How to cite this paper
Santhosh, M., NagendraPrasad, H., Nagashree, S., Manukumar, H., Mallesh, L & Mallu, P. (2019). Synthesis and characterization of Schiff base analogues of fluoroaniline and their antibiocidal activity against MRSA.Current Chemistry Letters, 8(3), 169-176.
Refrences
1. Schiff, H. (1864). Mittheilungen aus dem Universitätslaboratorium in Pisa: eine neue Reihe organischer Basen. Justus Lieb. Ann. Der. Chem., 131(1), 118-119.
2. Dhar, D. N., Taploo, C. L. (1982). Schiff-bases and their applications. J. Sci. Ind. Res., 41(8), 501-506.
3. Mittal, S. K., Rana, S., Kaur, N., Banks, C. E. (2018). A voltammetric method for Fe(III) in blood serum using a screen-printed electrode modified with a Schiff base ionophore. Analyst., 143(12), 2851-2861.
4. Hassan, A. M., Wahba, O. A., Naser, A. M., Eldin, A. M. (2016). Microwave synthesis and spectroscopic studies of some complex compounds as pigments and their applications in paints. J. Coat. Techn. Res., 13(3), 517-525.
5. Przybylski, P., Huczynski, A., Pyta, K., Brzezinski, B., Bartl, F. (2009). Biological properties of Schiff bases and azo derivatives of phenols. Cur. Org. Chem., 13(2), 124-148.
6. Kundu, A., Hariharan, P. S., Prabakaran, K., Anthony, S. P. (2015). Developing new Schiff base molecules for selective colorimetric sensing of Fe3+ and Cu2+ metal ions: Substituent dependent selectivity and colour change. Sen. Actu. B: Chem., 206, 524-530.
7. Karthik, C. S., Mallesha, L., Santhosh, M. V., Nagashree, S., Mallu, P. (2016). Synthesis, Characterization, Antimicrobial Activity, and Optical Properties of Schiff Bases Derived from 4-(Aminomethyl) Piperidine. Ind. J. Adv. Chem. Sci., 206, 212-216.
8. Munawar, K. S., Haroon, S. M., Hussain, S. A., Raza, H. (2018). Schiff Bases: Multipurpose Pharmacophores with Extensive Biological Applications. J.Bas. Appl. Sci., 14, 217-229.
9. Murtaza, S., Akhtar, M. S., Kanwal, F., Abbas, A., Ashiq, S., Shamim, S. (2017). Synthesis and biological evaluation of schiff bases of 4-aminophenazone as an anti-inflammatory, analgesic and antipyretic agent. J. Saudi Chem. Soc., 21, S359-S372.
10. Mishra, B. B., Kale, R. R., Singh, R. K., Tiwari, V. K. (2009). Alkaloids: future prospective to combat leishmaniasis. Fitoterapia., 80(2), 81-90.
11. Souza, A. O. D., Galetti, F., Silva, C. L., Bicalho, B., Parma, M. M., Fonseca, S. F. Andrade-Neto, M. (2007). Antimycobacterial and cytotoxicity activity of synthetic and natural compounds. Quim. Nova., 30(7), 1563-1566.
12. Carpintero, M., Cifuentes, M., Ferritto, R., Haro, R., Toledo, M. A. (2007). Automated liquid− liquid extraction workstation for library synthesis and its use in the parallel and chromatography-free synthesis of 2-alkyl-3-alkyl-4-(3H)-quinazolinones. J. Comb. Chem., 9(5), 818-822.
13. Kock, R., Schaumburg, F., Mellmann, A., Koksal, M., Jurke, A., Becker, K., Friedrich, A. W. (2013). Livestock-associated methicillin-resistant Staphylococcus aureus (MRSA) as causes of human infection and colonization in Germany. PloS One., 8(2), e55040-e55046.
14. Hennekinne, J. A., De Buyser, M. L., Dragacci, S. (2012). Staphylococcus aureus and its food poisoning toxins: characterization and outbreak investigation. FEMS Microb. Rev., 36(4), 815-836.
15. Paterson, G. K., Harrison, E. M., Holmes, M. A. (2014). The emergence of mecC methicillin-resistant Staphylococcus aureus. Trend. Micro., 22(1), 42-47.
16. Garcia-Alvarez, L., Holden, M. T., Lindsay, H., Webb, C. R., Brown, D. F., Curran, M. D., Walpole, E., Brooks, K., Pickard, D. J., Teale, C., Parkhill, J., Bentley, S. D., Edwards, G. F., Girvan, E. K., Kearns, A. M., Pichon, B., Hill, R. L., Larsen, A. R., Skov, R. L., Peacock, S. J., Maskell, D. J., Holmes M. A. (2011). Meticillin-resistant Staphylococcus aureus with a novel mecA homologue in human and bovine populations in the UK and Denmark: a descriptive study. Lancet Infect. Dis., 11(8), 595-603.
17. Lefeuvre, P., Cellier, G., Remenant, B., Chiroleu, F., Prior, P. (2013). Constraints on genome dynamics revealed from gene distribution among the Ralstonia solanacearum species. Plos one, 8(5), e63155-e633163.
18. Wu, A. M., Liu, J. H., Herp, A., Sudakevitz, D., Gilboa-Garber, N. (2012). Relative intensities of recognition factors at two combining sites of Ralstonia solanacearum lectin (RSL) for accommodating lFucα1→, dManα1→ and Galβ1→ 3/4GlcNAc glycotopes. FEBS let., 586(9), 1294-1299.
19. Xu, W. M., Han, F. F., He, M., Hu, D. Y., He, J., Yang, S., Song, B. A. (2012). Inhibition of tobacco bacterial wilt with sulfone derivatives containing an 1, 3, 4-oxadiazole moiety. J.Agri. Food Chem., 60(4), 1036-1041.
20 Karthik, C. S., Manukumar, H. M., Ananda, A. P., Nagashree, S., Rakesh, K. P., Mallesha, L., Krishnamurthy, N. B. (2018). Synthesis of novel benzodioxane midst piperazine moiety decorated chitosan silver nanoparticle against biohazard pathogens and as potential anti-inflammatory candidate: A molecular docking studies. Inter. Jour. Biol. Macro., 108, 489-502.
21 Mhaske, S. B., Argade, N. P. (2006). The chemistry of recently isolated naturally occurring quinazolinone alkaloids. Tetra., 62(42), 9787-9826.
22 Hosseinzadeh, L., Aliabadi, A., Kalantari, M., Mostafavi, A., Khajouei, M. R. (2016). Synthesis and cytotoxicity evaluation of some new 6-nitro derivatives of thiazole-containing 4-(3H)-quinazolinone. Res. Pharm.Sci., 11(3), 210-216.
23 Prasad, H. N., Karthik, C. S., Manukumar, H. M., Mallesha, L., Mallu, P. (2018). New approach to address antibiotic resistance: Miss loading of functional membrane microdomains (FMM) of methicillin-resistant Staphylococcus aureus (MRSA). Micro. Patho., 127, 106-105.
2. Dhar, D. N., Taploo, C. L. (1982). Schiff-bases and their applications. J. Sci. Ind. Res., 41(8), 501-506.
3. Mittal, S. K., Rana, S., Kaur, N., Banks, C. E. (2018). A voltammetric method for Fe(III) in blood serum using a screen-printed electrode modified with a Schiff base ionophore. Analyst., 143(12), 2851-2861.
4. Hassan, A. M., Wahba, O. A., Naser, A. M., Eldin, A. M. (2016). Microwave synthesis and spectroscopic studies of some complex compounds as pigments and their applications in paints. J. Coat. Techn. Res., 13(3), 517-525.
5. Przybylski, P., Huczynski, A., Pyta, K., Brzezinski, B., Bartl, F. (2009). Biological properties of Schiff bases and azo derivatives of phenols. Cur. Org. Chem., 13(2), 124-148.
6. Kundu, A., Hariharan, P. S., Prabakaran, K., Anthony, S. P. (2015). Developing new Schiff base molecules for selective colorimetric sensing of Fe3+ and Cu2+ metal ions: Substituent dependent selectivity and colour change. Sen. Actu. B: Chem., 206, 524-530.
7. Karthik, C. S., Mallesha, L., Santhosh, M. V., Nagashree, S., Mallu, P. (2016). Synthesis, Characterization, Antimicrobial Activity, and Optical Properties of Schiff Bases Derived from 4-(Aminomethyl) Piperidine. Ind. J. Adv. Chem. Sci., 206, 212-216.
8. Munawar, K. S., Haroon, S. M., Hussain, S. A., Raza, H. (2018). Schiff Bases: Multipurpose Pharmacophores with Extensive Biological Applications. J.Bas. Appl. Sci., 14, 217-229.
9. Murtaza, S., Akhtar, M. S., Kanwal, F., Abbas, A., Ashiq, S., Shamim, S. (2017). Synthesis and biological evaluation of schiff bases of 4-aminophenazone as an anti-inflammatory, analgesic and antipyretic agent. J. Saudi Chem. Soc., 21, S359-S372.
10. Mishra, B. B., Kale, R. R., Singh, R. K., Tiwari, V. K. (2009). Alkaloids: future prospective to combat leishmaniasis. Fitoterapia., 80(2), 81-90.
11. Souza, A. O. D., Galetti, F., Silva, C. L., Bicalho, B., Parma, M. M., Fonseca, S. F. Andrade-Neto, M. (2007). Antimycobacterial and cytotoxicity activity of synthetic and natural compounds. Quim. Nova., 30(7), 1563-1566.
12. Carpintero, M., Cifuentes, M., Ferritto, R., Haro, R., Toledo, M. A. (2007). Automated liquid− liquid extraction workstation for library synthesis and its use in the parallel and chromatography-free synthesis of 2-alkyl-3-alkyl-4-(3H)-quinazolinones. J. Comb. Chem., 9(5), 818-822.
13. Kock, R., Schaumburg, F., Mellmann, A., Koksal, M., Jurke, A., Becker, K., Friedrich, A. W. (2013). Livestock-associated methicillin-resistant Staphylococcus aureus (MRSA) as causes of human infection and colonization in Germany. PloS One., 8(2), e55040-e55046.
14. Hennekinne, J. A., De Buyser, M. L., Dragacci, S. (2012). Staphylococcus aureus and its food poisoning toxins: characterization and outbreak investigation. FEMS Microb. Rev., 36(4), 815-836.
15. Paterson, G. K., Harrison, E. M., Holmes, M. A. (2014). The emergence of mecC methicillin-resistant Staphylococcus aureus. Trend. Micro., 22(1), 42-47.
16. Garcia-Alvarez, L., Holden, M. T., Lindsay, H., Webb, C. R., Brown, D. F., Curran, M. D., Walpole, E., Brooks, K., Pickard, D. J., Teale, C., Parkhill, J., Bentley, S. D., Edwards, G. F., Girvan, E. K., Kearns, A. M., Pichon, B., Hill, R. L., Larsen, A. R., Skov, R. L., Peacock, S. J., Maskell, D. J., Holmes M. A. (2011). Meticillin-resistant Staphylococcus aureus with a novel mecA homologue in human and bovine populations in the UK and Denmark: a descriptive study. Lancet Infect. Dis., 11(8), 595-603.
17. Lefeuvre, P., Cellier, G., Remenant, B., Chiroleu, F., Prior, P. (2013). Constraints on genome dynamics revealed from gene distribution among the Ralstonia solanacearum species. Plos one, 8(5), e63155-e633163.
18. Wu, A. M., Liu, J. H., Herp, A., Sudakevitz, D., Gilboa-Garber, N. (2012). Relative intensities of recognition factors at two combining sites of Ralstonia solanacearum lectin (RSL) for accommodating lFucα1→, dManα1→ and Galβ1→ 3/4GlcNAc glycotopes. FEBS let., 586(9), 1294-1299.
19. Xu, W. M., Han, F. F., He, M., Hu, D. Y., He, J., Yang, S., Song, B. A. (2012). Inhibition of tobacco bacterial wilt with sulfone derivatives containing an 1, 3, 4-oxadiazole moiety. J.Agri. Food Chem., 60(4), 1036-1041.
20 Karthik, C. S., Manukumar, H. M., Ananda, A. P., Nagashree, S., Rakesh, K. P., Mallesha, L., Krishnamurthy, N. B. (2018). Synthesis of novel benzodioxane midst piperazine moiety decorated chitosan silver nanoparticle against biohazard pathogens and as potential anti-inflammatory candidate: A molecular docking studies. Inter. Jour. Biol. Macro., 108, 489-502.
21 Mhaske, S. B., Argade, N. P. (2006). The chemistry of recently isolated naturally occurring quinazolinone alkaloids. Tetra., 62(42), 9787-9826.
22 Hosseinzadeh, L., Aliabadi, A., Kalantari, M., Mostafavi, A., Khajouei, M. R. (2016). Synthesis and cytotoxicity evaluation of some new 6-nitro derivatives of thiazole-containing 4-(3H)-quinazolinone. Res. Pharm.Sci., 11(3), 210-216.
23 Prasad, H. N., Karthik, C. S., Manukumar, H. M., Mallesha, L., Mallu, P. (2018). New approach to address antibiotic resistance: Miss loading of functional membrane microdomains (FMM) of methicillin-resistant Staphylococcus aureus (MRSA). Micro. Patho., 127, 106-105.