Elongation of the side chain by linear alkyl groups increases the potency of salacinol, a potent α-glucosidase inhibitor from the Ayurvedic traditional medicine “Salacia,” against human intestinal maltase

2021 ◽  
Vol 33 ◽  
pp. 127751
Author(s):  
Katsuki Takashima ◽  
Mika Sakano ◽  
Eri Kinouchi ◽  
Shinya Nakamura ◽  
Shinsuke Marumoto ◽  
...  
Materials ◽  
2018 ◽  
Vol 11 (8) ◽  
pp. 1266 ◽  
Author(s):  
Alexandra Muñoz-Bonilla ◽  
Rocío Cuervo-Rodríguez ◽  
Fátima López-Fabal ◽  
José Gómez-Garcés ◽  
Marta Fernández-García

Herein, efficient antimicrobial porous surfaces were prepared by breath figures approach from polymer solutions containing low content of block copolymers with high positive charge density. In brief, those block copolymers, which were used as additives, are composed of a polystyrene segment and a large antimicrobial block bearing flexible side chain with 1,3-thiazolium and 1,2,3-triazolium groups, PS54-b-PTTBM-M44, PS54-b-PTTBM-B44, having different alkyl groups, methyl or butyl, respectively. The antimicrobial block copolymers were blended with commercial polystyrene in very low proportions, from 3 to 9 wt %, and solubilized in THF. From these solutions, ordered porous films functionalized with antimicrobial cationic copolymers were fabricated, and the influence of alkylating agent and the amount of copolymer in the blend was investigated. Narrow pore size distribution was obtained for all the samples with pore diameters between 5 and 11 µm. The size of the pore decreased as the hydrophilicity of the system increased; thus, either as the content of copolymer was augmented in the blend or as the copolymers were quaternized with methyl iodide. The resulting porous polystyrene surfaces functionalized with low content of antimicrobial copolymers exhibited remarkable antibacterial efficiencies against Gram positive bacteria Staphylococcus aureus, and Candida parapsilosis fungi as microbial models.


2016 ◽  
Vol 24 (16) ◽  
pp. 3705-3715 ◽  
Author(s):  
Genzoh Tanabe ◽  
Weijia Xie ◽  
Gorre Balakishan ◽  
Mumen F.A. Amer ◽  
Nozomi Tsutsui ◽  
...  

1995 ◽  
Vol 60 (12) ◽  
pp. 2097-2106 ◽  
Author(s):  
František Jursík ◽  
Ronald D. Archer

A series of new cobalt(III) octahedral complexes of the general formula Na[Co(ohb-aa)2] (ohb-aa = N-(o-hydroxybenzyl)amino acid anion); amino acid = glycine, (S)-α-alanine, α-aminoisobutyric acid, (S)-valine, (S)-norvaline and (S)-leucine) were prepared by the charcoal catalyzed reaction of the appropriate ligand with [Co(NH3)6]3+ in alkaline aqueous solution. Complexes obtained have, regardless of the amino acid used, the same facial all-trans symmetry (CoN2O4 chromophore) with the vicinal effects as the entire source of the optical activity. 13C NMR spectra reveal that the leucine derivative has, due to the steric reasons, a different ground state structure. Absorption maxima reflect a positive inductive effect from the amino acid side chain carbon atoms. Complexes of the ligands bearing electrophobic alkyl groups exhibit more negative E1/2 in comparison with the glycine derivative, reduction of which occurs at a more positive potential. Reduction potentials do not correlate with cobalt(III) Lewis acidity modulated by ligands.


CrystEngComm ◽  
2018 ◽  
Vol 20 (1) ◽  
pp. 128-132
Author(s):  
Phuong-Truc T. Pham ◽  
Victor G. Young ◽  
Mamoun M. Bader

The goal of this work is to examine the solid state structures of compounds that have been designed for increased conjugation and solubility, as these factors are important if these compounds are to be used in the solid state.


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