Results 101 to 110 of about 25,633 (260)

Synthesis, Bioactivities, and Antibacterial Mechanism of 5‑(Thioether)‑N‑phenyl/benzyl-1,3,4-oxadiazole-2-carboxamide/amine Derivatives

open access: yes
1,3,4-Oxadiazole thioethers have shown exciting antibacterial activities; however, the current mechanism of action involving such substances against bacteria is limited to proteomics-mediated protein pathways and differentially expressed gene analysis ...
Zengxue Wu (2629240)   +6 more
core   +1 more source

3-(4-Amino-1,2,5-oxadiazol-3-yl)-4-(4-nitro-1,2,5-oxadiazol-3-yl)-1,2,5-oxadiazole

open access: yesMolbank, 2014
The title compound 3-(4-amino-1,2,5-oxadiazol-3-yl)-4-(4-nitro-1,2,5-oxadiazol-3-yl)-1,2,5-oxadiazole (ANFF-1) was synthesized by: (1) by reaction of 3,4-bis(4-nitro-1,2,5-oxadiazol-3-yl)-1,2,5-oxadiazole (BNFF-1) with gaseous ammonia in toluene and (2)
Philip Pagoria   +5 more
doaj   +1 more source

Recent advancements in oxadiazole-based anticancer agents

open access: yes, 2017
Oxadiazole ring system occupies a significant position among heterocyclic templates for medicinal compounds due to its wide spectrum of biological activities.
Rasool, Irfan   +6 more
core   +1 more source

Bioactive Oxadiazoles 3.0

open access: yesInternational Journal of Molecular Sciences
Heterocycles are fundamental moieties for the construction of new compounds with perspective applications ranging from drugs to materials [...]
openaire   +3 more sources

Synthesis, Characterizations, Anti-Diabetic and Molecular Modeling Approaches of Hybrid Indole-Oxadiazole Linked Thiazolidinone Derivatives

open access: yesPharmaceuticals
Objective: To synthesize hybrid compounds of indole and oxadiazole in search of highly effective anti-diabetic therapeutic agent. Methods: With the goal of advancing diabetes research, our group designed and synthesized a library of 15 compounds based on
Shoaib Khan   +6 more
doaj   +1 more source

5-(Adamantan-1-yl)-3-[(4-benzylpiperazin-1-yl)methyl]-1,3,4-oxadiazole-2(3H)-thione

open access: yesActa Crystallographica Section E, 2012
The molecule of the title compound, C24H32N4OS, is a functionalized 1,3,4-oxadiazole-2-thione with substituted piperazine and adamantanyl substituents attached at the 3- and 5-positions, respectively, of the oxadiazole spacer with an approximately C ...
Ali A. El-Emam   +4 more
doaj   +1 more source

Synthesis of new oxadiazole derivatives as potent and selective FXR antagonists

open access: yes, 2019
In this comunication was reported that the manipulation of the oxadiazole scaffold, modifying both substituents at C-3 and C-5, led to the synthesis of a small library of derivatives some of which characterized by a potent FXR antagonistic activity and
Claudia Finamore   +5 more
core  

Electroluminescent devices based on polymeric thin films [PDF]

open access: yes, 2001
This thesis is concerned with the preparation of organic light-emitting diodes (LEDs) by using different thin film technologies: the Langmuir-Blodgett (LB) technique; spin-coating and thermal evaporation.
Young, J.G., Young, Jung Gun
core  

Synthesis of 2, 5-disubstituted-1, 3, 4-oxadiazole derivatives

open access: yes, 2019
Synthesis of a series of various 2, 5-disubstituted-1, 3, 4-oxadiazole derivatives (7a-7u) have been done. Synthesis of a series of intermediates (3a-3c and 5a-5c) have been also done, ethyl-2-phenoxyacetate (3a), ethyl 2-(2, 4-dichlorophenoxy)acetate ...
Sharma, Neetesh Kumar   +2 more
core   +1 more source

Synthesis and Antioxidant Activity of Styrylsulfonylmethyl 1,3,4-Oxadiazoles, Pyrazolyl/Isoxazolyl-1,3,4-oxadiazoles

open access: yesChemical and Pharmaceutical Bulletin, 2013
A new class of mono and bis heterocycles-styrylsulfonylmethyl 1,3,4-oxadiazoles, pyrazolyl/isoxazolyl-1,3,4-oxadiazoles were prepared and studied their antioxidant activity. The compound methyl substituted 2-(p-methylphenylamino-sulfonylmethyl)-5-[Z-(p-methylstyrylsulfonylmethyl)]-1,3,4-oxadiazole displayed slightly higher antioxidant activity than the
Mallikarjuna Reddy, Guda   +5 more
openaire   +3 more sources

Home - About - Disclaimer - Privacy