Background

Infectious diseases are among the leading health problems, accounting for 41% of global disease burden [1]. Diseases caused by bacteria and parasites are still challenging to public health. Their impact is particularly large in developing countries due to unavailability of relevant medicines and the emergence of widespread drug resistance [2,3,4]. The clinical efficacy of many existing antibiotics has been endangered by the emergence of MDR pathogens [5, 6]. To triumph over MDR pathogens, it is important to develop novel and more effective antimicrobial agents, especially with a different mechanism of action [7]. It is obvious that despite synthetic compounds, natural raw materials are the key sources for novel therapeutic agents for the management of various ailments like infectious diseases [8, 9].

Helminthiasis is among the most widespread parasitic infections in humans, distressing an enormous population of the world. Approximately two billions people are suffering from parasitic worms infections [10]. Majority of helminths mediated infections are limited to tropical regions and cause huge hazard to health leading to undernourishment, anaemia, eosinophilia, physical, mental sluggishness and pneumonia [11]. Parasitic infections also cause lymphatic filariasis leading to elephantiasis, onchocerciasis called river blindness and schistosomiasis. These infections are more common in populations living in endemic areas with poor hygiene and socio-economic problems [12]. Livestock and crops are also affected by parasitic worms thus leading to reduction in crops and milk production [13]. There is a substantial improvement in helminths control but due to emergence of anthelmintic resistance to currently available drugs. So, it is important to search alternative strategies against gastrointestinal nematodes [14]. Similarly, most of the available insecticidal from chemical sources are hazardous to human health and are associated with environmental risks [15]. Therefore, alternative resources must be explored to substitute the chemical pesticides. Pesticides from natural sources are advantageous as they are selective in targeting specific species and also have unique modes of action [16].

Isodon rugosus Wall. ex Benth. belongs to the family Lamiaceae. Isodon, an important genus of this family is a rich source containing a large number of bioactive compounds. The Isodon species have been used as anti-tumor, anticancer, antimicrobial, insecticide and anthelmintic [17, 18]. Isodon rugosus has been used ethnomedicinally as an antimicrobial and anthelmintic [19, 20]. This plant has also been used traditionally against skin infections and for the treatment of scabies [21, 22]. This specie has also been verified scientifically to possess variety of pharmacological activities [23]. Based on the published literature, the current study is designed to evaluate various fractions of I. rugosus for the antimicrobial, anthelmintic and insecticidal potentials along with identifications and sorting out of bioactive compounds by GC-MS analysis.

Methods

Plant collection and extraction

The plant was collected from Dir (KPK), Pakistan in the month of June and was identified by plant taxonomist at Department of Botany, Shaheed Benazir Bhuto University Dir (KPK), Pakistan. The plant sample was kept at the herbarium of the same university with voucher number 1016AZ. Fresh aerial parts (11 kg) were separated from the rest of the plant and rinsed with clean water to remove any dust particles followed by shade drying for 23 days. The dried plant parts were cut into small pieces and grinded into coarse powder with the help of a grinder. The powdered material (6 kg) was macerated in 80% methanol (25 L) for 18 days and the process was repeated three times. The filtrates were combined and concentrated under reduced pressure using rotary evaporator [24, 25]. A brown semisolid mass (380 g) of the crude methanolic extracts was obtained.

Fractionation

The crude methanolic extract was transferred into a separating funnel and diluted with 500 ml of distilled water. n-Hexane (500 ml) was added to it with vigorous shaking and kept for a while to form two layers. The n-hexane layer was separated and repeated the same procedure three times by adding 500 ml of n-hexane each time. All the n-hexane layers were combined and concentrated at reduced pressure using rotary evaporator. The final concentrated weight of n-hexane fraction was 19 g. In a similar way like n-hexane fraction, the chloroform and ethyl acetate fractions were extracted sequentially weighing 27 and 80 g respectively. The dry water residue (aqueous fraction) was collected at the end weighing 125 g [26, 27].

Extraction of crude saponins

The crude saponins from I. rugosus were obtained by adding 20 g of the plant powder in a conical flask having 100 ml of 20% ethanol. The sample was heated in water bath for 4 h at 55 °C with continuous stirring. The mixture was filtered and extracted again with 200 ml of 20% ethanol. The volume was heated up to 60 °C in water bath and got 40 ml of greenish color residue. The residue was added into the separating funnel followed by the addition of diethyl ether (20 ml) with vigorous shaking. After vigorous shaking, the separating funnel was put in a stand to get two distinct layers. The upper diethyl ether layer was discarded while the lower aqueous layer obtained was diluted with n-butanol (60 ml). This extract was washed with 10 ml of 5% sodium chloride solution. The solution was evaporated by keeping in water bath to obtained the dried saponins [26].

Extraction of Flavonoids

Plant sample having weight of 20 g was heated at 50 °C in 200 ml of HCl (2 M) under reflux for 30 min. The plant sample was filtered using Whatman No. 42 filter paper after getting cold. The filtrate obtained was poured into a separating funnel and added equal volume of ethyl acetate. The total amount of flavonoids present in the plant sample was precipitated, which were collected from the sample using a filter paper. The weight of flavonoids was 1.4 g (7%) [28].

Gas chromatography (GC) analysis

Ethyl acetate fraction was subjected to GC analysis and the GCMS was done by means of an Agilent USB-393752 gas chromatograph (Agilent Technologies, Palo Alto, CA, USA) with HHP-5MS phenylmethylsiloxane 5% with capillary column (30 m × 0.25 mm × 0.25 μm; Restek, Bellefonte, PA) equipped with an FID detector. Initially, the temperature of oven was maintained at 70 °C for 1 min, and then increased the required temperature slowly and step wise to 180 °C at the rate of 6 °C/min for 5 min, and at the final stage increased the temperature to 280 °C at the rate of 5 °C/min for 20 min. The temperatures of the Injector and detector were set at 220 °C and 290 °C, respectively. Helium was used as a carrier gas with a flow rate of 1 ml/min [29].

Gas chromatography–mass spectrometry (GC/MS) analysis

Ethyl acetate fraction was subjected to GC/MS analysis and the processed was done by means of an Agilent USB-393752 gas chromatograph (Agilent Technologies, Palo Alto, CA, USA) with a HHP-5MS phenylmethylsiloxane 5% with a capillary column (30 m × 0.25 mm × 0.25 μm film thickness; Restek, Bellefonte, PA) prepared with an Agilent HP-5973 mass selective detector in the electron impact mode (ionization energy: 70 ev) working under similar experimental background as illustrated for GC.

Identification of components

Identification of the compounds present in the ethyl acetate fraction of I. rugosus was carried out on the base of comparison of their relative retention indices of each component with those of the authentic compounds present in the literature. Further identifications of the compounds were carried out from the spectral data obtained from the Wiley and NIST libraries and additional identifications were carried out by completed comparisons of the fragmentation pattern of the mass spectra with the reported in literature [30].

Antibacterial investigations

Bacterial strains

Eight bacterial strains including Escherichia coli (739), Klebsiella pneumoniae (700603), Pseudomonas aeruginosa (27853), Enterococcus faecalis (29212), Proteus mirabilis (13315), Staphylococcus aureus (29213), Bacillus cereus and Salmonella typhi were used to investigate antibacterial potential of plant’s samples. The samples were provided by the Microbiology Laboratory of Department of Microbiology, Quaid-e-Azam University, Islamabad. Bacteria were preserved in freeze-dried condition at 4 °C in stab slant agar until later use.

Preparation and standardization of inoculums

Bacterial cultures were grown for 24 h at 37 °C and suspensions with cell density of 1 × 108 CFU/ml, were prepared using McFarland standard and was further diluted to a cell density of 1 × 106 CFU/ml using a UV visible spectrophotometer (Thermo electron corporation USA) at 625 nm and the standardization was maintained for the period of the study [31].

Antibacterial assay

Preliminary antibacterial activity of plant extracts were investigated using well assay technique [32, 33]. Briefly, Nutrient agar plates were prepared and inoculated with the test organisms aseptically under laminar flow hood and were properly labeled. Wells of 5 mm diameter were made in the plates using sterile cork borer. Samples were prepared having concentrations of 10 mg/ml. From each sample, 100 μl of extract was added into each well using micropipette. The standard drug ceftriaxone was used as positive control, which was added into the central well contained in nutrient agar media in each Petri plate. After inoculation and addition of the samples, the Petri plates were kept in incubator at 37 °C for 24 h. Diameter of inhibitory zones were determined around each bore after 24 h and were compared with positive control. Experiments were performed in triplicate and the data obtained was represented as mean ± SEM.

Determination of MICs

MICs were determined using microdilution method as described by National Committee for Clinical Laboratory Standards (NCCLS) [34]. Briefly, the plant’s samples were prepared at concentrations of 50 mg/ml (stock solution) in sterile distilled water and serially diluted with distilled water to 20, 17.5, 15, 12.5, 10, 7.5, 5, 2.5, 1 and 0.5 μg/ml using nutrient broth followed by inoculation with 0.2 ml suspension of the test organisms. After 24 h of incubation at 37 °C, the test tubes were visually observed for growth. The lowest concentration at which no growth of the microorganism was observed was considered as MIC of the plant extract against the relevant strains of the microorganisms.

Anthelmintic investigations

For the anthelmintic activity of I. rugosus, adult earthworms (Pherethima posthuma) and roundworms (Ascaridia galli) were used. Earthworms having average length of 7–8 cm and width 0.1–0.2 cm were collected from the muddy soil near Department of Pharmacy, University of Malakand, KPK, Pakistan. The selection of earthworms (P. posthuma) is based on close physiologic and anatomic resemblance with the human intestinal round worm parasites Ascaris lumbricoides [35]. Roundworms were collected from the intestines of chicken. The chickens were slaughtered, their intestines were dissected after the removal of fecal material with the help of normal saline and roundworms were collected from their intestines. These roundworms (A. galli) have close resemblance with that of the roundworm parasite (Ascaris lumbricoides) found in the human intestine. Both types of worms were divided into different groups, each group containing six (6) worms. All the extracts, their fractions, crude saponins and albendazole solutions were prepared in 10, 20 and 40 mg/ml. From each solution, 25 ml of the sample was transferred to sterilized Petri dishes (150 × 15 mm) followed by addition of earthworms using forceps. Observations were made for the time taken when the worms lost their motility as paralysis time and death was concluded when no movement was observed even with vigorous shaking in hot water at 50 °C. Both paralysis and death times were recorded for different fractions and were compared with the positive control [36].

Insecticidal investigations

Anti-beetle

The anti-beetle activity was carried out against R. dominica (grain borer) and T. castaneum (flour beetle) following the procedure previously described [37]. Various dilutions of extracts were prepared in methanol, i.e., 200, 100 and 50 mg/ml and filter paper was wetted with the 5 ml of each test sample solution in Petri dishes and kept overnight to evaporate the solvent. After evaporation of the solvents, 20 healthy insects were shifted to each Petri dish and kept for 24 h at room temperature with 50% of relative humidity. After 24 h, the results were checked by counting the number of dead and alive insects. Permethrin was used as positive control while the volatile solvents were used as negative control.

Anti-termite investigations

The anti-termite activity of crude saponins, methanolic extracts and resultant fractions of I. rugosus was conducted following standard procedure [38]. In this procedure the plant’s samples were assayed against Heterotermes indicola (termites). Sterilized filter papers were kept in Petri dishes equal to the size of the Petri dishes. Samples were prepared by dissolving 2 mg/ml of each extract of the plant in respective solvents. The filter papers were kept for 24 h so that the solvents become fully evaporated from it. Each filter paper was kept in the labeled Petri dishes. In each Petri dish, 25 termites were placed and were kept for 24 h at room temperature. After 24 h, the number of dead and alive termites was counted. Similarly, the results were also recorded on the second and third day. This activity was performed in triplicate and the average termites killed each day were recorded. Permethrin was used as positive control. The LD50 of each sample was calculated by graph prism pad software and Microsoft Excel.

Anti-Pharaoh (ants) investigations

The anti-Pharaoh activity was performed by the direct contact toxicity method described by Ahn et al. [37]. From each fraction, solutions of 0.5, 1, 2, 4, 6 and 8 mg/ml concentrations were prepared. Each concentration was added into Petri dish containing sterilized filter paper and kept for 12–15 h for evaporation of the solvent. After evaporation, 20 Pharaoh ants were added into each Petri dish. The Petri dishes containing distilled water treated filter paper served as a control. The Petri dishes were placed at room temperature for 24 h and numbers of dead and alive ants were observed in each Petri dish. Permethrin was used as positive control. The percent mortality of each sample was calculated and was compared with the positive control.

Statistical analysis

Each experiment was performed in three replicates and values were expressed as mean ± SEM. two way ANOVA followed by multiple comparison Bonferroni’s test. The P values less than 0.05 were considered as statistically significant. LD50 values were calculated by a linear regression analysis among the percent inhibition against the extract concentrations via Excel program and GraphPad Prism software.

Results

Gas chromatography mass spectroscopy

The GC-MS analysis of ethyl acetate fraction revealed the identifications of 57 compounds which have been enlisted in Table 1. Various parameters of major compounds in this fractions i.e., retention time, percent area, base peak, width etc. has also been summarized in Table 2. The GC-MS chromatogram of ethyl acetate fraction (Fig. 1) showed the peak areas for various compounds including the bioactive compounds. The structures of the bioactive compounds are shown in Fig. 2. The integration pattern of dominant compounds determined by GC-MS analysis is provided in Fig. 3.

Table 1 List of all compounds identified in the GC-MS analysis of ethyl acetate fraction of Isodon rugosus
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Table 2 Various parameters major compounds in GC-MS of ethyl acetate fraction of Isodon rugosus
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Fig. 1
figure 1

Chromatogram of Ethyl acetate fraction of Isodon rugosus

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Fig. 2
figure 2

Bioactive compounds identified in the ethyl acetate fraction of Isodon rugosus

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Fig. 3
figure 3

Mass spectra of bioactive compounds in ethyl acetate fraction of Isodon rugosus

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Antibacterial studies

Sensitivity pattern

The bacterial strains were exposed to different antibiotic groups to determine their susceptibility pattern as shown in Table 3. All strains were found resistant to more than three antibiotics and therefore were termed as multi drug resistant (MDR) strains.

Table 3 Antibiotic Susceptibility pattern of selected bacterial strains to different antibiotic groups
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Zone of inhibitions

Results of antibacterial activity (ZOI) are shown in Table 4. Among all the tested samples, flavonoids were most active against all the strains and its antibacterial potential was comparable to the standard drug ceftriaxone. Among other fractions, ethyl acetate was most effective against S. aureus and S. typhi displaying inhibitory zones of 29.3 ± 0.28 and 28.2 ± 0.35 mm respectively. Crude saponins were also effective against S. aureus, E. coli, B. cereus and K. pneumoniae causing inhibitory zones of 27.2 ± 0.23, 24.1 ± 0.52, 26.3 ± 0.34 and 21.3 ± 0.39 mm respectively. The crude methanolic extract and chloroform fraction were inactive against B. cereus, whereas the aqueous fraction was inactive against E. coli and E. faecalis. n-Hexane fraction was also inactive against E. coli. All the test samples were approximately least active against E. coli.

Table 4 Antibacterial activity of Isodon rugosus against various bacterial strains expressed in mm as ZOI
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Minimum inhibitory concentration (MICs)

Among all the tested samples, crude methanolic extract was found most effective against S. aureus and B. cereus with minimum inhibitory concentrations (MICs) of 2.50 ± 0.00 and 2.66 ± 1.30 μg/ml. MIC of n-hexane fraction against B. cereus was 1.33 ± 0.60 μg/ml which was comparable to positive control ceftriaxone displaying MIC of 0.83 ± 0.16 μg/ml. The chloroform fraction was most effective against K. pneumonia and E. coli, whose visible growth was inhibited at 1.16 ± 0.66 and 1.00 ± 0.00 μg/ml respectively. Saponins fraction was most potent against P. mirabilis, S. aureus and K. pneumonia with MICs of 1.00 ± 0.00, 0.83 ± 0.16 and 1.00 ± 0.00 μg/ml respectively. Flavonoids were also found equally effective against the tested microbes. All the results of minimum inhibitory concentrations (MICs) are summarized in Table 5.

Table 5 Minimum inhibitory concentrations for different fractions of Isodon rugosus against the tested bacterial strains expressed as μg/ml
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Anthelmintic activity

All the tested fractions were effective in concentration dependent manner as shown in Table 6. The saponins fraction was observed to be most effective against Pheretima posthuma with an average death time of 44.00 ± 2.00, 33.67 ± 3.05 and 27.67 ± 1.53 min at concentrations of 10, 20, 40 mg/ml respectively. The anthelmintic activity observed for saponins and chloroform fractions were comparable to the positive control albendazole. The order of anthelmintic activity for various fractions of the plant against Pheretima posthuma was in an ascending order of saponins > chloroform > ethyl acetate > n-hexane > methanolic extract > aqueous fraction. Moreover, crude saponins exhibited a significant result against Ascaridia galli with an average death time of 29.22 ± 0.61 min at 40 mg/ml concentration. Whereas, average death time for the standard drug albendazole was 33.6 ± 1.76 at the same tested concentration.

Table 6 Anthelmintic activity of aerial part of Isodon rugosus against Pheretima posthuma and Ascaridia galli
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Insecticidal activity

In finding out the insecticidal potentials of different fractions, saponins caused mortality to a significant level, i.e. 70.67 ± 1.20 and 76.65 ± 1.65% mortality against R. dominica and T. castaneum respectively at a concentration of 200 mg/ml, while at a concentration of 50 mg/ml saponins exhibited 61.66 ± 1.20 and 66.67 ± 0.67% mortality against R. dominica and T. castaneum respectively. Among other fractions, chloroform was more effective against R. dominica and T. castaneum showing 60.00 ± 1.15 and 70.33 ± 0.88% mortality against R. dominica and T. castaneum respectively at concentration of 200 mg/ml, while showed 51.00 ± 1.15 and 59.00 ± 0.57% mortality against R. dominica and T. castaneum respectively at a concentration of 50 mg/ml. The methanolic extract and n-hexane fraction also showed moderate insecticidal effects against both the insects as shown in Figs. 4 and 5.

Fig. 4
figure 4

Percent lethality of various samples of Isodon rugosus against Rhyzopertha dominica

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Fig. 5
figure 5

Percent lethality of various samples of Isodon rugosus against Tribolium castaneum

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Anti-termite activity

The anti-termite activity of various samples of I. rugosus showed prominent lethality against termites. The highest activity was attributed to saponins, killing almost all the termites on the first day as shown in Table 7. The second highest activity was shown by ethyl acetate fraction which demonstrated 93.00 ± 0.57% lethality on the first day and 100% lethality on the second day. Other fractions including chloroform, n-hexane and aqueous fractions showed moderate activity causing 77.32 ± 1.32, 50.33 ± 0.88 and 48.33 ± 0.88% lethality respectively on the first day. On the third day almost all the insects were killed by all the plant’s samples.

Table 7 Anti-termite effect of various samples of Isodon rugosus
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Anti-Pharaoh (ants) activity

The determination of anti-Pharaoh ants potentials of I. rugosus reveal that among all the plant’s samples, saponins showed 100% activity against Pharaoh at all the tested concentrations except at 0.5 mg/ml which was 96.33 ± 0.88%. The second highest activity can be attributed to the ethyl acetate fractions of I. rugosus which displayed 72.00 ± 1.15, 77.67 ± 0.67, 80.33 ± 0.33, 86.33 ± 0.88, 90.67 ± 0.67 and 100.0 ± 0.57% lethality at concentrations of 0.5, 1, 2, 4, 6 and 8 mg/ml respectively. The LD50 shown by saponins, ethyl acetate and chloroform fractions were smaller than 0.1 mg/ml, whereas LD50 for methanolic extract, n-hexane and aqueous fractions were 0.85, 1.13 and 3.37 mg/ml respectively as shown in Table 8.

Table 8 Anti-Pharaoh ant effect of various samples of Isodon rugosus
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Discussion

The origin and nature of drug used against specific diseases make a sound difference in the therapy and prognosis. The efficacy and safety of synthetic and natural drugs have been investigated and compared by multiple reporters [39, 40]. Similarly, the use of drugs derived from natural sources have been found comparatively safe and have been preferred against synthetic drugs [41]. Several groups of natural compounds have been reported to possess variety of potentials, for examples, flavonoids have been shown to possess antimicrobial activity that is also obvious in our current study [42]. Similarly, parasitic worms causing infections of human beings and animals are well-known to have negative health consequences and a significant reduction in body ability to resist other diseases. To find compounds with anthelmintic activity, a variety of substances have been investigated using different species of worms like earthworms, ascaris, heterakis and nippostrongylus [42, 43]. Among all these species, earthworms have been used generally for the preliminary evaluation of anthelmintic compounds in-vitro due to physiological similarity with intestinal worms, their reaction to anthelmintics and are easily accessible [44]. It has been established that all those anthelmintics which are toxic to earthworms are regarded as anthelmintic agents. To minimize losses caused by helminths infections, commercial anthelminthics have been used for decades. However, the threats of anthelminthic resistance, poor availability, risk of residue and high cost especially to low income people in developing countries have led to the need of other alternative control methods [45]. Screening and proper evaluation of the claimed medicinal plants could offer the possible alternatives that may both be sustainable and environmentally acceptable instead of those having toxic effect [46].

Results of the current study reveal that saponins were most effective against P. posthuma exhibiting an average death time of 27.67 ± 1.53 min which was comparable with the standard drug albendazole with average death time of 28.67 ± 1.53 at the same concentration (40 mg/ml). Furthermore, crude saponins were most effective against Ascaridia galli with average death time of 29.22 ± 0.61 min at 40 mg/ml. The average death time for standard drug albendazole was 33.6 ± 1.76 at the same concentration. Researchers have proven that saponins possess excellent anthelmintic potential which has also been depicted in our investigations [36].

In the current study, we observed that saponins were also active against insects in a similar way reported earlier [47]. Moreover, the saponins have also been reported to possess anthelmintic, antitussive, anticancer, fungicidal and antiviral properties [48,49,50,51]. Actually the saponins help the plants to protect against pests and parasites [49, 52,53,54,55]. Saponins may cause inhibition of food uptake in the insects’ gut and interrupt in their digestion which lead to stop their growth [47]. They are considered as first line choice for the proper eradication of insects due to their protease inhibitory properties and interaction with cholesterol by disturbing the synthesis of moulting hormones [56]. The saponins isolated from various plants have been reported to possess toxicity profile and have been demonstrated with prominent haemolytic potential. The haemolytic potential and toxicity profile of the saponins make it inevitable that the saponins of each and every plant should be subjected for the evaluation of safety profile in regards to the human body.

The GC-MS analysis showed 57 compounds in the ethyl acetate fraction of I. rugosus. The bioactive compounds identified were palmitic acid, hinokiol, α-amyrin, phytol, ethyl linolate, cyclohexanone, hinokione, methyl palmitate, ethyl palmitate and stigma sterol acetate. The literature survey of the bioactive compounds reveals the importance of I. rugosus regarding various biological activities. The compounds identified in this plant have been reported previously with significant biological activities. Cyclohexanone possess strong antibacterial activity [57]. Red and white wine containing succinic acid have been reported with strong antibacterial activity [58]. The succinic acid derivatives have been reported to treat the infants urinary tract infection [59]. Similarly, the succinic acid have also been reported for antibacterial potential produced by yeast during fermentation [60]. Palmitic acid have been reported to possess antimicrobial potential [61, 62]. Phytol have been reported for its antibacterial [63], antimicrobial [64] and insecticidal potentials [62]. Hinokiol isolated from Magnolia officinalis have been used for antibacterial activity [65]. Ethyl linolate have been used for the treatment of acne vulgaris [66] and topically as antibacterial agent [67]. In the same way, stigmasterol acetate has also been used as antibacterial agent [68]. Likewise, alpha-amyrin possess strong antibacterial activity [69]. Cyclohexanone have been reported to used as a solvent and as a building block in the production of various organic compounds such as insecticidal [70]. Methyl palmitate have been reported to possess insecticidal activity [71]. Palmitic acid have been reported to possess strong anti mosquitoes activities isolated from Acanthus montanus [72]. Ethyl palmitate is larvicidal and insecticidal agent and has been used in insecticidal sprays [73]. Similarly, hinokione isolated from Sabina vulgaris have been reported to possess insecticidal potential [74]. Stigmasterol acetate has mosquito repellent property [75]. Alpha-Amyrin have been reported for insecticidal activity [69].

Conclusions

It can be concluded that Isodon rugosus possess strong antibacterial, insecticidal and anthelmintic potentials. The gas chromatography-mass spectroscopy analysis also elucidated a collection of biologically important compounds putatively known for their antibacterial, insecticidal and anthelmintic potentials. Based on the experimental analysis, it may also be deduced that Isodon rugosus is a good source of antibacterial, insecticidal and anthelmintic compounds. The overwhelming role of ethyl acetate fraction in various biological assays and the GC-MS analysis confirm that this fraction might be an appropriate target for the isolation of bioactive compounds.