Identyfikatory
Warianty tytułu
Synthesis and biological activity of selected Mannich bases
Języki publikacji
Abstrakty
The Mannich reaction is important for the synthesis and modification of biologically active compounds. Mannich bases – substituted products containing different heterocyclic system in their structures seem to be suitable candidates for further chemical modifications and might be of interest as pharmacologically active compounds. The main goal of this article is to present synthesis and biological activity of selected Mannich bases. Based on a review of the chemical literature, Mannich bases showed a multipharmacological effects. The Mannich bases, containing various heterocyclic systems were identified as potent anticancer agents. Presented compounds exhibit cytotoxic, antiproliferate in vitro, anticonvulsant, antioxidative, antiinflaminatory and analgesic activity. Some of them can be used in a treatment of diabetes and hypertension.
Wydawca
Czasopismo
Rocznik
Tom
Strony
981--1008
Opis fizyczny
Bibliogr. 37 poz., schem.
Twórcy
autor
- Katedra i Zakład Technologii Leków Uniwersytet Medyczny im Piastów Śląskich we Wrocławiu ul. Borowska 211a, 50-556 Wrocław
autor
- Katedra i Zakład Technologii Leków Uniwersytet Medyczny im Piastów Śląskich we Wrocławiu ul. Borowska 211a, 50-556 Wrocław
Bibliografia
- [1] A. Nowicka, H. Liszkiewicz, W.P. Nawrocka, Wiad. Chem., 2014, 3-4, 161.
- [2] S.A. Shahzad, M. Yar, M. Bajda, B. Jadoon, Z.A. Khan, S.A.R. Naqvi, A.J. Shaikh, K. Hayat, A. Mahmmod, N. Mahmood, S. Filipek, Bioorg. Med. Chem., 2014, 22, 1008.
- [3] S. Ackland, G. Peters, Drug Resist Updat. 1999, 2, 205.
- [4] Y.J. Zhao, W. Wei, Z.G. Su, G.H. Ma, Int. J. Pharm., 2009, 379, 90.
- [5] V.R. Solomon, C. Hu, H. Lee, Bioorg. Med. Chem., 2010, 18, 1563.
- [6] A.Y. Shaw, C.Y. Chang, M.Y. Hsu, P.J. Lu, C.N. Yang, H.L. Chen, C.W. Lo, C.W. Shiau, M.K. Chern, Eur. J. Med. Chem., 2010, 45, 2860.
- [7] A.T. Taher, N.A. Khalil, E.M. Ahmed, Arch. Pharm. Res., 2011, 34, 1615.
- [8] A. Chaundhary, P.P. Sharma, G. Bhardwaj, V. Jain, P.V. Bharatam, B. Shrivastav, R.K. Roy, Med. Chem. Res., 2013, 22, 5654.
- [9] D. Sunil, A.M. Isloor, P. Shetty, B. Chandrakantha, K. Satyamoorthy, Med. Chem. Res., 2011, 20, 1024.
- [10] R.M. Kumbhare, K.V. Kumar, M.J. Ramaiah, T. Dadmal, S.N.C.V.L. Pushpavalli, D. Mukhopadhyay, B. Divya, T.A. Devi, U. Kosurkar, M. Pal-Bhadra, Eur. J. Med. Chem., 2011, 46, 4258.
- [11] G. Hu, G. Wang., N. Duan, X. Wen, T. Cao, S. Xie, W. Huang, Acta. Pharm. Sinc. B, 2012, 2, 312.
- [12] F.P.G. Euzebio, F.J.L. dos Santos, D. Pilo-Veloso, A.F.C. Alcantara, A.L.T.G. Ruiz, J.E. de Carvalho, M.A. Foglio, D.L. Farreira-Alves, A. de Fatima, Bioorg. Med. Chem., 2010, 18, 8172.
- [13] G Bartosz, Druga twarz tlenu, Wydawnictwo Naukowe PWN, Warszawa, 2008.
- [14] L. Ma, Y. Xiao, C. Li, Z.L. Xie, D.D. Li, Y.T. Wang, H.T. Ma, H.L. Zhu, M.H. Wang, Y.H. Ye, Bioorg. Med. Chem., 2013, 21, 6763.
- [15] N.G. Li, S.L. Song, M.Z. Shen, Y.P. Tang, Z.H. Shi, H. Tang, Q.P. Shi, Y.F. Fu, J.A. Duan, Bioorg. Med. Chem., 2012, 20, 6919.
- [16] R.V. Satyendra, K.A. Vishnumurthy, H.M. Vagdevi, K.P. Rajesh, H. Manjunatha, A. Shruthi, Eur. J. Med. Chem., 2011, 46, 3078.
- [17] J. Obniska, K. Kamiński, Acta Pol. Pharm., 2006, 63, 101.
- [18] J. Obniska, I. Chlebek, J. Pichor, M. Kopytko, K. Kamiński, Acta Pol. Pharm., 2009, 66, 639.
- [19] J. Obniska, K. Kamiński, I. Chlebek, Acta Pol. Pharm., 2009, 66, 663.
- [20] J. Obniska, H. Byrtus, K. Kamiński, M. Pawłowski, M. Szczesio, J. Karolak-Wojciechowska, Bioorg. Med. Chem., 2010, 18, 6134.
- [21] H. Byrtus, J. Obniska, A. Czopek, K. Kamiński, M. Pawłowski, Bioorg. Med. Chem., 2011, 19, 6149.
- [22] J. Obniska, S. Rzepka, K. Kamiński, Bioorg. Med. Chem., 2012, 20, 4872.
- [23] K. Kamiński, J. Obniska, I. Chlebek, B. Wiklik, S. Rzepka, Bioorg. Med. Chem., 2013, 21, 6821.
- [24] K. Kamiński, J. Obniska, I. Chlebek, P. Liana, E. Pękala, Eur. J. Med. Chem., 2013, 66, 12.
- [25] A.A. Kulkarni, S.B. Wankhede, N.D. Dhawale, P.B. Ydav, V.V. Deore, I.D. Gonjari, Arabian J. Chem., 2013 (in press).
- [26] K. Wiglusz, L. Trynda-Lemiesz, Postępy farmacji, 2011, 1, 20.
- [27] A.A. Radwan, K.E.H. elTahir, Arch. Pharm. Res., 2013, 36, 553.
- [28] E.P. Jesudason, S.K. Sridhar, E.J.P. Malar, P. Shanmugapandiyan, M. Inayathullah, V. Arul, D. Selvaraj, R. Jayakumar, Eur. J. Med. Chem., 2009, 44, 2307.
- [29] K. Manjunatha, B. Poojary, P.L. Lobo, J. Fernandes, N.S. Kumari, Eur. J. Med. Chem., 2010, 45, 5225.
- [30] Nithinchandra, B. Kalluraya, S. Aamir, A.R. Shabaraya, Eur. J. Med. Chem., 2012, 54, 597.
- [31] J. Gowda, A.M.A. Khader, B. Kalluraya, P. Shree, A.R. Shabaraya, Eur. J. Med. Chem., 2011, 46, 4100.
- [32] O.M. Abdelhafez, N.A. Abedelatif, F.A. Badria, Arch. Pharm. Res., 2011, 34, 1623.
- [33] M.M. Kamel, M.M. Anwar, A.M. Soliman, H.F. Abdel-Hamid, Res. Chem. Intermed, 2013, 39, 3417.
- [34] B. Singh, D.Chetia, S.K. Puri, K. Srivastava, A. Prakash, Med.Chem. Res., 2011, 20, 1523.
- [35] S.M. Siddiqui, A. Salahuddin, A. Azam, Med. Chem. Res., 2013, 22, 1313.
- [36] A.A. Siddiqui, R. Mishra, M. Shaharyar, Eur. J. Med. Chem., 2010, 45, 2283.
- [37] H. Wang, J. Yan, X. Song, L. Fan, J. Xu, G. Zhou, L. Jiang, D. Yang, Bioorg. Med. Chem., 2012, 20, 2119.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-df2d98c0-7049-407f-83d2-45a2dbfacdd2