Results 201 to 210 of about 25,633 (260)
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Bioorganic chemistry (Print), 2021
A series of novel 1,3,4-oxadiazole derivatives with substituted phenyl ring were designed and synthesized with an objective of discovering newer anti-cancer agents targeting thymidine phosphorylase enzyme (TP).
S. Bajaj +3 more
semanticscholar +1 more source
A series of novel 1,3,4-oxadiazole derivatives with substituted phenyl ring were designed and synthesized with an objective of discovering newer anti-cancer agents targeting thymidine phosphorylase enzyme (TP).
S. Bajaj +3 more
semanticscholar +1 more source
Poly‐1,3,4‐oxadiazoles. I. Polyphenylene‐1,3,4‐oxadiazoles
Journal of Polymer Science Part A: General Papers, 1965AbstractPolyphenylene‐1,3,4‐oxadiazoles have been prepared from benzenedicarboxylic acids or their derivatives and hydrazine by solution polycondensation in fuming sulfuric acid or polyphosphoric acid. These polymers were characterized by good thermal stability, and the molecular weights attained were high enough for the products to exhibit fiber‐or ...
Yoshio Iwakura +2 more
openaire +1 more source
European journal of medicinal chemistry, 2021
A total of forty-three compounds were synthesized, including thirty-two new ones. Among those compounds, seventeen were selected and tested on human tumor cell lines: PC-3 (prostate adenocarcinoma), HCT-116 (colorectal tumor), NCIH-460 (lung carcinoma ...
Valentina Nascimento e Melo de Oliveira +14 more
semanticscholar +1 more source
A total of forty-three compounds were synthesized, including thirty-two new ones. Among those compounds, seventeen were selected and tested on human tumor cell lines: PC-3 (prostate adenocarcinoma), HCT-116 (colorectal tumor), NCIH-460 (lung carcinoma ...
Valentina Nascimento e Melo de Oliveira +14 more
semanticscholar +1 more source
European journal of medicinal chemistry, 2020
With the increasing number of cases of inactive and drug-resistance tuberculosis, there is an urgent need to develop new potent molecules set for fighting this brutal disease.
S. Verma +5 more
semanticscholar +1 more source
With the increasing number of cases of inactive and drug-resistance tuberculosis, there is an urgent need to develop new potent molecules set for fighting this brutal disease.
S. Verma +5 more
semanticscholar +1 more source
Journal of Molecular Spectroscopy, 1967
Abstract The infrared absorption spectrum of 1,3,4-oxadiazole has been recorded in the region 5000-400 cm −1 in the vapor and in the liquid phases, in CS 2 and C 2 Cl 4 solutions. Also, the infrared absorption spectrum of liquid 2,5-dimethyl-1,3,4-oxadiazole was recorded in the same region. A tentative assignment of the fundamental vibrations of 1,
Daniel Højgaard Christensen +2 more
openaire +1 more source
Abstract The infrared absorption spectrum of 1,3,4-oxadiazole has been recorded in the region 5000-400 cm −1 in the vapor and in the liquid phases, in CS 2 and C 2 Cl 4 solutions. Also, the infrared absorption spectrum of liquid 2,5-dimethyl-1,3,4-oxadiazole was recorded in the same region. A tentative assignment of the fundamental vibrations of 1,
Daniel Højgaard Christensen +2 more
openaire +1 more source
1,3,4-Oxadiazole Bridges: A Strategy to Improve Energetics at the Molecular Level.
Angewandte Chemie, 2020Many energetic materials synthesized to date have limited applications because of low thermal and/or mechanical stability. This limitation can be overcome by introducing structural modifications such as a bridging group.
Jinchao Ma +5 more
semanticscholar +1 more source
Chinese Chemical Letters, 2020
A series of structurally novel 1,3,4-oxadiazole thioether derivatives ( 6a ― 6z ) containing a 6-fluoroquinazolinylpiperidinyl moiety were designed and synthesized using pharmacophore hybrid approach, and their structures were fully characterized by 1 H ...
Jun Shi +3 more
semanticscholar +1 more source
A series of structurally novel 1,3,4-oxadiazole thioether derivatives ( 6a ― 6z ) containing a 6-fluoroquinazolinylpiperidinyl moiety were designed and synthesized using pharmacophore hybrid approach, and their structures were fully characterized by 1 H ...
Jun Shi +3 more
semanticscholar +1 more source
Bioorganic & Medicinal Chemistry Letters, 2020
A new series of uracil analogues-1,2,4-oxadiazole hybrid derivatives were synthesized by a new, simple, and efficient method using for the first time HAP-SO3H as an heterogenous acid catalyst for the condensation and cyclization between amidoxime and ...
Az-eddine El Mansouri +6 more
semanticscholar +1 more source
A new series of uracil analogues-1,2,4-oxadiazole hybrid derivatives were synthesized by a new, simple, and efficient method using for the first time HAP-SO3H as an heterogenous acid catalyst for the condensation and cyclization between amidoxime and ...
Az-eddine El Mansouri +6 more
semanticscholar +1 more source
Pesticide Biochemistry and Physiology, 2020
In this study, thirty 1,3,4-oxadiazole sulfone derivatives containing 3,4-dichloroisothiazolamide moiety were designed and synthesized, and their antibacterial activities were evaluated.
Jie Xiang +4 more
semanticscholar +1 more source
In this study, thirty 1,3,4-oxadiazole sulfone derivatives containing 3,4-dichloroisothiazolamide moiety were designed and synthesized, and their antibacterial activities were evaluated.
Jie Xiang +4 more
semanticscholar +1 more source
European journal of medicinal chemistry, 2020
The inhibition or prevention of biofilm formation represents an emerging strategy in the war against antibiotic resistance, interfering with key players in bacterial virulence.
B. Parrino +12 more
semanticscholar +1 more source
The inhibition or prevention of biofilm formation represents an emerging strategy in the war against antibiotic resistance, interfering with key players in bacterial virulence.
B. Parrino +12 more
semanticscholar +1 more source

