[7]
Ball, P. Natural history or natural selection? J. Antimicrob. Chemother., 2000, 46(3), 17-24.
[18]
Eppakayala, L.; Sripelly, S.S.; Chary, M.T. 6 A Study on antibacterial activity of substituted 1, 8-Naphthyridine containing carbalehydes, methylene hydrazines, thiadizole amines and triazole Thiols. J. Adv. Drug Res., 2012, 2(2), 6-11.
[31]
Naik, T.R.R.; Naik, H.S.B.; Raghavendra, M.; Gopal, S.; Naik, K. Synthesis of Thieno[2,3-b]benzo[1,8]Naphthyridine-2-Carboxilic acids under microwave irradiation and intraction with DNA studies. ARKIVOC, 2006, 1-15, 84-94.
[32]
Bhambi, D.; Salvi, V.K.; Bapna, A.; Pemawat, G.; Talesara, G.L. Synthesis and antimicrobial evaluation of alkoxypthalimide derivatives of naphthyridine Indian J. Chem., 2009, 48(B), 697, 704.
[34]
Makhanya, T.R.; Gengan, R.M.; Ata, A. Synthesis and biological evaluation of novel fused indolo [3, 2-c][1, 8] naphthyridine derivatives as potential antibacterial agents. Synth. Commun., 2019, 49(6), 823-835.
[35]
Bhasker, G.V.; Satyanarayana, G.V.; Laxminarayana, E.; Latha, A.; Chary, M.T. Synthesis, antibacterial activity, and docking studies of some new 2-substituted-1, 8-naphthyridine derivatives. Indian J. Heterocyc CH., 2018, 28(02), 227-242.
[36]
Bhasker, G.V.; Satyanarayana, G.V.; Latha, A.; Laxminarayana, E.; Chary, M.T. Synthesis and antimicrobial activity of novel 1-[3-(1, 8-Naphthyridin-2-Yl) Phenyl]-3-Arylurea derivatives. Asian J. Chem., 2018, 30(4), 771-774.
[38]
Harvey, P.D.; Jones, M.T. Functional deficts in attenuated psuchosis syndrome and related conditions. Curr. Future Treat. Options. Res. Cogn., 2019.17100152
[41]
Ferrari, P.L.; Betti, L.; Cavallini, T.; Giannaccini, G.; Lucacchini, A.; Manera, C.; Martinelli, A.; Ortore, G.; Saccomanni, G.; Tuccinardi, T. Study on affinity profile toward native human and bovine adenosine receptors of a series of 1,8-naphthyridine derivatives. J. Med. Chem., 2004, 47(12), 3019-3031.
[65]
Bucha, M.; Eppakayala, L.; Sripelly, S.S.; Maringanti, T.C. An efficient synthesis of thiophene containing 1,8-Naphthyridine derivatives. JUSPS, 2015, 27(3), 167-174. Ultra Scientist
[69]
Thilagam, S.; Rajendran, S.P. Molecular docking and cytotoxic activity of 1,8-naphthyridine derivatives in human lung cancer. Indian J. Res., 2015, 4, 437-439.
[76]
Al-romaizan, A.N.; Jaber, T.S.; Ahmed, N.S. Naphthyridine derivatives: Design, synthesis and in vitro screening of their cytotoxic activity against MCF7 cell line. Open Chem., 2019, 17(1), 943-954.
[82]
Patil, P.T.; Warekar, P.P.; Patil, K.T.; Undare, S.S.; Jamale, D.K.; Vibhute, S.S.; Valekar, N.J.; Kolekar, G.B.; Deshmukh, M.B.; Anbhule, P.V. A simple and efficient one-pot novel synthesis of pyrazolo [3, 4-b][1, 8] naphthyridine and pyrazolo [3, 4-d] pyrimido [1, 2-a] pyrimidine derivatives as anti-inflammatory agents. Res. Chem. Intermed., 2018, 44(2), 1119-1130.
[84]
Bachand, B.; Nguyen-Ba, N.; Siddiqui, A.; Levesque, S.U.S.U.S. patent US 6,340,690,, 2002.
[89]
Yadav, A.; Kumari, R.; Yadav, A.; Mishra, J.P.; Srivatva, S.; Prabha, S. antioxidants and its functions in human body - a review. Res. Environ. Life Sci., 2016, 9(11), 1328-1331.
[91]
Pirasath, S.; Kumanan, T.; Guruparan, M. A Study on knowledge, awareness, and medication adherence in patients with hypertension from a Tertiary Care Centre from Northern Sri Lanka Int; J. Hyp, 2017.
[104]
Badawneh, M.; Aljamal, J. Antiplatelet aggregation activity of 4-phenyl-1,8- naphthyridine derivatives: Synthesis and evaluation. Int. J. Pharm. Pharm. Sci., 2016, 6, 290-304.
[110]
Johansson, S.G.; Bieber, T.; Dahl, R.; Friedmann, P.S.; Lanier, B.Q.; Lockey, R.F.; Motala, C.; Martell, J.A.; Platts-Mills, T.A.; Ring, J.; Thien, F. Revised nomenclature for allergy for global use: Report of the Nomenclature Review Committee of the World Allergy Organization. J. Allergy Clin. Immunol., 2004, 113(5), 832-836.
[112]
Fadel, S.; Hajbi, Y.; Khouili, M.; Lazar, S.; Suzenet, F.; Guillaumet, G. Synthesis of 3, 4-dihydro-1, 8-naphthyridin-2 (1H)-ones via microwave-activated inverse electron-demand Diels–Alder reactions. Beilstein J. Org. Chem., 2014, 10(1), 282-286.
[113]
Mohammed, S.; Khalid, M. A flexible synthesis of naphthyridine derivatives through diazotization, triflation, and Suzuki reaction. Indian J. Heterocy. Ch., 2019, 29(01), 21-25.