Synthesis and evaluation of antibacterial and antioxidant activity of novel 2-phenyl-quinoline analogs derivatized at position 4 with aromatically substituted 4H-1,2,4-triazoles
Published 2016 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Synthesis and evaluation of antibacterial and antioxidant activity of novel 2-phenyl-quinoline analogs derivatized at position 4 with aromatically substituted 4H-1,2,4-triazoles
Authors
Keywords
-
Journal
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY
Volume 31, Issue sup2, Pages 104-110
Publisher
Informa UK Limited
Online
2016-06-20
DOI
10.1080/14756366.2016.1190714
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Novel thiazolo[3,2-b]-1,2,4-triazoles derived from naproxen with analgesic/anti-inflammatory properties: Synthesis, biological evaluation and molecular modeling studies
- (2015) Deniz Sarigol et al. BIOORGANIC & MEDICINAL CHEMISTRY
- Design and synthesis of novel 2H-chromen-2-one derivatives bearing 1,2,3-triazole moiety as lead antimicrobials
- (2014) Khushbu Kushwaha et al. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
- Insights on the Antioxidant Potential of 1, 2, 4-Triazoles: Synthesis, Screening & QSAR Studies
- (2014) Sateesh Pokuri et al. CURRENT DRUG METABOLISM
- Synthesis of medicinally important quinazolines decorated with 1,4-disubstituted-1,2,3-triazoles using CuSO4·5H2O–Et3N catalytic system
- (2014) Monika Vashist et al. RSC Advances
- Synthesis and Evaluation of Antioxidant Properties of Novel 1,2,4-Triazole-Based Schiff Base Heterocycles
- (2013) Chandrashekar Aswathanarayanappa et al. ARCHIV DER PHARMAZIE
- New trifluoromethyl quinolone derivatives: Synthesis and investigation of antimicrobial properties
- (2013) Siva S. Panda et al. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
- Preparation of 8-hydroxyquinoline derivatives as potential antibiotics against Staphylococcus aureus
- (2013) Kim-Hung Lam et al. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
- Access to a new class of biologically active quinoline based 1,2,4-triazoles
- (2013) Rahul V. Patel et al. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
- Design, synthesis and evaluation of the antidepressant and anticonvulsant activities of triazole-containing quinolinones
- (2013) Xian-Qing Deng et al. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
- Bond dissociation free energy as a general parameter for flavonoid radical scavenging activity
- (2013) Višnja Stepanić et al. FOOD CHEMISTRY
- Synthesis and Antioxidant Activity of 1,2,4-Triazole linked Thieno[2,3- d]pyrimidine Derivatives
- (2013) Suresh Maddila et al. Letters in Drug Design & Discovery
- Synthesis and antimicrobial activity of novel bis-azaphenothiazines
- (2013) Khushbu Kushwaha et al. MEDICINAL CHEMISTRY RESEARCH
- Synthesis and QSAR studies of some novel disubstituted 1,2,4-triazoles as antimicrobial agents
- (2013) Siva S. Panda et al. MEDICINAL CHEMISTRY RESEARCH
- Evaluating the antioxidant capacity of natural products: A review on chemical and cellular-based assays
- (2012) Camilo López-Alarcón et al. ANALYTICA CHIMICA ACTA
- An efficient and convenient microwave-assisted chemical synthesis of (thio)xanthones with additional in vitro and in silico characterization
- (2012) Donatella Verbanac et al. BIOORGANIC & MEDICINAL CHEMISTRY
- Anti-HIV, antimycobacterial and antimicrobial studies of newly synthesized 1,2,4-triazole clubbed benzothiazoles
- (2012) Navin B. Patel et al. MEDICINAL CHEMISTRY RESEARCH
- Synthesis and antioxidant properties of novel quinoline–chalcogenium compounds
- (2012) Lucielli Savegnago et al. TETRAHEDRON LETTERS
- Design and synthesis of spiro[indole-thiazolidine]spiro[indole-pyrans] as antimicrobial agents
- (2011) Rajeev Sakhuja et al. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
- Synthesis and antimicrobial activity of some new 4-triazolylmethoxy-2H-chromen-2-one derivatives
- (2011) Siva S. Panda et al. MEDICINAL CHEMISTRY RESEARCH
- Open Babel: An open chemical toolbox
- (2011) Noel M O'Boyle et al. Journal of Cheminformatics
- Synthesis of New Quinoline Derivatives as Inhibitors of Human Tumor Cells Growth
- (2010) Aymn E. Rashad et al. ARCHIV DER PHARMAZIE
- Structure–activity relationship study of acridine analogs as haspin and DYRK2 kinase inhibitors
- (2010) Gregory D. Cuny et al. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
- Novel quinoline and naphthalene derivatives as potent antimycobacterial agents
- (2010) Ram Shankar Upadhayaya et al. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
- Design, synthesis and biological evaluation of novel triazole, urea and thiourea derivatives of quinoline against Mycobacterium tuberculosis
- (2009) Ram Shankar Upadhayaya et al. BIOORGANIC & MEDICINAL CHEMISTRY
- Synthesis and antimicrobial activities of novel quinoline derivatives carrying 1,2,4-triazole moiety
- (2009) Sumesh Eswaran et al. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
- 6-[2-(4-Aryl-1-piperazinyl)ethyl]-2H-1,4-benzoxazin-3(4H)-ones: Dual-acting 5-HT1 receptor antagonists and serotonin reuptake inhibitors
- (2008) Steven M. Bromidge et al. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
- Synthesis and antifungal activity of 1,2,3-triazole containing fluconazole analogues
- (2008) Nilkanth G. Aher et al. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
- Synthesis and antimycobacterial activities of novel 6-nitroquinolone-3-carboxylic acids
- (2008) Palaniappan Senthilkumar et al. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
- Antimicrobial studies of some novel quinazolinones fused with [1,2,4]-triazole, [1,2,4]-triazine and [1,2,4,5]-tetrazine rings
- (2008) Sarvesh Kumar Pandey et al. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
- Surprising Alteration of Antibacterial Activity of 5′′-Modified Neomycin against Resistant Bacteria
- (2008) Jianjun Zhang et al. JOURNAL OF MEDICINAL CHEMISTRY
- Physicochemical Properties of Antibacterial Compounds: Implications for Drug Discovery
- (2008) Rosemarie O’Shea et al. JOURNAL OF MEDICINAL CHEMISTRY
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started