Synthesis of novel coumarin appended bis(formylpyrazole) derivatives: Studies on their antimicrobial and antioxidant activities

Bioorganic and Medicinal Chemistry Letters

Volumn 26, Issue 2, 2016, Pages 690-694

  Nagamallu, Renuka ^a   Srinivasan, Bharath ^b   Ningappa, Mylarappa B ^c   Kariyappa, Ajay Kumar ^a  

^a UNIVERSITY OF MYSORE   (India)

^b GEORGIA INSTITUTE OF TECHNOLOGY   (United States)

^c CHILDREN S HOSPITAL OF PITTSBURGH   (United States)

Author keywords

Antimicrobial; Antioxidant; Coumarin; DPPH; Hydroxyl radical; MIC; Pyrazole

Indexed keywords

ANTIINFECTIVE AGENT; ANTIOXIDANT; ASCORBIC ACID; BUTYLATED HYDROXYANISOLE; CIPROFLOXACIN; COUMARIN DERIVATIVE; FLUCONAZOLE; PYRAZOLE DERIVATIVE; COUMARIN;

ANTIMICROBIAL ACTIVITY; ANTIOXIDANT ACTIVITY; ARTICLE; BACTERIAL STRAIN; CARBON NUCLEAR MAGNETIC RESONANCE; COMPARATIVE STUDY; CONTROLLED STUDY; DRUG POTENCY; DRUG SYNTHESIS; FUNGAL STRAIN; HYDROXYL RADICAL SCAVENGING ASSAY; MINIMUM INHIBITORY CONCENTRATION; PROTON NUCLEAR MAGNETIC RESONANCE; QUANTITATIVE STRUCTURE ACTIVITY RELATION; BACTERIAL INFECTIONS; BACTERIUM; CHEMISTRY; DRUG EFFECTS; FUNGUS; HUMAN; MICROBIAL SENSITIVITY TEST; MYCOSES; SYNTHESIS;

ANTI-INFECTIVE AGENTS; ANTIOXIDANTS; BACTERIA; BACTERIAL INFECTIONS; COUMARINS; FUNGI; HUMANS; MICROBIAL SENSITIVITY TESTS; MYCOSES; PYRAZOLES; QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 84952976272     PISSN: 0960894X     EISSN: 14643405     Source Type: Journal    
DOI: 10.1016/j.bmcl.2015.11.038     Document Type: Article

References (25)

1. M.E. Buyukokuroglu, I. Gulcin, M. Oktay, and O.I. Kufrevioglu Pharmacol. Res. 44 2001 491
2. Katsori Anna-Maria, and Hadjipavlon-Litina Dimitra Expert Opin. Ther. Pat. 24 2014 1323
3. A.M. Villar Food Chem. 110 2008 436
4. Figueroa-Guinez Roberto, Joaometos Maria, Vazquez-Rodriguez Saleta, Santana Lourdes, Uriarte Eugenio, Borges Fernanda, Olea-Azar Claudio, and Maya Juan Diego Curr. Top. Med. Chem. 15 2015 850
5. T. Nasr, S. Bondock, and M. Youns Eur. J. Med. Chem. 76 2014 539
6. D. Maity, D. Karthigeyan, T.K. Kundu, and T. Govindaraju Sens. Actuators, B 176 2013 831
7. K.K. Upadhyay, R.K. Mishra, A. Kumar, J.Z. Zhao, and R. Prasad J. Mol. Struct. 963 2010 228
8. I.I. Padilla-Martinez, I.Y. Flores-Larios, E.V. Garcia-Baez, J. Gonzalez, A. Cruz, and F.J. Martinez-Martinez Molecules 16 2011 915
9. Kuldipsinh P. Barot, Shailesh V. Jain, Laurent Kremer, Shubhra Singh, and Manjunath D. Ghate Med. Chem. Res. 24 2015 2771
10. G. Medina Fernanda, G. Marrero Joaquin, Macias-Alonso Mariana, C. Gonzalez Magdalena, Cordova-Guerrero Ivan, G. Teissier Garcia Ariana, and Osegueda-Robles Soraya Nat. Prod. Rep. 2015 10.1039/c4np00162a
11. L. Knorr Chem. Ber. 17 1883 546
12. G. Menozzi, L. Merello, P. Fossa, S. Schenone, A. Ranise, L. Mosti, F. Bondavalli, R. Loddo, C. Murgioni, V. Mascia, P. Lacolla, and E. Tamburini Bioorg. Med. Chem. 12 2004 5465
13. R. Nagamallu, and A.K. Kariyappa Bioorg. Med. Chem. Lett. 23 2013 6406
14. R. Kumar, S. Malik, and R. Chandra Indian J. Chem. 48B 2009 718
15. K.S. Girisha, B. Kalluraya, V. Narayana, and Padmashree Eur. J. Med. Chem. 45 2010 4640
16. S.K. Guniz, and Sevil Senkardes Eur. J. Med. Chem. 97 2015 786
17. M.A. Kira, Z.M. Nofal, and K.Z. Gadalla Tetrahedron Lett. 1970 4215
18. E.A. Tarik, A.I. Magdy, M.E.G. Zeinab, and M.E.A. Eman Synth. Commun. 43 2013 3329
19. B. El-Amraoui, J.F. Biard, M.J. Uriz, S. Rifai, and A. Fassouane J. Med. Mycol. 20 2010 70
20. T.W. Backman, Y. Cao, and T. Girke Nucleic Acids Res. 39 2011 W486
21. K. Roy, and I. Mitra Comb. Chem. High Throughput Screening 14 2011 450
22. B. Srinivasan, S. Tonddast-Navaei, and J. Skolnick Eur. J. Med. Chem. 2015 10.1016/j.ejmech.2015.08.021
23. S. Blois Marsden Nature 181 1958 1199
24. J. Jayaraman, T. Venugopal, R. Nagarajan, S. Kanagarathinam, and V.P. Marimuthu Med. Chem. Res. 21 2012 1850
25. P. Hochestein, and A.S. Atallah Mutat. Res. 202 1988 363