Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
Electrophoresis ; 2018 Jun 13.
Article in English | MEDLINE | ID: mdl-29897615

ABSTRACT

Apple pomace has been considered as a sustainable source for antioxidant phenolic compounds. Previous reports show extraction of total phenolic contents (TPC) by following various conventional and non-conventional techniques; however, a comparative study has not been reported. In the present work, conventional extraction was compared with several non-conventional extraction methods including ultrasound-assisted extraction (UAE), microwave-assisted extraction (MAE), high-speed homogenization (HH). Moreover, efficacy of combined treatments, including high-speed homogenization coupled with MAE and ultrasound-assisted enzymatic extraction (UAEE) was evaluated for the recovery of TPC. The results revealed that UAEE results in the highest TPC (4.62 mg GAE/g), moreover, it simultaneously enabled the recovery of low methoxy pectins with the degree of methylation ranging from 14.03- 28.85%. The LC-Q-Tof analysis revealed the presence of various phenolic acids and flavonoids. The DPPH radical scavenging assay showed that the phenolic rich extracts had IC50 values ranging from 27.1 to 54.6, depending on the extraction parameters. This article is protected by copyright. All rights reserved.

2.
Acta Pharm ; 63(2): 231-9, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23846145

ABSTRACT

3 Starting from 2-methyl-4-nitro-imidazole, new 5-(2-methyl- 4-nitro-1-imidazomethyl)-1,3,4-oxadiazole-2-thione () was synthesized and was subjected to Mannich reaction with appropriate amines to yield a new series of 3-substituted aminomethyl-5-(2-methyl-4-nitro-1-imidazomethyl)- 1,3,4-oxadiazole-2-thiones (4a-j). The structure of the title compounds was elucidated by elemental analysis and spectral data. The newly synthesized Mannich bases were screened for their antibacterial and antifungal activity. Many of these compounds exhibited potent antifungal activity.


Subject(s)
Antifungal Agents , Imidazoles , Mannich Bases , Oxadiazoles , Antifungal Agents/chemical synthesis , Antifungal Agents/chemistry , Antifungal Agents/pharmacology , Chemistry Techniques, Synthetic/methods , Enzyme Inhibitors/agonists , Enzyme Inhibitors/chemistry , Imidazoles/agonists , Imidazoles/chemical synthesis , Imidazoles/chemistry , Imidazoles/pharmacology , Mannich Bases/chemical synthesis , Mannich Bases/chemistry , Mannich Bases/pharmacology , Mass Spectrometry , Microbial Sensitivity Tests , Mitosporic Fungi/drug effects , Oxadiazoles/chemical synthesis , Oxadiazoles/chemistry , Oxadiazoles/pharmacology , Staphylococcus/drug effects , Structure-Activity Relationship
SELECTION OF CITATIONS
SEARCH DETAIL
...