The compound of 3β-hydroxy-sitosterol (1) and 2-metylester-1-H-pyrrole-4-carboxilyc acid were isolated from ethyl acetate extract of snake fruit (Salacca edulis Reinw) cv. Bongkok, (2). Inhibition of xanthine oxidase by the two compounds were evaluated against enzyme of xanthine oxidase. Compound 1 could be regarded as inactive, while compound 2 was found to be active with IC50 value of 48.86 μg mL-1.
How to cite this article:
Leni Herliani Afrianti Priyatno, Elin Yulinah Sukandar, Slamet Ibrahim and I. Ketut Adnyana, 2007. Xanthine Oxidase Inhibitor Activity of Terpenoid and Pyrrole Compounds Isolated from Snake Fruit (Salacca edulis Reinw.) cv. Bongkok. Journal of Applied Sciences, 7: 3127-3130.
The Salacca edulis Reinw. is known in Java, Sumatra and other island as snake fruit. There are some cv. of Salacca edulis Reinw such as Manonjaya, Bongkok, Banjarnegara, Condet, Pondoh, Bali, Enrekang and Sidempuan (Yustina and Farry, 1993). Snake fruit of Pondoh contains sucrose, glucose, fructose and volatile compounds as methyl esters of butanoic acids, 2-methylbutanoic acid, hexanoic acid, pentanoic acid and carboxylic acids (Supriyadi et al., 2002). Snake fruit (Salacca edulis Reinw) cv. Bongkok from Conggeang a sub district of Sumedang West Java. The fruit has more sour, bitter, an astringent taste and is not sweet than other snake fruit. According to survey in Conggeang, a price of snake fruit (Salacca edulis Reinw.) cv. Bongkok is very low, around five hundred rupiahs per kilogram. The production of snake fruit (Salacca edulis Reinw.) cv. Bongkok in Sumedang in 1992 until 1995 had decreased around 24% (Anonymous, 1993). The composition of the species is very attracted to study, its compound has not been known up to now.
The snake fruit has antioxidant activity (46.7±4.7 μmol TE g1) in rats fed cholesterol (Leontowicz, 2006). The potential beneficial role of antioxidants in preventing increase uric acid serum levels (Nieto et al., 2000). High uric acid level in blood known as gout can enhance cardiovascular disorder. Allopurinol is used commercially as anti gout with mechanism of action of xanthine oxidase inhibitors. Allopurinol is indicated when uricosuric drugs fail to reduce serum urate lower than 7.0 mg dL1. Xanthine oxidase catalyzes the oxidation of hypoxanthine and xanthine to uric acid. Xanthine oxidase is a complex metalloflavoprotein (Gerhard and Wolfgang, 1996).
MATERIALS AND METHODS
General experimental procedures: UV spectra were measured with a cvian conc. 100 instrument. IR spectra were determined with a Perkin Elmer FTIR Spectrum One spectrometer using KBr pellets. 1H and 13C NMR spectra were recorded with a JEOL AS400 operating at 400 (1H) and 100 (13C) MHZ using residual and deuterated solvent peaks as reference standards. Vacuum Liquid (VLC) and column chromatography were carried out using Merck silica gel 60 GF254 and silica gel G60 200-400 mesh. For TLC analysis, pre coated silica gel plates (Merck Kiesel-gel 60 GF254,0.25 mm) were used.
Plant material: The snake fruit (Salacca edulis Reinw.) cv. Bongkok was collected from Conggeang a sub district of Sumedang West Java, Indonesia and identified by Herbarium Bandungense, Institute Teknologi Bandung, Indonesia.
Extraction and isolation: The dried powdered snake fruit (Salacca edulis Reinw.) cv. Bongkok (3.15 kg) was macerated in ethyl acetate. The ethyl acetate extract (100 g) was fractionated into n-hexane/ethyl acetate soluble (24.67 g) and insoluble (75.33 g) fractions. A portion (20 g) of n-hexane/ethyl acetate soluble fraction was fractionated by VLC containing silica gel and n-hexane/ethyl acetate with composition of 10: 0 until 0:10 as an eluent solvent into eight major fractions A-H. Fraction B (2.41 g) was purified either by flash chromatography with internal diameter of column of 30 mm containing silica gel G60 200-400 mesh and n-heksan-kloroform (4:6) as a mobile phase to give compounds 1 (115 mg). The fraction F (3.90 g) was purified either by flash chromatography with internal diameter of column 30 mm (silica gel G60 200-400 mesh and n-hexane-chloroform-methanol (2.5: 6:1.5) as eluent to give compounds 2 (141.9 g).
Inhibition of xanthine oxidase in vitro: The inhibition of xanthine oxidase enzyme according to the method describe by Gerhard and Wolfgang (1996) and Kong et al. (2000). Xanthine was purchased from Sigma (USA), xanthine oxidase of bovine milk origin, was purchased from Sigma (USA). All other chemicals and reagents used were analytical grade and were purchased from SINDO Laboratory. The test compound is incubated with 0.1 units of xanthine oxidase, 40 μL EDTA and 1750 μL phosphate buffer solution (pH 7.8). Control solutions without test compound are incubated under identical conditions. Following addition 100 μL of xanthenes, the final volume is 2 mL, the change in absorbance is determined at 293 nm. The percent inhibition of xanthine oxidase is determined relative to control solution. The compound of extract dissolved initially in dimethyl sulfoxide (DMSO), were incorporated in the enzyme assay to assess their inhibitory activity at different concentration, in comparison with Allopurinol was used as the standard inhibitors (Elion et al., 1966). IC50 values of test compounds are calculated.
RESULTS AND DISCUSSION
For the first time 3β-hydroxy-sitosterol (1) and 2-metylester-1-H-pyrrole-4-carboxilyc acid (2) were detected in snake fruit (Salacca edulis Reinw.) cv. Bongkok. The structures of two compounds were elucidated and can be in Fig. 1.
Compound 1 was isolated from ethyl acetate extract of snake fruit (Salacca edulis Reinw.) cv Bongkok. The ethyl acetate was fractionated by VLC into eight major fraction namely fraction A to H fractionated and repeated purification of the fraction using flash chromatographic technique yielded compound 1 and 2. Compound 1 was a white crystal. The IR spectra indicated that compound 1 had high absorption from hydroxyl O-H (vmax 3435 cm1), alcohol secondary C-O (vmax 1063 cm1), Aliphatic of CH2 and CH3 (vmax 2934 dan 2865 cm1) and streching of aliphatic of CH2 and CH3 (vmax 1465 dan 1381 cm1), aromatic (vmax 1642 cm1). The 13C NMR spectra (Table 1), exhibited 28 signal of 29 carbons that distribution of 27 carbons of sp3 (δC 12.2-80.0 ppm) and two carbon atoms of sp3 (δC 121.9-140.9 ppm).
|Fig. 1:||Compounds 1 and 2|
The base of analysis of DEPT 135 that carbons signals of sp3 were six carbon atoms of methyl, 12 carbon atoms of methilen, seven carbon atoms of methine and one carbon atom quartener. Whereas the carbon signal of sp2 appears one carbon of ethilen and one carbon quartener. The 13C NMR spectra indicated that the compound 1 was triterpene of steroid groups. The 1H NMR spectra (Table 2), exhibited two singlet signal of methyl at δH 0,67 ppm (3H-18), 1,00 ppm (3H-19) and four doublet signal at δH 0.92 ppm (3H-21), 0.80 ppm (3H-26), 0.82 ppm (3H-27), 0.83 ppm (3H-29), one proton signal of vinylic at δH 5.35 ppm (1H, dd, J = 4.90; 3.05 Hz, H-6) and one proton signal of oxygenation at δH 3.52 ppm (1H, tt, J = 11.0; 4.25Hz, H-3). The 2D H-H COSY spectra, appears correlation ship between proton of H-3 (δH 3.52 ppm) with proton of H-2 and H-4, between proton of H-6 (δH 5.35 ppm) with H-7 and proton of H-8 (δH 1.49 ppm) with proton of H-7, H-9 and H-14. The 2D H-H COSY spectra indicated appears ring A and ring B of modified steroid groups. The 2D C-H HMBC spectra (Table 1) exhibited there was correlation of carbon at δC 140 ppm (C-5) with proton H-1, H-4 and H-19, also correlation between carbon at δC 36.3 (C-10) with proton H-9, H-6 and H-19, suggested that ring A and ring B of steroid group. The HMBC spectra showed the isoprene had been modified based on 2D C-H HMBC and H-H COSY spectrum, the carbon atom at δC 45.9 ppm (C-24) correlation with proton of H-28, whereas proton at δH 0.91 ppm (H-24) correlation with proton of H-28 of stigmastan group.
|Table 1:||1H,13C and 2D NMR data of compound 1|
|COSSY: Correlated Spectroscopy; HMBC: Hetero nuclear Multiple Bond Coherence|
|Table 2:||1H and 13C NMR data of compound 2|
|H: Proton; C: Carbon|
The correlation of HMBC spectra of compound 1 showed in Fig. 2. In the facts and comparison of study of 1H dan 13C NMR spectrum that the steroid compound of stigmastan group was β-sitosterol (Lendl et al., 2005; Castola et al., 2002), the compound 2 was derivate of triterpenoid penta siklik of stigmastan steroid. The name is 3β-hidroxy sitosterol.
The compound 2 was isolated as an amorphous orange solid. The UV spectrum of 1 exhibited absorptions at 217, 270, 314 nm, typical for a triazaridin chromophore and showed a bathochromic shifts on addition of NaOH.
|Fig. 2:||The correlation of HMBC spectra of compound 1|
The IR spectrum showed absorption from hydroxyl acid 3100-2500 cm1, N-H amina secondary (3260 and 3474 cm1), C-N (1283 cm1), C = C aliphatic (1659 and 1582 cm1), carbonyl acid and ester (1612 cm1) C-O-C ester un symmetry and symmetries (1228 and 1142 cm1). The 1H NMR and 1H-1H COSY spectra of 1 (Table 2) which showed three singlet proton signals consist one methoxy signal at δH 4.41 and two singlet proton signals of vinilic (δH 6.49 and δH 7.94).
|Table 3:||IC50 values of compounds 1-2 against inhibitor xhantine oxidase|
|IC50: Inhibition concentration at 50%|
The 13C NMR spectrum of 1 (Table 2), showed six signals of seven carbon consist one carbon atoms of C-sp3 and six carbon atoms of sp2. Seven carbon signals consist of one signal of methyl carbon (OCH3) at δC 61.12, two signals of methine carbon at δC 110.69 (C-3) and δC 140.90 (C-5), two signals of carbon quaternary at δC 110.69 (C-4) and δC 147.31 (C-2) and two signal of carbonyl carbon at δC 176,78 (C = O acid) and 170.34 (C = O ester). Support of structure 2 was obtained from the HMBC spectrum of 2 which showed, correlation between the carbon signal of C-2 with the proton signal of H-3 and H-5, while the carbon signal of C = O (acid) with the proton signal of H-3 and H-4. The carbon signal of C = O (ester) with the proton signal of H-3, H-5 and H-methyl.
The inhibition of xanthine oxidase of compound 1-2 (Table 3) were evaluated against enzyme of xanthine oxidase from Gerhard and Wolfgang (1996) and Kong et al. (2000). Compound 1 could be regarded as inactive, while compound 2 was found to be the most active with IC50 of 48.86 μg mL1.
The ethyl acetate extract was found to be active with IC50 value of 24.75 μg mL1. Whereas ethanol extract has IC50 value of 44.95 μg mL1.
The ethyl acetate extract of flesh of snake fruit (Salacca edulis Reinw.) cv. Bongkok contained 3β-hydroxy-sitosterol and 2-metylester-1-h-pyrrole-4-carboxilyc acid (2). The 3β-hydroxy-sitosterol is inactive to inhibit xanthin oxidase, while 2-metylester-1-H-pyrrole-4-carboxilyc acid is active with IC50 value of 48.86 μg mL1.
We would like to thank the Ministry of National Education of Republic of Indonesia (BPPs) and the Riset Unggulan Institut Teknologi Bandung for the financial support.
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