Suhair Hikmat1,
Tariq Al-qirim1 
,
Dania Alkabbani1,
Ghassan Shattat2,
Ghassan ABu Sheikha1,
Dima Sabbah1,
Reema Abu khalaf1,
Yusuf Al-hiari3
For correspondence:- Tariq Al-qirim Email: tariq.qirim@zuj.edu.jo Tel:+624291511
Received: 19 September 2016 Accepted: 15 December 2016 Published: 31 January 2017
Citation: Hikmat S, Al-qirim T, Alkabbani D, Shattat G, Sheikha GA, Sabbah D, et al. Synthesis and in vivo anti-hyperlipidemic activity of novel n-benzoylphenyl-2-furamide derivatives in Wistar rats. Trop J Pharm Res 2017; 16(1):193-201 doi: 10.4314/tjpr.v16i1.26
© 2017 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..
Purpose: To synthesize and evaluate the anti-hyperlipidemic activity of a novel series of N-(benzoylphenyl)-2-furamides (3a, 3b, 4a, 4b and 4c).
Methods: Compounds (3a, 3b, 4a, 4b and 4c) were successfully synthesized by reacting activated furan-2-carbonyl-chloride derivatives with aminobenzophenones at 60 °C for 36 h. Hyperlipidemia was induced in overnight fasted rats by intraperitoneal administration of Triton WR-1339 (300 mg/kg). to overnight fasted rats. The rats were divided into six groups: control, hyperlipidemic, hyperlipidemic plus compounds 3b, 4b, 4c, and hyperlipidemic plus bezafibrate-treated. Eighteen hours later, blood samples were collected and plasma lipid profile determined using enzymatic methods.
Results: At a dose of 15 mg/kg body weight, the elevated plasma triglyceride (TG) levels, total cholesterol (TC) and low density lipoprotein cholesterol (LDL-C) levels were significantly reduced by compounds 4b (p < 0.001) and 4c (p < 0.0001) 18 h later, compared to the hyperlipidemic group. Furthermore, compounds 4b and 4c significantly increased high density lipoprotein cholesterol (HDL-C) levels by 29 and 34 %, respectively.
Conclusion: The findings indicate the high potency of N-(benzolphenyl)-2-furamides (4b and 4c) as lipid-lowering agents. Thus, these compounds 4b and 4c may used as lead compounds for the development of new derivatives and agents for targeting dyslipidemia and cardiovascular diseases.
Introduction
Cardiovascular diseases have become a major health problem in developing countries. Hyperlipidemia is defined as high levels of lipids (fat, cholesterol and triglycerides) circulating in the bloodstream [1,2]. Epidemiological studies demonstrate that hyperlipidemia is the most prevalent indicator of susceptibility to atherosclerosis and heart diseases [3-5]. Thus, decreasing plasma lipid levels play a major role in the treatment and prevention of coronary heart diseases [6]. For this reason, many studies have been conducted to evaluate the potential lipid-lowering activity of synthetic and naturally compounds.
Triton WR-1339, a non-ionic detergent (oxyethylated tertiary octylphenol formaldehyde polymer) has been widely used in in vivo studies to produce acute hyperlipidemia in animal models in order to study the lipid-lowering effect of natural or chemical drugs [7]. Triton WR-1339 has been found to prevent the catabolism of triglycerol-rich lipoprotein by lipoprotein lipase [8,9].
There are many classes of lipid-lowering agents in existence. Fibrates and their derivatives including bezafibrate are class of drugs widely used to treat hypertriglyceridemia [10]. Bezafibrate significantly reduces serum triglyceride and free fatty acid levels [11]. The major mechanism of fibrates is by the induction of lipoprotein lipase and efficient reduction of apolipoprotein C-III-containing particles, which are markers for increased risk of atherosclerosis [12-14].
In the last decade, many studies have shown that furan derivatives have promising potentials as lipid-lowering agents [15-17]. Therefore, the present study focuses on the synthesis and pharmacological evaluation of a novel series of N-(benzoylphenyl)-2-furamides as models for their lipid-lowering activity ().
Methods
Materials and methods
All chemicals, reagents and solvents were of analytical grade and used directly without further purification. Chemicals and solvents were purchased from the corresponding companies (Sigma-Aldrich; St. Louis, MO, USA and Acros; Belgium).
Melting points (MP) were recorded using Gallenkamp melting point apparatus and were uncorrected. Infrared (IR) spectra were recorded using Shimadzu IR Affinity-1 spectrophotometer. All samples were prepared as potassium bromide (Acros, Belgium) discs. 1H and 13C NMR spectra were recorded using Bruker 300 MHz (Avance III, Switzerland Department of chemistry, the University of Jordan). Chemical Shifts are given in δ units using TMS as an internal reference. Chemical shifts are given in δ (ppm) using TMS as internal reference; deuterated solvents were used and stated with each compound. Thin Layer Chromatography (TLC) was performed on 20 x 20 cm aluminum plates pre-coated with fluorescent silica gel GF254 (Fluka, Germany) and visualized by UV light (at 254 and/or 360 nm).
Synthesis of the targeted compounds
5-(3-Hydroxyphenyl) furan-2-carboxylic acid (2): methyl-5-(3-hydroxyphenyl) furan-2-carboxylate (1) (1 g, 4.58 mmol) was treated with 10 mL of 10 % sodium hydroxide solution (6N) at 90 °C for 24 h. Then, the solution was neutralized with 10 % hydrochloric acid (2N), under ice conditions. The crude solid was filtered to afford methyl-5-(3-hydroxyphenyl) furan-2-carboxylic acid (2) as a white powder.
5-(3-Hydroxyphenyl) furan-2-carbonyl chloride (3): 5-(3-hydroxyphenyl) furan-2-carboxylic acid (2) (0.75 g, 3.675 mmol) was treated with oxalyl chloride (0.63 mL, 7.2 mmol). Thereafter, the solution was refluxed for 48 h and then evaporated under reduce pressure. The crude product was then co-evaporated twice with (10 mL) benzene to give 5-(3-hydroxyphenyl) furan-2-carbonyl chloride (3) as pale yellow solid.
N-(4-Benzoylphenyl)-5-(3-hydroxyphenyl)-2-furamide (3a): 5-(3-hydroxyphenyl) furan-2-carbonyl chloride (3) (0.5 g, 2.10 mmol) was dissolved in 10 mL dichloromethane (DCM). Then 100 mg of 4-(dimethylamino) pyridine (DMAP) was added. The mixture was stirred at room temperature for 15 min. Then 0.82 g, 4.20 mmol of 4-aminobenzophenon and 10 mL N, N dimethylformamide (DMF) were added to the reaction mixture.
The reaction mixture was heated at 60 °C for 36 h. Solvents were evaporated and the residue was purified by column chromatography using chloroform (100 %) as eluent to afford the targeted compound (3a) as a fine yellow solid.
N-(3-Benzoylphenyl)-5-(3-hydroxyphenyl)-2-furamide (3b): 5-(3-hydroxyphenyl) furan-2-carbonyl chloride (3) (0.5 g, 2.10 mmol) was dissolved in 10 mL of dichloromethane. Then, 100 mg of 4-(dimethylamino) pyridine was added. The mixture was stirred at room temperature for 15 min. Then (0.829 g, 4.206 mmol) of 3-aminobenzophenon and 10 mL of N, N dimethylformamide were added to the reaction mixture. The reaction mixture was heated at 60 °C for 36 h. Solvents were evaporated and the residue was purified by column chromatography using chloroform (100 %) as eluent to afford the targeted compound (3b) as a fine yellow solid.
N-(4-Benzoylphenyl)-5-methyl-2-furamide (4a): 5-methylfuran-2-carbonyl chloride (4) (0.5 g, 3.45 mmol) was dissolved in (10 ml) of dichloromethane. Then, 100 mg of 4-(dimethylamino) pyridine was added. The mixture was stirred at room temperature for 15 min. Then, (1.36 g, 6.91 mmol) of 4-aminobenzophenon was added to the reaction mixture. The reaction mixture was heated at 60 °C for 24 h. DCM was evaporated and the residue was purified by column chromatography using chloroform/methanol (80:20) as eluent to afford the targeted compound (4a) as a white powder.
N-(3-Benzoylphenyl)-5-methyl-2-furamide (4b): 5-methylfuran-2-carbonyl chloride (4) (1g, 6.91 mmol) was dissolved in (10 mL) of dichloromethane. Then, 100 mg of 4-(dimethylamino) pyridine was added. The mixture was stirred at room temperature for 15 min. Then (2.72 g, 13.83 mmol) of 3-aminobenzophenon was added to the reaction mixture. The reaction mixture was heated at 60 °C for 24 h. DCM was evaporated and the residue was purified by column chromatography using chloroform/methanol (80:20) as eluent to afford the targeted compound (4b) as a white powder.
N-(2-Benzoylphenyl)-5-methyl-2-furamide (4c): 5-methylfuran-2-carbonyl chloride (4) (0.8 g, 5.53 mmol) was dissolved in (10 mL) of dichloromethane. Then, 100 mg of 4-(dimethylamino) pyridine was added. The mixture was stirred at room temperature for 15 min. Then (2.18 g, 11.06 mmol) of 2-aminobenzophenon was added to the reaction mixture. The reaction mixture was heated at 60 °C for 24 h. DCM was evaporated and the residue was purified by column chromatography using chloroform/methanol (80:20) as eluent to afford the targeted compound (4c) as a white powder.
Animals and treatments
Male Wistar rats weighing 180 g were obtained from the animal house of the Faculty of Pharmacy, Al-Zaytoonah University of Jordan. The animals were provided ad libitum access only to tap water throughout the experimental duration and maintained in a 12 h light-dark cycle under standard laboratory conditions (22 ± 2 °C).
Principles of laboratory animal care as described in the European Community guidelines were followed [18]. All experiments were approved by the Animal Welfare Committee of the University (approval ref no. 6ZAWC/2016).
Triton model of hyperlipidemia
Acute hyperlipidemia was developed in animals by intraperitoneal administration of Triton WR-1339 (Tyloxapol, Sigma-Aldrich) to the rats at a dose of (300 mg/kg body weight) [19].
Determination of anti-hyperlipidemic activity
After injection of Triton, the overnight fasted rats were randomly divided into six groups of eight animals each. Normal control group (NCG) received an intraperitoneal administration of normal saline; hyperlipidemic control group (HCG) received an intraperitoneal injection of Triton WR-1339 dissolved in distilled water. In the third, fourth and fifth groups, hyperlipidemic rats were given intragastrically (15 mg/kg body weight) of compounds 3b, 4b and 4c respectively.
In the last group the hyperlipidemic rats were given intragastrically (100 mg/kg body weight) of bezafibrate (BF) [20,21]. At 18 h following triton administration animals were anaesthetized and blood samples were collected from the renal artery. The blood samples were immediately centrifuged (3000 rpm for 10 min) and the serum was used for lipid profile analysis by an enzymatic method with an automated analyzer (Model Erba XL-300, Mannheim, Germany).
Statistical analysis
All anti-hyperlipidemic activity data are presented as mean ± SEM (n = 8). The data were analyzed using Student’s t-test, and p < 0.05 was considered statistically significant (SPSS version 2015, IBM SPSS Statistics).
Results
Chemistry
According to the proposed aims, a series of N-(benzoylphenyl)-5-(3-hydroxyl phenyl)-2-furamide (3a and 3b) were synthesized starting from methyl-5-(3-hydroxyphenyl)furan-2-carboxylate (1) as shown in Scheme 1. Two different aminobenzophenone substitutions were used, 4-aminobenzophenone for compound N-(4-benzoylphenyl)-5-(3-hydroxyphenyl)-2-furamide (3a), and 3-aminobenzophenone for N-(3-benzoylphenyl)-5-(3-hydroxyphenyl)-2-furamide (3b).
At the same time, a series of N-(benzoylphenyl)-5-methyl-2-furamide (4a, 4b and 4c) were synthesized starting from 5-methylfuran-2-carbonylchloride (4) as shown in (Scheme 2). Three different aminobenzophenone substitutions were used, 4-aminobenzophenone for compound N-(4-benzoylphenyl)-5-methyl-2-furamide (4a), 3-aminobenzophenone for N-(3-benzoylphenyl)-5-methyl-2-furamide (4b), and 2-aminobenzophenone for N-(2-benzoylphenyl)-5-methyl-2-furamide (4c).
N-(4-Benzoylphenyl)-5-(3-hydroxyphenyl)-2-furamide (3a)
Yield 34 %; m.p.: 198-200 °C; Rf: 0.33 (CHCl3)/MeOH, 98:2); IR (KBr) cm-1: 3263 (N-H), 3055 (O-H), 1689 (CO, ketone), 1651 (CO, amide), 1597, 1527, 1411, 1311, 1280, 1180, 925, 848, 786, 702, 594, 509, 424, 385 cm-1. 1H-NMR (500 Hz, d6-DMSO) δ (ppm): 10.52 (br, s, 1H, CONH), 8.38 (s, 1H, OH), 7.96 (s, 1H, Ar-H), 7.71 (d, J = 1.35 Hz, 1H, furan-H), 7.66 (m, 6H, Ar-H), 7.55 (m,3H, Ar-H), 7.38 (d, J = 8.45 Hz, 1H, furan-H), 7.25 (m, 1H, Ar-H), 6.6 (m, 2H, Ar-H); 13C-NMR (d6-DMSO): δ = 195.3 (1C), 160.7 (1C), 142.7 (1C), 137.9 (2C), 132.8 (2C), 132.3 (1C), 132.2 (1C), 132.7 (2C), 129.8 (2C), 128.9 (4C), 128.4 (1C), 127.6(1C), 127.0 (1C), 119.0 (2C), 116.8 (1C), 116.6 (1C) ppm.
N-(3-Benzoylphenyl)-5-(3-hydroxyphenyl)-2-furamide (3b)
Yield: 32 %; m.p.: 200-202 °C; Rf: 0.30 (CHCl3/MeOH, 98:2); IR (KBr) cm-1: 3549 (N-H), 3278 (O-H), 1680 (CO, ketone), 1658 (CO, amide), 1589, 1543, 1481, 1435, 1404, 1311, 1280, 1165, 1126, 979, 902, 864, 786, 717, 648, 594. 1H-NMR (300 Hz, CDCl3) δ(ppm): 8.85 (br, s , 1H, CONH), 8.74 (s, 1H, OH), 8,48 (s, 1H, Ar-H), 8.34 (d, J = 3.0 Hz, 1H, furan-H), 7.96 (d, J = 9.0 Hz, 1H, furan-H), 7.87 (s,1H, Ar-H), 7.76 (m, 3H, Ar-H), 7.67 (m, 2H, Ar-H), 7.51 (m, 6H, Ar-H); 13C-NMR (CDCl3) δ (ppm): 196.6 (1C), 162.6 (1C), 159.7 (1C), 139.1 (1C), 138.3 (1C), 137.5 (1C), 137.4 (1C), 137.1 (1C), 137.0 (1C), 133.0 (1C), 132.8 (1C), 130.1 (2C), 129.7 (1C), 129.1 (1C), 128.5 (1C), 128.4(2C), 126.8 (1C), 126.4 (1C), 124.0 (1C), 122.4 (1C), 121.1 (1C), 119.6 (1C).
N-(4-Benzoylphenyl)-5-methyl-2-furamide (4a)
Yield: 45 %; m.p.: 106-108 °C; Rf: 0.5 (CHCl3/MeOH, 98:2); IR (KBr) cm-1: 3533 (N-H), 3008 (CH3), 1666.52 (CO, ketone), 1666.50 (CO, amide), 1589, 1519, 1404, 1319, 1280, 1249, 1211, 1134, 1018, 925, 848, 794, 748, 702, 624, 509. 1H-NMR (500 Hz, CDCl3) δ(ppm):8.20 (br, s, 1H, CONH), 7.88 (d, J = 8.65 Hz, 2H, Ar-H), 7.81 (m, 4H, Ar-H), 7.60 (t, J = 7.4 Hz, 1H, Ar-H), 7.54 (t, J = 8 Hz, 2H, Ar-H), 7.20 (d, J = 3.35 Hz,1H, furan-H), 6.21 (d, J = 2.65 Hz,1H, furan-H), 2.43 ppm (s, 3H, CH3); 13C-NMR(CDCl3) δ(ppm): 195.6 (1C), 156.2 (1C), 155.4 (1C), 145.8(1C), 141.6 (1C), 137.9 (1C), 133.0 (1C), 132.2 (1C), 131.6 (2C), 129.8 (2C), 128.3 (2C), 118.8(2C), 117.4 (1C), 109.3 (1C), 13.9 (1C).
N-(3-Benzoylphenyl)-5-methyl-2-furamide (4b)
Yield: 38 %: m.p.: 105-106 °C; Rf: 0.55 (CHCl3 /MeOH, 98:2); IR (KBr) cm-1: 3564 (N-H), 3062 (CH3), 1674.21 (CO, ketone), 1674.20(CO, amide), 1597, 1519, 1481, 1427, 1357, 1319, 1288, 1211, 1080, 1018, 964, 902, 871, 786, 725, 586, 509. 1H-NMR (500 Hz, CDCl3) δ(ppm): 8.17 (br, s, 1H, CONH), 8.12 (d, J = 1.0 Hz,1H, Ar-H), 7.93 (s, 1H, Ar-H), 7.84 (d, J = 1.3 Hz, 2H, Ar-H), 7.62 (t, J = 7.4Hz, 1H, Ar-H), 7.57 (d, J = 7.7 Hz,1H, Ar-H), 7.51 (t, J = 7 Hz, 3H, Ar-H), 7.17 (d, J = 3.35 Hz,1H, furan-H), 6.19 (d, J = 2.6 Hz,1H, furan-H), 2.42 ppm (s, 3H, CH3); 13C-NMR (CDCl3) δ(ppm): 196.2 (1C), 156.3 (1C), 155.2 (1C), 145.8(1C), 138.3 (1C), 137.7 (1C), 137.3 (1C), 132.6 (1C), 130.1 (2C), 129.1 (1C), 128.3 (2C), 125.9(1C), 123.8 (1C), 121.0 (1C), 117.0 (1C), 109.2 (1C), 13.9(1C).
N-(2-Benzoylphenyl)-5-methyl-2-furamide (4c)
Yield: 35 %: m.p.: 102-103 °C; Rf; 0.7 (CHCl3 /MeOH, 98:2); IR (KBr) cm-1: 3317 (N-H), 3124 (CH3), 1674.21 (CO, ketone), 1620.21(CO, amide), 1597, 1519, 1489, 1435, 1357, 1311, 1288, 1211, 1134, 1103, 1018, 925, 871, 802, 748, 694, 632, 516, 447, 385. 1H-NMR (400 Hz, CDCl3) δ(ppm):δ = 11.72 (br, s, 1H,CONH), 8.79 (d, J = 8.0 Hz,1H, furan-H), 7.72 (d, J = 8.0 Hz, 2H, Ar-H), 7.60 (t, J = 12.0 Hz,3H,Ar-H), 7.26 (s, 2H, Ar-H), 7.18 (d, J = 4.0 Hz,1H, Ar-H), 7.10 (t, J = 8.0 Hz, 1H, Ar-H), 6.15 (d, J = 4.0 Hz 1H, furan-H), 2.45 ppm (s, 3H, CH3);13C-NMR (CDCl3) δ(ppm): δ = 199.6 (1C), 156.9 (1C), 155.7 (1C), 146.27 (1C), 140.4 (1C), 138.8 (1C), 134.2 (1C), 133.7 (1C), 132.2 (2C), 129.7 (1C), 128.2 (2C), 123.2(1C), 121.9 (1C), 121.4 (1C), 116.7 (1C), 108.7 (1C), 13.9 (1C).
Anti-hyperlipidemic activity
The plasma total cholesterol (TC), triglyceride (TG), high-density lipoprotein-cholesterol (HDL-C), and low-density lipoprotein-cholesterol (LDL-C) levels in hyperlipidemic group (HCG) treated for 18 h are shown in (). Triton WR-1339 caused a significant increase in plasma TC, LDL-C (p < 0.001), and TG (p < 0.0001) levels, and a significant decrease in HDL-C level (p < 0.001) in hyperlipidemic control group (HCG) after 18 h of Triton WR-1339 administration in comparison with the normal control group (NCG).
The increase of plasma total cholesterol concentration in the HCG was 147 % after 18 h as compared to the NCG. Triglyceride level in the HCG was also elevated by 887 % after 18 h. At the same time, LDL-C level in HCG was also elevated by 49 % after 18 h as compared to the NCG. HDL level in HCG was decreased by 14 % after 18 h as compared to NCG.
Effect of compounds 3b, 4b, 4c and BF on plasma lipid profile in rats
The effect of compounds 3b, 4b, 4c and BF on plasma lipid profile on treated rats after 18 h are shown in . Interestingly, the elevated plasma TG levels produced by the acute injection of Triton WR-1339 were significantly (p < 0.0001) decreased by 71 and 67.5 % in compounds 4c and BF respectively and by 56 % in 4b (p < 0.001) after 18 h, in comparison to Triton treated hyperlipidemic control (HCG). Furthermore, total cholesterol levels were significantly (p < 0.01) reduced in 4b by 49 % and in 4c (p < 0.001) by 50 % after 18 h compared to hyperlipidemic control group (HCG).
After 18 h of treatment, LDL-cholesterol levels were lowered by (49 %, p < 0.0001) in 4c and (43.6 % p < 0.001) in compound 4b (). The HDL-C levels were significantly (p < 0.001) increased in compounds 4c and BF by 34 and 36.5 % respectively and in 4b by 29 % (p < 0.01) after 18 h compared to HCG treated rats. No significant differences in TC, TG, HDL-C and LDL-C levels were observed by compound 3b in treated rats after 18 h compared to HCG-treated rats.
Discussion
The results of the present study revealed the potential anti-hyperlipidemic activity of novel series of N-(benzoylphenyl)-2-furamides using Triton WR-1339-induced hyperlipidemic rats as a model for screening the lipid lowering potential [22].
Our results showed that the hyperlipidemia induced by Triton WR-1339 was significantly reduced by compounds 4b, 4c, and bezafibrate in comparison with the hyperlipidemic control group after 18 h. It was not surprising that the reduction in triglycerides levels of compounds 4b and 4c were significantly greater than the reduction in cholesterol levels; this could be explained by the significant elevation in plasma lipid profile following Triton WR-1339 administration which results mostly from the increase in VLDL (in which the triglycerides portion is several times greater than that of cholesterol) [23]. This result suggests that the compounds are able to restore, at least partially, the catabolism of lipoproteins.
In addition, 4b and 4c significantly increased the HDL-C levels after 18 h of Triton WR-1339 administration. Elevated HDL-C is reported to have a preventive action against atherogenesis [24].
The findings of this research work are in agreement with our previous data which indicated that the presence of an aromatic heterocyclic moiety connected to huge lipophilic aromatic rings through a carboxamide linkage is necessary for interaction with proper target(s) for hypolipidemic activity [25,26]. Also, the chemical nature and the electronic effect of the substituents bearing on the heterocycle ring play an important role in the determination of activity.
In the present study, the aromatic heterocycle is represented by furan ring and the aromatic lipophilic rings are benzophenones as shown in compounds 3b, 4b and 4c. Compounds 4b and 4c demonstrated much more activity than 3b. This result may be explained by the chemical nature of the substituent on position 5 of the furan ring. In compounds 4b and 4c, the substituent is methyl group, a small lipophilic group while compound 3b harbors a phenolic group that offers H-bond donor and acceptor motif. The size of the substituent on position 5 is a determinant for the activity and this result may indicate that the adjacent area in the target(s) which receives the furan ring is a small lipophilic site. Therefore, the presence of methyl group provides good hydrophobic interaction in the binding cleft. Interestingly, 4c exhibited better activity than 4b and this may be attributed to the possibility of intramolecular H-bond interaction which in turn affects drug/receptor interaction and thus, might infer that the binding site is lipophilic.
At the same time, if compounds 4b with 4c are compared, 4c is more active than 4b and this may be due to the possibility of intramolecular hydrogen bond formation which means that the amide hydrogen and the oxygen atom of the keto group are not involved in hydrogen bond formation with the target(s); this may suggest that the area in the active site of the target(s) which accommodates the ligand is lipophilic in nature.
Conclusion
Compounds 4b and 4c improve lipid profile in Triton-induced hyperlipidemic rats. These findings are in agreement with previous reports, and thus confirm that the presence of lipophilic moiety, carboxamide linkage and a heterocyclic ring (capable of hydrogen bond formation, furan ring) are three important requirements for the hypolipidemic activity of these novel compounds. Thus, there is a need for further investigations to elucidate the exact mechanism of action of these compounds which can serve as lead compounds in the search for therapeutic agents for targeting dyslipidemia and cardiovascular diseases.
Declarations
Acknowledgement
References
Archives
News Updates
Fulltext in PDF