Results 21 to 30 of about 55,807 (381)

Catechol-Based Hydrogel for Chemical Information Processing

Biomimetics, 2017
Catechols offer diverse properties and are used in biology to perform various functions that range from adhesion (e.g., mussel proteins) to neurotransmission (e.g., dopamine), and mimicking the capabilities of biological catechols have yielded important ...
Eunkyoung Kim, Zhengchun Liu, Yi Liu, William E. Bentley, Gregory F. Payne   +4 more
doaj   +1 more source

Application of nitroarene dioxygenases in the design of novel strains that degrade chloronitrobenzenes. [PDF]

, 2009
Widespread application of chloronitrobenzenes as feedstocks for the production of industrial chemicals and pharmaceuticals has resulted in extensive environmental contamination with these toxic compounds, where they pose significant risks to the health ...
Ju, Kou-San, Parales, Rebecca E
core   +1 more source

Surface-Enhanced Raman Scattering of Phenols and Catechols by a Molecular Analogue of Titanium Dioxide.

Analytical Chemistry, 2020
Surface-enhanced Raman spectroscopy (SERS) of semiconducting TiO2 was used for studying binding modes and surface reactions of molecules bound at the interface but is generally limited by low signal intensity and lack of authentic structural information.
Caiyun Liu, Junyi Hu, Subharanjan Biswas, Feng Zhu, J. Zhan, Guo Wang, C. Tung, Yifeng Wang   +7 more
semanticscholar   +1 more source

Catechol-Based Antimicrobial Polymers [PDF]

Molecules, 2021
Catechol is a key constituent in mussel adhesive proteins and is responsible for strong adhesive property and crosslinking formation. Plant-based polyphenols are also capable of chemical interactions similar to those of catechol and are inherently antimicrobial.
Seyedehfatemeh Razaviamri, Kan Wang, Bo Liu, Bruce P. Lee   +3 more
openaire   +3 more sources

Standardization transformation of C-lignin to catechol and propylene. [PDF]

Nat Commun
Shen X, Zhao Z, Wen J, Zhang J, Ji Y, Hou G, Liao Y, Zhang C, Yuan TQ, Wang F.   +9 more
europepmc   +3 more sources

Imine-Based Catechols and o-Benzoquinones: Synthesis, Structure, and Features of Redox Behavior

ACS Omega, 2020
Novel sterically hindered catechols of the type 3-(RN=CH)-4,6-DBCatH2 with iminoalkyl or iminoaryl groups in the third position of the aromatic ring have been synthesized and characterized in detail.
Tatiana V. Astaf’eva, M. Arsenyev, R. Rumyantcev, G. Fukin, V. Cherkasov, A. Poddel’sky   +5 more
semanticscholar   +1 more source

1st Symposium on Polydopamine and NanoTech Poland 2018: Conference Report

Biomimetics, 2018
The NanoTech Poland is an annual international conference with a strong scientific agenda focused on nanotechnology in energy, environment, and biomedicine.
Radosław Mrówczyński, Marco d’Ischia, Haeshin Lee, Stefan Jurga   +3 more
doaj   +1 more source

Catechols: a new class of carbonic anhydrase inhibitors.

Chemical Communications, 2020
To date, catechols have been only poorly investigated as carbonic anhydrase (CA) inhibitors. Here we report the first structural information on the CA inhibition mechanism of these molecules, showing that they adopt a peculiar binding mode to the enzyme ...
Katia D'Ambrosio, S. Carradori, S. Cesa, A. Angeli, S. Monti, C. Supuran, G. De Simone   +6 more
semanticscholar   +1 more source

Inhibition of Soybean 15-Lipoxygenase and Human 5-Lipoxygenase by Extracts of Leaves, Stem Bark, Phenols and Catechols Isolated From Lithraea caustica (Anacardiaceae)

Frontiers in Pharmacology, 2020
Lithraea caustica (Molina) Hook. and Arn. (Anacardiaceae), common name Litre, is an evergreen endemic plant used in the Mapuche Chilean folk medicine. The stem juice of L.
Alejandra Muñoz-Ramírez, Carolina Mascayano-Collado, Andrés Barriga, Javier Echeverría, Alejandro Urzúa   +4 more
doaj   +1 more source

Enzymatic functionalization of carbon-hydrogen bonds [PDF]

, 2011
The development of new catalytic methods to functionalize carbon–hydrogen (C–H) bonds continues to progress at a rapid pace due to the significant economic and environmental benefits of these transformations over traditional synthetic methods.
Arnold, Frances H., Coelho, Pedro S., Lewis, Jared C.   +2 more
core   +1 more source