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Medicinal Chemistry

Editor-in-Chief

ISSN (Print): 1573-4064
ISSN (Online): 1875-6638

Research Article

Synthesis, Molecular Docking and In Vivo Biological Evaluation of Iminostilbene Linked 1,2,3-Triazole Pharmacophores as Promising Anti- Anxiety and Anti-Inflammatory Agents

Author(s): Kariyappa N. Ankali, Javarappa Rangaswamy, Mallappa Shalavadi and Nagaraja Naik*

Volume 18, Issue 2, 2022

Published on: 29 July, 2021

Page: [260 - 272] Pages: 13

DOI: 10.2174/1573406417666210608141746

Price: $65

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Abstract

Background: Iminostilbene and 1,2,3-triazole ring containing compounds are considered as beneficial substrates in drug design.

Objectives: This study was aimed at the synthesis of novel series of iminostilbene linked 1,2,3- triazole pharmacophores (7c-n) by Cu(I) catalyzed 1,3 dipolar cycloaddition reaction between 5- (Prop-2-yn-1-yl)-5H-dibenzo[b,f]azepine (7b) and various substituted azidobenzene derivatives (3cn).

Methods: The chemical structures of compounds were confirmed by 1H NMR, 13C NMR, LC-MS and molecular docking studies were carried out through HEX docking software.

Results: The in vivo anti anxiety capacity of the compounds was evaluated by using “elevated plus maze” (EPM), anxiety model. The results exhibited that compounds (7d, 7e, 7j and 7k) have a higher anti anxiety effect close to diazepam. The anti-inflammatory activities of the synthesized compounds were evaluated by “Carrageenan-induced rat paw edema” model, compounds (7b, 7c, 7d, 7f, and 7j) demonstrated statistically significant inflammatory activity. Molecular docking analysis revealed that compounds (7d, 7e and 7j) bound to GABA(A) proteins show more efficiency when compared to the other analogues in the series.

Conclusion: These results suggest that compounds (7b, 7c, 7d, 7e, 7f, and 7j) can be considered as novel candidates for anti-anxiety and anti-inflammatory agents. Moreover, docking method was used to elucidate anti-anxiety effect of compounds. This study furnished insight into the molecular interactions of synthesized compounds with their physiological targets, and the potential to develop bioactive heterocyclic compounds.

Keywords: Iminostilbene, 1, 2, 3-triazole, click chemistry, anti-anxiety, anti-inflammatory, molecular docking.

Graphical Abstract
[1]
Jung, Y.H.; Ha, R.R.; Kwon, S.H.; Hong, S.I.; Lee, K.H.; Kim, S.Y.; Lee, S.Y.; Jang, C.G. Anxiolytic effects of Julibroside C1 isolated from Albizzia julibrissin in mice. Prog. Neuropsychopharmacol. Biol. Psychiatry, 2013, 44, 184-192.
[http://dx.doi.org/10.1016/j.pnpbp.2013.02.012] [PMID: 23481219]
[2]
The Diagnostic and Statistical Manual of Mental Disorders, 5th ed; American Psychiatric Association: Washington, DC, 2013.
[3]
Xiping, Z.; Dongxiao, S.W.; Qian, T.; Wenzhi, L.; Danyang, S.; Chun, C. The enhanced serotonin (5-HT) synthesis and anti-oxidative roles of Trp oligopeptide in combating anxious depression C57BL/6 mice. J. Funct. Foods, 2020, 67103859
[http://dx.doi.org/10.1016/j.jff.2020.103859]
[4]
Kunovac, J.L.; Stahl, S.M. Future directions in anxiolytic pharmacotherapy. Psychiatr. Clin. North Am., 1995, 18(4), 895-909.
[http://dx.doi.org/10.1016/S0193-953X(18)30030-3] [PMID: 8748388]
[5]
Abdullatif, A.; Ahmad, N.; Abed, N. A Anti-Inflammatory activity of natural products. Molecules, 2016, 21(10), 1321-1340.
[6]
Hiller, K.O.; Hodd, P.L.; Willson, R.L. Antiinflammatory drugs: protection of a bacterial virus as an in vitro biological measure of free radical activity. Chem. Biol. Interact., 1983, 47(3), 293-305.
[http://dx.doi.org/10.1016/0009-2797(83)90165-5] [PMID: 6317211]
[7]
Csetenyi, J.; Baker, K.M.; Frigerio, A.; Morselli, P.L. Iminostilbene--a metabolite of carbamazepine isolated from rat urine. J. Pharm. Pharmacol., 1973, 25(4), 340-341.
[http://dx.doi.org/10.1111/j.2042-7158.1973.tb10021.x] [PMID: 4146691]
[8]
LeDuc, B. Foye’s Principles of Medicinal Chemistry.6th ed.; Lemke, T.L.; Williams, D.A., Eds.; Lippincott Williams & Wilkins: Philadelphia, PA, 2007, p. 521;
[9]
Protiva, M. The place of dibenzo[b,f ]thiepin derivatives in medicinal chemistry: Structures and activities. J. Heterocycl. Chem., 1996, 33, 497-521.
[http://dx.doi.org/10.1002/jhet.5570330301]
[10]
Ueda, I.; Sato, Y.; Maeno, S.; Umio, S. Synthesis and pharmacological properties of 8-chloro-10-(2-dimethylaminoethoxy)dibenzo[b,f]thiepin and related compounds. Neurotropic and psychotropic agents. III. Chem. Pharm. Bull. (Tokyo), 1978, 26(10), 3058-3070.
[http://dx.doi.org/10.1248/cpb.26.3058] [PMID: 31984]
[11]
Kaushik, C.P.; Sangwan, J.; Luxmi, R.; Kumar, K. Pahwa. A. Synthetic routes for 1,4-disubstituted 1,2,3-triazoles: A review. Curr. Org. Chem., 2019, 23(8), 860-900.
[http://dx.doi.org/10.2174/1385272823666190514074146]
[12]
Zhi, Xu. 1,2,3-Triazole-containing hybrids with potential antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA). Eur. J. Med. Chem., 2020.
[13]
Wamhoff, H. 1,2,3-Triazoles and their benzo derivatives comprehensive heterocyclic chemistry.Oxford: Pergamon Press; , 1984, 5, pp. 670-732;
[14]
Kumar, H.V.; Kumar, C.K.; Naik, N. Synthesis of novel 3-chloro-1-(5H- dibenz[b,f]azepine-5yl) propan-1-one derivatives with antioxidant activity. Med. Chem. Res., 2011, 20, 101-108.
[http://dx.doi.org/10.1007/s00044-009-9292-7]
[15]
Vijay Kumar, H.; Naik, N. Synthesis and antioxidant properties of some novel 5H-dibenz[b,f]azepine derivatives in different in vitro model systems. Eur. J. Med. Chem., 2010, 45(1), 2-10.
[http://dx.doi.org/10.1016/j.ejmech.2009.09.016] [PMID: 19846240]
[16]
Rangaswamy, J.; Kumar, H.V.; Harini, S.T.; Naik, N. Synthesis of benzofuran based 1,3,5-substituted pyrazole derivatives: as a new class of potent antioxidants and antimicrobials--a novel accost to amend biocompatibility. Bioorg. Med. Chem. Lett., 2012, 22(14), 4773-4777.
[http://dx.doi.org/10.1016/j.bmcl.2012.05.061] [PMID: 22695127]
[17]
Harini, S.T.; Kumar, H.V.; Rangaswamy, J.; Naik, N. Synthesis, antioxidant and antimicrobial activity of novel vanillin derived piperidin-4-one oxime esters: preponderant role of the phenyl ester substituents on the piperidin-4-one oxime core. Bioorg. Med. Chem. Lett., 2012, 22(24), 7588-7592.
[http://dx.doi.org/10.1016/j.bmcl.2012.10.019] [PMID: 23116886]
[18]
Wuest, F.; Tang, X.; Kniess, T.; Pietzsch, J.; Suresh, M. Synthesis and cyclooxygenase inhibition of various (aryl-1,2,3-triazole-1-yl)-methanesulfonylphenyl derivatives. Bioorg. Med. Chem., 2009, 17(3), 1146-1151.
[http://dx.doi.org/10.1016/j.bmc.2008.12.032] [PMID: 19157881]
[19]
Brognini, G. J. Chem. Research,, 1993, 1263-1278.
[20]
Khan, M.A.; Saleem, A.; Ghouri, N.; Hameed, A.; Choudhary, M.I.; Basha, Z.F. Synthesis and in vitro evaluation of dibenzoazepine triazole derivatives: A novel class of antileishmanial agents. Lett. Drug Des. Discov., 2015, 12, 597-606.
[http://dx.doi.org/10.2174/1570180812999150225111959]
[21]
Abdoh, M.M.M.; Madan Kumar, S.; Vinay Kumar, K.S.; Manjunath, B.C.; Sadashiva, M.P.; Lokanath, K.N. 5-(Prop-2-yn-1-yl)-5H-dibenzo[b,f]azepine: orthorhombic polymorph. Acta Crystallogr., 2013, E69, o17.
[22]
Yousuf, S.; Khan, M.; Fazal, S.; Butt, M. Basha F. Z. 5-(Prop-2-ynyl)-5H- dibenzo[b,f]azepine. Acta Crystallogr., 2012, E68, o1101.
[23]
Ashwini, N.; Garg, M.; Mohan, C.D.; Fuchs, J.E.; Rangappa, S.; Anusha, S.; Swaroop, T.R.; Rakesh, K.S.; Kanojia, D.; Madan, V.; Bender, A.; Koeffler, H.P. Basappa; Rangappa, K.S. Synthesis of 1,2-benzisoxazole tethered 1,2,3-triazoles that exhibit anticancer activity in acute myeloid leukemia cell lines by inhibiting histone deacetylases, and inducing p21 and tubulin acetylation. Bioorg. Med. Chem., 2015, 23(18), 6157-6165.
[http://dx.doi.org/10.1016/j.bmc.2015.07.069] [PMID: 26299825]
[24]
Sharma, V.; Gilhotra, R.; Dhingra, D.; Gilhotra, N. Possible underlying influence of p38MAPK and NF-κB in the diminished anti-anxiety effect of diazepam in stressed mice. J. Pharmacol. Sci., 2011, 116(3), 257-263.
[http://dx.doi.org/10.1254/jphs.11026FP] [PMID: 21720097]
[25]
Pellow, S.; Chopin, P.; File, S.E.; Briley, M. Validation of open:closed arm entries in an elevated plus-maze as a measure of anxiety in the rat. J. Neurosci. Methods, 1985, 14(3), 149-167.
[http://dx.doi.org/10.1016/0165-0270(85)90031-7] [PMID: 2864480]
[26]
Morris, C.J. Carrageenan-induced paw edema in the rat and mouse. Methods Mol. Biol., 2003, 225, 115-121.
[http://dx.doi.org/10.1385/1-59259-374-7:115] [PMID: 12769480]
[27]
Ritchie, D.W. Evaluation of protein docking predictions using Hex 3.1 in CAPRI rounds 1 and 2. Proteins, 2003, 52(1), 98-106.
[http://dx.doi.org/10.1002/prot.10379] [PMID: 12784374]
[28]
Rangaswamy, J.; Vijay Kumar, H.; Harini, S.T.; Naik, N. Synthesis of novel benzofuran gathered C-2,4,6-substituted pyrimidine derivatives conjugated by sulfonyl chlorides: as a new series of potent antioxidants and antimicrobials drug candidate. J. Heterocycl. Chem., 2014, 52, 1349-1360.
[http://dx.doi.org/10.1002/jhet.2209]
[29]
Rangaswamy, J.; Vijay Kumar, H.; Harini, S.T.; Naik, N. An easy access to benzofurans via DBU induced condensation reaction of active 2-hydroxy acetophenones with phenacyl chlorides: A novel class of antioxidant agents. J. Heterocycl. Chem., 2015, 52, 938-943.
[http://dx.doi.org/10.1002/jhet.1971]
[30]
Charlier, C.; Michaux, C. Dual inhibition of cyclooxygenase-2 (COX-2) and 5-lipoxygenase (5-LOX) as a new strategy to provide safer non-steroidal anti-inflammatory drugs. Eur. J. Med. Chem., 2003, 38(7-8), 645-659.
[http://dx.doi.org/10.1016/S0223-5234(03)00115-6] [PMID: 12932896]

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