18979-53-8Relevant articles and documents
Allylphenols as a new class of human 15-lipoxygenase-1 inhibitors
Alavi, Seyed Jamal,Seyedi, Seyed Mohammad,Saberi, Satar,Safdari, Hadi,Eshghi, Hossein,Sadeghian, Hamid
, p. 259 - 266 (2020/10/12)
In this study, a series of mono- and diallylphenol derivative were designed, synthesized, and evaluated as potential human 15-lipoxygenase-1 (15-hLOX-1) inhibitors. Radical scavenging potency of the synthetic allylphenol derivatives was assessed and the results were in accordance with lipoxygenase (LOX) inhibition potency. It was found that the electronic natures of allyl moiety and para substituents play the main role in radical scavenging activity and subsequently LOX inhibition potency of the synthetic inhibitors. Among the synthetic compounds, 2,6-diallyl-4-(hexyloxy)phenol (42) and 2,6-diallyl-4-aminophenol (47) showed the best results for LOX inhibition (IC50 = 0.88 and 0.80 μM, respectively).
An amphiphilic pillar[5]arene: Synthesis, controllable self-assembly in water, and application in calcein release and TNT adsorption
Yao, Yong,Xue, Min,Chen, Jianzhuang,Zhang, Mingming,Huang, Feihe
supporting information, p. 15712 - 15715,4 (2020/08/24)
An amphiphilic pillar[5]arene was made. It could self-assemble to form vesicles and multiwalled microtubes in water. Dynamic light scattering, transmission electron microscopy, scanning electron microscopy, atomic force microscopy, and UV-vis and FTIR spectroscopy were employed to characterize its self-assembly process and the resultant assemblies. The vesicles could encapsulate calcein within their interiors under neutral conditions and release it in response to a decrease in pH. The microtubes, which have primary amine groups on their surfaces, could adsorb TNT through donor-acceptor interactions.
Synthesis of Y-Shaped liquid crystals and the influence of their structure on the phase behavior
Zuev, Vjacheslav V.
experimental part, p. 3 - 12 (2011/06/10)
A series of the Y-shaped liquid crystalline (LC) materials based on central 1,2,4-benzenetricarboxylic core was synthesized with variation of the arm length (two or three para-linked phenyl rings) in the Y-shaped mesogen and their dipole architecture (ether or ester terminal and linked groups). Our results indicate that main relationships between molecular structure and mesomorphic behavior well known for the calamitic LC are valid for the Y-shaped compounds too. Smectic mesophases might be obtained by lengthening the mesogen with an additional aromatic core in the arm or with an alkyl chain at the tail. The substitution of the alkoxy terminal groups on to alkanoyl also leads to the enhanced smectic behavior of the Y-shaped molecules. Taylor & Francis Group, LLC.
