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| REVIEW ARTICLE |
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| Year : 2014 | Volume
: 6
| Issue : 2 | Page : 69-80 |
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A review exploring biological activities of hydrazones
Garima Verma, Akranth Marella, Mohammad Shaquiquzzaman, Mymoona Akhtar, Mohammad Rahmat Ali, Mohammad Mumtaz Alam
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Jamia Hamdard, New Delhi, India
| Date of Submission | 18-Jul-2013 |
| Date of Decision | 14-Oct-2013 |
| Date of Acceptance | 31-Oct-2013 |
| Date of Web Publication | 20-Mar-2014 |
Correspondence Address:
Mohammad Mumtaz Alam
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Jamia Hamdard, New Delhi
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0975-7406.129170
 Abstract | | |
The development of novel compounds, hydrazones has shown that they possess a wide variety of biological activities viz. antimicrobial, anticonvulsant, antidepressant, anti-inflammatory, analgesic, antiplatelet, antimalarial, anticancer, antifungal, antitubercular, antiviral, cardio protective etc., Hydrazones/azomethines/imines possess-NHN = CH- and constitute an important class of compounds for new drug development. A number of researchers have synthesized and evaluated the biological activities of hydrazones. This review aims at highlighting the diverse biological activities of hydrazones. Keywords: Azomethine, biological activity, hydrazones
How to cite this article:
Verma G, Marella A, Shaquiquzzaman M, Akhtar M, Ali MR, Alam MM. A review exploring biological activities of hydrazones. J Pharm Bioall Sci 2014;6:69-80 |
How to cite this URL:
Verma G, Marella A, Shaquiquzzaman M, Akhtar M, Ali MR, Alam MM. A review exploring biological activities of hydrazones. J Pharm Bioall Sci [serial online] 2014 [cited 2022 Nov 30];6:69-80. Available from: https://www.jpbsonline.org/text.asp?2014/6/2/69/129170 |
Hydrazones, related to ketones and aldehydes belong to a class of organic compounds with the structure, R 1 R 2 C = NNH 2 [1] These compounds possess diverse biological and pharmacological properties such as antimicrobial, anti-inflammatory, analgesic, antifungal, anti-tubercular, antiviral, anticancer, antiplatelet, antimalarial, anticonvulsant, cardio protective, antihelmintic, antiprotozoal, [2] anti-trypanosomal, [3] antischistosomiasis etc. [4] These compounds contain C = N bond, which is conjugated with a lone pair of electrons of the functional nitrogen atom. [5] The nitrogen atoms of the hydrazones are nucleophilic and the carbon atom has both electrophilic and nucleophilic nature. [6] The α-hydrogen of hydrazones is more potent than that of acidic ketones.[7] The combination of hydrazones with other functional group leads to compounds with unique physical and chemical character.[8] Owing to their biological and pharmacological properties, they are considered important for the synthesis of heterocyclic compounds. [9]
| Biological Activity | |  |
Antimicrobial activity
The emerging bacterial resistance causes a widespread problem for the treatment of various infections. Therefore, the search for antimicrobials is a never-ending task. Now-a-days a number of hydrazone derivatives have been developed and evaluated for their antibacterial activity. Aslan et al., [10] investigated the antibacterial activity of sulfonyl derivatives (1). Certain steroidal hydrazines (2, 3) have been synthesized by Khan [11] which possess in-vitro antibacterial activity. Hydrazones bearing imidazoles (4) have been synthesized and screened for antibacterial activity against numerous bacterial strains by Abdel-Wahab et al.[12] Palekar et al., [13] synthesized different thiazolidinone derivatives (5, 6) using hydrazine hydrate and evaluated them for their in-vitro antibacterial activity. Wang et al., [14] synthesized hydrazone derivatives (7) with significant antibacterial activity. Hydrazone derivatives containing transition metal complex (8) were synthesized and evaluated for antimicrobial activity by Babahan et al.[15] Ozkay et al., [16] synthesized novel benzimidazole derivatives bearing hydrazone moiety (9) with antibacterial activity against different bacterial strains. Khalil et al., [17] synthesized hydrazone derivatives (10) and reported them as potential antibacterial agent. Hydrazone derivatives (11) synthesized by Abdel-Aziz and Mekawey [18] exhibited antibacterial activity with minimum inhibitory concentration (MIC) of 75 μg/mL. Good antibacterial activity of hydrazone derivatives (12) was reported by Bawa et al.[19] Hydrazone derivatives (13), synthesized by Sharma et al., [20] exhibited antibacterial activity against various bacterial strains. Antibacterial activity of certain hydrazone derivatives (14) was reported by Kendall et al.[21] Jubie et al. [22] synthesized hydrazone derivatives (15, 16) and reported them as promising antibacterial agents. Govindasami et al. [23] synthesized and evaluated vanillin related hydrazone derivatives for their antibacterial activity. Compounds 17 and 18 exhibited good activity.
Tuberculosis is a chronic, infectious and most prevalent disease all over the world. It is caused by different strains of the Mycobacterium tuberculosis. Lungs, liver and bones are most susceptible to infection. The activity of the newer agents is mostly tested against virulent H37Rv strain. Kamal et al., [24] synthesized nitroheterocyclic based 1, 2, 4-benzothiadizines (19), which exhibited MIC of 1 μg/mL. Raja et al., [25] synthesized hydrazone derivatives (20) and reported to have MIC of 6.25 μg/mL. Telvekar et al., [26] developed benzofuran-3-carbohydrazide derivatives (21) with good anti-tubercular activity. Hydrazone derivatives (22) synthesized by Gemma et al., [27] exhibited MIC of 6.25 μg/mL. Mahajan et al., [28] synthesized ferrocene-based hydrazone derivatives (23) with significant antitubercular activity. 1H-indole-2,3-dione based hydrazones (24), synthesized by Karali et al., [29] exhibited half maximal inhibitory concentration (IC 50 ) of 7.6 μg/mL. Hydrazones (25), synthesized by Eswaran et al., [30] exhibited a MIC of 6.25 μg/mL. Hydrazones (26, 27) synthesized by Imramovský et al., [31] based on isonicotinoylhydrazide, pyrazinamide, p-aminosalicylic acid, ethambutol, and ciprofloxacin exhibited MIC of 0.78 μg/mL and 3.13 μg/mL respectively. Hearn et al., [32] synthesized anti-tubercular agents (28, 29) which showed MIC of 0.06 μg/mL and 0.20 μg/mL respectively. Nayyar and Jain [33] synthesized disubstituted quinolone based hydrazides (30, 31) with good activity profiles. Turan-Zitouni et al., [34] synthesized thiazolyl hydrazones (32) having anti-tubercular activity with MIC of 2.5 μg/mL. 4-(adamantan-1-yl)-2-substituted quinoline based hydrazones (33) synthesized by Nayyar et al., [35] showed MIC of 1.00 μg/mL. Imramovský et al., [31] synthesized isonicotinyl derivatives (34) with a MIC of 3.13 μg/mL.
Fungal infections are generally observed as superficial or systemic infections in humans, animals as well as plants. The development of antifungal agents has surpassed the development of antibacterials. Secci et al., [36] developed novel Hydrazine derivative (35) and evaluated for in-vitro anti-Candidal activity which exhibited MIC of 0.25 μg/mL. Novel hydrazine thiazole derivatives (36) have been synthesized by Maillard et al., [37] and reported to exhibit anti-Candidal activity with MIC of 0.25 μg/mL. Altintop et al., [38] developed, evaluated novel hydrazone derivatives (37) for in-vitro anti-Candidal activity, and reported to have MIC of 0.05 μg/mL. Hydrazide derivatives (38) synthesized by Telvekar et al., [26] exhibited MIC of <15.62 μg/mL. Chimenti et al.[39] synthesized 2-thiazolylhydrazones (39) and reported to have potential activity against various strains of Candida species. Kocyigit-Kaymakcioglu et al. synthesized and evaluated the antifungal activity of various 3-acetyl-2,5-disubstituted-2,3-dihydro-1, 3, 4-oxadiazoles. Out of these, 4-Fluorobenzoic acid ([5-bromothiophen-2-yl] methylene) hydrazide (40) exhibited highest inhibitory activity against Candida albicans, with MIC value of 125 μg/mL. [40]
Virus is a small infectious agent, which can replicate only inside the living cell of an organism. It infects all types of organisms-humans, animals as well as plants. El-Sabbagh and Rady [41] evaluated the antiviral activity of hydrazone derivatives (41) against hepatitis A virus. Tian et al., [42] synthesized hydrazone derivatives (42, 43) as potential targets of human immunodeficiency virus-1 capsid protein. The half maximal effective concentration (EC 50 ) value of the agents was reported to be 0.21 and 0.17 μM respectively [Figure 1].
Analgesic and anti-inflammatory activity
A number of hydrazone derivatives have been developed to overcome gastrointestinal disturbance and toxicity. Mohamed Eissa et al., [43] developed anthranilic acid derivatives (44) and reported to have significant anti-inflammatory activity. Hydrazones containing 5-methyl-2 benzoxazolinones (45), developed by Salgin-Gökşen et al., [44] were reported to exhibit good analgesic and anti-inflammatory activity. Khan et al., [45] have described the anti-inflammatory activity of hydrazones derivatives of quinoxalinone (46). Rajitha et al., [46] have reported good anti-inflammatory activity of aryl hydrazone derivatives (47). Benzylidene hydrazides (48) with prominent analgesic and anti-inflammatory activity, exhibiting percentage inhibition of 68.66 have been synthesized by Bhandari et al. [47] Gökçe et al., [48] reported the analgesic and anti-inflammatory activity of 6-substituted-3 (2H)-pyridazinone-2-acetyl-2-(p-substituted benzal) hydrazone derivatives (49). Moldovan et al., [49] synthesized various hydrazone derivatives (50) with promising in-vivo anti-inflammatory activity. Kümmerle et al., [50] developed N-acylhydrazone derivatives (51, 52) with ED 50 value of 2.3 and 1.6 mg/kg respectively [Figure 2]. | Figure 2: Structure of hydrazones reported as analgesic and anti-inflammatory agents
Click here to view |
Anticancer activity
World Health Organization defines cancer as the rapid creation of abnormal cells that grow beyond their usual boundaries and which can invade adjoining parts of the body and spread to other organs. Dandawate et al., [51] developed plumbagin hydrazone derivatives (53) with high activity against breast cancer. Mohareb and Al-Omran [52] synthesized cyanoacetyl hydrazone with pregnanolone derivatives (54) active against multiple cancer cell lines. Aydın et al., [53] synthesized and evaluated flurbiprofen hydrazide derivatives (55) against ovarian and leukemia cancer cell lines. Cui et al., [54] synthesized acylhydrazones (56) and reported to have potent activity against the human promyelocytic leukemic cells (Hl-60). Al-Said et al., [55] synthesized certain compounds (57) and reported to have in-vitro anticancer activity against human breast cancer cell lines MCF7. Liu et al., [56] synthesized, evaluated acetyl hydrazone derivatives (58) for antitumor activity against A549, HCT11b, HepG2, PC-9 and A375 cell lines with an IC 50 value of 4-17 μM. Aryl hydrazone derivatives (59) synthesized by Vogel et al., [57] were reported to have an IC 50 of 6.7 nM against MDA-MB 231 and MCF-7 breast cancer cell lines. Xu et al., [58] screened hydrazone derivatives (60) for kinase inhibition in different cell lines. Benites et al., [59] synthesized hydrazone derivatives (61) and reported them to have significant antiproliferative activity. Hydrazone derivatives reported by Hayakawa et al., [60] (62, 63, 64) exhibited marked PI3 kinase p110 α inhibition. Zheng et al., [61] synthesized hydrazone derivatives (65) with the propensity to act against A549 lung cancer cell lines. Xia et al., [62] synthesized various hydrazones (66) with IC 50 value of 3.33 μM against A549 lung cancer cell lines. Gürsoy et al., [63] reported the anticancer activity of thiazolohydrazides (67) against prostate cancer. Despaigne et al., [64] have described acetylpyridine and benzoylpyridine derived hydrazones (68, 69) as agents against brain tumor [Figure 3].
Central nervous system (CNS) activity
CNS diseases can affect either brain or the spinal cord resulting in psychological and neurological disorder. Hydrazones are reported to have activity against various disorders of CNS. Salgin-Gökşen et al., [65] synthesized benzylidene hydrazone derivatives (70) and screened them for in-vitro monoamine oxidase inhibitory (MAO-B) activity for Parkinson's disease. Novel 2-Methoxy acyl hydrazone derivatives (71) synthesized by Cutshall et al., [66] were evaluated for inhibition of phosphodiasterase 10A (PDE10A), a PDE responsible for neurological and psychological disorders like schizophrenia. Certain anticonvulsant bishydrazones (72) and hydrazones (73) were developed by Kulandasamy et al.[67] de Oliveira et al., [68] synthesized and evaluated the antidepressant activity of hydrazones (74). Gökhan-Kelekçi et al., [69] synthesized hydrazone derivatives (75, 76), reported their selective MAO-B inhibition and hence useful in the treatment of depression [Figure 4].
Antiprotozoal activity
Protozoa are a diverse group of unicellular eukaryotic organisms affecting human beings, especially in tropical countries. Aryl hydrazone derivatives (77) synthesized by Siddiqui et al., [70] have been evaluated against HM1: IMSS strain of Entamoebica histolytica for anti-amoebic activity and reported to have IC 50 0.13 μM. Gerpe et al., [71] described the anti-Trypanosomal activity of 5-nitrofuran hydrazones (78). Caputto et al., [72] synthesized hydrazine derivatives (79) and reported to have activity against Trypanosoma cruzi (T. cruzi). Carvalho et al., [73] synthesized Cinamic N-acyl hydrazones (80) with good anti-Trypanosomal activity. dos Santos Filho et al., [74] synthesized hydrazone derivatives (81, 82) against T. cruzi. Trypanosomicidal activity of hydrazones (83, 84) has been reported by Porcal et al. [75] Hydrazone derivatives (85) developed by de Aquino et al., [76] have been reported to be useful in infections caused by Toxoplasma gondii. Caputto et al., [77] reported the inhibitory activity of hydrazones (86, 87) against cruzipain-a major cysteine protease of T. cruzi.
Malaria is a widespread infectious disease specifically of the tropics caused by Plasmodium. Antimalarial propensity of hydrazines (88) has been reported by Fattorusso et al.[78] against D10, W2 and 3D7 plasmodial strains with an IC 50 value of 39.2, 79.0 and 11.0 nM respectively. Acharya et al., [79] synthesized hydrazide derivatives (89) with an IC 50 of 160 nM/mL as against 280 nM/mL of the reference chloroquine [Figure 5].
Cardio protective activity
Cardiovascular disease is a class of diseases that involve the heart and blood vessels. Despite the extensive research, it still remains the major cause of mortalities world-wide. Bi et al., [80] reported hydrazone derivatives (90) to have potent activity against ischemia-reperfusion induced cardiac infarct size. Leal, et al., [81] synthesized acylhydrazone derivative (91) and reported to have high anti-hypertensive activity.
Antiplatelet activity
Antiplatelet drugs are the agents which decrease platelet aggregation and inhibit thrombus formation. Mashayekhi et al., [82] demonstrated the antiplatelet activity of hydrazone derivatives (92) containing indole moiety. Hydrazone derivatives (93, 94) synthesized by Lima et al., [83] were reported to inhibit platelet aggregation induced by collagen and thrombin [Figure 6]. | Figure 6: Structure of hydrazones reported as cardioprotective and antiplatelet agents
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| Conclusion | | |
The present review highlights the use of hydrazones as lead for the development of newer compounds. Biological activities of hydrazones include antibacterial, anticonvulsant, analgesic, anti-inflammatory, cardio protective, antiplatelet, anticancer etc., With proper designing, synthesis and structure activity relationship, a number of compounds can be developed with diverse biological activities.
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[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6]
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N
,
N
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N
-Dialkylhydrazones as Versatile Umpolung Reagents in Enantioselective Anion-Binding Catalysis
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Synthesis, Molecular Modeling, and Evaluation of Novel Sulfonylhydrazones as Acetylcholinesterase Inhibitors for Alzheimerćs Disease |
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Synthesis and evaluation of antioxidant phenolic diaryl hydrazones as potent antiangiogenic agents in atherosclerosis |
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Quinoline based mono- and bis-(thio)carbohydrazones: synthesis, anticancer activity in 2D and 3D cancer and cancer stem cell models |
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A versatile salicyl hydrazonic ligand and its metal complexes as antiviral agents |
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Synthesis and antifungal activity of substituted salicylaldehyde hydrazones, hydrazides and sulfohydrazides |
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