Schreierb P, Carlea R: Isotope ratio mass spectrometrical evaluation of betanin and isobetanin isolates for authenticity evaluation of purple pitaya-based solutions. Meals Chem 2006, 99:204?09. eight. Herbach KM, Stintzing FC, Carle R: Identification of heat-induced degradation items from purified betanin, phyllocactin and hylocerenin by high-performance liquid chromatography/electrospray ionization mass spectrometry. Fast Commun Mass Sp 2005, 19:2603?616. 9. Janeczko A: The presence and activity of progesterone in the plant kingdom. Steroids 2012, 77:169?73. 10. Nicholas HJ: Biosynthesis of -sitosterol and pentacyclic triterpenes of Dalvia officinalis. J Bio Chem 1962, 237:1676?680. 11. Patocka J: Biologically active pentacyclic triterpenes and their present medicine signification. J Appl Biomed 2013, 1:7?two. 12. Thao NTP, Hung TM, Lee MK, Kim JC, Min BS, Bae K: Triterpenoids from Camellia japonica and their cytotoxic activity. Chem Pharm Bull 2010, 58:121?24. 13. Lin L, Gao Q, Cui C, Zhao H, Fu L, Chen L, Yang B, Luo W, Zhao M: Isolation and identification of ent-kaurane-type diterpenoids from Rabdosia serra (MAXIM.) HARA leaf and their inhibitory activities against HepG-2, MCF-7, and HL-60 cell lines. Meals Chem 2012, 131:1009?014.DPPH no cost radical scavenging assayThe DPPH absolutely free radical scavenging assay has been widely employed to evaluate the antioxidant capacity, that is stable resulting from its resonance stability and particular blockade of benzene rings [27,28]. The purple chromogen radical DPPH is reduced by antioxidant compounds for the corresponding pale yellow hydrazine [29]. The antioxidant activity of plant extracts and antioxidant common were evaluated on the basis of radical scavenging impact of your steady DPPH free of charge radical. In its radical kind, DPPH has a characteristic absorption at 515 nm in ethanol, which d.