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Frontmatter
Published/Copyright:
March 9, 2022
Published Online: 2022-03-09
Published in Print: 2022-03-28
©2022 Walter de Gruyter GmbH, Berlin/Boston
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- Bioactive compounds from Matricaria chamomilla: structure identification, in vitro antiproliferative, antimigratory, antiangiogenic, and antiadenoviral activities
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- Chemical composition, antioxidant, and antimicrobial activities of two essential oils from Algerian propolis
- Stability of proteins involved in initiation of DNA replication in UV damaged human cells
- Bioguided isolation of antiplasmodial secondary metabolites from Persea americana Mill. (Lauraceae)
- Biological activities of some Salvia species
- Secondary metabolites of downy birch buds (Betula pubescens Erch.)
- (−)-Brunneusine, a new phenolic compound with antibacterial properties in aqueous medium from the leaves of Agelanthus brunneus (Engl.) Tiegh (LORANTHACEAE)
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Articles in the same Issue
- Frontmatter
- Research Articles
- Bioactive compounds from Matricaria chamomilla: structure identification, in vitro antiproliferative, antimigratory, antiangiogenic, and antiadenoviral activities
- Antimicrobial synergism and antibiofilm activities of Pelargonium graveolens, Rosemary officinalis, and Mentha piperita essential oils against extreme drug-resistant Acinetobacter baumannii clinical isolates
- Chemical composition, antioxidant, and antimicrobial activities of two essential oils from Algerian propolis
- Stability of proteins involved in initiation of DNA replication in UV damaged human cells
- Bioguided isolation of antiplasmodial secondary metabolites from Persea americana Mill. (Lauraceae)
- Biological activities of some Salvia species
- Secondary metabolites of downy birch buds (Betula pubescens Erch.)
- (−)-Brunneusine, a new phenolic compound with antibacterial properties in aqueous medium from the leaves of Agelanthus brunneus (Engl.) Tiegh (LORANTHACEAE)
- Novel thiazolyl-hydrazone derivatives including piperazine ring: synthesis, in vitro evaluation, and molecular docking as selective MAO-A inhibitor