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Search for "Candida albicans" in Full Text gives 55 result(s) in Beilstein Journal of Organic Chemistry.
Volatile organic compounds produced by the phytopathogenic bacterium Xanthomonas campestris pv. vesicatoria 85-10
Beilstein J. Org. Chem. 2012, 8, 579–596, doi:10.3762/bjoc.8.65
- development in Candida albicans [13], and Hogan et al. [14] concluded that either the bacteria modulate the fungal behavior or that C. albicans (or related fungi) responded to the presence of antagonistic bacteria in such a way that it was advantageous for the bacteria. Volatiles were also shown to support
Synthesis of szentiamide, a depsipeptide from entomopathogenic Xenorhabdus szentirmaii with activity against Plasmodium falciparum
Beilstein J. Org. Chem. 2012, 8, 528–533, doi:10.3762/bjoc.8.60
- different Gram-positive (Micrococcus luteus, Bacillus subtilis, Staphylococcus aureus) and Gram-negative (Escherichia coli, Pseudomonas aeroginosa) bacteria, as well as yeast (Candida albicans, Saccharomyces cerivisiae). However, consistent with the published data [12], no antibacterial or antifungal
Synthesis and characterization of new diiodocoumarin derivatives with promising antimicrobial activities
Beilstein J. Org. Chem. 2011, 7, 1688–1696, doi:10.3762/bjoc.7.199
- bacteria, namely Staphylococcus aureus (NCTC-7447), Bacillus cereus (ATCC-14579), and two Gram-negative bacteria, namely Escherichia coli (NCTC-10410), Serratia marcescens (IMRU-70); and against two species of fungi, namely Aspergillus fumigatus (MTCC-3008) and Candida albicans (MTCC-227). The tested
Advances in synthetic approach to and antifungal activity of triazoles
Beilstein J. Org. Chem. 2011, 7, 668–677, doi:10.3762/bjoc.7.79
- -lactams and terminal alkynes of bile acids in the presence of a Cu(I) catalyst (click chemistry) by Vatmurge et al. The synthesized compounds were evaluated for their antifungal activity against different fungal strains such as Candida albicans, Cryptococcus neoformans, Benjaminiella poitrasii, Yarrowia
- ]. Holla et al. synthesized triazole derivatives by the 1,3-dipolar cycloaddition reaction of 4-azido-8-trifluoromethylquinoline with ethyl acetoacetate and acetylacetone, respectively, and tested for antifungal activity against Candida albicans. Among the various synthesized compounds, 1-(1-(8
- ) Second generation of triazoles Voriconazole (VCZ, 11) Posaconazole (PCZ, 12) Ravuconazole (RCZ, 13) First generation of triazoles Fluconazole Fluconazole (9, Figure 8) is a fungistatic agent active against Candida albicans, Candida tropicalis, and Candida glabrata. Fluconazole is also used to treat
Sordarin, an antifungal agent with a unique mode of action
Beilstein J. Org. Chem. 2008, 4, No. 31, doi:10.3762/bjoc.4.31
- , early antifungal screens in the 1970s excluded sordarin, but two decades later, renewed appreciation of that natural product arose as a consequence of its potent in vitro inhibition of protein synthesis in Candida albicans, a pathogenic fungus. Unlike traditional antifungal agents, which target only the
- by stabilizing the EF2/ribosome complex. Strong activity against Saccharomyces cerevisiae [9][10], Candida albicans [11][12], and a number of pathogenic fungi make sordarin a promising antimycotic agent. Review Total syntheses of sordarin and its congeners To date, three total syntheses of sordarin
- Glycosyl analogs Sordarin and congeners exhibit good activity against some fungal species, for instance, Candida albicans [11][12], but are inactive toward others. Modifications to both the glycosyl unit and the diterpene core have been pursued in an effort to engender activity against the greatest
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