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The structure-activity relationship of aromatic compounds in advanced oxidation processes:a review.
Chemosphere, 2022Advanced oxidation processes (AOPs) are widely used as efficient technologies to treat highly toxic and harmful substances in wastewater. Taking the most representative aromatic compounds (monosubstituted benzenes, substituted phenols and heterocyclic ...
Mingzhu Ren +6 more
semanticscholar +1 more source
Anti-Inflammation Activity of Flavones and Their Structure-Activity Relationship.
Journal of Agricultural and Food Chemistry, 2021Flavones are an important class of bioactive constituents in foods, and their structural diversity enables them to interact with different targets. In particular, flavones are known for their anti-inflammatory activity.
Xiang Wang +5 more
semanticscholar +1 more source
A systematic review of synthetic tyrosinase inhibitors and their structure-activity relationship
Critical reviews in food science and nutrition, 2021Tyrosinase is a copper-containing oxidation enzyme, which is responsible for the production of melanin. This enzyme is widely distributed in microorganisms, animals and plants, and plays an essential role in undesirable browning of fruits and vegetables,
Zhiyun Peng +6 more
semanticscholar +1 more source
ACS Applied Materials and Interfaces, 2021
Oxygen reduction reaction (ORR) is an efficiency-determining process at the cathode in several energy storage and conversion devices, typically such as metal-air batteries and fuel cells.
Guangdi Nie +4 more
semanticscholar +1 more source
Oxygen reduction reaction (ORR) is an efficiency-determining process at the cathode in several energy storage and conversion devices, typically such as metal-air batteries and fuel cells.
Guangdi Nie +4 more
semanticscholar +1 more source
Structure–activity relationship of avocadyne
Food & Function, 2021Structural components including the terminal triple bond, the presence and (R)-stereochemistry of the hydroxyl groups, and number of carbons in avocadyne's aliphatic linear chain are critical to its ability to modulate fatty acid oxidation.
Matthew Tcheng +12 more
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Structure and Activity Relationships in Molluscicides
Journal of Pharmaceutical Sciences, 1968Noninfected snails of the Biomphalari and Bulinus types (intermediate hosts for Schistosoma mansoni and Schistosoma hematobium , respectively) can oxidize instantly and intensively p -phenylenediamine dihydrochloride and its derivatives to the corresponding colored trivalent nitrogen-free radicals.
I, Nabih, M T, Elwasimi
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Structure–activity relationships in nitrothiophenes
Bioorganic & Medicinal Chemistry, 2006The structure and electronic properties of a series of biologically active 2-nitrothiophenes (1) have been calculated using both semi-empirical and ab initio molecular orbital methods. Multi-linear regression analysis suggests that there is a reasonable correlation between the experimental activity of the derivatives against either Escherichia coli or ...
John O, Morley, Thomas P, Matthews
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Antibacterial activities with the structure-activity relationship of coumarin derivatives.
European journal of medicinal chemistry, 2020The development of drug-resistant bacteria, as well as multidrug-resistant pathogens related to substantial mortality, is an important global health threat.
Hua-Li Qin +3 more
semanticscholar +1 more source
Structure-activity relationships of chemokines
Journal of Leukocyte Biology, 1995Abstract Structural analysis of chemokines has revealed that the α/β structural-fold is highly conserved among both the CXC and CC chemokine classes. Although dimerization and aggregation is often observed, the chemokines function as monomers.
I, Clark-Lewis +7 more
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Bioorganic chemistry (Print), 2020
Morpholine is a versatile moiety, a privileged pharmacophore and an outstanding heterocyclic motif with wide ranges of pharmacological activities due to different mechanisms of action.
A. Kumari, R. Singh
semanticscholar +1 more source
Morpholine is a versatile moiety, a privileged pharmacophore and an outstanding heterocyclic motif with wide ranges of pharmacological activities due to different mechanisms of action.
A. Kumari, R. Singh
semanticscholar +1 more source

