Cargando…

Antibacterial structure–activity relationship studies of several tricyclic sulfur-containing flavonoids

A structure–activity relationship study concerning the antibacterial properties of several halogen-substituted tricyclic sulfur-containing flavonoids has been performed. The compounds have been synthesized by cyclocondensation of the corresponding 3-dithiocarbamic flavanones under acidic conditions....

Descripción completa

Detalles Bibliográficos
Autores principales:	Bahrin, Lucian G, Hopf, Henning, Jones, Peter G, Sarbu, Laura G, Babii, Cornelia, Mihai, Alina C, Stefan, Marius, Birsa, Lucian M
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Beilstein-Institut 2016
Materias:	Full Research Paper
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902053/ https://www.ncbi.nlm.nih.gov/pubmed/27340492 http://dx.doi.org/10.3762/bjoc.12.100

Ejemplares similares

Tricyclic flavonoids with 1,3-dithiolium substructure
por: Bahrin, Lucian G, et al.
Publicado: (2012)

An Improved Synthetic Method for Sensitive Iodine Containing Tricyclic Flavonoids
por: Birsa, Mihail Lucian, et al.
Publicado: (2022)

The Cytotoxic Properties of Some Tricyclic 1,3-Dithiolium Flavonoids
por: Sarbu, Laura G., et al.
Publicado: (2019)

A novel synthetic flavonoid with potent antibacterial properties: In vitro activity and proposed mode of action
por: Babii, Cornelia, et al.
Publicado: (2018)

[2.2]Paracyclophane derivatives containing tetrathiafulvalene moieties
por: Sarbu, Laura G, et al.
Publicado: (2015)

The Antibacterial Synthetic Flavonoid BrCl-Flav Exhibits Important Anti-Candida Activity by Damaging Cell Membrane Integrity
por: Babii, Cornelia, et al.
Publicado: (2021)

[2.2]Paracyclophane Derivatives as Building Blocks for Coordination Polymers
por: Birsa, Mihail Lucian, et al.
Publicado: (2023)

Selenium halide-induced bridge formation in [2.2]paracyclophanes
por: Sarbu, Laura G, et al.
Publicado: (2014)

An Approach to Paracyclophane-Based Tetrathiafulvalenes: Synthesis and Characterization of a Pseudo-Geminal [2.2]Paracyclophane 1,3-Dithia-2-Thione
por: Bahrin, Lucian G., et al.
Publicado: (2020)

Nitrogen-Based Linkers with a Mesitylene Core: Synthesis and Characterization
por: Bahrin, Lucian Gabriel, et al.
Publicado: (2021)

4-Bromo-2-[5-methyl-2-(morpholin-4-yl)-1,3-thiazol-4-yl]phenol
por: Bahrin, Lucian G., et al.
Publicado: (2013)

Health Benefits of Key Constituents in Cichorium intybus L.
por: Birsa, Mihail Lucian, et al.
Publicado: (2023)

Hydroxy Chalcones and Analogs with Chemopreventive Properties
por: Birsa, Mihail Lucian, et al.
Publicado: (2023)

The preparation of new functionalized [2.2]paracyclophane derivatives with N-containing functional groups
por: Hopf, Henning, et al.
Publicado: (2015)

rac-1-(5-Bromo-2-hydroxyphenyl)-1-oxopropan-2-yl morpholine-4-carbodithioate
por: Sarbu, Laura G., et al.
Publicado: (2013)

Synthesis of a library of tricyclic azepinoisoindolinones
por: Miller, Bettina, et al.
Publicado: (2012)

Synthetic Flavonoid BrCl-Flav—An Alternative Solution to Combat ESKAPE Pathogens
por: Moldovan, Cristina-Veronica, et al.
Publicado: (2022)

Improved Tricyclic Inhibitors of Trypanothione Reductase by Screening and Chemical Synthesis
por: Richardson, John L, et al.
Publicado: (2009)

Dipolar addition to cyclic vinyl sulfones leading to dual conformation tricycles
por: Wong, Steven S Y, et al.
Publicado: (2013)

Ynamide Carbopalladation: A Flexible Route to Mono-, Bi- and Tricyclic Azacycles
por: Campbell, Craig D, et al.
Publicado: (2015)

Intraannular photoreactions in pseudo-geminally substituted [2.2]paracyclophanes
por: Hopf, Henning, et al.
Publicado: (2011)

Attempts to prepare an all-carbon indigoid system
por: Yildizhan, Şeref, et al.
Publicado: (2015)

Five-membered ring annelation in [2.2]paracyclophanes by aldol condensation
por: Hopf, Henning, et al.
Publicado: (2014)

Synthetic Studies on Tricyclic Diterpenoids: Direct Allylic Amination Reaction of Isopimaric Acid Derivatives
por: Timoshenko, Mariya A., et al.
Publicado: (2015)

A tandem Mannich addition–palladium catalyzed ring-closing route toward 4-substituted-3(2H)-furanones
por: John, Jubi, et al.
Publicado: (2014)

The preparation of several 1,2,3,4,5-functionalized cyclopentane derivatives
por: Kelch, André S, et al.
Publicado: (2013)

Building complex carbon skeletons with ethynyl[2.2]paracyclophanes
por: Dix, Ina, et al.
Publicado: (2014)

The chemical behavior of terminally tert-butylated polyolefins
por: Klein, Dagmar, et al.
Publicado: (2015)

Synthesis of fused tricyclic amines unsubstituted at the ring-junction positions by a cascade condensation, cyclization, cycloaddition then decarbonylation strategy
por: Coldham, Iain, et al.
Publicado: (2012)

Synthesis of a tricyclic lactam via Beckmann rearrangement and ring-rearrangement metathesis as key steps
por: Kotha, Sambasivarao, et al.
Publicado: (2015)

Stereoselective synthesis of tricyclic compounds by intramolecular palladium-catalyzed addition of aryl iodides to carbonyl groups
por: Saadi, Jakub, et al.
Publicado: (2016)

Sulfur-containing spiroketals from Breynia disticha and evaluations of their anti-inflammatory effect
por: Nakashima, Ken-ichi, et al.
Publicado: (2023)

Modulating the activity of short arginine-tryptophan containing antibacterial peptides with N-terminal metallocenoyl groups
por: Albada, H Bauke, et al.
Publicado: (2012)

Capacity Fade Analysis of Sulfur Cathodes in Lithium–Sulfur Batteries
por: Yan, Jianhua, et al.
Publicado: (2016)

THE ANTIBACTERIAL PROPERTIES OF SULFUR
por: Weld, Julia T., et al.
Publicado: (1947)

The Bicycle and Tricycle for Physicians
Publicado: (1883)

Inclusion complexes of β-cyclodextrin with tricyclic drugs: an X-ray diffraction, NMR and molecular dynamics study
por: Castiglione, Franca, et al.
Publicado: (2017)

Complementarity of solution and solid state mechanochemical reaction conditions demonstrated by 1,2-debromination of tricyclic imides
por: Štrbac, Petar, et al.
Publicado: (2022)

Conformational Analysis of Acyclic α‐Fluoro Sulfur Motifs
por: Erdeljac, Nathalie, et al.
Publicado: (2020)

Reversible intramolecular photocycloaddition of a bis(9-anthrylbutadienyl)paracyclophane – an inverse photochromic system. (Photoactive cyclophanes 5)
por: Hopf, Henning, et al.
Publicado: (2009)

Cannot write session to /tmp/vufind_sessions/sess_2a1a2g2d5j050rr188f4gjkvh6