Electron ionization mass spectrometric study of N‐substituted hydrazones of isomeric hydroxybenzaldehydes and isomeric pyridinecarboxaldehydes bearing an <i>N</i>‐(<i>E</i>)‐stilbenyloxyalkylcarbonyltryptophyl substituent

Prukała, Dorota

doi:10.1002/rcm.2534

Rapid Comm Mass Spectrometry

2006

DOI: 10.1002/rcm.2534

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Electron ionization mass spectrometric study of N‐substituted hydrazones of isomeric hydroxybenzaldehydes and isomeric pyridinecarboxaldehydes bearing an N‐(E)‐stilbenyloxyalkylcarbonyltryptophyl substituent

Dorota Prukała

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Cited by 2 publications

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Current literature in mass spectrometry

2007

J. Mass Spectrom.

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In order to keep subscribers up‐to‐date with the latest developments in their field, John Wiley & Sons are providing a current awareness service in each issue of the journal. The bibliography contains newly published material in the field of mass spectrometry. Each bibliography is divided into 11 sections: 1 Reviews; 2 Instrumental Techniques & Methods; 3 Gas Phase Ion Chemistry; 4 Biology/Biochemistry: Amino Acids, Peptides & Proteins; Carbohydrates; Lipids; Nucleic Acids; 5 Pharmacology/Toxicology; 6 Natural Products; 7 Analysis of Organic Compounds; 8 Analysis of Inorganics/Organometallics; 9 Surface Analysis; 10 Environmental Analysis; 11 Elemental Analysis. Within each section, articles are listed in alphabetical order with respect to author (6 Weeks journals ‐ Search completed at 15th. Nov. 2006)

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2007

J. Mass Spectrom.

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Synthesis and biological evaluation of some stilbene-based analogues

et al. 2010

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The phytoalexin 3,5,4 0 -trihydroxy-trans-stilbene (resveratrol) has attracted considerable attention from biologists and chemists due to its diverse biological properties. Owing to the biological importance of this compound, we have synthesized new stilbene-based analogues by using substituted benzyl chlorides and substituted aldehydes in a two-step reaction and evaluated their in vitro antioxidant, antibacterial and antifungal potential. Most of the compounds displayed moderate to significant radical scavenging activity. (E)-1-(3,4-difluorophenyl)-2-(4-fluorophenyl)ethene (4c) showed nearer equipotent antibacterial activity against Staphylococcus aureus. (E)-1,2-bis (4-fluorophenyl)ethene (4a), (E)-1-(3-fluorophenyl)-2-(4-fluorophenyl)ethene (4b), (E)-1-(2,4-dichlorophenyl)-2-(3, 4-dichlorophenyl)ethene (4f), (E)-1-(2,4-dichlorophenyl)-2-(3-chlorophenyl)ethene (4g), (E)-1-(2,4-dichlorophenyl)-2-(4-fluorophenyl)ethene (4j) (E)-1-(4-fluorophenyl)-2-(3-chlorophenyl)ethene (4l) and (E)-1-(4-chlorophenyl)-2-(4-fluorophenyl)ethene (4n) inhibited the growth of Penicillium chrysogenum.

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Electron ionization mass spectrometric study of N‐substituted hydrazones of isomeric hydroxybenzaldehydes and isomeric pyridinecarboxaldehydes bearing an N‐(E)‐stilbenyloxyalkylcarbonyltryptophyl substituent

Cited by 2 publications

References 12 publications

Current literature in mass spectrometry

Current literature in mass spectrometry

Synthesis and biological evaluation of some stilbene-based analogues

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