Results 1 to 10 of about 44,072 (262)

Extraction of Anthraquinone from Fermented Morinda officinalis and Its Antioxidant and Hypoglycemic Activities

open access: yesShipin gongye ke-ji, 2022
Objective: Optimization of the extraction process of anthraquinone from fermented Morinda officinalis and investigated its antioxidant and hypoglycemic activities. Methods: Taking the extraction ratio of anthraquinone as the evaluation index, the optimal
Dong PENG   +6 more
doaj   +1 more source

Anthraquinone contamination levels and exposure risk assessment in tea for sale in border areas

open access: yesZhongguo shipin weisheng zazhi, 2023
ObjectiveTo investigate the contamination levels of anthraquinone (9,10-anthraquinone as representative) in tea for sale in border areas in China, and to assess the exposure level and health risk of anthraquinone for residents.MethodsThe content of ...
XIE Qianqian   +5 more
doaj   +1 more source

Anthraquinones as Inhibitors of SOS RAS-GEF Activity

open access: yesBiomolecules, 2021
Recent breakthroughs have reignited interest in RAS GEFs as direct therapeutic targets. To search for new inhibitors of SOS GEF activity, a repository of known/approved compounds (NIH-NACTS) and a library of new marine compounds (Biomar Microbial ...
Alberto Fernández-Medarde   +6 more
doaj   +1 more source

In Silico-Based Discovery of Natural Anthraquinones with Potential against Multidrug-Resistant E. coli

open access: yesPharmaceuticals, 2022
E. coli is a Gram-negative bacterium that causes different human infections. Additionally, it resists common antibiotics due to its outer protective membrane. Natural products have been proven to be efficient antibiotics.
Hani A. Alhadrami   +4 more
doaj   +1 more source

Mechanisms of HIV-1 Nucleocapsid Protein Inhibition by Lysyl-Peptidyl-Anthraquinone Conjugates [PDF]

open access: yes, 2016
The Nucleocapsid protein NCp7 (NC) is a nucleic acid chaperone responsible for essential steps of the HIV-1 life cycle and an attractive candidate for drug development.
Alice Sosic   +12 more
core   +2 more sources

Anthraquinones with Antiplasmodial Activity from the Roots of Rennellia elliptica Korth. (Rubiaceae)

open access: yesMolecules, 2010
Dichloromethane root extract of Rennellia elliptica Korth. showed strong inhibition of Plasmodium falciparum growth in vitro with an IC50 value of 4.04 µg/mL.
Faridahanim Mohd Jaafar   +5 more
doaj   +1 more source

Electric-field control of interfering transport pathways in a single-molecule anthraquinone transistor [PDF]

open access: yes, 2015
It is understood that molecular conjugation plays an important role in charge transport through single-molecule junctions. Here, we investigate electron transport through an anthraquinone based single-molecule three-terminal device.
Hummelen, J. C.   +4 more
core   +3 more sources

Electrochemical control of quantum interference in anthraquinone-based molecular switches [PDF]

open access: yes, 2010
Using first-principles calculations we analyze the electronic transport properties of a recently proposed anthraquinone based electrochemical switch. Robust conductance on/off ratios of several orders of magnitude are observed due to destructive quantum ...
Jakob Schiötz   +3 more
core   +2 more sources

Anthraquinone in Indonesian infusion tea: analysis by HPLC–UV and risk assessment

open access: yesChemical and Biological Technologies in Agriculture, 2019
Background Detection of anthraquinone in tea samples marketed in Europe is raising a concern due to the possible carcinogenicity of this compound. The European Union has set a very low maximum residue level (MRL) for anthraquinone residue in tea (0.02 mg/
Retno Yusiasih   +4 more
doaj   +1 more source

Crystal structure and Hirshfeld surface analysis of 3,4-dihydro-2H-anthra[1,2-b][1,4]dioxepine-8,13-dione

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2020
The title compound, C17H12O4, was synthesized from the dye alizarin. The dihedral angle between the mean plane of the anthraquinone ring system (r.m.s. deviation = 0.039 Å) and the dioxepine ring is 16.29 (8)°. In the crystal, the molecules are linked by
Sofia Zazouli   +4 more
doaj   +1 more source

Home - About - Disclaimer - Privacy