Synthesis and Characterization of Novel Hydrazone Derivatives of Isonicotinic Hydrazide and Their Evaluation for Antibacterial and Cytotoxic Potential

Hydrazones are active compounds having an azomethine –NHN=CH group and are widely studied owing to their ease of preparation and diverse pharmacological benefits. Novel isonicotinic hydrazone derivatives of vanillin aldehyde and salicyl aldehyde were synthesized that had azomethine linkages and were characterized by UV–Visible, FTIR, EI-MS, 1H-NMR and 13C-NMR spectroscopy. The compounds were screened for their antibacterial activity against Staphylococcus aureus, Bacillus subtilus, and Escherichia coli using disc diffusion and minimum inhibitory concentration (MIC) methods. For cytotoxicity, a brine shrimp lethality test was performed to calculate the lethal concentration (LC50). The results demonstrated appreciable antibacterial activities against the applied strains, amongst which the compounds coded NH3 and NH5 showed maximum inhibition and MIC responses. In terms of cytotoxic activity, the maximum effect was observed in compound NH5 and NH6 treatments with minimum survival percentages of 36.10 ± 3.45 and 32.44 ± 2.0, respectively. These hydrazones could be potential candidates in antitumorigenic therapy against various human cancer cells.


Introduction
New complex diseases are likely to affect humans because of changing global climatic conditions [1]. There is a continuous need to discover new remedies to combat diseases caused by resistant pathological strains to improve human life [2]. A variety of compounds have been synthesized or isolated from various natural sources, the majority of which have been reported to have significant therapeutic potentials [3][4][5][6][7]. Amongst them, the hydrazones, a class of synthetic organic compounds, are being recognized due to their wide range of pharmacological benefits, including antimicrobial, anti-inflammatory, antifungal [8], anticancer, antioxidant, cardioprotective, antiprotozoal and many other activities [9][10][11]. These compounds possess an -HC=N-NH-bond, which is the active site [12], and further combining hydrazones with numerous functional groups leads to the formation of products with unique biological properties [13].
Hydrazones possesses some particular properties which make them a potential candidate for designing new moieties. They contain a C=N bond in conjugated form with a functional nitrogen electron pair. They are distinguished from other members of this class (imines, oximes) by the presence of two interlinked nitrogen atoms [14][15][16]. These nitrogen atoms are nucleophilic, while the carbon has both an electrophilic and nucleophilic nature and further combining hydrazones with numerous functional groups leads to the formation of products with unique biological properties [13,17].
Isoniazid is a first-line antitubercular drug and it acts by inhibiting enoyl reductase (InHA) in Mycobacterium Tuberculosis. This drug is a prodrug and needs to be activated by KatG catalase-peroxidase [18]. A number of hydrazone derivatives have been synthesized from isoniazid and were found to have potentiated activities against various bacterial and fungal strains [19], including hydrazones with benzohydrazide and menthone [11,18,20]. Furthermore, metal complexes of isonicotinic hydrazones including, copper, zinc, manganese, nickel showed enhanced activities against microbes, tumor and free radicals [21,22].
Hydrazones are usually synthesized by heating hydrazides with different aldehydes using solvents such as acetone, ethanol that can be easily confirmed from its spectral data [9]. Further, they can be used as an intermediate in Wolff Kishner reductions to reduce the carbonyl functionality of aldehyde and ketones into alkanes [23]. Based on the aforementioned literature, the current research project has been designed to synthesize new hydrazone derivatives of alkylated vanillin aldehyde and salicyl aldehyde with isonicotinic hydrazide, with the aim to achieve biologically active derivatives having potential antibacterial and cytotoxic properties. The structure of acylhydrazone is given below in Figure 1.
Melting points were determined on an Electrothermal 9100 melting point apparatus (Weiss-Gallenkamp, Loughborough, UK). The purity of the compounds was confirmed by Thin-Layer Chromatography (TLC) using Kieselgel 60 F 254 (Merck). EI-MS was performed on a JEOL JMS 600 mass spectrometer. 1 H-NMR Bruker signals appeared at 300 and 400 MHz in CH 3 OH-d 4 and that of 13 C-NMR at 75 MHz in CHCl 3 -d 4 . Fourier-transform infrared spectroscopy (FT-IR) spectra were obtained on a Shimadzu, IR Prestige-21 (Shimadzu, Tokyo, Japan).

General Procedure for the Synthesis of Isonicotinic Hydrazid-Based Hydrazone Derivatives
The synthesis of isoniazid-based hydrazones was accomplished in 2 steps (Figure 2). In the first step, each 4-hydroxy-3-methoxy-benzaldehyde (Vanillin)/4-hydroxybenzaldehyde was alkylated with 5mmol of bromo alkyl derivatives and 5 mmol of K 2 CO 3 in acetone as a solvent under reflux conditions. After completion of the reaction, the solvent was evaporated. The solid residue thus obtained was extracted three times with biphasic system of water and dichloromethane. The combined organic phase was evaporated over a rotary evaporator. The crude product was then subjected to column to obtain the desired product in a good yield. In the next step, 2 mmol of each alkoxy benzaldehyde derivative was reacted with 2 mmol of isoniazid in ethanol followed by the addition of a few drops of acetic acid. The reaction mixture was refluxed for 2.5 to 3 h and the progress of the reaction was observed via TLC. After the completion of the reaction, the precipitate was filtered, washed with cold distilled water and dried. The desired compound was further purified by washing it twice with 30% ethyl acetate: hexane. The products obtained were in excellent yields. The data are summarized in Table 1 and the compounds are shown as their code names (i.e., NH1-NH6).  evaporated. The solid residue thus obtained was extracted three times with biphasic system of water and dichloromethane. The combined organic phase was evaporated over a rotary evaporator. The crude product was then subjected to column to obtain the desired product in a good yield. In the next step, 2 mmol of each alkoxy benzaldehyde derivative was reacted with 2 mmol of isoniazid in ethanol followed by the addition of a few drops of acetic acid. The reaction mixture was refluxed for 2.5 to 3 h and the progress of the reaction was observed via TLC. After the completion of the reaction, the precipitate was filtered, washed with cold distilled water and dried. The desired compound was further purified by washing it twice with 30% ethyl acetate: hexane. The products obtained were in excellent yields. The data are summarized in Table 1 and the compounds are shown as their code names (i.e., NH1-NH6).  evaporated. The solid residue thus obtained was extracted three times with biphasic system of water and dichloromethane. The combined organic phase was evaporated over a rotary evaporator. The crude product was then subjected to column to obtain the desired product in a good yield. In the next step, 2 mmol of each alkoxy benzaldehyde derivative was reacted with 2 mmol of isoniazid in ethanol followed by the addition of a few drops of acetic acid. The reaction mixture was refluxed for 2.5 to 3 h and the progress of the reaction was observed via TLC. After the completion of the reaction, the precipitate was filtered, washed with cold distilled water and dried. The desired compound was further purified by washing it twice with 30% ethyl acetate: hexane. The products obtained were in excellent yields. The data are summarized in Table 1 and the compounds are shown as their code names (i.e., NH1-NH6).  evaporated. The solid residue thus obtained was extracted three times with biphasic system of water and dichloromethane. The combined organic phase was evaporated over a rotary evaporator. The crude product was then subjected to column to obtain the desired product in a good yield. In the next step, 2 mmol of each alkoxy benzaldehyde derivative was reacted with 2 mmol of isoniazid in ethanol followed by the addition of a few drops of acetic acid. The reaction mixture was refluxed for 2.5 to 3 h and the progress of the reaction was observed via TLC. After the completion of the reaction, the precipitate was filtered, washed with cold distilled water and dried. The desired compound was further purified by washing it twice with 30% ethyl acetate: hexane. The products obtained were in excellent yields. The data are summarized in Table 1 and the compounds are shown as their code names (i.e., NH1-NH6).  evaporated. The solid residue thus obtained was extracted three times with biphasic system of water and dichloromethane. The combined organic phase was evaporated over a rotary evaporator. The crude product was then subjected to column to obtain the desired product in a good yield. In the next step, 2 mmol of each alkoxy benzaldehyde derivative was reacted with 2 mmol of isoniazid in ethanol followed by the addition of a few drops of acetic acid. The reaction mixture was refluxed for 2.5 to 3 h and the progress of the reaction was observed via TLC. After the completion of the reaction, the precipitate was filtered, washed with cold distilled water and dried. The desired compound was further purified by washing it twice with 30% ethyl acetate: hexane. The products obtained were in excellent yields. The data are summarized in Table 1 and the compounds are shown as their code names (i.e., NH1-NH6).  evaporated. The solid residue thus obtained was extracted three times with biphasic system of water and dichloromethane. The combined organic phase was evaporated over a rotary evaporator. The crude product was then subjected to column to obtain the desired product in a good yield. In the next step, 2 mmol of each alkoxy benzaldehyde derivative was reacted with 2 mmol of isoniazid in ethanol followed by the addition of a few drops of acetic acid. The reaction mixture was refluxed for 2.5 to 3 h and the progress of the reaction was observed via TLC. After the completion of the reaction, the precipitate was filtered, washed with cold distilled water and dried. The desired compound was further purified by washing it twice with 30% ethyl acetate: hexane. The products obtained were in excellent yields. The data are summarized in Table 1 and the compounds are shown as their code names (i.e., NH1-NH6).

Antibacterial Activity 2.3.1. Bacterial Strains Used
All the synthesized compounds were screened for antibacterial activities using minimum inhibitory concentrations (MIC) and zone of inhibitions against Gram (+)and Gram (−) bacterial strains. ATCC strains of the test microorganism selected for antibacterial assay were Gram-positive bacteria; Staphylococcus aureus ATCC 25923, Bacillus subtilus ATCC 11774, and Gram-negative bacteria; Escherichia coli ATCC 10536. The bacterial strains' stock cultures were kept in Nutrient agar (Oxoid, UK) at 4 • C and inocula were prepared by transferring several single colonies of microbes to a sterile Mueller Hinton broth. The bacterial cell suspension was mixed until homogeneity to give a final density of 5 × 10 5 cfu/mL

Paper Disc Diffusion Method for Zone of Inhibition Assay
Preliminary screenings of synthesized compounds were conducted on agar plates using the disc diffusion method. The plates were prepared using Mueller-Hinton agar following the autoclave process (121 • C for 30 min). After cooling, the plates were inoculated with the suspension of microorganisms (S. aureus, B. subtilis and E. coli). The paper discs impregnated with the test compounds (1000 µg mL −1 in dimethyl sulfoxide) were placed on the solidified medium and incubated at 37 • C for 24 hours before recording the zone of inhibition in millimeters [24,25].

Microplate Assay of Minimum Inhibitory Concentration (MIC)
The minimum inhibitory concentrations of test microorganisms and reference material were determined using the tetrazolium microplate assay method [26]. The assay was performed using a 96-well clear microtiter plate. Freshly harvested bacterial cell and fungal cell suspensions were seeded at 5 × 10 5 cfu/mL in each well of the 96-well plate. Different concentrations, 500 to 10 µg/mL, of the test compounds were diluted in series with Muller-Hinton broth. A volume of 200 µL of each concentration was added in triplicate to the wells and the plates were then incubated for 18-24 h at 37 • C ± 0.5. After incubation, in each well, 50 µL of 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide MTT, having a concentration of 0.2 mg/mL, was added and the plate was incubated at 37 • C for 30 min. An appropriate solvent blank (DMSO) was included as the negative control and the bacterial suspension was included as the positive control. The absorbance was measured at 570 nm with a reference wavelength of 650 nm by adding DMSO using a spectrophotometer and the percentage reduction of the dye (indicating the bacterial growth inhibition) was calculated [27].

Morphological Changes Studied by Atomic Force Microscopy (AFM)
All the strains were grown on tryptic soya agar for 24 h at 37 • C. A volume of 10 µL of polylysine was added to the freshly cleaved mica slides and dried. A few drops of diluted culture, with a density of 10 5 cfu, was applied to these slides and dried at an ambient temperature, and they were subjected to atomic force microscopy (AFM) for morphological analysis. For test compounds, 5-10 µL of samples was taken from MIC wells and applied on polylysine slides, dried and subjected to AFM. The morphological changes with and without test compounds were recorded and compared.

Cytotoxicity
The cytotoxicities of synthesized hydrazones were recorded by employing an in vitro brine shrimp lethality bioassay technique [28]. The eggs of Artemia salina (brine shrimp) were allowed to incubate at 30 • C for 48 h under a light and dark cycle using artificial sea water before subjecting them to the sample solutions. The hatched larvae (nauplii) were collected with using a Pasteur pipette and were transferred to freshly prepared sea water (commercial salt and double-distilled water). The stock solutions of each compound were prepared at 500 µg/mL concentration in DMSO and sea water at 1:1, and further serial dilutions of 25, 50, 100, 200 and 300 µg/mL were prepared using sea water. Using a 2mL volume from each dilution, sea water containing 10 nauplii was added to a test tube and incubated for 24 h. A solvent mixture with nauplii containing no test compound was used as the control. After due time, the number of nauplii that survived was determined using a magnifying glass. The experiment was performed in triplicate and the median lethal concentration (LC 50 ) ± SEM was calculated using regression analysis.

Antibacterial Assay
The antibacterial sensitivities of test compounds were assayed using the paper disc diffusion method using Amikacin for comparison, as shown in Table 2. From the screening, it was concluded that compounds show varied responses against S. aureus, B. subtilis, and E. coli. Against the S. aureus compounds NH1 and NH5, optimum inhibitions of 24 mm and 22 mm, respectively, were found. Against B. subtilis, the compound NH5 showed a maximum inhibition of 25 mm, while NH3, NH4 and NH6 presented 23 mm zones of inhibition. In the case of E. coli, the compound NH3 was found to have a significant inhibitory effect of 33 mm, while the compounds NH1 and NH5 showed 25 mm and 24 mm zones of inhibition, respectively. In order to determine the MIC of synthesized compounds, ceftriaxone and amoxicillin were used as standards to compare antibacterial effects. Ceftriaxone was used against Staphylococcus aureus and Bacillus subtilis, while amoxicillin was used against Escherichia coli. The compounds were tested in a concentration range of 25-500 µg/mL and the percent inhibitions were recorded as mentioned in Table 3. Ceftriaxone showed a significant effect with an IC 50 of 50 µg/mL, inhibiting 55 ± 0.3% of S. aureus, and in the case of B. subtilis, the IC 50 was 50 µg/mL inhibiting 55 ± 0.7% of the population (Figures 3 and 4). Similarly, amoxicillin exhibited a significant effect against E. coli at IC 50 of 50µg/mL inhibiting 66 ± 0.5% of microbial growth, as shown in Figure 5.    The synthesized compounds also showed inhibition at various percentages. Among the synthesized compounds (NH1-NH6), the highest inhibitory effect was presented by NH3 against all bacterial strains. At a dose of 200 µg/mL, it inhibited the growth by 60 ± 1.5% of S. aureus, 53 ± 0.7% of B. subtilis and 65 ± 0.3 of E. coli, respectively, as mentioned in Tables 3-5

Morphological Observations Using Atomic Force Microscopy
To visualize the surface morphological changes in bacterial cultures, the atomic force microscopy was utilized. AFM has the capability to record the changes in biological samples without any damaging effect. The AFM images of normal bacterial cultures of S. aureus, B. subtilis and E. coli were taken as mentioned in Figures 3-5, respectively. Upon treatment with standard drugs, surface morphological changes were clearly visible.
The structural damages were significant as no clear cellular boundaries are visible. Similarly, in the case of newly synthesized compounds, the antimicrobial effect was obvious, as recorded by AFM. The irregular cellular shape, disoriented colonies and lack of clear boundaries signify the antimicrobial efficacies of these compounds.

Cytotoxic Activities
The cytotoxic activities were assessed using brine shrimp lethality assay. The LC 50 obtained for synthesized compounds are presented in Figure 6. The LC 50 observed for the test compounds were between 162.5 (NH6) and 240 (NH3) µg/mL, indicating their toxic nature as per Meyer's and Clarkson toxicity scale their LC 50 is below 1000µg/mL. Since the brine shrimp lethality test has a strong correlation with cytotoxicity in human cancer cells, it can be used for the screening of anticancer potential. However, due to its lower sensitivity to distinguish between strong, moderate and weak effects, more delicate procedures are required for testing on human cancer cell lines [29].

Discussion
This study reports the synthesis of vanillinaldehyde and salicylaldehyde hydrazones with isoniazid employing azomethine linkage. The detailed principal peaks are given for each compound. The FTIR spectral analysis supported the presence of the characteristic functional groups present in the synthesized compound. The presence of peaks at naldehyde and salicylaldehyde hydrazones . The detailed principal peaks are given for upported the presence of the characteristic compound. The presence of peaks at ῡ = of an imine linkage (C=N) in all the com-NH6. The existence of the ester functional ined with the appearance of peaks at ῡ = 4.42 cm −1 were assigned to (N-H) in all the rated at ῡ = 1112.43-1163.08 cm −1 and amide = 1639.49-1745.10 cm −1 for all compounds C-H) peak appeared at around 2926.01 to l shifts (δ, ppm) of 1.04 to 5.46 are assigned of the series, from NH1 to NH6, which are 3.91, 3.91 and 3.93 ppm are assigned to the H1, respectively. The resonance peaks bewere assigned to the azomethine (−CH=N-) m are assigned to the aromatic protons. In four key resonance signals were observed. H=N-) and the terminal alkyl groups in all from δ 10.49 to 133.11. The carbonyl carbon -168.08 and carbonyl carbon of ester linkage respectively. The signals of −OCH3 carbon d NH5 resonates at δ 56.62, 56.75 and 57.19, h benzene and pyridine rings in all six com-112 to 152. These spectroscopic data conrazones mentioned above. The λ max (nm) d according to their UV-Vis spectra are in ded that the synthesized compounds were ntial due to their antibacterial and cytotoxic nds, NH3 was found to have promising and to have high cytotoxicity behavior. Studncer activity using human cancer cell lines se. These hydrazones can be further modiation of other biological properties.  These spectroscopic data conrazones mentioned above. The λ max (nm) d according to their UV-Vis spectra are in ded that the synthesized compounds were ntial due to their antibacterial and cytotoxic nds, NH3 was found to have promising and to have high cytotoxicity behavior. Studncer activity using human cancer cell lines se. These hydrazones can be further modiation of other biological properties.  H-NMR signals at chemical shifts (δ, ppm) of 1.04 to 5.46 are assigned yl chain in each of these compounds of the series, from NH1 to NH6, which are o the aromatic ring. The signals at δ 3.91, 3.91 and 3.93 ppm are assigned to the OCH3 protons of NH3, NH5 and NH1, respectively. The resonance peaks be-6 ppm and 8.29 ppm in the spectra were assigned to the azomethine (−CH=N-) ydrazones. Signals at δ 6.97-8.94 ppm are assigned to the aromatic protons. In MR spectra of all these hydrazones, four key resonance signals were observed. δ 143.19-144.02 for azomethine (−CH=N-) and the terminal alkyl groups in all ds, NH1-NH6, appeared in the range from δ 10.49 to 133.11. The carbonyl carbon l group roughly appeared at δ 164.08-168.08 and carbonyl carbon of ester linkage nd NH2 resonates at δ 167.7-168.7, respectively. The signals of −OCH3 carbon o the aromatic ring of NH1, NH3 and NH5 resonates at δ 56.62, 56.75 and 57.19, ly. Peaks of aromatic carbons of both benzene and pyridine rings in all six comhowing chemical shifts δ range from 112 to 152. These spectroscopic data cone successful syntheses of the six hydrazones mentioned above. The λ max (nm) these six hydrazones were calculated according to their UV-Vis spectra are in range of 320 to 330 nm.
sions esults obtained in this study concluded that the synthesized compounds were ields and exhibited appreciable potential due to their antibacterial and cytotoxic s. Amongst the synthesized compounds, NH3 was found to have promising anl properties, while NH6 was observed to have high cytotoxicity behavior. Studbe undertaken to assess their anticancer activity using human cancer cell lines their true potential for therapeutic use. These hydrazones can be further modietal coordination for further investigation of other biological properties. . The 1 H-NMR signals at chemical shifts (δ, ppm) of 1.04 to 5.46 are assigned to side alkyl chain in each of these compounds of the series, from NH1 to NH6, which are adjacent to the aromatic ring. The signals at δ 3.91, 3.91 and 3.93 ppm are assigned to the aromatic-OCH3 protons of NH3, NH5 and NH1, respectively. The resonance peaks between 8.26 ppm and 8.29 ppm in the spectra were assigned to the azomethine (−CH=N-) of these hydrazones. Signals at δ 6.97-8.94 ppm are assigned to the aromatic protons. In the 13CNMR spectra of all these hydrazones, four key resonance signals were observed. These are δ 143.19-144.02 for azomethine (−CH=N-) and the terminal alkyl groups in all compounds, NH1-NH6, appeared in the range from δ 10.49 to 133.11. The carbonyl carbon of the acyl group roughly appeared at δ 164.08-168.08 and carbonyl carbon of ester linkage of NH1 and NH2 resonates at δ 167.7-168.7, respectively. The signals of −OCH3 carbon adjacent to the aromatic ring of NH1, NH3 and NH5 resonates at δ 56.62, 56.75 and 57.19, respectively. Peaks of aromatic carbons of both benzene and pyridine rings in all six compounds showing chemical shifts δ range from 112 to 152. These spectroscopic data confirmed the successful syntheses of the six hydrazones mentioned above. The λ max (nm) values of these six hydrazones were calculated according to their UV-Vis spectra are in the λmax range of 320 to 330 nm.

Conclusions
The results obtained in this study concluded that the synthesized compounds were of good yields and exhibited appreciable potential due to their antibacterial and cytotoxic properties. Amongst the synthesized compounds, NH3 was found to have promising antibacterial properties, while NH6 was observed to have high cytotoxicity behavior. Studies should be undertaken to assess their anticancer activity using human cancer cell lines to reveal their true potential for therapeutic use. These hydrazones can be further modified for metal coordination for further investigation of other biological properties.  . The 1 H-NMR signals at chemical shifts (δ, ppm) of 1.04 to 5.46 are assigned to side alkyl chain in each of these compounds of the series, from NH1 to NH6, which are adjacent to the aromatic ring. The signals at δ 3.91, 3.91 and 3.93 ppm are assigned to the aromatic-OCH3 protons of NH3, NH5 and NH1, respectively. The resonance peaks between 8.26 ppm and 8.29 ppm in the spectra were assigned to the azomethine (−CH=N-) of these hydrazones. Signals at δ 6.97-8.94 ppm are assigned to the aromatic protons. In the 13CNMR spectra of all these hydrazones, four key resonance signals were observed. These are δ 143.19-144.02 for azomethine (−CH=N-) and the terminal alkyl groups in all compounds, NH1-NH6, appeared in the range from δ 10.49 to 133.11. The carbonyl carbon of the acyl group roughly appeared at δ 164.08-168.08 and carbonyl carbon of ester linkage of NH1 and NH2 resonates at δ 167.7-168.7, respectively. The signals of −OCH3 carbon adjacent to the aromatic ring of NH1, NH3 and NH5 resonates at δ 56.62, 56.75 and 57.19, respectively. Peaks of aromatic carbons of both benzene and pyridine rings in all six compounds showing chemical shifts δ range from 112 to 152. These spectroscopic data confirmed the successful syntheses of the six hydrazones mentioned above. The λ max (nm) values of these six hydrazones were calculated according to their UV-Vis spectra are in the λmax range of 320 to 330 nm.

Conclusions
The results obtained in this study concluded that the synthesized compounds were of good yields and exhibited appreciable potential due to their antibacterial and cytotoxic properties. Amongst the synthesized compounds, NH3 was found to have promising antibacterial properties, while NH6 was observed to have high cytotoxicity behavior. Studies should be undertaken to assess their anticancer activity using human cancer cell lines to reveal their true potential for therapeutic use. These hydrazones can be further modified for metal coordination for further investigation of other biological properties. = 1639.49-1745.10 cm −1 for all compounds of the series. The presence of an aromatic (C-H) peak appeared at around 2926.01 to 2975.26 cm −1 . The 1 H-NMR signals at chemical shifts (δ, ppm) of 1.04 to 5.46 are assigned to side alkyl chain in each of these compounds of the series, from NH1 to NH6, which are adjacent to the aromatic ring. The signals at δ 3.91, 3.91 and 3.93 ppm are assigned to the aromatic-OCH 3 protons of NH3, NH5 and NH1, respectively. The resonance peaks between 8.26 ppm and 8.29 ppm in the spectra were assigned to the azomethine (−CH=N-) of these hydrazones. Signals at δ 6.97-8.94 ppm are assigned to the aromatic protons. In the 13CNMR spectra of all these hydrazones, four key resonance signals were observed. These are δ 143.19-144.02 for azomethine (−CH=N-) and the terminal alkyl groups in all compounds, NH1-NH6, appeared in the range from δ 10.49 to 133.11. The carbonyl carbon of the acyl group roughly appeared at δ 164.08-168.08 and carbonyl carbon of ester linkage of NH1 and NH2 resonates at δ 167.7-168.7, respectively. The signals of −OCH 3 carbon adjacent to the aromatic ring of NH1, NH3 and NH5 resonates at δ 56.62, 56.75 and 57.19, respectively. Peaks of aromatic carbons of both benzene and pyridine rings in all six compounds showing chemical shifts δ range from 112 to 152. These spectroscopic data confirmed the successful syntheses of the six hydrazones mentioned above. The λ max (nm) values of these six hydrazones were calculated according to their UV-Vis spectra are in the λ max range of 320 to 330 nm.

Conclusions
The results obtained in this study concluded that the synthesized compounds were of good yields and exhibited appreciable potential due to their antibacterial and cytotoxic properties. Amongst the synthesized compounds, NH3 was found to have promising antibacterial properties, while NH6 was observed to have high cytotoxicity behavior. Studies should be undertaken to assess their anticancer activity using human cancer cell lines to reveal their true potential for therapeutic use. These hydrazones can be further modified for metal coordination for further investigation of other biological properties.

Acknowledgments:
The authors wish to thanks researcher support project number (RSP-2021/110) at King Saud University Riyadh Saudi Arabia for financial support.

Conflicts of Interest:
The authors declare no conflict of interest.