Results 21 to 30 of about 207,327 (249)

Tetrazolium salts [PDF]

open access: yes, 1956
Tetrazolium salts, as the name indicates, are quartenary. Substitution is possible on positions 2, 3, and 5 of the ring as is shown in type formula (I).
Richardson, Andrew Garnett
core   +1 more source

Unlocking Zenith Electronic State of Ni Sites in Ligand-Engineered COFs for Efficient •O<sub>2</sub> <sup>-</sup>-Driven Uranium Photoreduction. [PDF]

open access: yesAdv Sci (Weinh)
We develop a ligand engineering strategy to construct Ni‐diketimine‐linked COFs with precisely tuned Ni electronic states. By varying the coordinated diketone units, we achieve an optimal electronic configuration that enhances O2 adsorption and lowers the energy barrier for •O2− generation.
Wu G   +5 more
europepmc   +2 more sources

Comparative Evaluation on Impacts of Fibronectin, Heparin–Chitosan, and Albumin Coating of Bacterial Nanocellulose Small-Diameter Vascular Grafts on Endothelialization In Vitro

open access: yesNanomaterials, 2021
In this study, we contrast the impacts of surface coating bacterial nanocellulose small-diameter vascular grafts (BNC-SDVGs) with human albumin, fibronectin, or heparin–chitosan upon endothelialization with human saphenous vein endothelial cells (VEC) or
Max Wacker   +10 more
doaj   +1 more source

Tetrazolium Salts and Identification of Corynebacterium diphtheriae.

open access: yesExperimental Biology and Medicine, 1962
SummaryA simple method for detection of C. diphtheriae by means of nitro blue tetrazolium (NO2BT) is presented. This procedure is based on the marked reducing activity of C. diphtheriae and the very sensitive indicator properties of NO2BT.
B, MONIS, J F, REBACK
openaire   +2 more sources

Trinuclear silver(I) complex of non-steroidal anti-inflammatory drug naproxen: Synthesis, characterization, and in vitro cytotoxicity

open access: yesMacedonian Journal of Chemistry and Chemical Engineering, 2021
Herein, a new silver(I) complex with the non-steroidal anti-inflammatory drug naproxen and nitrogen donor 3-picoline ligands was synthesized, characterized, and subsequently tested for its cytotoxicity against different types of cancer cell lines ...
Sema Caglar   +3 more
doaj   +1 more source

Improving alkynyl(aryl)iodonium salts: 2-anisyl as a superior aryl group [PDF]

open access: yes, 2014
The majority of alkynyl(aryl)iodonium salts reported in the literature are derived from iodobenzene. This article describes the effects of varying this iodoarene building block on the synthesis, reactivity and stability of these salts.
Moran, Wesley   +3 more
core   +1 more source

Functionalized formazans: A review on recent progress in their pharmacological activities

open access: yesJournal of Advanced Research, 2015
This review provides an up to date information about the diverse pharmaceutical activities of formazans. The bibliography includes 97 references which have been published during the period from 1980 to 2013. The covered biological activities of the title
Ahmad S. Shawali, Nevien A. Samy
doaj   +1 more source

An effective "three-in-one" screening assay for testing drug and nanoparticle toxicity in human endothelial cells. [PDF]

open access: yesPLoS ONE, 2018
Evaluating nanoparticle (NP) toxicity in human cell systems is a fundamental requirement for future NP biomedical applications. In this study, we have designed a screening assay for assessing different types of cell death induced by NPs in human ...
Marcela Filipova   +7 more
doaj   +1 more source

Citotoxicidad del glifosato en células mononucleares de sangre periférica humana

open access: yesBiomédica: revista del Instituto Nacional de Salud, 2007
Introducción. El glifosato es un herbicida de amplio espectro, no selectivo, utilizado comúnmente en agricultura para eliminar malezas. Los estudios que han evaluado la toxicidad del glifosato en animales y en ambiente muestran que las formulaciones ...
Adriano Martínez   +2 more
doaj   +1 more source

The influence of salt formation on electrostatic and compression properties of flurbiprofen salts [PDF]

open access: yes, 2013
Salt formation is an effective method of improving physicochemical properties of acidic and basic drugs. The selection of a salt form most suitable for drug development requires a well-designed screening strategy to ensure various issues are addressed in
Conway, Barbara R   +6 more
core   +1 more source

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