Advances in the Study of Oxyresveratrol

Life International Journal of Pharmacology ISSN 1811-7775 Life science alert ansinet Asian Network for Scientific Information

International Journal of Pharmacology 10 (1): 44-54. 2014 ISSN 1811-7775 DOI: 10.3923/ijp.2011.11.51 2014 Asian Network for Scientific Information Advances in the Study of Oxyresveratrol 'Li Xu, 'Chao Liu, ‘Wei Xiang, 'Hu Chen, Xiaoli Qin and ‘Xianzhi Huang 'College of Biotechnology, Southwest University, Chongqing, 400716, China 'College of Food Science, Southwest University, Chongqing, 400716, China Abstract: As a representative substance of stilbenes, oxyresveratrol has various kinds of biological activities including antineoplastic activity, antioxidant activity, tyrosinase inhibitory activity and ability of boosting the immune system. In this study, physical and chemical properties, extraction and separation, structural identification, medicinal activity and pharmacokinetics of oxyresveratrol and its derivatives were reviewed. Future perspectives and challenges involved in the use of oxyresveratrol were also very key discussed. Key words: Oxyresveratrol, physical and chemical properties, extraction and separation, biological activities and pharmacokinetics, derivative INTRODUCTION Oxyresveratrol is a hydroxyl-substituted stilbene found in the roots, leaves, stem and fruit of many widely distributed plants including Moraceae, Liliaceae, Gnetaceae, etc., (Xiong et al., 2008; Ti et al., 2011) in China. The common representatives of plants harboring oxyresveratrol are Smilax china L. (Smilacaceae) (Xiong et al., 2008; Ruan et al., 2005; Huang et al., 2008a. b; Zhao et al., 2008; Huang et al., 2009a; Ban et al., 2006a, b: Ban et al., 2007; Jeon et al., 2007), Morus alba T.. (Moraceae) (Zhang et al., 2009; Tu et al., 2005; Ilu et al., 1996; Xu et al., 2009; Schultz et al., 1995; Andrabi et al., 2004; Qiu et al., 1996a; Lee et al., 2003, Djapic et al., 2003; Chung et al., 2003; Syah et al., 2004; Ferlinahayati et al., 2008; Shi et al., 2012), Arlocarpus heterophyllus L.. (Moraceae) (Fang et al, 2008; Chuanasa et al., 2008: Sasivimolphan et al., 2009; Likhitwitayawuid et al., 2005; Likhitwilayawuid et al., 2006; Hakim et al., 2002; Maneechai et al., 2009; Qiao et al., 2011; Maneechai et al., 2012), Veratrum nigrum L. (Liliaceae) (Zhao et al., 2008) and Scirpus maritimus (Cyperaceae) (Powell et al., 1987). Oxyresveratrol can be transported to tissues at high rates and can result in a bioavailability of around 50% in plants (Qiu et al., 1996b). In addition, oxyresveratrol not only has a potent inhibitory effect on cyclooxygenase activity (Shin et al., 1998b), ral liver mitochondrial ATPase activity (Nimmanpisut et al., 1976) and dopa oxidase activity (Song et al., 2007) also possesses antitumor activity (Li et al., 2010; Mouihate et al., 2006), antiviral activity (Chuanasa et al., 2008; Sasivimolphan et al., 2009; Likhitwilayawuid et al., 2005; Lipipun et al., 2011; Galindo et al., 2011; Jagtap and Bapat, 2010) and neuroprotective activity (Hom et al., 2003; Breuer et al.. 2006). According to recent studies (Song et al., 2007; Choi et a7, 2004, 2006; Chun et al., 2009; Likhitwitayawuid et al., 2006b; Rodriguez-Bonilla et al., 2010; Han et al., 2007; Guengerich et al., 2003, Chun et al., 2001), oxyresveratrol derivatives have important and significant biological activities than itself. Thus, oxyresveratrol is a potential substance to be utilized to produce medicines, cosmetics and health supplements. Resveratrol (3, 5, 4'-trihydroxysitlbene), a well-known representative of stilbene, is a phytoalexin used to improve the ability of plant against pathogens and against environmental deterioration. Due to the similar structure. oxyresveratrol may be an important plant natural substance with the same physiological functions. Now though oxyresveratrol have been found to possess a wide range of pharmacological properties and more and more to be of high value in promotion and utilization, no comprehensive report is available for this compound. In order to meet the needs of relevant intellectuals and other researchers, the following provides a detailed review of this particular hydroxystilbene. CHARACTERISTICS OF OXYRESVERATROL C Oxyresveratrol (2, 4, 3, 5-tetrahydroxystilbene; Fig. 1) is a derivative of resveratrol. Its linking C double bond has a trans conformation and allows the formation of a conjugated system throughout the molecule. Its dihedral angle between the benzene rings is 9.39 degrees. In the crystal, molecules are connected into a three-dimensional architecture through O-H-O hydrogen bonds between hydroxy groups of Corresponding Author: Li Xu and Xianzhi Huang, College of Biotechnology, Southwest University, Chongqing 400716, China Tel: 023-68250191 Fax: -023-68250191 44

HO OH Int. J. Pharmacol., 10 (1): 44-54, 2014 OH Fig. 1: Molecular structure of oxyresveratrol OH Oxyresveratrol and solvent water molecules (Deng et al., 2012). Additionally, as a natural hydroxystilbene. oxyresveratrol is a yellow solid with a melting-point of 199-204°C (>>98%), a molecular formula of CH, and a molecular weight of 244.24; oxyresveratrol shows blue fluorescence under UV light in a TLC reaction and also turns blue when mixed with FeCl. (Xiong et al., 2008; Ruan et al., 2005; Hu et al., 1996; Zhao et al., 1998). As can be seen from the structure, its chemical properties are unstable. In order to provide a reference for extraction separation and preservation process, factors that could influence the stability of oxyresveratrol were studied in our laboratory. The results showed that pure water is the most suitable solvent, -40°C is the most suitable temperature, 5.38 is the optimum pII value and dark environment is necessary for the storage of oxyresveratrol (Liu 2013). EXTRACTION AND SEPARATION In recent decades, oxyresveratrol has been isolated by using ethanol bathing from the Smilax china T.. (Smilacaceae) (Xiong et al., 2008; Ruan et al., 2005; Iluang et al., 2008a; Zhao et al., 2008; Iluang et al., 2009a; Ban et al., 2006a, b; Ban et al., 2007, Jeon et al., 2007; Zhang et al., 2009), Morus alba L. (Moraceae) (Fu et al.. 2005; Hu et al., 1996; Xu et al., 2009; Schultz et al., 1995; Andrabi et al., 2001; Qiu et al., 1996a; Lee et al., 2003; Djapic et al., 2003; Chung et al., 2003; Syah et al., 2004; Ferlinghayati et al., 2008), Artocarpus heterophyllus L.. (Moraceae) (Fang et al., 2008; Chuanasa et al., 2008: Sasivimolphan et al., 2009; Likhitwitayawuid et al., 2005; Likhitwitayawuid et al., 2006a, Hakim et al., 2002; Manocchi et al., 2009), Veratrum nigrum T.. (Liliaceae) (Zhao et al, 2008), Scirpus maritimus (Cyperaceae) (Powell et al., 1987) and others. Additionally, Tsuruga et al. (1991) extracted oxyresveratrol with chloroform and methanol from the fiuits of melaleuca leucadendron (Myrtaceae). At present, the main extraction reagents used to obtain oxyresveratrol from plants are ethanol (Maneechai et al., 2009), acetone (Djapic et al., 2003) and other organic solvents; the procedure begins with bathing the plant in the solvent and then using a chromato bar to purify oxyresveratrol. Lorenz et al. (2003) obtained pure solid oxyresveratrol (yield: 1.71 g) from 500 g mulberry wood shavings with 6.0 L of 96% (v/v) ethanol for two days at room temperature. Likewise, Zhang et al. (2008) also yielded oxyresveratrol that appeared as yellowish oil (1.01 g, 0.16%) from Ramulus mori by cutting the dried samples (6.50 kg) into small pieces followed by soaking with 70% ethanol (30 L) at ambient temperature for 24 h. In order to establish a more effective extraction technology. we optimized the ultrasonic-assisted extraction conditions of oxyresveratrol from the bark of cultured black mulberry. The optimal conditions were as follows: Extraction temperature: 50°C, Ratio of solution to solid (v/g): 20:1. Ultrasonic power: 196.23 W, Extraction time: 113 min, Ethanol concentration: 70.98%, Acetic acid concentration: 0.77% (Xu et al., 2013). Furthermore, with the development of science and technology, an increasing number of related methods of extraction and separation were invented. Tong et al. (2011) used ethanol fractionation, silica gel column chromatography and Sephadex LH-20 gel filtration chromatography to isolate and enrich oxyresveratrol sample from mulberry, used Nuclear Magnetic Resonance (NMR), HPLC-MS to identify its chemical structure and molecular weight; used High Performance Liquid Chromatography (HPLC) to detect its mass fraction (99%). Luo et al. (2012) developed a new method for the separation and purification of oxyresveratrol by High-Speed Counter-current Chromatography (HSCCC) from the extract of Ramulus mori using n-hexane: ethyl acelate methyl water (1:1:1:2, v/v) as the solvent system, the upper phase as the stationary phase, the lower phase as the mobile phase, 2.0 ml, min of flow-rate, 900 r min¯¹ of rotation speed and 75 mg of injection amount. llowever, the content of oxyresveratrol in plants is very low, thus only a small amount can be obtained. In this case, our research group (Xu et al., 2009) gained a chinese patent on a process of utilizing ethanol and enzymes to extract oxyresveratrol and to convert mulberroside A to oxyresveratrol and the process significantly improved extracting efficiency. Chemical synthesis is a complex process and can produce considerable toxic waste. Bioconversion. however, is an eco-friendly and efficient method for improving the yield. Organic synthesis is another available method for obtaining abundant oxyresveratrol. Thus, Kim et al. (2010) produced oxyresveratrol by 45

Int. J. Pharmacol., 10 (1): 44-54, 2014 enzymatic hydrolysis of mulberroside a using B-glucosidase. At the same time, Sun et al. (2010) also obtained oxyresveratrol with 311 yield of 30% Stom 3. 5-dihydroxyacetophenone and 2. 4dimethoxybenzaldehyde, via methylation, willgerodtkindler reaction, perkin condensations, subsequent decarboxylation and demethylation isomerization process. IDENTIFICATION AND ANALYSIS For oxyresveratrol, there are a variety of determination methods, for instance crystal color and melting point. As mentioned previously, a characteristic blue fluorescence under UV light in a TLC reaction also reflects the presence of oxyresveratrol (Hu et al., 1996; Ruan et al., 2005; Zhao et al., 1998). Based others' studies, Maneechai et al. (2009) developed a Thin Layer Chromatography (TLC) method for the quantitative analysis of oxyresveratrol content in Artocarpus lakoocha (Moraceae) heart wood and in the traditional drug 'Puag-Haad'. The reversed-phase high performance liquid chromatography (RE-HPLC) can also be utilized to accurately detect oxyresveratrol. In this procedure, a Zorbax SB-C, column (250×4.6 mm, 5 μm) with a simple linear gradient of acetonitrile-0.01% phosphoric acid at a wavelength of 320 nm and a column temperature of 30°C was used (Huang et al., 2008a). Shao et al. (2007) also utilized HPLC (connected an Agilent Zorbax XDB-C₁ column to a Zorbax XDB-C,, guard column) to determinate oxyresveratrol with A (acetonitrile) and B (0.02% aqueous phosphoric acid, v/v) as eluents at the temperature of 30°C. In addition, Ayinampudi et al. (2011) further described the methods for quantitative analysis of oxyresveratrol in different parts of mortis species by Iligh Performance Thin Layer Chromatography (HPTLC) and HPLC These methods were found to be precise and reproducible. MODIFICATION AND DERIVATIZATION Oxyresveratrol has been reported to have a stronger inhibitory effect on the dopa oxidase activity of tyrosinase than kojic acid (Shin et al., 1998b, Liang et al., 2012). However, another experiment suggested that oxyresveratrol revealed high cell toxicity in the melanoma cell line (Gomez-Cordoves et al., 2001). Furthermore, the quantity of this ingredient was limited in cell transmission and had many synthetic stops for organic synthesis (Zhang et al., 1998; Alonso et al., 1997). Accordingly, Choi et al. (2004) evaluated the effects of synthetic benzyl amide 2,6-dimethoxy-Nphenylbenzamide which is an oxyresveratrol derivative with an amide connection chain between the two benzene rings (Compound 1. Fig. 2) QII the ultraviolet B (UV B)-induced hyperpigmentation of the skin and found that (1) The skin returned to its original color after treatment. with compound when LV B-induced hyperpigmentation was elicited on brownish guinea pig skin, (2) Melanin level in the hyperpigmented area was significantly decreased in the compound 1-treated animals, (3) A 31.7% inhibition of melanin production among the cultured melanoma cells by compound 1 al 100 μM in vitro, while the compound had no effect on the tyrosinase enzyme function. Likhitwitayawuid et al. (2006a) studied 8 different Oxyresveratrol derivations, the results showed the biological activities of 2, 1, 3, 5-tetrahydroxybibenzyl and cis-2, 1, 3, 5-tetramethoxystilbene (compound 2 and compound 3. Fig. 2) were much better than that of Oxyresveratrol. Compound 2 exhibited more potent. tyrosinase inhibitory activity than oxyresveratrol and had no cytotoxicity. It also was a non-competitive inhibitor of mushroom tyrosinase with L-dopa as the substrate and demonstrated a slightly higher affinity to the enzyme than oxyresveratrol. Compared with the common anticanker agents ellipticine and doxorubicin, compound 3 showed very strong cell toxicity against the human cancer cells KB, BC and NCI-H187. Simultaneously, Choi et al. (2006) synthesized 2, 6-dimethoxy-N-(4-methoxyphenyl)benzamide (DMPB) (compound 1, Fig. 2) using a combination of benzoic acid and aniline, exhibiting significant depigmentation ability on the UV B-induced hyperpigmentation of the brown guinea pig skin without. significant cytotoxicity. The results confirmed that DMPB has conquered the shortcoming of oxyresveratrol and could be used to produce cosmetic products. What's more, Song et al. (2007) pointed out. Tha hydroxyl-substituted 2-phenyl-naphthalenes as new inhibitors of mushroom tyrosinase, exerted potent inhibitory effects on cyclooxygenase. rat liver mitochondrial ATPase and tyrosinase. Among them, 7-(3, 5-dihydroxyphenyl)-1, 3-naphthalenediol (compound 5, Fig. 2), an isostere of oxyresveratrol, demonstrated an IC value of 0.49 µM;, 5-(6-hydroxy-2naphthyl)-1, 3-benzenediol (compound 6, Fig. 2) demonstrated an IC, value of 16.52 µM; 4-(6-hydroxy-2naphthyl)-1, 3-benzenediol (compound 7. Fig. 2) demonstrated an ICs, value of 0.034 μM. Likewise, Chun et al. (2009) results indicated that 2, 2, 4, 6-tetramethoxystilbene (compound 8, Fig. 2), a methoxy derivative of oxyresveratrol, was a very selective and potent competitive inhibitor of human cytochrome P4501B1 (CYP1B1), as well as a suppressor of CYP1B1 expression, which could be a valuable tool for determining 46

OMe myh OMe Int. J. Pharmacol., 10 (1): 44-54, 2014 OH ΟΠΙ Compound 1 HO Compound 2 HO. OMe Compound 4 OH OH Compound 5 OMc OH McO Me0 OMe Compound 3 OH HO OMe kmyt QUI OH Compound 6 HO OH Compound 7 Fig. 2: Structure of compounds 1-8 the enzymatic properties of human CYPIBI. Recently, Song et al. (2012) gol. a more varied approach which increased effect on antityrosinase as well as antioxidant and other activities, as can be expected by zx-Oxyresveratrol due to the combination of the chemical properties of azo compounds and oxyresveratrol. Several problems are associated with low stability and bioavailability of oxyresveratrol and the ease with which it is oxidized by prooxidant agents. These issues have limited its use in the food and pharmaceutical industries. Rodriguez-Bonilla et al. (2010) applied cyclodextrins and oxy resveratrol to produce oxyresveratrol/SS-cyclodextrin complexes which slowed the rapid metabolism and elimination of oxyresveratrol, thereby its bioavailability was improved. BIOLOGICAL ACTIVITIES Antineoplastic activity: There is growing evidence demonstrating the inhibitory effect of oxyresveratrol on cancer. In Hu et al. (1996) studied the inhibitory effect of oxyresveratrol on Protein Kinase C (PKC) which probably scives as a receptor for the tumor promoters and found that oxyresveratrol showed noncompetitive inhibition (Nishizuka, 1984). Likewise, Li et al. (2010) investigated. the cytotoxicity of oxyresveratrol together with resveratrol Compound 8 in IIT-29 human colon cancer cells by MTT assay and found oxyresveratrol have about 2-fold more polent. cytotoxic activity than resveratrol. Furthermore, a related study (Wu et al., 2010) indicated that oxyresveratrol demonstrated in vitro anti-breast tumor cell activity. Accordingly, Mouihate et al. (2006) found that oxyresveratrol could dampen neuroimmune responses in vivo, suggesting that the oxyresveratrol-induced dampening of neuroimmune responses was largely due to its inhibitory effect on tumor necrosis factor- (TNF-α) production. However, this study also showed that oxyresveratrol demonstrated no direct effect on the NF-kappa B signaling pathway in vivo. Thus the author considered that oxyresveratrol could be used in pathological conditions where excessive detrimental TNF-a was produced. Whitening and skin care effects: In early. Mongolsuk et al. (1957) found oxyresveratrol in Artocarpus lakoocha (Moraccac) (Charocnlarp et al.. 1981) and proved that it has an obvious whitening effect. Later, the whitening effect of oxyresveratrol had been verified by some related experiments in guinea pigs (Tengamnuay et al., 2003) and humans. (Tengammuay et al., 2006). With in-depth research, more and more studies showed that excessive amount of 47

Int. J. Pharmacol., 10 (1): 44-54, 2014 melanin would cause pigmentation disorders which had great hann to human health and tyrosinase was the key enzyme in the production of melanin. The addition of inhibitors that inhibit tyrosinase activity in whitening cosmetics, achieved skin whitening through restraint of melanin formation (Lu et al., 2001). Moreover, Shin et al. (1998a) concluded the mechanism of whitening effect of oxyresveratrol: in vivo tyrosinase could convert tyrosine into dopa quinine and then formed melanin with a series of chemical reactions. When L-dopa was used as a substrate, oxyresveratrol inhibited dopa oxidase activity of tyrosinase in a noncompetitive marmer. Additionally, K. values suggested that oxyresveratrol exhibited about a 150-fold more potent inhibitory effect than resveratrol and exerted more effective inhibition on the enzyme than the well known inhibitors of azelaic acid. curcumin, kojic acid (Zheng et al., 2011) and mimosine. The effect was clear even though they were determined by similar assay systems 11 different laboratories (Lu et al., 2001). On the other hand, some similar studies found that compared with mulberroside A, oxyresveratrol had better performance in inhibiting ultraviolet B (LYB) irradiation-induced melanogenesis in brown guinea pig skin (Park et al., 2011), compared with dioscin and Mulberroside A oxyresveratrol showed stronger tyrosinase inhibitory activity (Liang et al., 2012; Kim et al., 2012). Oxyresveratrol also demonstrated a potent inhibitory effect on mushroom lyrosinase activity. which was 32-fold stronger than kojic acid (Kim et al., 2002). Recently, through scientific studies and investigations, Zheng el al. (2012) suggested oxyresveratrol as a good source of natural tyrosinase. inhibitor with a great potential and it can be used in foods as anti-browning agents and in cosmetics as skin-whitening agents. Antioxidant activity: As a bioactive compound, oxyresveratrol has demonstrated strong antioxidant. activity (Zhang and Shi, 2012; Schonfeld et al., 2009; Aftab et al., 2010). Especially, it has been shown to effectively scavenge free radicals such as 2,2'Azinobis-(3-ethylbenzthiazoline-6-sulphonate) (ABTS) and 2,2-diphenyl-1-pieryl-hydrazyl (DPPII) with a TEAC value 3.11 mM (Zhao et al., 2008). Chung et al. 2003 proved that oxyresveratrol could inhibit the expression of nitric oxide synthase and the accumulation of nitrite which produces a protective effect on cells after inflammatory injury and improves the antioxidant capacity of cells. Oxyresveratrol also was found to be nearly twice as strong as resveratrol in antioxidation (TBARS methods) (Nasapon et al., 2010). Another study found that compared with resveratrol or trans-4-hydroxystibene. oxyresveratrol was a more effective scavenger for DPPH used as a general free radical model and was a potential protectant against reactive oxygen and nitrogen species (ROS/RNS) (Lorenz et al., 2003). In our laboratory, the radical scavenging capacities and antioxidant activities of resveratrol, oxyresveratrol and mulberroside a from Cortex mori also were investigated. The results showed that oxyresveratrol has higher DPPII radical scavenging capacity than resveratrol and mulberroside A (Wang et al, 2011). Furthermore, oxyresveratrol demonstrated higher DNA protective effects than both trolox and ascorbic acid (well-known antioxidants) and might become a promising anti-aging drug and riboflavin stabilizer (Chatsumpun et al., 2011). Neuroprotective activity: Oxyresveratrol is a potent neuroprotectant and may be a potential drug for the treatment of acute ischemic stroke (Horn et al., 2003). Jagtap and Bapat (2010) reported that oxyresveratrol lowered the activity of neurodegenerative diseases, which destroy microglia and then lead to loss of cell activity after dramatic morphological changes in our brains and in this process nerve issue would secrete a host of soluble factors, which were beneficial to other major types of glial cells in the brain but could be deleterious to neurons. In addition, oxyresveratrol not only prevented neurological deficits but also reduced the infarct volume and apoptotic DNA fragmentation in middle cerebral artery occluded rats (Andrabi et al., 2004). Likewise, Breuer et al. (2006) demonstrated that oxyresveratrol potentially exerted direct protective effects on the brain by crossing the blood-brain barrier and proved an excellent complementary drug for the treatment of neurodegenerative diseases that involved oxidative/nitrosative stress especially in stroke. Oxyresveratrol non-competitively inhibited SS-secretase (Jeon et al., 2007), prevented amyloid protein (25-35)induced neuronal cell damage by interfering with the increase of Cat and inhibited glutamate release and reactive oxygen species generation (Ban et al., 2007). Oxyresveratrol was also a potential nutritional candidate for protection against neurodegeneration in Parkinson's disease (Liu and Long, 2003). Compared with resveratrol, oxyresveratrol exhibited a wider effective dosage range as an intracellular antioxidant for reducing oxidative stress induced by 6-hydroxydopamine, which markedly attenuated 6-hydroxydopamine (6-OHDA) induced phosphorylation of c-Jun N-terminal kinase and c-Jun; Furthermore, oxyresveratrol increased the basal levels of SIRTI, which might disclose new pathways accounting for the neuroprotective effects of oxyresveratrol (Chao et al., 2008). 48

Int. J. Pharmacol., 10 (1): 44-54, 2014 Weber et al. (2012) analyzed the neuroprotective ability of oxyresveratrol by using an in vitro model of stretch-induced trauma in co-cultures of neurons and glia and by exposing cultures to high levels of glutamate. The results showed that oxyresveratrol significantly inhibited trauma produced marked neuronal death when measured 24 h post-injury but it was not inhibited by oxyresveratrol when cultures exposed to high glutamate for 21 h. Protective function of hepatic damage: Currently, alcohol toxicosis has been attracted more and more attention. As well known, alcohol is harmful to the liver and can lead to many diseases, such as alcoholic hepatitis, hepatic fibrosis and cirrhosis. Thus, a new drug which can efficiently protect and repair our liver would be an important discover. Zhang et al. (2008) studied the activity of oxyresveratrol on the liver of mice intoxicated with ethanol and demonstrated that oxyresveratrol from Romulus mori could protect mice against ethanol-induced hepatic damage. Oxyresveratrol also increased glutathione levels and antioxidant enzymes activities and reduced iron concentration and mitochondrial permeability transition lo keep the related physiological indexes to the basal level, as well as allenuated the degree of tissue damage and the regulation of the expression of TNF-α. The molecular mechanisms behind the liver-protecting effects of oxyresveratrol, however, are still unclear and require further study. Ilypoglycemic activity: Oxyresveratrol could decrease the level of blood sugar in mice and inhibits the activity of a-glucosidase, therefore oxyresveratrol could be used to produce a novel hypoglycemic drug that could cure or prevent diabetes mellitus (Lu and Wang, 2010). In addition, Nasapon et al (2010) reported that oxyresveratrol showed strong antiglycation activities, the IC value was 2.0 μg mL (5 times higher than that of aminoguanidine). Antiviral and antibacterial activities: Artocarpus lakoocha (Moraceae), a Thai traditional plant. had shown to possess in vitro anti-herpes simplex virus activity and oxyresveratrol was a major constituent previously purified from it (Sasivimolphan et al., 2009; Likhitwitayawuid et al., 2005). In Chuanasa et al. (2008) concluded that oxyresveratrol revealed inhibitory activity at the early and late phases of viral replication with pretreatment in the one-step growth assay of HSV-1 and IISV-2 that had significantly delayed in herpetic skin lesion development (p<0.05). At the same time, topical application of oxyresveratrol (30%) ointment five times daily markedly delayed the development of skin lesions and protected mice from death (p<0.0001). Another study demonstrated that 10% oxyresveratrol in cream form was significantly effective for cutaneous HSV infection (Lipipun et al., 2011). Likewise, oxyresveratrol showed a broad spectrum of anti-varicella zoster virus activity and the mechanism of action was different from that of acyclovir (Sasivimolphan et al., 2009). In addition. possessed oxyresveratrol potential anti-HTV activity agams a wild-type Human immunodeficiency virus type 1 (HIV-1) isolate and was found to be a modest inhibitor of HIV (EC = 28.2 μM) (Likhitwitayawuid et al., 2005). In Galindo et al. (2011), a new study showed that oxyresveratrol displayed an excellent inhibitory activity on African Swine fever virus replication and inhibited viral DNA replication, late viral protein synthesis and viral factory formation but allowed early protein synthesis. In the same year, Mazimba et al. (2011) found that oxyresveratrol showed activities against Staphylococcus aureus, Bacillus subtilis, Mihirococcus flavus. Streptococcus faecalis. Salmonella abony and Pseudomonas aeruginosa. Oxyresveratrol also was evaluated for its antifungal activity and its cytotoxicity and its structure was established by 1D and 2D NMR, HRMS, CD and optical rotation measurements (Basset et al., 2012). Recently Sasivimolphan et al. (2012) evaluated the physicochemical properties of the optimized microemulsion and examined the permeating ability of oxyresveratrol in microemulsion and the efficacy of oxyresveratrol microemulsion culaneous Herpes simplex virus type 1 (HSV-1) infection in mice, demonstrated that topical oxyresveratrol microemulsion at 20-30% (w/w) was suitable for cutaneous IISV-1 mouse infection. PHARMACOKINETICS wzn A previous study demonstrated that oxyresveratrol was transported to tissues at high rates in rats (Qiu et al., 1996b). A sensitive and simple IIPLC method had been and developed validated for the pharmacokinetic profiles of oxyresveratrol in rat plasma (Huang et al., 2008a) and then oxyresveratrol was quantitatively determined by this method in rat lissues including heart, liver, spleen, lung and kidney after oral administration of Smilax china L. (Smilacaceae) extract (Huang et al., 2009a). The cumulative excretion of oxyresveratrol was 0.29% in bile samples and 0.84% in urine samples (Iluang et al., 2009b). The main metabolites of oxyresveratrol were monoglucuronided monosulfated oxyresveratrol (Huang et al., 2010). Mei et al. (2012) found that when incubated anaerobically 49

Int. J. Pharmacol., 10 (1): 44-54, 2014 with intestinal bacteria, the permeation of oxyresveratrol which underwent extensive hepatic glucuronidation and across Caco-2 cells was much more rapid than Mulberroside A. That further revealed a key role of intestinal bacterial conversion in absorption and systemic exposure of oxyresveratrol in the oral route in humans and rals. CONCLUSION AND FUTURE PERSPECTIVES With the rapid development of the economy, our lives have greally transformed. On the other hand, il. is easy for us to be infected by diseases, thus the rate of tumour, cerebral and vascular diseases, diabetes and heart. disease increases. In addition, the concept of health has attracted more and more attention and women in growing numbers take their appearance into consideration and are eager to find ways to make themselves look more beautiful. These problems have increased the burden of our society but give oxyresveratrol an opportunity to serve mankind. Oxyresveratrol has anti-tumor and anti-oxidant activities and can lower blood fat and blood sugar levels. Besides, oxyresveratrol can enhance the immune system and inhibit the activity of tyrosinase. Owing to these functions, oxyresveratrol could be utilized to develop and produce cosmetics, health supplements and drugs. Moreover, a lot of substances with important and significant activity could be derived from oxyresveratrol, which would become important in the future. Meanwhile. consumers in developed countries are becoming disillusioned with modern healthcare and are seeking allenatives. Since herbal medicines serve the health needs of about 80% of the world's population, thus oxyresveratrol is an important bioactive phytochemical that can be used as a promising source of medicine. For this purpose, oxyresveratrol should typically be subject.ed to precise scientific standardization in order to confirm the combination of traditional and modem wisdom in the light of a rational phytotherapy. It was well known that the Morus (Moraceae) plant is adapted to grow all over the world Every year, there are a large number of waste branches of mulberry especially in China. Many reports had pointed out that oxyresveratrol exists in mulberry and its concentration is low. While mulberroside A concentration is high and it can be converted to oxyresveratrol (Kim et al., 2010; Mei et al., 2012; Park et al., 2011; Wu, 2012). Thus, based on 3-year cooperation with Chongqing Huanshaotang Bio-Tech Co., Ltd and exploratory study on the pilot and the later development of the extraction and separation technology of oxyresveratrol and mulberrosideA, we think mulberry could provide the raw material for exploiting oxyresveratrol in the future. Currently, the study on oxyresveratrol is a very hot. field in scientific research. Oxyresveratrol and its various derivatives possess significant potential as therapeutic agents for a wide range of diseases and ailments. This promise needs to be effectively studied at the clinical level, so as to firmly establish the usefulness of these compounds in the treatment or prevention of diseases in humans. ACKNOWLEDGEMENTS This study was supported by the Fundamental Research Funds for the Central Universities (No. XDJK2013C053) and the Modern Agricultural Industry Technology System Special Funds (No. CARS-22). REFERENCES Aftab, N., K. Likhitwitayawuid and A. Vieira, 2010. Comparative antioxidant activities and synergism of resveratrol and oxyresveratrol. Nat. Prod. Res., 24: 1726-1733. Alonso, E., D.J. Ramon and M. Yus, 1997. Simple synthesis of 5-substituted resorcinols: A revisited Carmily of interesting bioactive molecules. J. Org. Chem., 62: 117-121 Andrabi, S.A., M.G. Spina, P. Lorenz, L. Ebmeyer, G. Wolf and T.F. Hom, 2004. Oxyresveratrol (trans-2, 3, 4, 5-tetrahydroxystilbene) is neuroprotective and inhibits the apoptotic cell death in transient cerebral ischemia. Brain Res., 1017: 98-107. Ayinampudi, S.R., Y.II. Wang, B. Avula, T.J. Smillie and I.A. Khan, 2011 Quantitative analysis ¢»[ oxyresveratrol in different plant parts of Morus species and related genera by HPTLC and HPLC. J. Planar Chromatography-Modem TLC. 24: 125-129. Ban, J. Y., S.Y. Jeon, K. Bac, K.S. Song and Y.H. Scong. 2006a. Catechin and epicatechin from Smilacis chinae rhizome protect cultured rat cortical neurons against amyloid protein (25-35)-induced neurotoxicity through inhibition of cytosolic calcium elevation. Life Sci., 79: 2251-2259. Ban, J. Y., S.Y. Jeon T.T.H. Nguyen, K. Bae, K.S. Seonga and Y.H. Song, 2006b. Neuroprotective effect of oxyresveratrol from Smilacis chinac rhizome on amyloid SS protein (25-35)-Induced neurotoxicity in cultured rat cortical neurons. Biol. Pharm. Bull., 29: 2419-2424. 50

Int. J. Pharmacol., 10 (1): 44-54, 2014 Ban, J.Y, SO. Cho, S.Y. Jeon, K. Bae, K.S. Song and Y.II. Seong, 2007. 3,1-Dihydroxybenzoic acid from Smilacis chinae rhizome protects amyloid protein (25-35)-induced neurotoxicity in cultured ral cortical neurons. Neurosci. Lett., 420: 184-188. Basset, C., A.M.S. Rodrigues, V. Eparvier, M.R.R. Silva and N.P. Lopes et al., 2012. Secondary metabolites from Spirotropis longifolia (DC) Baill and their antifungal activity against human pathogenic fungi. Phytochemistry, 74: 166-172. Breuer, C., G. Wolf, S.A. Andrabi, P. Lorenz and T.F. Hom, 2006. Blood-brain barrier permeability to the neuroprotectant oxyresveratrol. Neurosci. Lett., 393: 113-118. Chao, J., M.S. Yu, Y.S. Ho, M. Wang and R.C.C. Chang, 2008. Dietary oxyresveratrol prevents parkinsonian mimetic 6-hydroxydopamine neurotoxicity. Free Radical Biol. Med., 45: 1019-1026. Charoenlarp, P., P. Radomyos and T. Harinasuta, 1981. Treatment of laeniasis with Pung-Hand: A crude extract of Artocarpus lakoocha wood. Southeast Asian J. Trop. Med. Public Health, 12: 568-570. Chatsumpun, M., T. Chuanasa, B. Sritularak and K. Likhitwitayawuid, 2011. Oxyresveratrol protects against DNA damage induced by photosensitized riboflavin. Nat. Prod. Commun, 6: 41-44. Choi, S.Y., S. Kim, J.S. Hwang, B.G. Lee, H. Kim and S. Y. Kim, 2004. Benzylamide derivative compound B-induced allenuales The ultraviolet. hyperpigmentation in the brownish guinea pig skin. Biochem. Pharmacol., 67: 707-715. Choi, S.Y., L.S. Hwang, S. Kim and S.Y. Kim, 2006. Synthesis, discovery and mechanism of 2. 6-dimethoxy-N-(4-methoxyphenyl) benzamide as potent depigmenting agent in the skin. Biochem. Biophys. Res. Commun., 3-19: 39-19. Chuanasa, T., J. Phromjai, V. Lipipun, K. Likhitwitayawuid and M. Suzuki et al., 2008. Anti-herpes simplex virus (IISV-1) activity of oxyresveratrol derived from Thai medicinal plant: Mechanism of action and therapeutic efficacy on culaneous HSV-1 infection in mice. Antiviral Res., 80: 62-70. Chun Y.J., S. Kim, D. Kim, S.K. Lee and F.P. Guengerich 2001. A new selective and potent inhibitor of human cytochrome P450 1B1 and its application to antimutagenesis. Cancer Res., 61: 8164-8170. Chun, Y.J., Y.K. Oh, B.J. Kim, D. Kim, S.S. Kim, ILK. Choi and M. Y. Kim, 2009. Potent inhibition of human cytochrome P450 1B1 by tetramethoxystilbene. Toxicol. Lett., 189: 84-89. Chung, K.O., B.Y. Kim, M.H. Lee, Y.R. Kim, H. Y. Chung, J.H. Park and JO. Moon 2003. In-vitro and in-vivo Anti-inflammatory effect of oxyresveratrol from Morus alba .. J. Pharm. Phamacol., 55: 1695-1700. Deng, H., X. He, Y. Xu and X. Hu, 2012. Oxyresveratrol from mulberry as a dihydrate. Acta Cryst., 68: 01318-01319. Djapic, N., Z. Djarmatim, S. Filip and R.M. Jankov, 2003. A stilbene from the heartwood of Maclura pomifera. J. Serbian Chem. Soc., 68: 235-237. Fang, S.C., C.L. IIsu and G.C. Yen, 2008. Anti-inflammatory effects of phenolic compounds isolated from the fruits of Artocarpus heterophyllus. J. Agric. Food Chem., 56: 4463-4468. Ferlinahayali, Y.M. Syah, L.D. Juliawaly, S.A. Achmad and E.II. Ilakim et al., 2008. Phenolic constituents from the wood of Morus australis with cytotoxic activity. Z Naturforsch C, 63: 35-39. Fu, D.X., L. Chen, A.J. Ilou, Q. Yao and W. Y. Zhang, 2005. Chemical constients of Morus nigra. Chinese Trad. Herbal Drugs, 36: 1296-1299. Galindo, I., B. Hernaez, J. Berna. J. Fenoll, J.L. Cenis. J.M. Escribank and C. Alonso, 2011. Comparative inhibitory activity of the stilbenes resveratrol and oxyresveratrol on African swine fever virus replication. Antiviral Res., 91: 57-63. Gomez-Cordoves, C., B. Bartolome, W. Vieira and V.M. Virador, 2001. Effects of wine phenolics ankl sorghum tannins on tyrosinase activity and growth of melanoma cells. J. Agric. Food Chem., 49: 1620-1624. Guengerich, F.P., Y.J. Chun, D. Kim, E.M.J. Gillam and T. Shimada, 2003. Cytochrome P450 1B1: A target for inhibition in anticarcinogenesis strategies. Mutation Res./Fundam. Mol. Mechanisms Mutagenesis, 523: 173-182. Hakim, E.H., U.Z. Ulinnuha, Y.M. Syah and prenylated EL Ghisalberti, 2002. Antoindonesianins N and 0, new stilbene and prenylated arylbenzofuran derivatives from Artocarpus gomezianus. Fitoterapia, 73: 597-603. Ilan, X.L., Z.J. Fang and J.II. Chen, 2007. Stilbene compounds inhibit proliferation of tumor cells and induce apoptosis of Bel-7402 cells. Chin. J. Biochem. Mol. Biol., 23: 963-970. Hom, T.F.W., S.A. Andrabi, P. Lorenz and G. Wolf, 2003. Reduced infarct sizes in a rat stroke model: Effects on nitric oxide and intracellular calcium. Soc. Neurosci., 776: 11-11 Ilu, C.Q, Z.D. Chen, R.F. Yao and C. Xu, 1996. Inhibition of protein kinade C by stilbene derivatives from Morus alba L. Nal. Prod. Res. Dev.. 8: 13-16. 51

Int. J. Pharmacol., 10 (1): 44-54, 2014 Huang, H.L., D.A. Guo and P. Li, 2008a. Determination of stilbenodids in Smilax china I.. by HPLC. Chinese J. New Drugs, 17: 2122-2124. Huang, H., J. Zhang, G. Chen, Z. Lu and X. Wang et al.. 2008b. High performance liquid chromatographic method for the determination and pharmacokinetic studies of oxyresveratrol and resveratrol in rat plasma after oral administration of Smilax china extract. Biomed. Chromatogr., 22: 421-427. Huang, H.L., G.T. Chen, Z.Q. Lu JQ. Zhang and D.A. Guo, 2009a. Distdbution study of two constituents in rat after oral administration of Smilax china extract. China J. Chinese Materia Med., 34: 2512-2515. Huang, H..., J.Q. Zhang, G.T. Chena, Z.Q. Lu, N. Sha and D.A. Gou 2009b. Simultaneous determination of Oxyresveratrol and resveratrol in rat bile and urine by HPLC after oral administration of smilax China extract. Nat. Prod. Commun., 1: 825-830. Iluang, II., G. Chen, Z. Lu, J. Zhang and D.A. Guo, 2010. Identification of seven metabolites of oxyresveratrol in rat urine and bile using liquid chromatography/landem mass spectrometry. Biomed. Chromatogr., 24: 426-432. Jagtap, L.B. and V.A. Bapat 2010. Artocarpus: A review of its traditional uses, phytochemistry and pharmacology. J. Ethnopharmacol., 129: 142-166. Jeon, S.Y., S.II. Kwon, Y.II. Seong, K. Bae and J.M. Hur et al., 2007. B-secretase (BACE1)-inhibiting stilbenoids from Smilax Rhizoma. Phytomedicine. 14: 403-408. Kim, Y.M., J. Yun, CK. Lee, H. Lee, K.R. Min and Y. Kim, 2002. Oxyresveratrol and hydroxystilbene compounds inhibitory effect on tyrosinase and mechanism of action. J. Biol. Chem., 277: 16340-16344. Kim, J.K., M. Kim, S.G. Cho, M.K. Kim, S.W. Kim and Y.H. Lin, 2010. Biotransformation of mulbertoside A from Morus alba results in enhancement of tyrosinase inhibition. J. Ind. Microbiol. Biotechnol., 37: 631-637. Kim, J.K., K.T. Park, II.S. Lee, M. Kim and Y.II. Lim, 2012. Evaluation of the inhibition of mushroom tyrosinase and cellular tyrosinase activities of oxyresveratrol: Comparison with mulberroside A. J. Enzyme Inhibition Med. Chem., 27: 195-503. Lee, K.T., K.S. Lee, J.H. Jeong, B.K. Jo, M.Y. Heo and II.P. Kim, 2003. Inhibitory effects of Ramulus mori melanogenesis. J. Cosmetic Sci.. extracts on 54: 133-142. Li, H., W.K. WIL, Z. Zheng, C.T. Che and Z..J. Li et al., 2010. 3,3,4,5,5' Pentahydroxy-trans-stilbene, a resveratrol derivative, induces apoptosis in colorectal carcinoma cells via oxidative stress. Eur. J. Pharmacol., 637: 55-61. Liang, C., J.H. Lim, S.H. Kim and D.S. Kim, 2012. Dioscin: A synergistic tyrosinase inhibitor from the roots of Smilax china. Food Chem., 134: 1146-1148. Likhitwilayawuid K., B. Stitularak, K. Benchanak, V. Lipipun, J. Mathew and R.F. Schinazi, 2005. Phenolics with antiviral activity from Millettia erythrocalyx and Artocarpus lakoocha. Nat. Prod. Res., 19: 177-182. Likhitwilayawuil K., S. Chaiwiriya, B. Stitularak and V. Lipipun, 2006. Antiherpetic flavones from the heartwood of Artocarpus gomezianus. Chem. Biodiversity, 3: 1138-1143. Likhitwitayawuid, K., A. Sornsute, B. Sritularak and P. Ploypradith, 2006b. Chemical transformations of oxyresveratrol (trans-2,4,3,5-tetrahydroxystilbene) into a potent tyrosinase inhibitor and a strong cyloloxic agent. Bioorganic Med. Chem. Lell, 16: 5650-5653. Lipipun, V., P. Sasivimolphan, Y. Yoshida, T. Daikoku and B. Sritularak et al., 2011. Topical Cream-based oxyresveratrol in the treatment of cutaneous HSV-1 infection in mice. Antiviral Res., 91: 154-160. Liu, B. and J.S. Hong, 2003. Role of microglia in inflammation-mediated neurodegenerative diseases: Mechanisms and strategies for therapeutic intervention. J. Pharmacol. Exp. Ther., 301: 1-7. Liu, J.C., 2013. Study on stability of the stilbene compounds from mulberry. Southwestern University, China Lorenz, P., S. Roychowdhury, M. Engelmarmi, G. Wolf and T.F. Hom, 2003. Oxyresveratrol and resveratrol are potent antioxidants and free radical scavengers: Effect on nitrosative and oxidative stress derived from microglial cells. Nitric Oxide, 9: 61-76. Lu, Y., M.Q. Zhou, K.S. Weng and G.X. Liu, 2001. Inhibition of lyrosinase Helivily by three While-making ingredients. Flavour Fragrance Cosmetics, 68: 15-17. Lu, Y.II. and II.J. Wang, 2010. Studies on usages of oxyresveratrol. State Intellectual Property Office of Peoples Republic of China, 200910200593.5. Luo, J., P.W. Sun, S. Liu and X.Z. Li, 2012. Separation of phenols from Ramulus mori. by High-speed coumiler-current chromatography. Nal Prod. Res. Dev., 21: 186-189. Maneechai, S., K. Likhitwitayawuid. B. Sritularak C. Palanuvej, N. Ruangrungsi and P. Sirisa-Ard, 2009. Quantitative analysis of oxyresveratrol content in Artocarpus lakoocha and Puag-Haad. Med. Principles Practice, 18: 223-227. Maneechai, S., W. De-Ekmamkul, K. Umehara, H. Noguchi and K. Likhitwitayawuid, 2012. Flavonoid and stilbenoid production in callus cultures of Artocarpus lakoocha. Phytochemistry, 81: 42-49. 52

Int. J. Pharmacol., 10 (1): 44-54, 2014 Mazimba, O., R.R.T. Majinda and D. Motlhanka, 2011. Antioxidant and antibacterial constituents from Morus nigra. Afr. J. Pharm. Pharmacol., 5: 751-754. Mei, M., JQ Ruan, W.J. Wu, R.N. Zhou a J.P. Lei et al., 2012. In vitro pharmacokinetic characterization of mulberroside a, the main polyhydroxylated stilbene mulberry (Morus alba L.) and is bacterial metabolite oxyresveratrol in traditional oral use. J. Agric. Food Chem., 60: 2299-2308. in Mongolsuk, S., A. Robertson and R. Towers, 1957. 2:43:5-Tetrahydroxystilbene from Artocarpus lakoocha. J. Chem. Soc., 1957; 2230-2233. Mouihate, A., T.I. IIorn and Q.J. Pittman, 2006. Oxyresveratrol dampens neuroimmune responses In vivo: A selective effect. on TNF-a. Am. J. Physiol. Regulatory Integrative Compar. Physiol., 291: R1 215-R1221. Nasapon, P., P. Ampai, S. Maitree and P. Leelapornpisid. 2010. Anliglycation and antioxidant activities of oxyresveratrol extracted from the heartwood of Artocarpus lakoocha Roxb. Maejo Int. J. Sci. Technol., 1: 154-161. Nimmanpisut S., P. Chudapongse and K. Ratanabanangkoon, 1976. Effects of 2,4,3, 5-tetrahydroxystilbene on oxidative phosphorylation by rat liver mitochondria. Biochem. Pharmacol., 25: 1245-1248. Nishizuka, Y., 1984. The role of protein kinase C in cell surface signal transduction and tumour promotion. Nature, 308: 693-698. Park, K.T., J.K. Kim, D. Hwang, Y. You and Y.H. Lim, 2011. Inhibitory effect of mulberroside A and its derivatives on melanogenesis induced by ultraviolet Birradiation. Food Chem. Toxicol., 19: 3038-3015. Powell, R.G., R. Bajaj and J.L. McLaughlin, 1987. Bioactive stilbenes of Scirpus maritimus. 1. Nat. Prod.. 50: 293-296. Qiao, X., T. Zhao, M. Wang, C. Lei and A. Hou, 2011. Flavonoids from Artocarpus hypargyreus. China J. Chinese Maleria Med., 36: 2975-2979. Qiu, F., K. Komatsu, K. Kawasaki, K. Saito, X. Yao and Y. Kano, 1996a. A novel stilbene glucoside, oxyresveratrol 3-0-beta-glucopyranoside, from the root bark of Morus alba. Planta Medica, 62: 559-561. Qiu, F., K. Komatsu, K. Saito, K. Kawasaki, X. S. Yao and Y. Kano, 1996b. Pharmacological properties of traditional medicines. 22. Pharmacokinetic study of mulberroside A and its metabolites in rat. Biol. Pharm. Bull, 19: 1463-1467. Rodriguez-Bonilla, P., J.M. Lopez-Nicolas and F. Garcia-Carmona, 2010. Use of reversed phase high pressure liquid chromatography for the physicochemical and thermodynamic characterization of oxyresveratrol/beta-cyclodextrin complexes. J. Chromatography B, 878: 1569-1575. Ruan, JL., J. Zou and Y.L. Cai, 2005. A study of the Anti-inflammatory components of Smilax china. IIerald Med., 24: 670-672. Sasivimolphan, P., V. Lipipun, K. Likhitwitayawuid, M. Takemoto, P. Pramyothin M. Hallori arkl K. Shiraki, 2009. Inhibitory activity of oxyresveratrol on Wild-type and Drug-resistant Varicella-zoster virus replication in vitro. Antiviral Res., 84: 95-97. Sasivimolphan, P., V. Lipipun, G. Ritthidej, K. Chitphet and Y. Yoshida et al., 2012. Microemulsion-based oxyresveratrol for topical treatment of Herpes Simplex Virus (HSV) infection: Physicochemical properties and efficacy in cutaneous HSV-1 infection in mice. AAPS Pharm. Sci. Tech., 13: 1266-1275. Schonfeld, P., N. Kruska and G. Reiser, 2009. Antioxidative activity of the olive oil constituent. Hydroxy-1-aryl-isochromans in cells and Cell-free systems. Biochimica Biophys. Acta-General Subjects, 1790: 1698-1704. Schultz, T.P., W.B. Harms, T.H. Fisher, K.D. McMurtrey, J. Minn and D.D. Nicholas, 1995. Durability of angiosperm heartwood: The importance of extractives. Holzforschung-Int. J. Biol. Chem. Phys. Technol. Wood, 49: 29-34. Shao, B., H.Z. Guo, Y.J. Cui, A.H. Liu and H.L.. Yu et al.. 2007. Simultaneous determination of six major stilbenes and flavonoids in Smilax china by high performance liquid chromatography. J. Pharm. Biomed. Anal., 44: 737-742. Shi, YW, C.P. Wang, X. Wang, Y.L. Zhang and L. Liu et al., 2012. Uricosuric and nephroprotective properties of Ramulus Mori ethanol extract in hyperuricemic mice. J. Ethnopharmacol., 143: 896-904. Shin, N.H., S.Y. Ryu, E.J. Choi, S.H. Kang, L.M. Chang K.R. Min and Y. Kim, 1998a. Oxyresveratrol as the potent inhibitor on dopa oxidase activity of mushroom tyrosinase. Biochem. Biophys. Res. Commun., 243: 801-803. on Shin, N.H., S.Y. Ryu, H. Lee, K.R. Min and Y. Kim, 1998b. Inhibitory effects of hydroxystilbenes cyclooxygenase from sheep seminal vesicles. Planta Medica, 61: 283-281. Song, S., II. Lee, Y. Jin, Y.M. IIa, S. Bae, II. Y. Chung and II. Suh, 2007. Syntheses of hydroxy substituted 2-phenyl-naphthalenes as inhibitors of tyrosinase. Bioorganic Med. Chem. Lett., 17: 461-464. 53

Int. J. Pharmacol., 10 (1): 44-54, 2014 Song, Y.M., Y.M. Ha, J.A. Kim, K.W. Chung and Y. Uchara et al., 2012. Synthesis of novel azo-resveratrol. azo-oxyresveratrol and their derivatives as potent tyrosinase inhibitors. Bioorg. Med. Chem. Lell, 22: 7451-7455. Sun, H.Y, C.F. Xiao and W. Wei, 2010. Synthesis of Oxyresveratrol. Chinese J. Organic Chem.. 30: 1574-1579. Syah, Y.M., S.A. Achmad, E.L. Ghisalberti, E.H. Hakim L. Makmur and N.H. Soekamto, 2004. Astilbene dimer andalasin B, from the root trunk of Morus macroura. J. Chem. Res., 2001: 339-310. Tengamnuay, P., K Pengrungruangwong and K. Likhitwitayawuid, 2003. A potent tyrosinase inhibitor from Artocarpus lakoocha heartwood extract. Proceedings of the IFSCC Conference, September 22-24, 2003, Seoul, Korea, pp: 201-212. Tengammuay, P., K. Pengrungruangwong, 1. Pheansri and K. Likhitwitayawuid, 2006. Artocarpus lakoocha heartwood extract as a novel cosmetic ingredient: Evaluation of the in vitro Anti-tyrosinase and in vivo skin whitening activities. Int. J. Cosmetic Sci.. 28: 269-276. Ti, H.H., P. Wu and L.D. Lin, 2011. Stilbenes and flavonoids from Artocarpus nitidus subsp linganensis. Fitoterapia, 82: 662-665. Tong, Z.Y., XP. Yan, S.X. Li, J. Zhou, G.X. Cai. QY. Zheng and D. Huang, 2011. Isolation and identification of oxyresveratrol in Mulberry branch. Sci. Sericult, 37: 0918-0951. Tsuruga, T., Y.T. Chun, Y. Ebizuka and U. Sankawa, 1991. Biologically active constituents of Melaleuca leucadendron Inhibitors of induced histamine release from rat mast cells. Chem. Pharm. Bull., 39: 3276-3278. Wang, Y.C., C. Wu, L. Chen, Y. Zheng, L. Xu and X.Z. Iluang, 2011. Antioxidant activities of resveratrol, oxyresveratrol, csveratrol, mulberroside a from cortex mori. Food Sci., 32: 135-138. Weber, J.T., M. Lamont, L. Chibrikova, D. Fekkes and A.S. Vlug, 2012. Potential neuroprotective effects of oxyresveratrol AgHirus. Traumatic injury. Eur. J. Pharmacol., 680 55-62. Wu, L.S., XI. Wang, H. Wang, H.W. Yang, A.Q. Jia, 2010. Cytotoxic polyphenols against breast tumor cell in Smilax china L. J. Ethnopharmacol., 130: 460-464. Wu, C., 2012. Study on the extraction and purification processes of mulberroside a from Mulberry branch bark and its activities. Southwestern University. China. Xiong, Y., D.A. Guo and H.L. Huang, 2008. Chemical constituents from Lubers of Smilux china L. Modem Chinese Med., 10: 20-22. Xu, L., C. Wu, J.C. Liu, M.D. Yu and Q. Y. Xia, 2009. Studies on oxyresveratrol extraction methods. State Intellectual Property Office of Peoples Republics of China, 200910101202,X. Xu, L., J. Liu, C. Liu, C. Wu, C.H. Wang and X.Z. Huang, 2013. Response surface optimization of ultrasonic-assisted oxyresveratrol extraction from the bark of cultured black mulberry (Morus nigra L.). Separat. Sci. Technol., 18: 2779-2785. Zhang, J.T., W. Dai and R.G. Harvey, 1998. Synthesis of higher oxidized metabolites of dibenz[a,/anthracene implicated in the mechanism of carcinogenesis. Org. Chem., 63: 8125-8132. Zhang, Z., J. Jin and L. Shi, 2008. Protective function of cis-mulberroside A and oxyresveratrol from Ramulus mori against Ethanol-induced hepatic damage. Environ. Toxicol. Pharmacol., 26: 325-330. Zhang, Z. J. Jin and L. Shi, 2009. Antioxidant properties of ethanolic extract from Ramulus mori (Sangzhi). Food Sci. Technol. Int., 15: 435-444. Zhang, Z. and L. Shi, 2012. Delection of antioxidant active compounds in mori ramulus by HPLC-MS-DPPH]. China J. Chin. Mater. Med., 37: 800-802. Zhao, W.J., Y.T. Guo Y. Tezuka and T. Kikuchi, 1998. Chemical research on the stilbenes from Veratrum nigrum L. var. ussuriense Nakai. Chinese J. Med. Chem., 8: 35-37. Zhao, Z.X, J. Jin, W. Fang and J.L. Ruan, 2008. Antioxidant activity of polyphenolic constituents from Smilax china. IIerald Med., 27: 765-767. Zheng, Z.P., Q. Zhu, C.L. Fan, H. Y. Tan and M. Wang. 2011. Phenolic tyrosinase inhibitors from the stems of Cudrania cochinchinensis. Food Function. 2: 259-264. Zheng, Z.P., H.Y. Tan and M.F. Wang, 2012. Tyrosinase inhibition constituents from the roots of Morus australis. Fitoterapia, 83: 1008-1013. 54

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