Novel (3,5-di-tert-butyl-2-hydroxy-phenylcarbamoyl)-alkanoic acids as potent antioxidants
- Author
- LODYATO, Vladimir I1 2 ; YURKOVA, Irina L1 ; SOROKIN, Viktor L1 ; SHADYRO, Oleg I1 ; DOLGOPALETS, Vladimir I2 ; KISEL, Mikhail A2
[1] Department of Chemistry of the Belarusiun State University, Skaryna av., 4, 220050 Minsk, Belarus
[2] Institute of Bioorgunic Chemistry of the Belarus National Academy of Sciences, Kuprevich St., 5/2, 220141 Minsk, Belarus - Source
Bioorganic & medicinal chemistry letters (Print). 2004, Vol 14, Num 16, pp 4253-4256, 4 p
- ISSN
- 0960-894X
- Scientific domain
- Biochemistry, molecular biology, biophysics; Pharmacology drugs
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Acide carboxylique Antioxydant Benzène dérivé Carboxamide Composé aliphatique Composé amphiphile Phénols Relation structure activité Synthèse chimique Acide alcanoïque([(3,5-di-tert-butyl-2-hydroxyphényl)carbamoyl])
- Keyword (en)
- Carboxylic acid Antioxidant Benzene derivatives Carboxamide Aliphatic compound Amphiphilic compound Phenols Structure activity relation Chemical synthesis
- Keyword (es)
- Acido carboxílico Antioxidante Benceno derivado Carboxamida Compuesto alifático Compuesto anfifílico Fenoles Relación estructura actividad Síntesis química
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02N General and cellular metabolism. Vitamins
- Discipline
- Pharmacological treatments
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 15956313
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1016/j.bmcl.2004.06.003 
https://dx.doi.org/10.1016/j.bmcl.2004.06.003
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