Synthesis, Characterization, Anti-Inflammatory and in Vitro Antimicrobial Activity of Some Novel Alkyl/Aryl Substituted Tertiary Alcohols

The synthesis of some novel alkyl/aryl substituted tertiary alcohols was accomplished in two steps. The synthetic route involves preparation of Grignard reagents by treating alkyl/aryl bromides with magnesium turnings in dry ether. Then substituted chalcones were reacted with the Grignard reagents t...

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Main Authors: Rafiuzzaman SaeedulHaq, Muhammad Baseer, Farzana Latif Ansari, Zaman Ashraf
Format: Article
Language:English
Published: MDPI AG 2011-12-01
Series:Molecules
Subjects:
Online Access:http://www.mdpi.com/1420-3049/16/12/10337/
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spelling doaj-a80542b546ff4784bb494788332830ec2020-11-24T23:54:10ZengMDPI AGMolecules1420-30492011-12-011612103371034610.3390/molecules161210337Synthesis, Characterization, Anti-Inflammatory and in Vitro Antimicrobial Activity of Some Novel Alkyl/Aryl Substituted Tertiary AlcoholsRafiuzzaman SaeedulHaqMuhammad BaseerFarzana Latif AnsariZaman AshrafThe synthesis of some novel alkyl/aryl substituted tertiary alcohols was accomplished in two steps. The synthetic route involves preparation of Grignard reagents by treating alkyl/aryl bromides with magnesium turnings in dry ether. Then substituted chalcones were reacted with the Grignard reagents to afford alkyl/aryl substituted tertiary alcohols 1-10. The structures of the synthesized compounds were assigned on the basis of FT-IR, 1H-NMR, 13C-NMR and mass spectroscopic data. The in vivo anti-inflammatory activity of the synthesized compounds was evaluated using the carrageenan-induced hind paw edema method and was compared with that of ibuprofen. Some of the newly synthesized compounds showed promising anti-inflammatory activity. The tertiary alcohols 1-10 were also screened for antibacterial activity against ten bacterial strains using seven Gram-positive and three Gram-negative bacteria and for antifungal activity against Aspergillus Flavus, Aspergillus Niger and Aspergillus pterus. Tertiary alcohols 1-10 were found to exhibit good to excellent antimicrobial activities compared to levofloxacin and fluconazole used as standard drugs.http://www.mdpi.com/1420-3049/16/12/10337/tertiary alcoholsanti-inflammatory activityantibacterial activityantifungal activity
collection DOAJ
language English
format Article
sources DOAJ
author Rafiuzzaman SaeedulHaq
Muhammad Baseer
Farzana Latif Ansari
Zaman Ashraf
spellingShingle Rafiuzzaman SaeedulHaq
Muhammad Baseer
Farzana Latif Ansari
Zaman Ashraf
Synthesis, Characterization, Anti-Inflammatory and in Vitro Antimicrobial Activity of Some Novel Alkyl/Aryl Substituted Tertiary Alcohols
Molecules
tertiary alcohols
anti-inflammatory activity
antibacterial activity
antifungal activity
author_facet Rafiuzzaman SaeedulHaq
Muhammad Baseer
Farzana Latif Ansari
Zaman Ashraf
author_sort Rafiuzzaman SaeedulHaq
title Synthesis, Characterization, Anti-Inflammatory and in Vitro Antimicrobial Activity of Some Novel Alkyl/Aryl Substituted Tertiary Alcohols
title_short Synthesis, Characterization, Anti-Inflammatory and in Vitro Antimicrobial Activity of Some Novel Alkyl/Aryl Substituted Tertiary Alcohols
title_full Synthesis, Characterization, Anti-Inflammatory and in Vitro Antimicrobial Activity of Some Novel Alkyl/Aryl Substituted Tertiary Alcohols
title_fullStr Synthesis, Characterization, Anti-Inflammatory and in Vitro Antimicrobial Activity of Some Novel Alkyl/Aryl Substituted Tertiary Alcohols
title_full_unstemmed Synthesis, Characterization, Anti-Inflammatory and in Vitro Antimicrobial Activity of Some Novel Alkyl/Aryl Substituted Tertiary Alcohols
title_sort synthesis, characterization, anti-inflammatory and in vitro antimicrobial activity of some novel alkyl/aryl substituted tertiary alcohols
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2011-12-01
description The synthesis of some novel alkyl/aryl substituted tertiary alcohols was accomplished in two steps. The synthetic route involves preparation of Grignard reagents by treating alkyl/aryl bromides with magnesium turnings in dry ether. Then substituted chalcones were reacted with the Grignard reagents to afford alkyl/aryl substituted tertiary alcohols 1-10. The structures of the synthesized compounds were assigned on the basis of FT-IR, 1H-NMR, 13C-NMR and mass spectroscopic data. The in vivo anti-inflammatory activity of the synthesized compounds was evaluated using the carrageenan-induced hind paw edema method and was compared with that of ibuprofen. Some of the newly synthesized compounds showed promising anti-inflammatory activity. The tertiary alcohols 1-10 were also screened for antibacterial activity against ten bacterial strains using seven Gram-positive and three Gram-negative bacteria and for antifungal activity against Aspergillus Flavus, Aspergillus Niger and Aspergillus pterus. Tertiary alcohols 1-10 were found to exhibit good to excellent antimicrobial activities compared to levofloxacin and fluconazole used as standard drugs.
topic tertiary alcohols
anti-inflammatory activity
antibacterial activity
antifungal activity
url http://www.mdpi.com/1420-3049/16/12/10337/
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AT farzanalatifansari synthesischaracterizationantiinflammatoryandinvitroantimicrobialactivityofsomenovelalkylarylsubstitutedtertiaryalcohols
AT zamanashraf synthesischaracterizationantiinflammatoryandinvitroantimicrobialactivityofsomenovelalkylarylsubstitutedtertiaryalcohols
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