Abstract
Quinolines are nitrogen-containing bicyclic compounds that are widely found throughout Nature in various forms. Quinoline derivatives are utilized in the areas of medicine, food, catalysts, dyes, materials, refineries, electronics, etc. The quinoline nucleus is present in numerous biological compounds, e.g., antimalarial, antimicrobial, antimycobacterial, antidepressant, anticonvulsant, antiviral, anticancer, antihypertensive, platelet-derived growth factor (PDGF) receptor tyrosine kinase (RTK) inhibitory, antiinflammatory, antioxidant, and anti-human immunodeficiency virus (HIV) agents. However, owing to the swift development of new molecules containing this nucleus, many research reports have been generated in a brief span of time. There therefore seems to be a requirement to collect recent information in order to understand the current status of the quinoline nucleus in medicinal chemistry research, focusing in particular on the numerous attempts to synthesize and investigate new structural prototypes with more effective antimalarial, antimicrobial, and anticancer activity.
Similar content being viewed by others
Abbreviations
- Candida utilis :
-
C. utilis
- Aspergillus flavus :
-
A. flavus
- Beer yeast:
-
B. yeast
- Candida albicans :
-
C. albicans
- Micrococcus luteus :
-
M. luteus
- Eberthella typhosa :
-
E. typhosa
- Bacillus subtilis :
-
B. s.
- Pseudomonas aeruginosa :
-
P. a.
- Aspergillus clavatus :
-
A. c.
- Methicillin-resistant Staphylococcus aureus :
-
MRSA
- Staphylococcus aureus :
-
S. aureus
- Pseudomonas aeruginosa :
-
P. aeruginosa
- Escherichia coli :
-
E. coli
- Shigella dysenteriae :
-
S. dysenteriae
- Quinolone-resistant S. aureus :
-
QRSA
- Clostridium tetani :
-
C. t.
- Vibrio cholera :
-
V. c.
References
S. Emami, E. Ghafouri, M.A. Faramarzi, N. Samadi, H. Irannejad, A. Foroumadi, Eur. J. Med. Chem. 68, 185–190 (2013)
N.C. Desai, G.M. Kotadiya, A.R. Trivedi, Bioorg. Med. Chem. Lett. 24, 3126–3131 (2014)
A. Barteselli, S. Parapini, N. Basilico, D. Mommoa, A. Sparatore, Bioorg. Med. Chem. 22, 5757–5765 (2014)
S. Vandekerckhove, T. Desmet, H.G. Tran, C.d. Kock, P.J. Smith, K. Chibale, M. D’hooghe, Bioorg. Med. Chem. Lett. 24, 1214–1217 (2014)
B. Vivekanand, K.M. Raj, B.H.M. Mruthyunjayaswamy, J. Mol. Str. 1079, 214–224 (2015)
C. Gomez, P. Ponien, N. Serradji, A. Lamouri, A. Pantel, E. Capton, V. Jarlier, G. Anquetin, A. Aubry, Bioorg. Med. Chem. 21, 948–956 (2013)
K. Plevova, K. Briestenska, F. Colobert, J. Mistrikova, V. Milata, F.R. Leroux, Tetrahedron Lett. 56, 5112–5115 (2015)
R. Abonia, D. Insuasty, J. Castillo, B. Insuasty, J. Quiroga, M. Nogueras, J. Cobo, Eur. J. Med. Chem. 57, 29–40 (2012)
M.M. Alam, M. Shaharyar, H. Hamid, S. Nazreen, S. Haider, M.S. Alam, Med. Chem. 7(6), 663–673 (2011)
L. Feng, K. Lv, M. Liu, S. Wang, J. Zhao, X. You, S. Li, J. Cao, H. Guo, Eur. J. Med. Chem. 55, 125–136 (2012)
N.K. Shah, N.M. Shah, M.P. Patel, R.G. Patel, J. Serb. Chem. Soc. 77(3), 279–286 (2012)
T. Djemel, A. Messai, D. Luneau, E. Jeanneau, J. Chem. Crystallogr. 45, 300–309 (2015)
N.Y. Jadhav, S.M. Hipparagi, M.B. Raju, S.S. Shyale, S.D. Kadam, R. Sen, Ph. Tech. Med. 3(2). ISSN 2278-1099 (2014)
A.R. Bhatt, A. Tazeem, I. Azam, F.Athar. Choi, Eur. J. Med. Chem. 46, 3158–3166 (2011)
N.C. Desai, A.M. Dodiya, Arab. J. Chem. 7, 906–913 (2014)
S.F. Cui, Y. Ren, S.L. Zhang, X.M. Peng, G.L.V. Damu, R.X. Geng, Z. Cheng-He, Bioorg. Med. Chem. Lett. 23, 3267–3272 (2013)
R. Dhanapal, P.T. Perumal, Natl. J. Chembiosis 4(2), 10–13 (2013)
B. Garudachari, M.N. Satyanarayana, B. Thippeswamy, C.K. Shivakumar, N. Shivananda, G. Hegde, A.M. Isloor, Eur. J. Med. Chem. 54, 900–906 (2012)
S.B. Ghodile, P.T. Kosankarb, R.D. Raut, Int. J. Pharm. Chem. 4(04), 134–136 (2014)
M. Guo, C.J. Zheng, M.X. Song, Y. Wu, L.P. Sun, Y.J. Li, Y. Liu, H.R. Piao, Bioorg. Med. Chem. Lett. 23, 4358–4361 (2013)
M. Gupta, N. Upmanyu, S. Pramanika, C.K. Tyagi, A. Chandekar, Int. J. Drug. Dev. Res. 3(2), 233–239 (2011)
H.H. Jardosh, M.P. Patel, Arab. J. Chem. (2014) (in press)
N.D. Jayanna, H.M. Vagdevi, J.C. Dharshan, T.R.P. Kekuda, J. Chem. 2013, 1–7 (2013)
S.D. Joshi, U.A. More, D. Parkale, T.M. Aminabhavi, A.K. Gadad, M.N. Nadagouda, R. Jawarkar, Med. Chem. Res. 24(11), 3892–3911 (2015)
H.G. Kathrotiya, M.P. Patel, Eur. J. Med. Chem. 63, 675–684 (2013)
J.A. Makawana, M.P. Patel, R.G. Patel, Med. Chem. Res. 21, 616–623 (2012)
P.G. Mandhane, R.S. Joshi, P.S. Mahajan, M.D. Nikam, D.R. Nagargoje, C.H. Gill, Arab. J. Chem. 8, 474–479 (2015)
B.M. Mistry, S. Jauhari, Med. Chem. Res. 22, 647–658 (2013)
A. Wube, A. Hüfner, W. Seebacher, M. Kaiser, R. Brun, R. Bauer, F. Bucar, Molecules 19, 14204–14220 (2014)
S. Vandekerckhove, S.V. Herreweghe, J. Willems, B. Danneels, T. Desmet, C. de Kock, P.J. Smith, K. Chibale, M.V. D’hooghe, Eur. J. Med. Chem. 92, 91–102 (2015)
R.K. Arafa, G.H. Hegazy, G.A. Piazza, A.H. Abadi, Eur. J. Med. Chem. 63, 826–832 (2013)
A.K. El-Damasy, S.H. Seo, N.C. Cho, S.B. Kang, A.N. Pae, K.S. Kim, G. Keum, Eur. J. Med. Chem. 101, 754–768 (2015)
Y.F. Chen, Y.C. Lin, P.K. Huang, H.C. Chan, S.C. Kuo, K.H. Lee, L.J. Huang, Bioorg. Med. Chem. 21, 5064–5075 (2013)
S.M.F. da Luana, M.C.T. Nathalia, M.T.de.S. Alessandra, C.C. Helena, C.M. Raquel, F.D. Rafael, E.I.M.O. Maria, P.S.J. Floriano, H.B. Leilane, M.R.B. Rommel, A.V. Bárbara, O. de Riethe, F.F. Vitor, C.C. Anna, C.S.B. da Fernanda, B.V.de.S. Maria Cecília, Molecules 19, 6651–6670 (2014)
J.A. Makawana, C.B. Sangani, L. Lin, H.L. Zhu, Bioorg. Med. Chem. Lett. 24, 1734–1736 (2014)
L. Matesic, J.M. Locke, K.L. Vine, M. Ranson, J.B. Bremner, D. Skropeta, Tetrahedron 68, 6810–6819 (2012)
M. Naveen, D. Rambabu, R.R. Mohan, M. Chaitanya, S.K. Chitta, M.K. Arunasree, G.R. Krishna, C.M. Reddy, M.V.B. Rao, P. Manojit, Bioorg. Med. Chem. 20, 759–768 (2012)
N. Perin, R. Nhili, K. Ester, W. Laine, G.K. Zamola, M. Kralj, M.H.D. Cordonnier, M. Hranjec, Eur. J. Med. Chem. 80, 218–227 (2014)
J. Sun, H. Zhu, Z.M. Yang, H.L. Zhu, Eur. J. Med. Chem. 60, 23–28 (2013)
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Narwal, S., Kumar, S. & Verma, P.K. Synthesis and therapeutic potential of quinoline derivatives. Res Chem Intermed 43, 2765–2798 (2017). https://doi.org/10.1007/s11164-016-2794-2
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11164-016-2794-2