Multi technique investigation on interaction between 5-(2-thiazolylazo)-2,4,6-triaminopyrimidine and HSA and BSA

References

• Abdullah, S. M., Fatma, S., Rabbani, G., & Ashraf, J. M. (2017). A spectroscopic and molecular docking approach on the binding of tinzaparin sodium with human serum albumin. Journal of Molecular Structure, 1127, 283–288. https://doi.org/10.1016/j.molstruc.2016.07.108
   Web of Science ®Google Scholar
• Ahmad, E., Rabbani, G., Zaidi, N., Ahmad, B., & Khan, R. H. (2012). Pollutant-induced modulation in conformation and β-lactamase activity of human serum albumin. PLoS One, 7(6), e38372. https://doi.org/10.1371/journal.pone.0038372
   PubMed Web of Science ®Google Scholar
• Ahmad, E., Rabbani, G., Zaidi, N., Singh, S., Rehan, M., Khan, M. M., Rahman, S. K., Quadri, Z., Shadab, M., Ashraf, M. T., Subbarao, N., Bhat, R., & Khan, R. H. (2011). Stereo-selectivity of human serum albumin to enantiomeric and isoelectronic pollutants dissected by spectroscopy, calorimetry and bioinformatics. PLoS One, 6(11), e26186. https://doi.org/10.1371/journal.pone.0026186
   PubMed Web of Science ®Google Scholar
• Almutairi, F. M., Ajmal, M. R., Siddiqi, M. K., Amir, M., & Khan, R. H. (2020). Multi-spectroscopic and molecular docking technique study of the azelastine interaction with human serum albumin. Journal of Molecular Structure, 1201, 127147. https://doi.org/10.1016/j.molstruc.2019.127147
   Web of Science ®Google Scholar
• Baig, M. H., Rahman, S., Rabbani, G., Imran, M., Ahmad, K., & Choi, I. (2019). Multi-spectroscopic characterization of human serum albumin binding with cyclobenzaprine hydrochloride: Insights from biophysical and in silico approaches. International Journal of Molecular Sciences, 20(3), 662. https://doi.org/10.3390/ijms20030662
   PubMed Web of Science ®Google Scholar
• Bradshaw, T., Stevens, M., & Westwell, A. (2001). The discovery of the potent and selective antitumour agent 2-(4-amino-3-methylphenyl)benzothiazole (DF 203) and related compounds. Current Medical Chemistry, 8(2), 203–210. https://doi.org/10.2174/0929867013373714
   PubMed Web of Science ®Google Scholar
• Dezhampanah, H., Esmaili, M., & Khorshidi, A. (2017). Milk β-casein as a vehicle for delivery of bis (indolyl) methane: Spectroscopy and molecular docking studies. Journal of Molecular Structure, 1136, 50–58. https://doi.org/10.1016/j.molstruc.2017.01.065
   Web of Science ®Google Scholar
• Dezhampanah, H., & Firouzi, R. (2017). An Investigation on intermolecular interaction between Bis(indolyl)methane and HSA and BSA using multi technique methods. Journal of Biomolecular Structure & Dynamics, 35(16), 3615–3626. https://doi.org/10.1080/07391102.2016.1264890
   PubMed Web of Science ®Google Scholar
• Dezhampanah, H., Firouzi, R., Shoeili, Z. M., & Binazir, R. (2020). Intermolecular investigation on interaction of two ternary copper (II) Schiff base complexes with bovine serum albumin. Journal of Molecular Structure, 1205, 127557. https://doi.org/10.1016/j.molstruc.2019.127557
   Web of Science ®Google Scholar
• Gup, R., Giziroglu, E., & Kırkan, B. (2007). Synthesis and spectroscopic properties of new azo-dyes and azo-metal complexes derived from barbituric acid and aminoquinoline. Dyes and Pigments, 73(1), 40–46. https://doi.org/10.1016/j.dyepig.2005.10.005
   Web of Science ®Google Scholar
• Haque, A., Hsieh, M.-F., Hassan, S. I., Faizi, M. S. H., Saha, A., Dege, N., Rather, J. A., & Khan, M. S. (2017). Synthesis, characterization, and pharmacological studies of ferrocene-1H-1, 2, 3-triazole hybrids. Journal of Molecular Structure, 1146, 536–545. https://doi.org/10.1016/j.molstruc.2017.06.027
   Web of Science ®Google Scholar
• Ishtikhar, M., Rabbani, G., Khan, S., & Khan, R. H. (2015). Biophysical investigation of thymoquinone binding to ‘N’and ‘B’ isoforms of human serum albumin: Exploring the interaction mechanism and radical scavenging activity. RSC Advances, 5(24), 18218–18232. https://doi.org/10.1039/C4RA09892G
   Web of Science ®Google Scholar
• P. I., Jha, K. K., & Vijayakumar, M. (2016). Synthesis, characterization and pharmacological evaluation of substituted 4-aryl thiazole-2-amino acetanilides. Indian Journal of Pharmaceutical and Biological Research, 4(03), 74–79. https://doi.org/10.30750/ijpbr.4.3.10
   Google Scholar
• Kamal, A., Srikanth, Y., Khan, M. N. A., Shaik, T. B., & Ashraf, M. (2010). Synthesis of 3,3-diindolyl oxyindoles efficiently catalysed by FeCl3 and their in vitro evaluation for anticancer activity . Bioorganic & Medicinal Chemistry Letters, 20(17), 5229–5231. https://doi.org/10.1016/j.bmcl.2010.06.152
   PubMed Web of Science ®Google Scholar
• Keshavayya, J. (2019). Synthesis, structural investigations and in vitro biological evaluation of N, N-dimethyl aniline derivatives based azo dyes as potential pharmacological agents. Journal of Molecular Structure, 1186, 404–412. https://doi.org/10.1016/j.molstruc.2019.03.042
   Web of Science ®Google Scholar
• Kong, D., Qin, C., Fan, P., Li, B., & Wang, J. (2015). Spectroscopic studies on interaction of BSA and Eu(III) complexes with H5ph-dtpa and H5dtpa ligands . Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 140, 372–381. https://doi.org/10.1016/j.saa.2015.01.004
   PubMed Web of Science ®Google Scholar
• Lakowicz, J. R. (2013). Principles of fluorescence spectroscopy. Springer Science & Business Media.
   Google Scholar
• Loh, S. H., Park, J.-Y., Cho, E. H., Nah, S.-Y., & Kang, Y.-S. (2017). Animal lectins: Potential receptors for ginseng polysaccharides. Journal of Ginseng Research, 41(1), 1–9. https://doi.org/10.1016/j.jgr.2015.12.006
   PubMed Web of Science ®Google Scholar
• Mahran, M. A., William, S., Ramzy, F., & Sembel, A. M. (2007). Synthesis and in vitro evaluation of new benzothiazole derivatives as schistosomicidal agents. Molecules (Basel, Switzerland), 12(3), 622–633. https://doi.org/10.3390/12030622
   PubMed Web of Science ®Google Scholar
• Maliyappa, M., Keshavayya, J., Mallikarjuna, N., Krishna, P. M., Shivakumara, N., Sandeep, T., Sailaja, K., & Nazrulla, M. A. (2019). Synthesis, characterization, pharmacological and computational studies of 4, 5, 6, 7-tetrahydro-1, 3-benzothiazole incorporated azo dyes. Journal of Molecular Structure, 1179, 630–641. https://doi.org/10.1016/j.molstruc.2018.11.041
   Web of Science ®Google Scholar
• Maradiya, H. R. (2010). Synthesis and dyeing performance of some novel thiazole azo disperse dyes. Journal of Saudi Chemical Society, 14(1), 77–81. https://doi.org/10.1016/j.jscs.2009.12.012
   Web of Science ®Google Scholar
• Mohammadi, A., & Ghasemi, Z. (2020). A simple pyrimidine based colorimetric and fluorescent chemosensor for sequential detection of copper (II) and cyanide ions and its application in real samples. Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 228, 117730. https://doi.org/10.1016/j.saa.2019.117730
   PubMed Web of Science ®Google Scholar
• Mohseni-Shahri, F. S., Moeinpour, F., & Nosrati, M. (2018). Spectroscopy and molecular dynamics simulation study on the interaction of sunset yellow food additive with pepsin. International Journal of Biological Macromolecules, 115, 273–280. https://doi.org/10.1016/j.ijbiomac.2018.04.080
   PubMed Web of Science ®Google Scholar
• Naveenraj, S., & Anandan, S. (2013). Binding of serum albumins with bioactive substances–nanoparticles to drugs. Journal of Photochemistry and Photobiology C: Photochemistry Reviews, 14, 53–71. https://doi.org/10.1016/j.jphotochemrev.2012.09.001
   Web of Science ®Google Scholar
• Naveenraj, S., Solomon, R. V., Mangalaraja, R. V., Venuvanalingam, P., Asiri, A. M., & Anandan, S. (2018). A multispectroscopic and molecular docking investigation of the binding interaction between serum albumins and acid orange dye. Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 192, 34–40. https://doi.org/10.1016/j.saa.2017.10.075
   PubMed Web of Science ®Google Scholar
• Rabbani, G., Ahmad, E., Zaidi, N., & Khan, R. H. (2011). pH-dependent conformational transitions in conalbumin (ovotransferrin), a metalloproteinase from hen egg white. Cell Biochemistry and Biophysics, 61(3), 551–560. https://doi.org/10.1007/s12013-011-9237-x
   PubMed Web of Science ®Google Scholar
• Rabbani, G., & Ahn, S. N. (2019). Structure, enzymatic activities, glycation and therapeutic potential of human serum albumin: A natural cargo. International Journal of Biological Macromolecules, 123, 979–990. https://doi.org/10.1016/j.ijbiomac.2018.11.053
   PubMed Web of Science ®Google Scholar
• Rabbani, G., Baig, M. H., Lee, E. J., Cho, W.-K., Ma, J. Y., & Choi, I. (2017). Biophysical study on the interaction between eperisone hydrochloride and human serum albumin using spectroscopic, calorimetric, and molecular docking analyses. Molecular Pharmaceutics, 14(5), 1656–1665. https://doi.org/10.1021/acs.molpharmaceut.6b01124
   PubMed Web of Science ®Google Scholar
• Rabbani, G., & Choi, I. (2018). Roles of osmolytes in protein folding and aggregation in cells and their biotechnological applications. International Journal of Biological Macromolecules, 109, 483–491. https://doi.org/10.1016/j.ijbiomac.2017.12.100
   PubMed Web of Science ®Google Scholar
• Rabbani, G., Kaur, J., Ahmad, E., Khan, R. H., & Jain, S. (2014). Structural characteristics of thermostable immunogenic outer membrane protein from Salmonella enterica serovar Typhi. Applied Microbiology and Biotechnology, 98(6), 2533–2543. https://doi.org/10.1007/s00253-013-5123-3
   PubMed Web of Science ®Google Scholar
• Rabbani, G., Khan, M. J., Ahmad, A., Maskat, M. Y., & Khan, R. H. (2014). Effect of copper oxide nanoparticles on the conformation and activity of β-galactosidase. Colloids and Surfaces B: Biointerfaces, 123, 96–105. https://doi.org/10.1016/j.colsurfb.2014.08.035
   PubMed Web of Science ®Google Scholar
• Rabbani, G., Lee, E. J., Ahmad, K., Baig, M. H., & Choi, I. (2018). Binding of tolperisone hydrochloride with human serum albumin: Effects on the conformation, thermodynamics, and activity of HSA. Molecular Pharmaceutics, 15(4), 1445–1456. https://doi.org/10.1021/acs.molpharmaceut.7b00976
   PubMed Web of Science ®Google Scholar
• Rahman, S., Rehman, M. T., Rabbani, G., Khan, P., AlAjmi, M. F., Hassan, M. I., Muteeb, G., & Kim, J. (2019). Insight of the interaction between 2, 4-thiazolidinedione and human serum albumin: A spectroscopic, thermodynamic and molecular docking study. International Journal of Molecular Sciences, 20(11), 2727. https://doi.org/10.3390/ijms20112727
   PubMed Web of Science ®Google Scholar
• Rajendiran, N., & Thulasidhasan, J. (2015). Study of the binding of thiazolyazoresorcinol and thiazolyazocresol dyes with BSA and adenine by spectral, electrochemical and molecular docking methods. Molecules, 12, 13.
   Google Scholar
• Rudra, S., Dasmandal, S., Patra, C., Patel, B. K., Paul, S., & Mahapatra, A. (2018). Characterization of domain-specific interaction of synthesized dye with serum proteins by spectroscopic and docking approaches along with determination of in vitro cytotoxicity and antiviral activity. Journal of Biomolecular Structure & Dynamics, 36(14), 3773–3790. https://doi.org/10.1080/07391102.2017.1400468
   PubMed Web of Science ®Google Scholar
• Sharma, A. S., Anandakumar, S., & Ilanchelian, M. (2014). A combined spectroscopic and molecular docking study on site selective binding interaction of toluidine blue O with human and bovine serum albumins. Journal of Luminescence, 151, 206–218. https://doi.org/10.1016/j.jlumin.2014.02.009
   Web of Science ®Google Scholar
• Umadevi, P., & Lalitha, P. (2012). Synthesis and antimicrobial evaluation of imino substituted 1, 3, 4 oxa and thiadiazoles. International Journal of Pharmacy and Pharmaceutical Sciences, 4, 523–527.
   Google Scholar
• Venkatesh, P., Pandeya, S. (2009). Synthesis, characterisation and anti-inflammatory activity of some 2-amino benzothiazole derivatives. International Journal of ChemTech Research, 1(4), 1354-1358.
   Google Scholar
• Wang, Q., Huang, C-r., Jiang, M., Zhu, Y.-Y., Wang, J., Chen, J., & Shi, J-h. (2016). Binding interaction of atorvastatin with bovine serum albumin: Spectroscopic methods and molecular docking. Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 156, 155–163. https://doi.org/10.1016/j.saa.2015.12.003
   PubMed Web of Science ®Google Scholar
• Wu, J., Bi, S.-Y., Sun, X.-Y., Zhao, R., Wang, J.-H., & Zhou, H.-F. (2019). Study on the interaction of fisetholz with BSA/HSA by multi-spectroscopic, cyclic voltametric, and molecular docking technique. Journal of Biomolecular Structure & Dynamics, 37(13), 3496–3505. https://doi.org/10.1080/07391102.2018.1518789
   PubMed Web of Science ®Google Scholar
• Yasmeen, S., & Rabbani, G. (2017). Calorimetric and spectroscopic binding studies of amoxicillin with human serum albumin. Journal of Thermal Analysis and Calorimetry, 127(2), 1445–1455. https://doi.org/10.1007/s10973-016-5555-y
   Web of Science ®Google Scholar
• Yazdanbakhsh, M., Yousefi, H., Mamaghani, M., Moradi, E., Rassa, M., Pouramir, H., & Bagheri, M. (2012). Synthesis, spectral characterization and antimicrobial activity of some new azo dyes derived from 4, 6-dihydroxypyrimidine. Journal of Molecular Liquids, 169, 21–26. https://doi.org/10.1016/j.molliq.2012.03.003
   Web of Science ®Google Scholar
• Yu, X.,Yang, Y.,Shiyu, L.,Yao, Q.,Heting, L.,Xiaofang, L., &Pinggui, Y. (2011). The fluorescence spectroscopic study on the interaction between imidazo[2,1-b]thiazole analogues and bovine serum albumin. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 83(1), 322–328. https://doi.org/10.1016/j.saa.2011.08.038
   PubMed Web of Science ®Google Scholar