Results 11 to 20 of about 103,024 (350)

Novel 1, 2, 4-Triazoles as Antifungal Agents

open access: yesBioMed Research International, 2022
The development of innovative antifungal agents is essential. Some fungicidal agents are no longer effective due to resistance development, various side effects, and high toxicity.
Zahra Kazeminejad   +5 more
semanticscholar   +1 more source

Synthesis methods of 1,2,3-/1,2,4-triazoles: A review

open access: yesFrontiers in Chemistry, 2022
Triazole, comprising three nitrogen atoms and two carbon atoms, is divided into two isomers 1,2,3-triazole and 1,2,4-triazole. Compounds containing a triazole are one of the significant heterocycles that exhibit broad biological activities, such as ...
J. Dai   +3 more
semanticscholar   +1 more source

1,2,3-Triazoles of 8-Hydroxyquinoline and HBT: Synthesis and Studies (DNA Binding, Antimicrobial, Molecular Docking, ADME, and DFT)

open access: yesACS Omega, 2021
A new series of 1,2,3-triazole hybrids containing either 2- or 4-hydroxyphenyl benzothiazole (2- or 4-HBT) and naphthalen-1-ol or 8-hydroxyquinoline (8-HQ) was synthesized in high yields and fully characterized.
Nidhi Nehra, Ram Kumar Tittal, V. Ghule
semanticscholar   +1 more source

1,2,4-Triazoles as Important Antibacterial Agents

open access: yesPharmaceuticals, 2021
The global spread of drug resistance in bacteria requires new potent and safe antimicrobial agents. Compounds containing the 1,2,4-triazole ring in their structure are characterised by multidirectional biological activity.
M. Strzelecka, P. Świątek
semanticscholar   +1 more source

Design and antiproliferative and antioxidant activities of furan-based thiosemicarbazides and 1,2,4-triazoles: their structure-activity relationship and SwissADME predictions

open access: yesMedicinal Chemistry Research, 2021
Due to the limited number of drugs in current clinical use, the diverse biological applications of furan have encouraged the preparation of a wide variety of thiosemicarbazide and triazole derivatives for the purpose of developing new drug agents.
Yusuf Sıcak
semanticscholar   +1 more source

1,2,3-Triazoles as Biomimetics in Peptide Science

open access: yesMolecules, 2021
Natural peptides are an important class of chemical mediators, essential for most vital processes. What limits the potential of the use of peptides as drugs is their low bioavailability and enzymatic degradation in vivo.
Naima Agouram   +2 more
semanticscholar   +1 more source

Application of triazoles in the structural modification of natural products

open access: yesJournal of Enzyme Inhibition and Medicinal Chemistry, 2021
Nature products have been extensively used in the discovery and development of new drugs, as the most important source of drugs. The triazole ring is one of main pharmacophore of the nitrogen-containing heterocycles.
Hong-Yan Guo   +3 more
semanticscholar   +1 more source

The Overview on the Pharmacokinetic and Pharmacodynamic Interactions of Triazoles

open access: yesPharmaceutics, 2021
Second generation triazoles are widely used as first-line drugs for the treatment of invasive fungal infections, including aspergillosis and candidiasis. This class, along with itraconazole, voriconazole, posaconazole, and isavuconazole, is characterized
A. Czyrski   +4 more
semanticscholar   +1 more source

An insight on medicinal attributes of 1,2,4-triazoles

open access: yesEuropean journal of medicinal chemistry, 2020
The present review aims to summarize the pharmacological profile of 1,2,4-triazole, one of the emerging privileged scaffold, as antifungal, antibacterial, anticancer, anticonvulsant, antituberculosis, antiviral, antiparasitic, analgesic and anti ...
R. Aggarwal, Garima Sumran
semanticscholar   +1 more source

Regioselectivity in the Thermal Rearrangement of Unsymmetrical 4-Methyl-4H-1,2,4-triazoles to 1-Methyl-1H-1,2,4-triazoles

open access: yesMolecules, 2001
The rearrangement of 4-methyl-3,5-diaryl-4H-1,2,4-triazoles to the corresponding 1-methyl-3,5-diaryl-1H-1,2,4-triazoles showed regioselectivity comparable to that observed for the alkylation of 3,5-diaryl-1H-1,2,4-triazoles.
Per H.J. Carlsen, Odd R. Gautun
doaj   +1 more source

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