Results 51 to 60 of about 1,970,027 (229)

Assessing the Effects of Alloxydim Phototransformation Products by QSAR Models and a Phytotoxicity Study

open access: yesMolecules, 2018
Once applied, an herbicide first makes contact with leaves and soil. It is known that photolysis can be one of the most important processes of dissipation of herbicides in the field.
Juan J. Villaverde   +4 more
doaj   +1 more source

QSAR studies on Withanolide analogs for anticancer activity [PDF]

open access: yes, 2011
Withanolides are a group of pharmacologically active compounds present in most prodigal amounts in roots and leaves of Withania somnifera (Indian ginseng), one of the most important medicinal plants of Indian systems of medicine.
Dharmendra Kumar Yadav   +2 more
core   +2 more sources

An Investigation on the Quantitative Structure-Activity Relationships of the Anti-Inflammatory Activity of Diterpenoid Alkaloids

open access: yesMolecules, 2017
Diterpenoid alkaloids are extracted from plants. These compounds have broad biological activities, including effects on the cardiovascular system, anti-inflammatory and analgesic actions, and anti-tumor activity.
Xiao Li   +4 more
doaj   +1 more source

Toward Novel Antioxidant Drugs: Quantitative Structure-Activity Relationship Study of Eugenol Derivatives

open access: yesWalisongo Journal of Chemistry, 2021
The study of the Quantitative Structure-Activity Relationship (QSAR) of eugenol compound and its derivatives towards antioxidant activities was conducted using electronic and molecular descriptors.
Priyagung Dhemi Widiakongko   +1 more
doaj   +1 more source

Evaluating Molecular Properties Involved in Transport of Small Molecules in Stratum Corneum: A Quantitative Structure-Activity Relationship for Skin Permeability

open access: yesMolecules, 2018
The skin permeability (Kp) defines the rate of a chemical penetrating across the stratum corneum. This value is widely used to quantitatively describe the transport of molecules in the outermost layer of epidermal skin and indicate the significance of ...
Chen-Peng Chen   +3 more
semanticscholar   +1 more source

Quantitative structure-activity relationship for antimalarial activity of artemisinin [PDF]

open access: yes, 2010
The increase in resistance to older drugs and the emergence of new types of infection have created an urgent need for discovery and development of new compounds with antimalarial activity.
Hasan, Mohamed Noor   +1 more
core  

LIPOPHILICITY AND ANTIFUNGAL ACTIVITY OF SOME 2-SUBSTITUTED BENZIMIDAZOLE DERIVATIVES [PDF]

open access: yesChemical Industry and Chemical Engineering Quarterly, 2011
In the present paper, the antifungal activity of some 2-methyl and 2-amino-benzimidazole derivatives was evaluated against yeast Saccharomyces cere¬visiae. The tested compounds displayed in vitro antifungal activity and mini¬mum inhibitory concentration (
SANJA O. PODUNAVAC-KUZMANOVIĆ   +1 more
doaj  

Quantitative structure-activity relationship to elucidate human CYP2A6 inhibition by organosulfur compounds

open access: yesADMET and DMPK, 2019
CYP2A6 is a human enzyme responsible for the metabolic elimination of nicotine, and it is also involved in the activation of procarcinogenic nitrosamines, especially those present in tobacco smoke.
Daniela Andrea Ramirez   +3 more
doaj   +1 more source

A practical overview of quantitative structure-activity relationship [PDF]

open access: yes, 2009
Quantitative structure-activity relationship (QSAR) modeling pertains to the construction of predictive models of biological activities as a function of structural and molecular information of a compound library.
Isarankura-Na-Ayudhya, Chartchalerm   +3 more
core  

The effect of lipophilicity on the antibacterial activity of some 1-benzylbenzimidazole derivatives [PDF]

open access: yes, 2008
In the present paper, the antibacterial activity of some 1-benzylbenzimidazole derivatives were evaluated against the Gram-negative bacteria Escherichia coli. The minimum inhibitory concentration was determined for all the compounds.
D. D. CVETKOVIC   +2 more
core   +1 more source

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