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Current Bioactive Compounds

Editor-in-Chief

ISSN (Print): 1573-4072
ISSN (Online): 1875-6646

Research Article

Design and Synthesis of 2-Substituted Benzothiazole Derivatives as Antioxidant and Antimicrobial Agents

Author(s): Ravi K. Nishad, Karuna S. Shukla and Pooja A. Chawla*

Volume 16, Issue 8, 2020

Page: [1242 - 1248] Pages: 7

DOI: 10.2174/1573407216666200128160438

Price: $65

Abstract

Background: An upsurge in the number of antibiotic-resistant microbial infections has warranted the discovery and development of new antibiotics. This is a matter of great concern for effective therapy for a search of novel antimicrobial agents. Literature has a number of reports of involvement of oxidative stress due to an imbalance between the generation and neutralization of free radicals in many diseases. Heterocyclic compounds have been involved in the treatment of various disorders. Benzothiazole is one such heterocyclic nucleus having benzene ring merged with the thiazole ring. Among the various substitutions possible in this nucleus, substitutions at position-2 have already been reported with potential bioactivities. Thus, different substituted compounds have been synthesized which could serve as antimicrobials and antioxidants.

Methods: Benzothiazole derivatives (B1-B7) were synthesized by two-step reactions and the structures were confirmed through infrared, mass and NMR spectroscopy. The compounds were evaluated for in vitro antioxidant and antimicrobial activities using standard methods.

Results: The results of antibacterial and antifungal activity showed that compound B4 exhibited maximum activity against all the tested strains of microorganisms with the zone of inhibition 17.1-18.5 mm and MIC value 1.1-1.5 μg/mL. Compound B5 exhibited potent antioxidant activity.

Conclusion: The compounds substituted with halogen on the aryl ring showed increased antimicrobial activity as seen in the case of compound B4 (6-fluoro). The compounds substituted with a hydroxyl group (B5) exhibited good antioxidant activity.

Keywords: Benzothiazole, heterocycles, antioxidant, microorganism, antimicrobial, spectrometer.

Graphical Abstract
[1]
Saeed, S.; Rashid, N.; Jones, P.G.; Ali, M.; Hussain, R. Synthesis, characterization and biological evaluation of some thiourea derivatives bearing benzothiazole moiety as potential antimicrobial and anticancer agents. Eur. J. Med. Chem., 2010, 45(4), 1323-1331.
[http://dx.doi.org/10.1016/j.ejmech.2009.12.016] [PMID: 20056520]
[2]
Jian, H.; Fenglian, Ge.; Wang, Z.; Wen, W. One-pot synthesis of 2-trifluoromethyl and 2-difluoromethyl substituted benzo-1,3-diazoles. Tetrahedron Lett., 2007, 48, 3251-3254.
[http://dx.doi.org/10.1016/j.tetlet.2007.03.015]
[3]
Huang, S.T.; Hsei, I.J.; Chen, C. Synthesis and anticancer evaluation of bis(benzimidazoles), bis(benzoxazoles), and benzothiazoles. Bioorg. Med. Chem., 2006, 14(17), 6106-6119.
[http://dx.doi.org/10.1016/j.bmc.2006.05.007] [PMID: 16714116]
[4]
Palmer, P.J.; Trigg, R.B.; Warrington, J.V. Benzothiazolines as antituberculous agents. J. Med. Chem., 1971, 14(3), 248-251.
[http://dx.doi.org/10.1021/jm00285a022] [PMID: 4994696]
[5]
Burger, A.; Sawhney, S.N. Antimalarials. 3. Benzothiazole amino alcohols. J. Med. Chem., 1968, 11(2), 270-273.
[http://dx.doi.org/10.1021/jm00308a018] [PMID: 5654216]
[6]
Siddiqui, N.; Pandeya, S.N.; Khan, S.A.; Stables, J.; Rana, A.; Alam, M.; Arshad, M.F.; Bhat, M.A. Synthesis and anticonvulsant activity of sulfonamide derivatives-hydrophobic domain. Bioorg. Med. Chem. Lett., 2007, 17(1), 255-259.
[http://dx.doi.org/10.1016/j.bmcl.2006.09.053] [PMID: 17046248]
[7]
Suresh, C.H.; Rao, J.V.; Jayaveera, K.N.; Subudhi, S.K. Synthesis and anthelmintic activity of 3-(2-hydrozino benzothiazole)-substituted indole-2-one. Int. J. Pharm., 2013, 2, 257-261.
[8]
Siddiqui, N.; Alam, M.; Siddiqui, A.A. Synthesis and analgesic activity of some 2-[4-(alkyl thioureido) phenyl sulphonamido]-6-substituted benzothiazoles. Asian J. Chem., 2004, 16, 1005-1008.
[9]
Gurupadayya, B.M.; Gopal, M.; Padmashali, B.; Vaidya, V.P. Synthesis and bological activities of fuorobenzothiazoles. Indian J. Heterocycl. Chem., 2005, 15, 169-172.
[10]
Singh, S.P.; Segal, S. Study of fungicidal activities of some benzothiazoles. Indian J. Chem., 1988, 27B, 941-943.
[11]
Gupta, A. Synthesis of C-6 methyl substituted benzothiazole derivatives and antifungal activity against Aspergillus niger. Ther. Res. Skin. Dis., 2018, 1(2), 36-40.
[http://dx.doi.org/10.32474/TRSD.2018.01.000106]
[12]
Singh, Y.; Kaur, B.; Kaur, A.; Gupta, V.K.; Gupta, M. Synthesis, spectral studies and biological activity of 2, 3-disubstituted imidazo [2, 1-b] benzothiazole derivatives. Indian J. Pharm. Biol. Res., 2018, 6, 1-8.
[13]
Capobianco, J.O.; Cao, Z.; Shortridge, V.D.; Ma, Z.; Flamm, R.K.; Zhong, P. Studies of the novel ketolide ABT-773: transport, binding to ribosomes and inhibition of protein synthesis in Streptococcus pneumoniae. Antimicrob. Agents Chemother., 2000, 44, 1562-1567.
[14]
Shukla, K.S.; Pandey, S.; Chawla, P. Synthesis of some 5-(substituted benzylidene-2, 4-dioxothiazolidin-3-yl) benzoic acid derivatives by conventional and microwave-assisted methods and evaluation of their potential as antimicrobial agents. Anti. Inf. Agents, 2019, 17(2), 115-129.
[http://dx.doi.org/10.2174/2211352516666181024151213]
[15]
Fang, J.; Seki, T.; Maeda, H. Therapeutic strategies by modulating oxygen stress in cancer and inflammation. Adv. Drug Deliv. Rev., 2009, 61(4), 290-302.
[http://dx.doi.org/10.1016/j.addr.2009.02.005] [PMID: 19249331]
[16]
ndian Pharmacopoeia. Controller of Publication: Delhi, A-100, Vol II (P-Z), 1996.
[17]
Tortora, G.J.; Funke, B.R.; Case, C.L. Microbiology- An Introduction, 8th ed; Pearson Education Pvt, Ltd.: Singapore, 2009, pp. 588-617.
[18]
Hugo, W.B.; Russell, A.D. Pharmaceutical Microbiology, 6th ed; Blackwell science Ltd., 1998, pp. 243-245.
[19]
Koppireddi, S.; Komsani, J.R.; Avula, S.; Pombala, S.; Vasamsetti, S.; Kotamraju, S.; Yadla, R. Novel 2-(2,4-dioxo-1,3-thiazolidin-5-yl)acetamides as antioxidant and/or anti-inflammatory compounds. Eur. J. Med. Chem., 2013, 66, 305-313.
[http://dx.doi.org/10.1016/j.ejmech.2013.06.005] [PMID: 23811092]
[20]
Mishra, G.; Sachan, N.; Chawla, P. Synthesis and evaluation of thiazolidinedione-coumarin adducts as antidiabetic, anti-inflammatory and antioxidant agents. Lett. Org. Chem., 2015, 12, 429-445.
[http://dx.doi.org/10.2174/1570178612666150424235603]
[21]
Song, E.Y.; Kaur, N.; Park, M.Y.; Jin, Y.; Lee, K.; Kim, G.; Lee, K.Y.; Yang, J.S.; Shin, J.H.; Nam, K.Y.; No, K.T.; Han, G. Synthesis of amide and urea derivatives of benzothiazole as Raf-1 inhibitor. Eur. J. Med. Chem., 2008, 43(7), 1519-1524.
[http://dx.doi.org/10.1016/j.ejmech.2007.10.008] [PMID: 18023932]
[22]
Kalsi, P.S. Spectroscopy of Organic Compound; New Age International: Delhi, India, 2004.
[23]
Pavia, D.L.; Lampman, G.M.; Kriz, G.S. Introduction to Spectroscopy; Cengage Learning: Boston, 2008.

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