*Corresponding Author:
A. Husain
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Jamia Hamdard, New Delhi-110 062, India
E-mail: [email protected]
Date of Submission 27 January, 2009
Date of Revision 12 July 2008
Date of Acceptance 01 February 2008
Indian J Pharm Sci, 2009, 71 (1): 62-66  

Abstract

In the present investigation, two new series, 1-(4-benzylphenyl)-3-(5-substituted-1,3,4-oxadiazol-2-yl)-1-propanone and 1-(4-ethylphenyl)-3-(5-substituted-1,3,4-oxadiazol-2-yl)-1-propanone from β-(4-benzylbenzoyl)propionic acid and β-(4-ethylbenzoyl)propionic acid, respectively, were synthesized and tested for antiinflammatory, analgesic, lipid peroxidation, ulcerogenic and antibacterial actions. A fair number of compounds were found to have good antiinflammatory activity in carrageenan-induced rat paw edema test, while a few compounds showed significant antibacterial activity. The newly synthesized compounds showed very low ulcerogenic action.

Keywords

Oxadiazoles, aroylpropionic acid, antiinflammatory, analgesic, antibacterial

A diversity of useful biological effects is possessed by heterocyclic compounds containing the fivemembered oxadiazole nucleus [1]. In particular, compounds bearing 1,3,4-oxadiazole nucleus are known to exhibit unique antiedema and antiinflammatory activity [2-5]. Differently substituted oxadiazole moiety has also been found to have other interesting activities such as analgesic [3,4], antimicrobial [6,7], antitubercular [8], anticonvulsant [9] and antitumor activities [5]. The most prevalent side effects of commonly used NSAIDs are the occurrence of gastrointestinal damage with gastric upset and irritation. Studies suggest that the direct tissue contact of these agents plays an important role in the production of gastric side effects [10,11]. Aroylpropionic acids are good antiinflammatory agents but produce gastrointestinal side effects and these side effects are due to presence of free carboxylic group in the molecule [12,13]. Therefore, it was considered worthwhile to synthesize some new β-aroylpropionic acid derivatives by converting the free terminal carboxylic group into oxadiazolyl moiety with the hope to get better molecules.

As shown in Scheme 1, The starting materials, β-(4- benzylbenzoyl)propionic acid 3 and β-(4-ethylbenzoyl) propionic acid 4, were prepared by condensing diphenylmethane or ethylbenzene with succinic anhydride in presence of anhydrous aluminium chloride following Friedel-Craft’s acylation reaction conditions. Reaction between β-(4-benzylbenzoyl) propionic acid 3 or β-(4-ethylbenzoyl)propionic acid 4 with aryl acid hydrazides 2a-l in phosphorous oxychloride (reaction time varies from 2 to 5 h) afforded title compounds 5a-l and 6a-e. Both analytical and spectral data [1H NMR, Mass (HREIMS) and IR] of the synthesized compounds are in agreement with the proposed structures.

Scheme

Scheme 1: Synthetic route for the preparation of 1,3,4-oxadiazoles, 5a-l, 6a-e

Melting points were determined with the help of open glass capillaries using Kjeldahl flask containing liquid paraffin and are uncorrected. Purity of the compounds was checked by TLC on silica gel plates and spots were visualized by exposure to iodine vapors. 1H NMR spectra were recorded on Varian E-360 MHz or Bruker spectropsin DPX-300MHz with tetramethylsilane as internal standard in solvent CDCl3.The IR spectra were recorded on a Perkin- Elmer 1600 FTIR spectrophotometer in potassium bromide pellets. Mass spectra were recorded on a Jeol JMS-D 300 instrument fitted with a JMS 2000 data system at 70 eV.

Ethyl esters of aromatic acids (1a-l) and aryl acid hydrazides (2a-l) were synthesized according to the literature method [14].

Aryl hydrazide 2a (1 mol) was dissolved in phosphorous oxychloride (5 ml) and to it was added compound 3 (equimolar; 1 mmol). The reaction mixture, after refluxing for 4h, was cooled to room temperature and poured onto crushed ice. On neutralization of the contents with sodium bicarbonate solution (20%), a solid mass separated out, which was filtered and washed with water. It was crystallized from methanol to give 5a. Similarly 5b-l and 6a-e were prepared (Table 1).

Compound R MP (0) Yield (%) Molecular formula Molecularweight
3 - 178-180 48 C17H16O3 268.31
4 - 110 64 C12H14O3 206.24
5a C6H5 154 52 C24H20N2O2 368.43
5b 3-NO2 C6H4 178-180 56 C24H19N3O4 413.43
5c 4-F-C6H4 142-144 54 C24H19FN2O2 386.42
5d 4-OCH3-C6H4 172-174 63 C25H22N2O3 398.46
5e C6H5-COC6H4 188 58 C31H24N2O3 472.54
5f 2-Cl-C6H4 160-162 56 C24H19ClN2O2 402.88
5g 4-Cl-C6H4 172-174 66 C24H19ClN2O2 402.88
5h 3,4-(OCH3)2-C6H3 166-168 59 C26H24N2O4 428.48
5i C6H5-CH2 154 63 C25H22N2O2 382.46
5j C6H5-OCH2 166 54 C25H22N2O3 398.46
5k 1-C10H7-OCH2 170-172 52 C29H24N2O3 448.52
5l 2-C10H7-OCH2 190-192 50 C29H24N2O3 448.52
6a C6H5 122-124 62 C29H18N2O2 306.36
6b 3-NO2 C6H4 128-130 60 C19H17N3O4 351.36
6c 4-F-C6H4 116-118 55 C19H17FN2O2 324.35
6d 4-OCH3-C6H4 134-136 63 C20H20N2O3 336.38
6e C6H5-COC6H4 154-156 57 C26H22N2O3 410.47

Table 1: Physical Constants Of The Title Compounds

In general, IR spectral data (cm-1) of the compounds revealed bands at 3100-3030 (C-H); 1665-1650 (C=O); 1440-1420 (C-N) and 810-750 (aromatic) and 830-815 (p-disubstituted). 1H-NMR spectral studies of the title compounds showed two triplets of two protons each at around δ 2.6 and δ 3.5 which could be assigned to two methylene protons (-CH2-CH2-). A signal was observed at around δ 4.02 in case of compounds 5a-l, which could be accounted for the methylene group (-CH2-) present between two phenyl rings. There appeared signals (triplet at around δ 1.26 for CH3CH2- and quartet at around δ 2.69 for CH3CH2-), for ethyl function in case of compounds 6a-e. Aromatic protons appeared in the region 7.03- 8.06 ppm. Other peaks were observed at appropriate places. The mass spectra showed acylium fragments containing benzylphenyl/ethylphenyl and aryl moieties as major peaks followed by peaks with loss of CO besides the molecular ion peaks in reasonable intensities supporting the structure.

Antiinflammatory activity of the compounds was evaluated by carrageenan-induced paw edema test in rats [15], at a dose of 20 mg/kg po, using indomethacin as standard drug at same dose level. Swiss rats of either sex (150-200 g) were divided into control, standard, and test groups, each comprising of six rats. The protocol of animal experiments has been approved by the Institutional Animal Ethics Committee (IAEC). Freshly prepared suspension of carrageenan (0.05 ml, 1% w/v solution in 0.9% saline) was injected under the planter aponeurosis of the left hind paw of each rat. One group was kept as control and the animals of other groups were pre-treated with the test drugs suspended in 1% carboxymethylcellulose (CMC) given orally 30 min before carrageenan injection. The foot volume was measured using the mercury displacement technique, with the help of plethysmograph, both in control as well as test animals including standard drug animals, before and after 3 h of carrageenan injection. The percentage inhibition of inflammation was calculated using the formula, % inhibition = (1- Vt/Vc)x100, where, Vt and Vc are the mean relative changes in the volume of paw edema in the test and control, respectively. The results are summarised in Table 2.

Compound Antiinflammatory activity* Analgesic activity* Ulcerogenic activity* Antimicrobial activity
  (% inhibition ± SEM) (% protection ± SEM) (severity index) (MIC; µg/ml)
5a     0.416
25.92±1.04 32.44±0.84
5b 19.40±1.60 24.42±0.98 0.750 >100
5c 33.33±1.07 19.08±0.65 0.833 50 >100
5d 52.60±0.59 40.07±0.90 0.666 >100 >100
5e 29.63±1.18 32.44±1.13 0.583
5f 36.36±1.38 51.31±0.42 0.916 >100 >100
5g 46.00±1.16 45.80±0.29 1.083 25 50
5h 56.20±2.32 54.12±0.62 0.333
5i 13.64±1.06 19.08±1.33 0.583
5j 19.35±2.20 14.33±1.50 0.666 >100
5k 35.60±1.28 19.08±0.65 0.833
5l 29.63±1.33 26.42±1.44 0.583
6a 25.92±2.83 24.42±1.50 0.916
6b 13.00±3.61 19.08±0.66 1.083
6c 29.63±1.54 26.42±1.44 0.833 50 >100
6d 35.60±1.96 45.12±0.11 0.750
6e 32.33±1.65 29.17±1.18 0.333
Indomethacin 64.25±2.03 nt 2.666    
Aspirin nt 61.86±0.22 nt    
Nitrofurazone       12.5 6.5

Table 2: Results Of Antiinflammatory, Analgesic, Ulcerogenic And Antibacterial Activities

Analgesic activity was carried out by acetic acid induced writhing method [16] using albino mice (25- 30 g) of either sex on groups of six animals each. A 1% aqueous acetic acid solution (i.p. injection; 0.1 ml) was used as writhing induced agent. Mice were kept individually in the test cage, before acetic acid injection and habituated for 30 min. Screening of analgesic activity was performed after oral administration of test drugs at the dose of 20 mg/kg. All compounds were dissolved in 1% carboxymethylcellulose (CMC) solution. One group was kept for the control experiment and received po administration of 1% CMC. Aspirin was used as standard at the dose of 100 mg/kg po. After 1 h of drug administration 0.10 ml of 1% acetic acid solution was given to mice intraperitoneally. Stretching movements consisting of arching of the back, elongation of body and extension of hind limbs were counted for 5-15 min of acetic acid injection. The analgesic activity was expressed in terms of % protection. % Analgesic activity =(n – n’/n) x 100 where n = mean number of writhes of control group and n’ = mean number of writhes of test group. The percent protection in mice brought about by administration of the drugs is shown in Table 2.

Acute ulcerogenesis test was done according to Cioli et al [11]. Albino rats (150-200 g) were divided into different groups consisting of six animals in each group. Ulcerogenic activity was evaluated after oral administration of test compounds or indomethacin at the dose of 60 mg/kg. Control rats received oral administration of vehicle (suspension of 1% methylcellulose). Food but not water was removed 24 h before administration of the test compounds. After the drug treatment, the rats were fed normal diet for 17 h and then sacrificed. The stomach was removed and opened along the greater curvature, washed with distilled water and cleaned gently by dipping in saline. The gastric mucosa of the rats was examined by means of a magnifying glass. For each stomach, the severity of mucosal damage was assessed according to the following scoring system: 0.5- redness; 1.0- spot ulcers; 1.5- hemorrhagic streaks; 2.0- ulcers<3, but ≤5; 3.0- ulcers>5. The mean score of each treated group minus the mean score of the control group was considered as severity index of gastric mucosal damage.

Antibacterial activity of newly synthesized compounds was determined against the bacterial strains gram positive (Staphylococcus aureus; NCTC-6571) and gram negative (Escherichia coli; ATCC-25922). The test was carried out according to the turbidity method [17]. A solution of the compounds was prepared in dimethylformamide (DMF) and a series of doubling dilutions prepared with sterile pipettes. To each of a series of sterile stoppered test tubes a standard volume of nutrient broth medium was added. A control tube containing no antimicrobial agent was included. The inoculum consisting of an overnight broth culture of microorganisms was added to separate tubes. The tubes were incubated at 37° for 24 h and examined for turbidity. The tube with highest dilution showing no turbidity was MIC. Nitrofurazone was used as standard drug.

The antiinflammatory activity (Table 2), revealed that the compounds 5d and 5h showed very good antiinflammatory activity (52.60 and 56.20% inhibition, respectively), which was comparable to that of indomethacin (64.25% inhibition). Amongst the compounds subjected to analgesic activity (Table 2), compounds 5f and 5h were found to possess significant activity (51.31 and 54.12% protection, respectively), while the standard drug aspirin showed 61.86% activity. All the synthesized compounds showed very low ulcerogenic activity (0.416- 1.083 severity index), whereas the standard drug indomethacin showed high severity index of 2.666 (Table 2). The results indicate that the compounds are almost devoid of ulcerogenic action. From the antibacterial results (Table 2), it was observed that the compound 5g was the most active among the tested compounds with MIC- 25 μg/ml against S. aureus and MIC- 50 μg/ml against E. coli. The rest of the compounds were moderate or inactive in their action.

Acknowledgements

Financial support provided by the DST, New Delhi, under SERC-fast track scheme is gratefully acknowledged. Thanks are due to Ranbaxy Research Laboratories for providing spectral data of the compounds. We are also thankful to Mrs. Shaukat Shah, In-charge animal house, for providing animals for pharmacological studies and Prof. (Mrs.) P. K. Pillai for helping in carrying out antimicrobial activity of the compounds.

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