References
- Akhtar, J., Khan, A. A., Ali, Z., Haider, R., & Shahar Yar, M. (2017). Structure-activity relationship (SAR) study and design strategies of nitrogen-containing heterocyclic moieties for their anticancer activities. European Journal of Medicinal Chemistry, 125, 143–189. https://doi.org/10.1016/j.ejmech.2016.09.023
- Dasari, S., Abbas, Z., Kumar, P., & Patra, A. K. (2016). Photosensitized samarium(iii) and erbium(iii) complexes of planar N,N-donor heterocyclic bases: Crystal structures and evaluation of biological activity. CrystEngComm, 18(23), 4313–4322. https://doi.org/10.1039/C5CE02387D
- Dufour, C., & Dangles, O. (2005). Flavonoid–serum albumin complexation: Determination of binding constants and binding sites by fluorescence spectroscopy. Biochimica et Biophysica Acta (BBA) - General Subjects, 1721(1-3), 164–173. https://doi.org/10.1016/j.bbagen.2004.10.013
- Gichumbi, J. M., Friedrich, H. B., & Omondi, B. (2016). Application of arene ruthenium(II) complexes with pyridine-2-carboxaldimine ligands in the transfer hydrogenation of ketones. Journal of Molecular Catalysis A: Chemical, 416, 29–38. https://doi.org/10.1016/j.molcata.2016.02.012
- Haribabu, J., Jeyalakshmi, K., Arun, Y., Bhuvanesh, N. S. P., Perumal, P. T., & Karvembu, R. (2015). Synthesis, DNA/protein binding, molecular docking. RSC Advances, 5(57), 46031–46049. https://doi.org/10.1039/C5RA04498G
- Hu, Y.-Q., Gao, C., Zhang, S., Xu, L., Xu, Z., Feng, L.-S., Wu, X., & Zhao, F. (2017). Quinoline hybrids and their antiplasmodial and antimalarial activities. European Journal of Medicinal Chemistry, 139, 22–47. https://doi.org/10.1016/j.ejmech.2017.07.061
- Jain, S., Chandra, V., Kumar Jain, P., Pathak, K., Pathak, D., & Vaidya, A. (2019). Comprehensive review on current developments of quinoline-based anticancer agents. Arabian Journal of Chemistry, 12(8), 4920–4946. https://doi.org/10.1016/j.arabjc.2016.10.009
- Kaur, H., Lim, S. M., Ramasamy, K., Vasudevan, M., Shah, S. A. A., & Narasimhan, B. (2020). Diazenyl schiff bases: Synthesis, spectral analysis, antimicrobial studies and cytotoxic activity on human colorectal carcinoma cell line (HCT-116). Arabian Journal of Chemistry, 13(1), 377–392. https://doi.org/10.1016/j.arabjc.2017.05.004
- Khan, M. S., Khalid, M., Ahmad, M. S., Ahmad, M., Ashafaq, M., Rahisuddin, … Shahid, M. (2019). Synthesis, spectral and crystallographic study, DNA binding and molecular docking studies of homo dinuclear Co(II) and Ni(II) complexes. Journal of Molecular Structure, 1175, 889–899. https://doi.org/10.1016/j.molstruc.2018.08.048
- Kiran, T., Prasanth, V. G., Balamurali, M. M., Vasavi, C. S., Munusami, P., Sathiyanarayanan, K. I., & Pathak, M. (2015). Synthesis, spectroscopic characterization and in vitro studies of new heteroleptic copper (II) complexes derived from 2-hydroxy napthaldehyde Schiff’s bases and N, N donor ligands: Antimicrobial, DNA binding and cytotoxic investigations. Inorganica Chimica Acta, 433, 26–34. https://doi.org/10.1016/j.ica.2015.04.033
- Liberto, N. A., Simões, J. B., de Paiva Silva, S., da Silva, C. J., Modolo, L. V., de Fátima, Â., Silva, L. M., Derita, M., Zacchino, S., Zuñiga, O. M. P., Romanelli, G. P., & Fernandes, S. A. (2017). Quinolines: Microwave-assisted synthesis and their antifungal, anticancer and radical scavenger properties. Bioorganic & Medicinal Chemistry, 25(3), 1153–1162. https://doi.org/10.1016/j.bmc.2016.12.023
- Lunagariya, M. V., Thakor, K. P., Kanthecha, D. N., & Patel, M. N. (2018). Synthesis, characterization and biological applications of substituted pyrazolone core based platinum(II) organometallic compounds. Journal of Organometallic Chemistry, 854, 49–63. https://doi.org/10.1016/j.jorganchem.2017.11.012
- Lunagariya, M. V., Thakor, K. P., Varma, R. R., Waghela, B. N., Pathak, C., & Patel, M. N. (2018). Synthesis, characterization and biological application of 5-quinoline 1,3,5-trisubstituted pyrazole based platinum(ii) complexes. MedChemComm, 9(2), 282–298. https://doi.org/10.1039/C7MD00472A
- Mehta, J. V., Gajera, S. B., Raval, D. B., Thakkar, V. R., & Patel, M. N. (2016). Biological assessment of substituted quinoline based heteroleptic organometallic compounds. MedChemComm, 7(8), 1617–1627. https://doi.org/10.1039/C6MD00251J
- Meier-Menches, S. M., Gerner, C., Berger, W., Hartinger, C. G., & Keppler, B. K. (2018). Structure–activity relationships for ruthenium and osmium anticancer agents – towards clinical development. Chemical Society Reviews, 47(3), 909–928. https://doi.org/10.1039/C7CS00332C
- Mühlgassner, G., Bartel, C., Schmid, W. F., Jakupec, M. A., Arion, V. B., & Keppler, B. K. (2012). Biological activity of ruthenium and osmium arene complexes with modified paullones in human cancer cells. Journal of Inorganic Biochemistry, 116, 180–187. https://doi.org/10.1016/j.jinorgbio.2012.06.003
- Mungra, D. C., Kathrotiya, H. G., Ladani, N. K., Patel, M. P., & Patel, R. G. (2012). Molecular iodine catalyzed synthesis of tetrazolo[1,5-a]-quinoline based imidazoles as a new class of antimicrobial and antituberculosis agents. Chinese Chemical Letters, 23(12), 1367–1370. https://doi.org/10.1016/j.cclet.2012.11.007
- Oliveri, V., & Vecchio, G. (2016). 8-Hydroxyquinolines in medicinal chemistry: A structural perspective. European Journal of Medicinal Chemistry, 120, 252–274. https://doi.org/10.1016/j.ejmech.2016.05.007
- Özel, A., Barut, B., Demirbaş, Ü., & Biyiklioglu, Z. (2016). Investigation of DNA binding, DNA photocleavage, topoisomerase I inhibition and antioxidant activities of water soluble titanium(IV) phthalocyanine compounds. Journal of Photochemistry and Photobiology B: Biology, 157, 32–38. https://doi.org/10.1016/j.jphotobiol.2016.02.005
- Pages, B. J., Ang, D. L., Wright, E. P., & Aldrich-Wright, J. R. (2015). Metal complex interactions with DNA. Dalton Transactions, 44(8), 3505–3526. https://doi.org/10.1039/C4DT02700K
- Patel, M. N., Gandhi, D. S., Parmar, P. A., & Mehta, J. V. (2017). Molecular docking, free radical scavenging, and DNA interaction studies of drug-based coordination compounds. Monatshefte für Chemie - Chemical Monthly, 148(5), 901–908. https://doi.org/10.1007/s00706-016-1816-5
- Phadte, A. A., Banerjee, S., Mate, N. A., & Banerjee, A. (2019). Spectroscopic and viscometric determination of DNA-binding modes of some bioactive dibenzodioxins and phenazines. Biochemistry and Biophysics Reports, 18, 100629. https://doi.org/10.1016/j.bbrep.2019.100629
- Pradeepa, S. M., Bhojya Naik, H. S., Vinay Kumar, B., Indira Priyadarsini, K., Barik, A., & Jayakumar, S. (2015). Synthesis and characterization of cobalt(II), nickel(II) and copper(II)-based potential photosensitizers: Evaluation of their DNA binding profile, cleavage and photocytotoxicity. Inorganica Chimica Acta, 428, 138–146. https://doi.org/10.1016/j.ica.2014.12.032
- Prasad, P., Sasmal, P. K., Majumdar, R., Dighe, R. R., & Chakravarty, A. R. (2010). Photocytotoxicity and near-IR light DNA cleavage activity of oxovanadium(IV) Schiff base complexes having phenanthroline bases. Inorganica Chimica Acta, 363(12), 2743–2751. https://doi.org/10.1016/j.ica.2010.03.016
- Ramana, M. M. V., Betkar, R., Nimkar, A., Ranade, P., Mundhe, B., & Pardeshi, S. (2015). In vitro DNA binding studies of antiretroviral drug nelfinavir using ethidium bromide as fluorescence probe. Journal of Photochemistry and Photobiology B: Biology, 151, 194–200. https://doi.org/10.1016/j.jphotobiol.2015.08.012
- Rijt, S. H. v., Kostrhunova, H., Brabec, V., & Sadler, P. J. (2011). Functionalization of osmium arene anticancer complexes with (poly)arginine: Effect on cellular uptake, internalization, and cytotoxicity. Bioconjugate Chemistry, 22(2), 218–226. https://doi.org/10.1021/bc100369p
- Romero-Canelón, I., Salassa, L., & Sadler, P. J. (2013). The contrasting activity of iodido versus chlorido ruthenium and osmium arene azo- and imino-pyridine anticancer complexes: Control of cell selectivity, cross-resistance, p53 dependence, and apoptosis pathway. Journal of Medicinal Chemistry, 56(3), 1291–1300. https://doi.org/10.1021/jm3017442
- Saha, S., Jana, S., Gupta, S., Ghosh, A., & Nayek, H. P. (2016). Syntheses, structures and biological activities of square planar Ni(II), Cu(II) complexes. Polyhedron, 107, 183–189. https://doi.org/10.1016/j.poly.2016.01.034
- Scalese, G., Correia, I., Benítez, J., Rostán, S., Marques, F., Mendes, F., Matos, A. P., Costa Pessoa, J., & Gambino, D. (2017). Evaluation of cellular uptake, cytotoxicity and cellular ultrastructural effects of heteroleptic oxidovanadium(IV) complexes of salicylaldimines and polypyridyl ligands. Journal of Inorganic Biochemistry, 166, 162–172. https://doi.org/10.1016/j.jinorgbio.2016.11.010
- Shaban, S. Y., El-Kemary, M. A., Samir, G., El-Baradei, H., & Puchta, R. (2015). Norfloxacin La(III)-based complex: Synthesis, characterization, and DNA-binding studies. Journal of Coordination Chemistry, 68(17-18), 3247–3258. https://doi.org/10.1080/00958972.2015.1065320
- Shiro, T., Fukaya, T., & Tobe, M. (2015). The chemistry and biological activity of heterocycle-fused quinolinone derivatives: A review. European Journal of Medicinal Chemistry, 97, 397–408. https://doi.org/10.1016/j.ejmech.2014.12.004
- Suntharalingam, K., Lin, W., Johnstone, T. C., Bruno, P. M., Zheng, Y.-R., Hemann, M. T., & Lippard, S. J. (2014). A breast cancer stem cell-selective, mammospheres-potent osmium(VI) nitrido complex. Journal of the American Chemical Society, 136(41), 14413–14416. https://doi.org/10.1021/ja508808v
- Tanaka, K., Tainaka, K., & Okamoto, A. (2007). Methylcytosine-selective fluorescence quenching by osmium complexation. Bioorganic & Medicinal Chemistry, 15(4), 1615–1621. https://doi.org/10.1016/j.bmc.2006.12.023
- Teng, P., Li, C., Peng, Z., Anne Marie, V., Nimmagadda, A., Su, M., Li, Y., Sun, X., & Cai, J. (2018). Facilely accessible quinoline derivatives as potent antibacterial agents. Bioorganic & Medicinal Chemistry, 26(12), 3573–3579. https://doi.org/10.1016/j.bmc.2018.05.031
- Thakor, K. P., Lunagariya, M. V., Bhatt, B. S., & Patel, M. N. (2018). Synthesis, characterization and biological applications of some substituted pyrazoline based palladium (II) compounds. Applied Organometallic Chemistry, 32(11), e4523. https://doi.org/10.1002/aoc.4523
- Thakor, K. P., Lunagariya, M. V., Bhatt, B. S., & Patel, M. N. (2019). Bipyrazole-based palladium(II) complexes as DNA intercalator and artificial metallonuclease. Monatshefte für Chemie - Chemical Monthly, 150(2), 233–245. https://doi.org/10.1007/s00706-018-2316-6
- Thakor, K. P., Lunagariya, M. V., & Patel, M. N. (2017). Acetyl pyridine-based palladium(II) compounds as an artificial metallonucleases. Journal of Biomolecular Structure and Dynamics, 35(13), 2925–2937. https://doi.org/10.1080/07391102.2016.1236748
- Tušek-Božić, L., Juribašić, M., Scarcia, V., & Furlani, A. (2010). Platinum(II) complexes of 8-quinolylmethylphosphonates: Synthesis, characterization and antitumour activity. Polyhedron, 29(12), 2527–2536. https://doi.org/10.1016/j.poly.2010.05.022
- Upadhyay, A., Kushwaha, P., Gupta, S., Dodda, R. P., Ramalingam, K., Kant, R., Goyal, N., & Sashidhara, K. V. (2018). Synthesis and evaluation of novel triazolyl quinoline derivatives as potential antileishmanial agents. European Journal of Medicinal Chemistry, 154, 172–181. https://doi.org/10.1016/j.ejmech.2018.05.014
- van Rijt, S. H., Mukherjee, A., Pizarro, A. M., & Sadler, P. J. (2010). Cytotoxicity, hydrophobicity, uptake, and distribution of osmium(II) anticancer complexes in ovarian cancer cells. Journal of Medicinal Chemistry, 53(2), 840–849. https://doi.org/10.1021/jm901556u
- Varma, R. R., Pursuwani, B. H., Suresh, E., Bhatt, B. S., & Patel, M. N. (2020). Single crystal, DNA interaction and cytotoxicity studies of rhenium(I) organometallic compounds. Journal of Molecular Structure, 1200, 127068. https://doi.org/10.1016/j.molstruc.2019.127068
- Zheng, Y., Tice, C. M., & Singh, S. B. (2017). Conformational control in structure-based drug design. Bioorganic & Medicinal Chemistry Letters, 27(13), 2825–2837. https://doi.org/10.1016/j.bmcl.2017.04.079