Copyright (c) 2024 Ketan Vashisht, Pooja Sethi, Anshul Bansal, Hardeep Singh Tuli, Ammar Abdulrahman Jairoun, Moyad Shahwan, Seema Ramniwas, Ritu Chauhan
This work is licensed under a Creative Commons Attribution 4.0 International License.
Path of Pyrazoles from Synthetic Factors to Anti-inflammatory Potential: A Review
Corresponding Author(s) : Pooja Sethi
Asian Journal of Chemistry,
Vol. 36 No. 6 (2024): Vol 36 Issue 6, 2024
Abstract
Pyrazoles, a class of heterocyclic compounds, have garnered considerable attention in drug development due to their intriguing properties, particularly those containing a pyrazole moiety. Pyrazole, a pivotal chemical in the creation of potent bioactive agents, encompasses five heterocyclic members. The discovery of certain pyrazole compounds exhibiting robust biological activities has spurred interest in this field of inquiry. Heterocyclic compounds incorporating nitrogen and its derivatives have historically served as crucial sources of medicinal compounds. Given that the heterocyclic group constitutes a vast reservoir of organic molecules, its significance in both theoretical and applied chemistry has grown significantly. Extensive literature indicates that researchers have employed diverse synthetic strategies in recent years to produce substituted pyrazole derivatives with promising biological potential as anti-HIV, anti-inflammatory, antitumor and antimicrobial agents. Inflammation, a multifaceted biological response essential for the body’s defense mechanisms, can also contribute to various pathological conditions when dysregulated. Understanding the underlying molecular mechanisms offers a foundation for targeted interventions against inflammatory disorders. These insights fuel ongoing endeavors to discover effective and innovative anti-inflammatory agents with potential therapeutic applications. This review delves into the synthesis and characterization of various pyrazole derivatives, emphasizing structural modifications influencing their anti-inflammatory efficacy. The insights provided herein are invaluable for the rational design and synthesis of novel anti-inflammatory agents. Furthermore, the review concludes with a discussion on future perspectives, underscoring the imperative for further research to optimize the therapeutic potential of pyrazole derivatives as anti-inflammatory agents.
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- M.H. Helal, S.A. El-Awdan, M.A. Salem, T.A. Abd-Elaziz, Y.A. Moahamed, A.A. El-Sherif and G.A.M. Mohamed, Spectrochim. Acta A Mol. Biomol. Spectrosc., 135, 764 (2015); https://doi.org/10.1016/j.saa.2014.06.145
- A.-G.E. Amr and M.M. Abdulla, Bioorg. Med. Chem., 14, 4341 (2006); https://doi.org/10.1016/j.bmc.2006.02.045
- Y.A. Ammar, E.A. Fayed, A.H. Bayoumi, M.A. Saleh and M.E. El-Araby, Am. J. PharmTech. Res., 5, 245 (2015).
- S.M. Sondhi, N. Singh, M. Johar and A. Kumar, Bioorg. Med. Chem., 13, 6158 (2005); https://doi.org/10.1016/j.bmc.2005.06.063
- A.P. Keche, G.D. Hatnapure, R.H. Tale, A.H. Rodge, S.S. Birajdar and V.M. Kamble, Bioorg. Med. Chem. Lett., 22, 3445 (2012); https://doi.org/10.1016/j.bmcl.2012.03.092
- B. Tozkoparan, M. Ertan, P. Kelicen and R. Demirdamar, Farmaco, 54, 588 (1999); https://doi.org/10.1016/S0014-827X(99)00068-3
- R.S.M. Bafail and W.A. Samman, Trop. J. Pharm. Res., 23, 67 (2024); https://doi.org/10.4314/tjpr.v23i1.9
- A.Y.A. Alzahrani, W.S. Shehab, A.H. Amer, M.G. Assy, S.M. Mouneir, M.A. Aziz and A.M. Abdel Hamid, RSC Adv., 14, 995 (2024); https://doi.org/10.1039/D3RA07078F
- A.M.R. Raauf, T.N.-A. Omar, M.F. Mahdi and H.R. Fadhil, Nat. Prod. Res., 38, 253 (2024); https://doi.org/10.1080/14786419.2022.2117174
- R. Surendra Kumar, I.A. Arif, A. Ahamed and A. Idhayadhulla, Saudi J. Biol. Sci., 23, 614 (2016); https://doi.org/10.1016/j.sjbs.2015.07.005
- D. Vasudha, A. Jagadeesh, S.N. Mali, R.R. Bhandare and A.B. Shaik, Chem. Phys. Impact, 8, 100500 (2024); https://doi.org/10.1016/j.chphi.2024.100500
- N.A. Khalil, M. Eman, E.M. Ahmed and H.B.E. Nassan, Med. Chem. Res., 22, 1021 (2013); https://doi.org/10.1007/s00044-012-0098-7
- C.S. Yadav, I. Azad, A.R. Khan, M. Nasibullah, N. Ahmad, D. Hansda, S.N. Ali, K. Shrivastav, M. Akil and M.B. Lohani, Results Chem., 7, 101326 (2024); https://doi.org/10.1016/j.rechem.2024.101326
- M.H.M. Helal, M.A. Salem, M.S.A. El-Gaby and M. Aljahdali, Eur. J. Med. Chem., 65, 517 (2013); https://doi.org/10.1016/j.ejmech.2013.04.005
- V. Kamat, R. Santosh, B. Poojary, S.P. Nayak, M. Sankaranarayanan, B.K. Kumar, S. Faheem, S. Khanapure, D.A. Barretto and S.K. Vootla, ACS Omega, 5, 25228 (2020); https://doi.org/10.1021/acsomega.0c03386
- F.A. Hassan, Int. J. Appl. Sci. Technol., 2, 180 (2012).
- D.M. Sirsat, P.S. Bhale, H.V. Chavan, S.M. Karape and M.T. Bachute, Rasayan J. Chem., 13, 1589 (2020); https://doi.org/10.31788/RJC.2020.1335768
- A.A. Marzouk, E.S. Taher, M.Sh.A. Shaykoon, P. Lan, W.H. Abd-Allah, A.M. Aboregela and M.F. El-Behairy, Bioorg. Chem., 111, 104883 (2021); https://doi.org/10.1016/j.bioorg.2021.104883
- A. Shaabani, M.T. Nazeri and R. Afshari, Mol. Divers., 23, 751 (2019); https://doi.org/10.1007/s11030-018-9902-8
- D. Dewangan, T. Kumar, A. Alexander, K. Nagori and D.K. Tripathi, Curr. Pharma Res., 1, 369 (2011); https://doi.org/10.33786/JCPR.2011.v01i04.010
- M. Govindaraju, B.N. Mylarappa and K.A. Kumar, Int. J. Pharm. Pharm. Sci., 5, 734 (2013).
- F. Giornal, S. Pazenok, L. Rodefeld, N. Lui, J.-P. Vors and F.R. Leroux, J. Fluor. Chem., 152, 2 (2013); https://doi.org/10.1016/j.jfluchem.2012.11.008
- S. Sun, L. Chen, J. Huo, Y. Wang, S. Kou, S. Yuan, Y. Fu and J. Zhang, J. Agric. Food Chem., 70, 3447 (2022); https://doi.org/10.1021/acs.jafc.2c00092
- D. Huang, F. Liu, S. Wen, Y. Wang, W. Fang, Z. Zhang and S. Ke, Phytochem. Lett., 59, 117 (2024); https://doi.org/10.1016/j.phytol.2024.01.006
- D. Huang, M. Huang, W. Liu, A. Liu, X. Liu, X. Chen, H. Pei, J. Sun, D. Yin and X. Wang, Chem. Pap., 71, 2053 (2017); https://doi.org/10.1007/s11696-017-0198-4
- D. Xia, X. Cheng, X. Liu, C. Zhang, Y. Wang, Q. Liu, Q. Zeng, N. Huang, Y. Cheng and X. Lv, J. Agric. Food Chem., 69, 8358 (2021); https://doi.org/10.1021/acs.jafc.1c01189
- Z.-Q. Long, L.-L. Yang, J.-R. Zhang, S.-T. Liu, Jiao Xie, P.-Y. Wang, J.-J. Zhu, W.-B. Shao, L.-W. Liu and S. Yang, J. Agric. Food Chem., 69, 8380 (2021); https://doi.org/10.1021/acs.jafc.1c02460
- G.M. Nitulescu, G. Stancov, O.C. Seremet, G. Nitulescu, D.P. Mihai, C.G. Duta-Bratu, S.F. Barbuceanu and O.T. Olaru, Molecules, 28, 5359 (2023); https://doi.org/10.3390/molecules28145359
- G. Li, Y. Cheng, C. Han, C. Song, N. Huang and Y. Du, RSC Med. Chem., 13, 1300 (2022); https://doi.org/10.1039/D2MD00206J
- F.K. Keter and J. Darkwa, Biometals, 25, 9 (2012); https://doi.org/10.1007/s10534-011-9496-4
- M. Ahmadi, S. Bekeschus, K.-D. Weltmann, T. von Woedtke and K. Wende, RSC Med. Chem., 13, 471 (2022); https://doi.org/10.1039/D1MD00280E
- E.M. Gedawy, A.E. Kassab and A.M. El Kerdawy, Eur. J. Med. Chem., 189, 112066 (2020); https://doi.org/10.1016/j.ejmech.2020.112066
- L.S. Pavase, D.V. Mane and K.G. Baheti, J. Heterocycl. Chem., 55, 913 (2018); https://doi.org/10.1002/jhet.3118
- A.L. Franks and J.E. Slansky, Anticancer Res., 32, 1119 (2012).
- G. Kollias, E. Douni, G. Kassiotis and D. Kontoyiannis, Ann. Rheum. Dis., 58, i32 (1999); https://doi.org/10.1136/ard.58.2008.i32
- D. Laveti, M. Kumar, R. Hemalatha, R. Sistla, V.G.M. Naidu, V. Talla, V. Verma, N. Kaur and R. Nagpal, Inflamm. Allergy Drug Targets, 12, 349 (2013); https://doi.org/10.2174/18715281113129990053
- E. Kadusevicius, Int. J. Mol. Sci., 22, 6637 (2021); https://doi.org/10.3390/ijms22126637
- J.K. Gierse, J.J. McDonald, S.D. Hauser, S.H. Rangwala, C.M. Koboldt and K. Seibert, J. Biol. Chem., 271, 15810 (1996); https://doi.org/10.1074/jbc.271.26.15810
- R. Sohail, M. Mathew, K.K. Patel, S.A. Reddy, Z. Haider, M. Naria, A. Habib, Z.U. Abdin, W.R. Chaudhry and A. Akbar, Cureus, 15, e37080 (2023); https://doi.org/10.7759/cureus.37080
- Y. Lee, C. Rodriguez and R. Dionne, Curr. Pharm. Des., 11, 1737 (2005); https://doi.org/10.2174/1381612053764896
- G. Dannhardt and W. Kiefer, Eur. J. Med. Chem., 36, 109 (2001); https://doi.org/10.1016/S0223-5234(01)01197-7
- V. Sharma, P. Bhatia, O. Alam, M. Javed Naim, F. Nawaz, A. Ahmad Sheikh and M. Jha, Bioorg. Chem., 89, 103007 (2019); https://doi.org/10.1016/j.bioorg.2019.103007
- S. Sanghi, E.J. MacLaughlin, C.W. Jewell, S. Chaffer, P.J. Naus, L.E. Watson and D.E. Dostal, Cardiovasc. Hematol. Disord. Drug Targets, 6, 83 (2006); https://doi.org/10.2174/187152906777441803
- S. Grosch, T.J. Maier, S. Schiffmann and G. Geisslinger, J. Natl. Cancer Inst., 98, 736 (2006); https://doi.org/10.1093/jnci/djj206
- F.S. Lehmann and C. Beglinger, Curr. Top. Med. Chem., 5, 449 (2005); https://doi.org/10.2174/1568026054201703
- P. Rao and E.E. Knaus, J. Pharm. Pharm. Sci., 11, 81s (2008); https://doi.org/10.18433/J3T886
- G. Kaur and O. Silakari, Bioorg. Chem., 80, 24 (2018); https://doi.org/10.1016/j.bioorg.2018.05.014
- P. Sethi, R. Khare and R. Choudhary, Asian J. Chem., 32, 2594 (2020); https://doi.org/10.14233/ajchem.2020.22813
- P. Sethi, P. Dogra, G.K. Gupta, S. Mostafa and S. Kaur, Res. J. Chem. Environ., 22, 73 (2018).
- A. Kumar, K.K. Bhagat, A.K. Singh, H. Singh, T. Angre, A. Verma, H. Khalilullah, M. Jaremko, A.-H. Emwas and P. Kumar, RSC Adv., 13, 6872 (2023); https://doi.org/10.1039/D3RA00056G
- M.A. Ragab, W.M. Eldehna, A. Nocentini, A. Bonardi, H.E. Okda, B. Elgendy, T.S. Ibrahim, M.M. Abd-Alhaseeb, P. Gratteri, C.T. Supuran, A.A. Al-Karmalawy and M. Elagawany, Eur. J. Med. Chem., 250, 115180 (2023); https://doi.org/10.1016/j.ejmech.2023.115180
- M.M.M. El-Miligy, A.K. Al-Kubeisi, M.G. Bekhit, S.R. El-Zemity, R.A. Nassra and A.A. Hazzaa, J. Enzyme Inhib. Med. Chem., 38, 294 (2023); https://doi.org/10.1080/14756366.2022.2147164
- S.S. Dhotre, G.T. Pawar, R.P. Pawar and S.R. Vaidya, Research Square, (2023).
- K. Vashisht, P. Sethi, P. Mishra and A. Bansal, Res. J. Chem. Environ., 26, 184 (2022); https://doi.org/10.25303/2610rjce1840198
- K. Mehta, M. Khambete, A. Abhyankar and A. Omri, Pharmaceuticals, 16, 377 (2023); https://doi.org/10.3390/ph16030377
- M. Lusardi, A. Spallarossa and C. Brullo, Int. J. Mol. Sci., 24, 7834 (2023); https://doi.org/10.3390/ijms24097834
- M.M. Fouad, The Utility of Thiocarbohydrazide for Generating Novel Triazole and Pyrazole Derivatives Containing a Sulfur Moiety as Anti-microbial Agents, ChemRxiv., (2023); https://doi.org/10.26434/chemrxiv-2023-9b6v1
- R. Matta, J. Pochampally, B.N. Dhoddi, S. Bhookya, S. Bitla and A.G. Akkiraju, BMC Chem., 17, 61 (2023); https://doi.org/10.1186/s13065-023-00965-8
- B. Kurban, B.N. Saðlýk, D. Osmaniye, S. Levent, Y. Özkay and Z.A. Kaplancýklý, ACS Omega, 8, 31500 (2023); https://doi.org/10.1021/acsomega.3c04635
- X. Gu and S. Ma, Anticancer. Agents Med. Chem., 22, 1643 (2022); https://doi.org/10.2174/1871520621666210901102832
- Y. Kong, S. Liu, S. Wang, B. Yang, W. He, H. Li, S. Yang, G. Wang and C. Dong, Sci. Rep., 13, 7756 (2023); https://doi.org/10.1038/s41598-023-33403-9
- M. Bonesi, M.R. Loizzo, G.A. Statti, S. Michel, F. Tillequin and F. Menichini, Bioorg. Med. Chem. Lett., 20, 1990 (2010); https://doi.org/10.1016/j.bmcl.2010.01.113
- S. Kantevari, D. Addla, P.K. Bagul, B. Sridhar and S.K. Banerjee, Bioorg. Med. Chem., 19, 4772 (2011); https://doi.org/10.1016/j.bmc.2011.06.085
- H. Ye and I.C. Shaw, Food Chem. Toxicol., 129, 328 (2019); https://doi.org/10.1016/j.fct.2019.04.008
- H. Yuseran, E. Hartoyo, T. Nurseta and H. Kalim, Clin. Nutr. Open Sci., 35, 77 (2021); https://doi.org/10.1016/j.yclnex.2020.10.001
- M. Kumar, Z. Abbas, P. Siwach, J. Sharma, A. Rani, S. Sharma, P. Aggarwal, P. Show, S. Haque, V.K. Garg and H.S. Tuli, J. Adv. Biotechnol. Exp. Ther., 6, 386 (2023); https://doi.org/10.5455/jabet.2023.d134
- M. Song, B. Liu, S. Yu, S. He, Y. Liang, S. Li, Q. Chen and X. Deng, Lett. Drug Design Discov., 17, 502 (2020); https://doi.org/10.2174/1570180816666190731113441
- M.A. Abdelgawad, M.B. Labib and M. Abdel-Latif, Bioorg. Chem., 74, 212 (2017); https://doi.org/10.1016/j.bioorg.2017.08.014
- R. Ayman, M.S. Abusaif, A.M. Radwan, A.M. Elmetwally and A. Ragab, Eur. J. Med. Chem., 249, 115138 (2023); https://doi.org/10.1016/j.ejmech.2023.115138
- A. Masih, A.K. Agnihotri, K. Srivastava, N. Pandey, H.R. Bhat and U.P. Singh, J. Biochem. Mol. Toxicol., 35, e22656 (2021); https://doi.org/10.1002/jbt.22656
- T. Akaishi and K. Abe, Eur. J. Pharmacol., 819, 190 (2018); https://doi.org/10.1016/j.ejphar.2017.12.008
- Y. Fu, J. Ma, X. Shi, X.-Y. Song, Y. Yang, S. Xiao, J. Li, W.-J. Gu, Z. Huang, J. Zhang and J. Chen, Biochem. Pharmacol., 135, 126 (2017); https://doi.org/10.1016/j.bcp.2017.03.013
- M. Law, J.L. Morales, L.F. Mottram, A. Iyer, B.R. Peterson and A. August, Int. J. Biochem. Cell Biol., 43, 1228 (2011); https://doi.org/10.1016/j.biocel.2011.04.016
- J. Ishikawa, K. Ohga, T. Yoshino, R. Takezawa, A. Ichikawa, H. Kubota and T. Yamada, J. Immunol., 170, 4441 (2003); https://doi.org/10.4049/jimmunol.170.9.4441
- N.R. Trindade, P.R. Lopes, L.M. Naves, J.O. Fajemiroye, P.H. Alves, N.O. Amaral, L.M. Liao, A.C.S. Rebelo, C.H. Castro, V.A. Braga, R. Menegatti and G.R. Pedrino, Front. Physiol., 9, 1073 (2018); https://doi.org/10.3389/fphys.2018.01073
- L. de Oliveira, I.F. Florentino, D.P. Silva, F. Pazini, F.S. de Carvalho, G. Sanz, B.G. Vaz, F.F. da Rocha, J.O. Fajemiroye, P.C. Ghedini, L.M. Lião, R. Menegatti, E.A. Costa and T.S. de Oliveira, Can. J. Physiol. Pharmacol., 101, 216 (2023); https://doi.org/10.1139/cjpp-2022-0428
- S.M. Haghighi, M. Fathalipour, A. Purkhosrow, S. Oftadehgan, M. Abbasi, A. Khalafi-Nezhad and E. Sattarinezhad, Trends Pharm. Sci., 9, 105 (2023); https://doi.org/10.30476/TIPS.2023.98280.1185
- F.E. Silverstein, G. Faich, J.L. Goldstein, L.S. Simon, T. Pincus, A. Whelton, R. Makuch, G. Eisen, N.M. Agrawal, W.F. Stenson, A.M. Burr, W.W. Zhao, J.D. Kent, J.B. Lefkowith, K.M. Verburg and G.S. Geis, JAMA, 284, 1247 (2000); https://doi.org/10.1001/jama.284.10.1247
- N.H. Amin, M.T. El-Saadi, A.A. Hefny, A.H. Abdelazeem, H.A. Elshemy and K.R. Abdellatif, Future Med. Chem., 10, 2521 (2018); https://doi.org/10.4155/fmc-2018-0224
- K.F. Croom and M.A. Siddiqui, Drugs, 69, 1513 (2009); https://doi.org/10.2165/00003495-200969110-00008
- Y. Yin, C.-J. Chen, R.-N. Yu, L. Shu, T.-T. Zhang and D.-Y. Zhang, Bioorg. Med. Chem., 27, 1562 (2019); https://doi.org/10.1016/j.bmc.2019.02.054
- G.J. Southan, D. Gauld, A. Lubeskie, B. Zingarelli, S. Cuzzocrea, A.L. Salzman, C. Szabó and D.J. Wolff, Biochem. Pharmacol., 54, 409 (1997); https://doi.org/10.1016/S0006-2952(97)00196-2
- P.P. Kattimani, R.R. Kamble, A.R. Nesaragi, M.Y. Kariduraganavar, S.D. Joshi, S.S. Dodamani and S.S. Jalalpure, Synth. Commun., 51, 3125 (2021); https://doi.org/10.1080/00397911.2021.1964530
- Y.-R. Li, C. Li, J.-C. Liu, M. Guo, T.-Y. Zhang, L.-P. Sun, C.-J. Zheng and H.-R. Piao, Bioorg. Med. Chem. Lett., 25, 5052 (2015); https://doi.org/10.1016/j.bmcl.2015.10.028
- S. Hussain and D. Kaushik, J. Saudi Chem. Soc., 19, 274 (2015); https://doi.org/10.1016/j.jscs.2012.04.002
- K.R.A. Abdellatif, M.A. Abdelgawad, M.B. Labib and T.H. Zidan, Bioorg. Med. Chem. Lett., 25, 5787 (2015); https://doi.org/10.1016/j.bmcl.2015.10.047
- P. Khloya, S. Kumar, P. Kaushik, P. Surain, D. Kaushik and P.K. Sharma, Bioorg. Med. Chem. Lett., 25, 1177 (2015); https://doi.org/10.1016/j.bmcl.2015.02.004
- K.R.A. Abdellatif, M.A. Abdelgawad, H.A.H. Elshemy, S.S.R. Alsayed and G. Kamel, Arch. Pharm. Res., 38, 1932 (2015); https://doi.org/10.1007/s12272-015-0606-7
- R. Sribalan, G. Banuppriya, M. Kirubavathi, A. Jayachitra and V. Padmini, Bioorg. Med. Chem. Lett., 26, 5624 (2016); https://doi.org/10.1016/j.bmcl.2016.10.075
- S.N. Thore, S.V. Gupta and K.G. Baheti, J. Saudi Chem. Soc., 20, 259 (2016); https://doi.org/10.1016/j.jscs.2012.06.011
- L.Z. Chen, W.W. Sun, L. Bo, J.Q. Wang, C. Xiu, W.J. Tang, J.B. Shi, H.P. Zhou and X.H. Liu, Eur. J. Med. Chem., 138, 170 (2017); https://doi.org/10.1016/j.ejmech.2017.06.044
- M.A. Bhat, A.F. Ahmed, Z.-H. Wen, M.A. Al-Omar and H.A. Abdel-Aziz, Med. Chem. Res., 26, 1557 (2017); https://doi.org/10.1007/s00044-017-1870-5
- M.N. Kumbar, R.R. Kamble, J.P. Dasappa, P.K. Bayannavar, H.A. Khamees, M. Mahendra, S.D. Joshi, S. Dodamani, V.P. Rasal and S. Jalalpure, J. Mol. Struct., 1160, 63 (2018); https://doi.org/10.1016/j.molstruc.2018.01.047
- R.C. Kulkarni, J.M. Madar, S.L. Shastri, F. Shaikh, N.S. Naik, R.B. Chougale, L.A. Shastri, S.D. Joshi, S.R. Dixit and V.A. Sunagar, Chem. Data Coll., 17-18, 497 (2018); https://doi.org/10.1016/j.cdc.2018.11.004
- M.F. El Shehry, E.F. Ewies and E.M. Zayed, Russ. J. Gen. Chem., 89, 492 (2019); https://doi.org/10.1134/S1070363219030216
- G.S. Hassan, D.E. Abdel Rahman, E.A. Abdelmajeed, R.H. Refaey, M. Alaraby Salem and Y.M. Nissan, Eur. J. Med. Chem., 171, 332 (2019); https://doi.org/10.1016/j.ejmech.2019.03.052
- G. Mustafa, A. Angeli, M. Zia-ur-Rehman, N. Akbar, S. Ishtiaq and C.T. Supuran, Bioorg. Chem., 91, 103110 (2019); https://doi.org/10.1016/j.bioorg.2019.103110
- P.S. Bhale, B.P. Bandgar, S.B. Dongare, S.N. Shringare, D.M. Sirsat and H.V. Chavan, Phosphorus Sulfur Silicon Rel. Elem., 194, 843 (2019); https://doi.org/10.1080/10426507.2019.1565760
- R. Kenchappa and D.B. Yadav, Chem. Data Coll., 28, 100453 (2020); https://doi.org/10.1016/j.cdc.2020.100453
- K.R.A. Abdellatif, E.K.A. Abdelall, M.B. Labib, W.A.A. Fadaly and T.H. Zidan, Bioorg. Chem., 105, 104418 (2020); https://doi.org/10.1016/j.bioorg.2020.104418
- D.G. Raut, A.S. Lawand, V.D. Kadu, M.G. Hublikar, S.B. Patil, D.G. Bhosale and R.B. Bhosale, Polycycl. Aromat. Compd., 42, 70 (2022); https://doi.org/10.1080/10406638.2020.1716028
- S.G. Nayak, B. Poojary and V. Kamat, Arch. Pharm., 353, 2000103 (2020); https://doi.org/10.1002/ardp.202000103
- A.K. Kadambar, B. Kalluraya, S. Singh, B.C. Revanasiddappa and V. Agarwal, J. Heterocycl. Chem., 58, 654 (2021); https://doi.org/10.1002/jhet.4172
- K. Bhuvaneswari, N. Nagasundaram and A. Lalitha, J. Chin. Chem. Soc., 68, 27 (2021); https://doi.org/10.1002/jccs.202000265
- S.S. Abd El-Karim, H.S. Mohamed, M.F. Abdelhameed, A. El-Galil E. Amr, A.A. Almehizia and E.S. Nossier, Bioorg. Chem., 111, 104827 (2021); https://doi.org/10.1016/j.bioorg.2021.104827
- M. Mantzanidou, E. Pontiki and D. Hadjipavlou-Litina, Molecules, 26, 3439 (2021); https://doi.org/10.3390/molecules26113439
- D. Kumar, R.R. Kumar, S. Pathania, P.K. Singh, S. Kalra and B. Kumar, Bioorg. Chem., 114, 105068 (2021); https://doi.org/10.1016/j.bioorg.2021.105068
- S.A. Domiati, K.H. Abd El Galil, M.A.S. Abourehab, T.M. Ibrahim and H.M. Ragab, J. Enzyme Inhib. Med. Chem., 37, 2179 (2022); https://doi.org/10.1080/14756366.2022.2109025
- T.K.S. Muhammed, A. Das, C.S. Chandran, B.C. Revanasiddappa, K. Sreeraj and K.V. Shijith, J. Mol. Struct., 1255, 132415 (2022); https://doi.org/10.1016/j.molstruc.2022.132415
- P. Gudimani, N.U. Hebbar, S.L. Shastri, L.A. Shastri, A.K. Shettar, J.H. Hoskeri, S. Joshi and V.A. Sunagar, J. Mol. Struct., 1285, 135405 (2023); https://doi.org/10.1016/j.molstruc.2023.135405
- A.H.H. Ahmed, M.F.A. Mohamed, R.M. Allam, A. Nafady, S.K. Mohamed, A.E. Gouda and E.A.M. Beshr, Bioorg. Chem., 129, 106171 (2022); https://doi.org/10.1016/j.bioorg.2022.106171
- K.R.A. Abdellatif, W.A.A. Fadaly, G.M. Kamel, Y.A.M.M. Elshaier and M.A. El-Magd, Bioorg. Chem., 82, 86 (2019); https://doi.org/10.1016/j.bioorg.2018.09.034
References
M.H. Helal, S.A. El-Awdan, M.A. Salem, T.A. Abd-Elaziz, Y.A. Moahamed, A.A. El-Sherif and G.A.M. Mohamed, Spectrochim. Acta A Mol. Biomol. Spectrosc., 135, 764 (2015); https://doi.org/10.1016/j.saa.2014.06.145
A.-G.E. Amr and M.M. Abdulla, Bioorg. Med. Chem., 14, 4341 (2006); https://doi.org/10.1016/j.bmc.2006.02.045
Y.A. Ammar, E.A. Fayed, A.H. Bayoumi, M.A. Saleh and M.E. El-Araby, Am. J. PharmTech. Res., 5, 245 (2015).
S.M. Sondhi, N. Singh, M. Johar and A. Kumar, Bioorg. Med. Chem., 13, 6158 (2005); https://doi.org/10.1016/j.bmc.2005.06.063
A.P. Keche, G.D. Hatnapure, R.H. Tale, A.H. Rodge, S.S. Birajdar and V.M. Kamble, Bioorg. Med. Chem. Lett., 22, 3445 (2012); https://doi.org/10.1016/j.bmcl.2012.03.092
B. Tozkoparan, M. Ertan, P. Kelicen and R. Demirdamar, Farmaco, 54, 588 (1999); https://doi.org/10.1016/S0014-827X(99)00068-3
R.S.M. Bafail and W.A. Samman, Trop. J. Pharm. Res., 23, 67 (2024); https://doi.org/10.4314/tjpr.v23i1.9
A.Y.A. Alzahrani, W.S. Shehab, A.H. Amer, M.G. Assy, S.M. Mouneir, M.A. Aziz and A.M. Abdel Hamid, RSC Adv., 14, 995 (2024); https://doi.org/10.1039/D3RA07078F
A.M.R. Raauf, T.N.-A. Omar, M.F. Mahdi and H.R. Fadhil, Nat. Prod. Res., 38, 253 (2024); https://doi.org/10.1080/14786419.2022.2117174
R. Surendra Kumar, I.A. Arif, A. Ahamed and A. Idhayadhulla, Saudi J. Biol. Sci., 23, 614 (2016); https://doi.org/10.1016/j.sjbs.2015.07.005
D. Vasudha, A. Jagadeesh, S.N. Mali, R.R. Bhandare and A.B. Shaik, Chem. Phys. Impact, 8, 100500 (2024); https://doi.org/10.1016/j.chphi.2024.100500
N.A. Khalil, M. Eman, E.M. Ahmed and H.B.E. Nassan, Med. Chem. Res., 22, 1021 (2013); https://doi.org/10.1007/s00044-012-0098-7
C.S. Yadav, I. Azad, A.R. Khan, M. Nasibullah, N. Ahmad, D. Hansda, S.N. Ali, K. Shrivastav, M. Akil and M.B. Lohani, Results Chem., 7, 101326 (2024); https://doi.org/10.1016/j.rechem.2024.101326
M.H.M. Helal, M.A. Salem, M.S.A. El-Gaby and M. Aljahdali, Eur. J. Med. Chem., 65, 517 (2013); https://doi.org/10.1016/j.ejmech.2013.04.005
V. Kamat, R. Santosh, B. Poojary, S.P. Nayak, M. Sankaranarayanan, B.K. Kumar, S. Faheem, S. Khanapure, D.A. Barretto and S.K. Vootla, ACS Omega, 5, 25228 (2020); https://doi.org/10.1021/acsomega.0c03386
F.A. Hassan, Int. J. Appl. Sci. Technol., 2, 180 (2012).
D.M. Sirsat, P.S. Bhale, H.V. Chavan, S.M. Karape and M.T. Bachute, Rasayan J. Chem., 13, 1589 (2020); https://doi.org/10.31788/RJC.2020.1335768
A.A. Marzouk, E.S. Taher, M.Sh.A. Shaykoon, P. Lan, W.H. Abd-Allah, A.M. Aboregela and M.F. El-Behairy, Bioorg. Chem., 111, 104883 (2021); https://doi.org/10.1016/j.bioorg.2021.104883
A. Shaabani, M.T. Nazeri and R. Afshari, Mol. Divers., 23, 751 (2019); https://doi.org/10.1007/s11030-018-9902-8
D. Dewangan, T. Kumar, A. Alexander, K. Nagori and D.K. Tripathi, Curr. Pharma Res., 1, 369 (2011); https://doi.org/10.33786/JCPR.2011.v01i04.010
M. Govindaraju, B.N. Mylarappa and K.A. Kumar, Int. J. Pharm. Pharm. Sci., 5, 734 (2013).
F. Giornal, S. Pazenok, L. Rodefeld, N. Lui, J.-P. Vors and F.R. Leroux, J. Fluor. Chem., 152, 2 (2013); https://doi.org/10.1016/j.jfluchem.2012.11.008
S. Sun, L. Chen, J. Huo, Y. Wang, S. Kou, S. Yuan, Y. Fu and J. Zhang, J. Agric. Food Chem., 70, 3447 (2022); https://doi.org/10.1021/acs.jafc.2c00092
D. Huang, F. Liu, S. Wen, Y. Wang, W. Fang, Z. Zhang and S. Ke, Phytochem. Lett., 59, 117 (2024); https://doi.org/10.1016/j.phytol.2024.01.006
D. Huang, M. Huang, W. Liu, A. Liu, X. Liu, X. Chen, H. Pei, J. Sun, D. Yin and X. Wang, Chem. Pap., 71, 2053 (2017); https://doi.org/10.1007/s11696-017-0198-4
D. Xia, X. Cheng, X. Liu, C. Zhang, Y. Wang, Q. Liu, Q. Zeng, N. Huang, Y. Cheng and X. Lv, J. Agric. Food Chem., 69, 8358 (2021); https://doi.org/10.1021/acs.jafc.1c01189
Z.-Q. Long, L.-L. Yang, J.-R. Zhang, S.-T. Liu, Jiao Xie, P.-Y. Wang, J.-J. Zhu, W.-B. Shao, L.-W. Liu and S. Yang, J. Agric. Food Chem., 69, 8380 (2021); https://doi.org/10.1021/acs.jafc.1c02460
G.M. Nitulescu, G. Stancov, O.C. Seremet, G. Nitulescu, D.P. Mihai, C.G. Duta-Bratu, S.F. Barbuceanu and O.T. Olaru, Molecules, 28, 5359 (2023); https://doi.org/10.3390/molecules28145359
G. Li, Y. Cheng, C. Han, C. Song, N. Huang and Y. Du, RSC Med. Chem., 13, 1300 (2022); https://doi.org/10.1039/D2MD00206J
F.K. Keter and J. Darkwa, Biometals, 25, 9 (2012); https://doi.org/10.1007/s10534-011-9496-4
M. Ahmadi, S. Bekeschus, K.-D. Weltmann, T. von Woedtke and K. Wende, RSC Med. Chem., 13, 471 (2022); https://doi.org/10.1039/D1MD00280E
E.M. Gedawy, A.E. Kassab and A.M. El Kerdawy, Eur. J. Med. Chem., 189, 112066 (2020); https://doi.org/10.1016/j.ejmech.2020.112066
L.S. Pavase, D.V. Mane and K.G. Baheti, J. Heterocycl. Chem., 55, 913 (2018); https://doi.org/10.1002/jhet.3118
A.L. Franks and J.E. Slansky, Anticancer Res., 32, 1119 (2012).
G. Kollias, E. Douni, G. Kassiotis and D. Kontoyiannis, Ann. Rheum. Dis., 58, i32 (1999); https://doi.org/10.1136/ard.58.2008.i32
D. Laveti, M. Kumar, R. Hemalatha, R. Sistla, V.G.M. Naidu, V. Talla, V. Verma, N. Kaur and R. Nagpal, Inflamm. Allergy Drug Targets, 12, 349 (2013); https://doi.org/10.2174/18715281113129990053
E. Kadusevicius, Int. J. Mol. Sci., 22, 6637 (2021); https://doi.org/10.3390/ijms22126637
J.K. Gierse, J.J. McDonald, S.D. Hauser, S.H. Rangwala, C.M. Koboldt and K. Seibert, J. Biol. Chem., 271, 15810 (1996); https://doi.org/10.1074/jbc.271.26.15810
R. Sohail, M. Mathew, K.K. Patel, S.A. Reddy, Z. Haider, M. Naria, A. Habib, Z.U. Abdin, W.R. Chaudhry and A. Akbar, Cureus, 15, e37080 (2023); https://doi.org/10.7759/cureus.37080
Y. Lee, C. Rodriguez and R. Dionne, Curr. Pharm. Des., 11, 1737 (2005); https://doi.org/10.2174/1381612053764896
G. Dannhardt and W. Kiefer, Eur. J. Med. Chem., 36, 109 (2001); https://doi.org/10.1016/S0223-5234(01)01197-7
V. Sharma, P. Bhatia, O. Alam, M. Javed Naim, F. Nawaz, A. Ahmad Sheikh and M. Jha, Bioorg. Chem., 89, 103007 (2019); https://doi.org/10.1016/j.bioorg.2019.103007
S. Sanghi, E.J. MacLaughlin, C.W. Jewell, S. Chaffer, P.J. Naus, L.E. Watson and D.E. Dostal, Cardiovasc. Hematol. Disord. Drug Targets, 6, 83 (2006); https://doi.org/10.2174/187152906777441803
S. Grosch, T.J. Maier, S. Schiffmann and G. Geisslinger, J. Natl. Cancer Inst., 98, 736 (2006); https://doi.org/10.1093/jnci/djj206
F.S. Lehmann and C. Beglinger, Curr. Top. Med. Chem., 5, 449 (2005); https://doi.org/10.2174/1568026054201703
P. Rao and E.E. Knaus, J. Pharm. Pharm. Sci., 11, 81s (2008); https://doi.org/10.18433/J3T886
G. Kaur and O. Silakari, Bioorg. Chem., 80, 24 (2018); https://doi.org/10.1016/j.bioorg.2018.05.014
P. Sethi, R. Khare and R. Choudhary, Asian J. Chem., 32, 2594 (2020); https://doi.org/10.14233/ajchem.2020.22813
P. Sethi, P. Dogra, G.K. Gupta, S. Mostafa and S. Kaur, Res. J. Chem. Environ., 22, 73 (2018).
A. Kumar, K.K. Bhagat, A.K. Singh, H. Singh, T. Angre, A. Verma, H. Khalilullah, M. Jaremko, A.-H. Emwas and P. Kumar, RSC Adv., 13, 6872 (2023); https://doi.org/10.1039/D3RA00056G
M.A. Ragab, W.M. Eldehna, A. Nocentini, A. Bonardi, H.E. Okda, B. Elgendy, T.S. Ibrahim, M.M. Abd-Alhaseeb, P. Gratteri, C.T. Supuran, A.A. Al-Karmalawy and M. Elagawany, Eur. J. Med. Chem., 250, 115180 (2023); https://doi.org/10.1016/j.ejmech.2023.115180
M.M.M. El-Miligy, A.K. Al-Kubeisi, M.G. Bekhit, S.R. El-Zemity, R.A. Nassra and A.A. Hazzaa, J. Enzyme Inhib. Med. Chem., 38, 294 (2023); https://doi.org/10.1080/14756366.2022.2147164
S.S. Dhotre, G.T. Pawar, R.P. Pawar and S.R. Vaidya, Research Square, (2023).
K. Vashisht, P. Sethi, P. Mishra and A. Bansal, Res. J. Chem. Environ., 26, 184 (2022); https://doi.org/10.25303/2610rjce1840198
K. Mehta, M. Khambete, A. Abhyankar and A. Omri, Pharmaceuticals, 16, 377 (2023); https://doi.org/10.3390/ph16030377
M. Lusardi, A. Spallarossa and C. Brullo, Int. J. Mol. Sci., 24, 7834 (2023); https://doi.org/10.3390/ijms24097834
M.M. Fouad, The Utility of Thiocarbohydrazide for Generating Novel Triazole and Pyrazole Derivatives Containing a Sulfur Moiety as Anti-microbial Agents, ChemRxiv., (2023); https://doi.org/10.26434/chemrxiv-2023-9b6v1
R. Matta, J. Pochampally, B.N. Dhoddi, S. Bhookya, S. Bitla and A.G. Akkiraju, BMC Chem., 17, 61 (2023); https://doi.org/10.1186/s13065-023-00965-8
B. Kurban, B.N. Saðlýk, D. Osmaniye, S. Levent, Y. Özkay and Z.A. Kaplancýklý, ACS Omega, 8, 31500 (2023); https://doi.org/10.1021/acsomega.3c04635
X. Gu and S. Ma, Anticancer. Agents Med. Chem., 22, 1643 (2022); https://doi.org/10.2174/1871520621666210901102832
Y. Kong, S. Liu, S. Wang, B. Yang, W. He, H. Li, S. Yang, G. Wang and C. Dong, Sci. Rep., 13, 7756 (2023); https://doi.org/10.1038/s41598-023-33403-9
M. Bonesi, M.R. Loizzo, G.A. Statti, S. Michel, F. Tillequin and F. Menichini, Bioorg. Med. Chem. Lett., 20, 1990 (2010); https://doi.org/10.1016/j.bmcl.2010.01.113
S. Kantevari, D. Addla, P.K. Bagul, B. Sridhar and S.K. Banerjee, Bioorg. Med. Chem., 19, 4772 (2011); https://doi.org/10.1016/j.bmc.2011.06.085
H. Ye and I.C. Shaw, Food Chem. Toxicol., 129, 328 (2019); https://doi.org/10.1016/j.fct.2019.04.008
H. Yuseran, E. Hartoyo, T. Nurseta and H. Kalim, Clin. Nutr. Open Sci., 35, 77 (2021); https://doi.org/10.1016/j.yclnex.2020.10.001
M. Kumar, Z. Abbas, P. Siwach, J. Sharma, A. Rani, S. Sharma, P. Aggarwal, P. Show, S. Haque, V.K. Garg and H.S. Tuli, J. Adv. Biotechnol. Exp. Ther., 6, 386 (2023); https://doi.org/10.5455/jabet.2023.d134
M. Song, B. Liu, S. Yu, S. He, Y. Liang, S. Li, Q. Chen and X. Deng, Lett. Drug Design Discov., 17, 502 (2020); https://doi.org/10.2174/1570180816666190731113441
M.A. Abdelgawad, M.B. Labib and M. Abdel-Latif, Bioorg. Chem., 74, 212 (2017); https://doi.org/10.1016/j.bioorg.2017.08.014
R. Ayman, M.S. Abusaif, A.M. Radwan, A.M. Elmetwally and A. Ragab, Eur. J. Med. Chem., 249, 115138 (2023); https://doi.org/10.1016/j.ejmech.2023.115138
A. Masih, A.K. Agnihotri, K. Srivastava, N. Pandey, H.R. Bhat and U.P. Singh, J. Biochem. Mol. Toxicol., 35, e22656 (2021); https://doi.org/10.1002/jbt.22656
T. Akaishi and K. Abe, Eur. J. Pharmacol., 819, 190 (2018); https://doi.org/10.1016/j.ejphar.2017.12.008
Y. Fu, J. Ma, X. Shi, X.-Y. Song, Y. Yang, S. Xiao, J. Li, W.-J. Gu, Z. Huang, J. Zhang and J. Chen, Biochem. Pharmacol., 135, 126 (2017); https://doi.org/10.1016/j.bcp.2017.03.013
M. Law, J.L. Morales, L.F. Mottram, A. Iyer, B.R. Peterson and A. August, Int. J. Biochem. Cell Biol., 43, 1228 (2011); https://doi.org/10.1016/j.biocel.2011.04.016
J. Ishikawa, K. Ohga, T. Yoshino, R. Takezawa, A. Ichikawa, H. Kubota and T. Yamada, J. Immunol., 170, 4441 (2003); https://doi.org/10.4049/jimmunol.170.9.4441
N.R. Trindade, P.R. Lopes, L.M. Naves, J.O. Fajemiroye, P.H. Alves, N.O. Amaral, L.M. Liao, A.C.S. Rebelo, C.H. Castro, V.A. Braga, R. Menegatti and G.R. Pedrino, Front. Physiol., 9, 1073 (2018); https://doi.org/10.3389/fphys.2018.01073
L. de Oliveira, I.F. Florentino, D.P. Silva, F. Pazini, F.S. de Carvalho, G. Sanz, B.G. Vaz, F.F. da Rocha, J.O. Fajemiroye, P.C. Ghedini, L.M. Lião, R. Menegatti, E.A. Costa and T.S. de Oliveira, Can. J. Physiol. Pharmacol., 101, 216 (2023); https://doi.org/10.1139/cjpp-2022-0428
S.M. Haghighi, M. Fathalipour, A. Purkhosrow, S. Oftadehgan, M. Abbasi, A. Khalafi-Nezhad and E. Sattarinezhad, Trends Pharm. Sci., 9, 105 (2023); https://doi.org/10.30476/TIPS.2023.98280.1185
F.E. Silverstein, G. Faich, J.L. Goldstein, L.S. Simon, T. Pincus, A. Whelton, R. Makuch, G. Eisen, N.M. Agrawal, W.F. Stenson, A.M. Burr, W.W. Zhao, J.D. Kent, J.B. Lefkowith, K.M. Verburg and G.S. Geis, JAMA, 284, 1247 (2000); https://doi.org/10.1001/jama.284.10.1247
N.H. Amin, M.T. El-Saadi, A.A. Hefny, A.H. Abdelazeem, H.A. Elshemy and K.R. Abdellatif, Future Med. Chem., 10, 2521 (2018); https://doi.org/10.4155/fmc-2018-0224
K.F. Croom and M.A. Siddiqui, Drugs, 69, 1513 (2009); https://doi.org/10.2165/00003495-200969110-00008
Y. Yin, C.-J. Chen, R.-N. Yu, L. Shu, T.-T. Zhang and D.-Y. Zhang, Bioorg. Med. Chem., 27, 1562 (2019); https://doi.org/10.1016/j.bmc.2019.02.054
G.J. Southan, D. Gauld, A. Lubeskie, B. Zingarelli, S. Cuzzocrea, A.L. Salzman, C. Szabó and D.J. Wolff, Biochem. Pharmacol., 54, 409 (1997); https://doi.org/10.1016/S0006-2952(97)00196-2
P.P. Kattimani, R.R. Kamble, A.R. Nesaragi, M.Y. Kariduraganavar, S.D. Joshi, S.S. Dodamani and S.S. Jalalpure, Synth. Commun., 51, 3125 (2021); https://doi.org/10.1080/00397911.2021.1964530
Y.-R. Li, C. Li, J.-C. Liu, M. Guo, T.-Y. Zhang, L.-P. Sun, C.-J. Zheng and H.-R. Piao, Bioorg. Med. Chem. Lett., 25, 5052 (2015); https://doi.org/10.1016/j.bmcl.2015.10.028
S. Hussain and D. Kaushik, J. Saudi Chem. Soc., 19, 274 (2015); https://doi.org/10.1016/j.jscs.2012.04.002
K.R.A. Abdellatif, M.A. Abdelgawad, M.B. Labib and T.H. Zidan, Bioorg. Med. Chem. Lett., 25, 5787 (2015); https://doi.org/10.1016/j.bmcl.2015.10.047
P. Khloya, S. Kumar, P. Kaushik, P. Surain, D. Kaushik and P.K. Sharma, Bioorg. Med. Chem. Lett., 25, 1177 (2015); https://doi.org/10.1016/j.bmcl.2015.02.004
K.R.A. Abdellatif, M.A. Abdelgawad, H.A.H. Elshemy, S.S.R. Alsayed and G. Kamel, Arch. Pharm. Res., 38, 1932 (2015); https://doi.org/10.1007/s12272-015-0606-7
R. Sribalan, G. Banuppriya, M. Kirubavathi, A. Jayachitra and V. Padmini, Bioorg. Med. Chem. Lett., 26, 5624 (2016); https://doi.org/10.1016/j.bmcl.2016.10.075
S.N. Thore, S.V. Gupta and K.G. Baheti, J. Saudi Chem. Soc., 20, 259 (2016); https://doi.org/10.1016/j.jscs.2012.06.011
L.Z. Chen, W.W. Sun, L. Bo, J.Q. Wang, C. Xiu, W.J. Tang, J.B. Shi, H.P. Zhou and X.H. Liu, Eur. J. Med. Chem., 138, 170 (2017); https://doi.org/10.1016/j.ejmech.2017.06.044
M.A. Bhat, A.F. Ahmed, Z.-H. Wen, M.A. Al-Omar and H.A. Abdel-Aziz, Med. Chem. Res., 26, 1557 (2017); https://doi.org/10.1007/s00044-017-1870-5
M.N. Kumbar, R.R. Kamble, J.P. Dasappa, P.K. Bayannavar, H.A. Khamees, M. Mahendra, S.D. Joshi, S. Dodamani, V.P. Rasal and S. Jalalpure, J. Mol. Struct., 1160, 63 (2018); https://doi.org/10.1016/j.molstruc.2018.01.047
R.C. Kulkarni, J.M. Madar, S.L. Shastri, F. Shaikh, N.S. Naik, R.B. Chougale, L.A. Shastri, S.D. Joshi, S.R. Dixit and V.A. Sunagar, Chem. Data Coll., 17-18, 497 (2018); https://doi.org/10.1016/j.cdc.2018.11.004
M.F. El Shehry, E.F. Ewies and E.M. Zayed, Russ. J. Gen. Chem., 89, 492 (2019); https://doi.org/10.1134/S1070363219030216
G.S. Hassan, D.E. Abdel Rahman, E.A. Abdelmajeed, R.H. Refaey, M. Alaraby Salem and Y.M. Nissan, Eur. J. Med. Chem., 171, 332 (2019); https://doi.org/10.1016/j.ejmech.2019.03.052
G. Mustafa, A. Angeli, M. Zia-ur-Rehman, N. Akbar, S. Ishtiaq and C.T. Supuran, Bioorg. Chem., 91, 103110 (2019); https://doi.org/10.1016/j.bioorg.2019.103110
P.S. Bhale, B.P. Bandgar, S.B. Dongare, S.N. Shringare, D.M. Sirsat and H.V. Chavan, Phosphorus Sulfur Silicon Rel. Elem., 194, 843 (2019); https://doi.org/10.1080/10426507.2019.1565760
R. Kenchappa and D.B. Yadav, Chem. Data Coll., 28, 100453 (2020); https://doi.org/10.1016/j.cdc.2020.100453
K.R.A. Abdellatif, E.K.A. Abdelall, M.B. Labib, W.A.A. Fadaly and T.H. Zidan, Bioorg. Chem., 105, 104418 (2020); https://doi.org/10.1016/j.bioorg.2020.104418
D.G. Raut, A.S. Lawand, V.D. Kadu, M.G. Hublikar, S.B. Patil, D.G. Bhosale and R.B. Bhosale, Polycycl. Aromat. Compd., 42, 70 (2022); https://doi.org/10.1080/10406638.2020.1716028
S.G. Nayak, B. Poojary and V. Kamat, Arch. Pharm., 353, 2000103 (2020); https://doi.org/10.1002/ardp.202000103
A.K. Kadambar, B. Kalluraya, S. Singh, B.C. Revanasiddappa and V. Agarwal, J. Heterocycl. Chem., 58, 654 (2021); https://doi.org/10.1002/jhet.4172
K. Bhuvaneswari, N. Nagasundaram and A. Lalitha, J. Chin. Chem. Soc., 68, 27 (2021); https://doi.org/10.1002/jccs.202000265
S.S. Abd El-Karim, H.S. Mohamed, M.F. Abdelhameed, A. El-Galil E. Amr, A.A. Almehizia and E.S. Nossier, Bioorg. Chem., 111, 104827 (2021); https://doi.org/10.1016/j.bioorg.2021.104827
M. Mantzanidou, E. Pontiki and D. Hadjipavlou-Litina, Molecules, 26, 3439 (2021); https://doi.org/10.3390/molecules26113439
D. Kumar, R.R. Kumar, S. Pathania, P.K. Singh, S. Kalra and B. Kumar, Bioorg. Chem., 114, 105068 (2021); https://doi.org/10.1016/j.bioorg.2021.105068
S.A. Domiati, K.H. Abd El Galil, M.A.S. Abourehab, T.M. Ibrahim and H.M. Ragab, J. Enzyme Inhib. Med. Chem., 37, 2179 (2022); https://doi.org/10.1080/14756366.2022.2109025
T.K.S. Muhammed, A. Das, C.S. Chandran, B.C. Revanasiddappa, K. Sreeraj and K.V. Shijith, J. Mol. Struct., 1255, 132415 (2022); https://doi.org/10.1016/j.molstruc.2022.132415
P. Gudimani, N.U. Hebbar, S.L. Shastri, L.A. Shastri, A.K. Shettar, J.H. Hoskeri, S. Joshi and V.A. Sunagar, J. Mol. Struct., 1285, 135405 (2023); https://doi.org/10.1016/j.molstruc.2023.135405
A.H.H. Ahmed, M.F.A. Mohamed, R.M. Allam, A. Nafady, S.K. Mohamed, A.E. Gouda and E.A.M. Beshr, Bioorg. Chem., 129, 106171 (2022); https://doi.org/10.1016/j.bioorg.2022.106171
K.R.A. Abdellatif, W.A.A. Fadaly, G.M. Kamel, Y.A.M.M. Elshaier and M.A. El-Magd, Bioorg. Chem., 82, 86 (2019); https://doi.org/10.1016/j.bioorg.2018.09.034