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Antifungal compounds applications

Since the initial reports of HSQC-1,1-ADEQUATE spectra are very recent,49,50 there are only the reports by the author and co-workers in the literature. Aside from the initial work done using strychnine (1) as a model compound, applications to the complex antifungal agent posaco-nazole (47)96 and the cyclin-dependant kinase inhibitor dinaciclib (48)97 are the only other applications that have been reported. [Pg.277]

The application of this catalyst is nicely illustrated in a synthesis of ambruticin.63 Ambruticin 261 is an antifungal compound. The tetrahydropyran on the left hand side of the molecule and the dihydropyran on the right both contain two stereogenic centres which could be controlled in a hetero Diels-Alder reaction via 262 and 263. [Pg.563]

This chapter will describe some natural antifungal compounds produced by LAB, the factors that influence their production by this group of bacteria, and some practical applications of such antifungal compounds. In addition, the effect that these bacteria have on the production of mycotoxin by toxigenic fungi will be discussed, along with their potential as mycotoxin binders (by adsorption) in Uquid systems. [Pg.334]

Potential applications of lactic acid bacteria as antifungal compounds... [Pg.341]

Phytotoxicity Assays. Compounds identified with antifungal activity were used for plant tests to determine disease resistance potentials. Soybean varieties Essex, KS5292, Crawford and Hutchenson at 2-4 true leaf stage, two plants per pot, two pots per treatment were used for the test. Antifungal compounds were incorporated into a spray formulation for application onto soybean plants. Two ml volumes of 0, 10, 100, 250 and 500 xg/ml concentrations were applied to the plants followed by incubation on a greenhouse bench at 30 C. Phytotoxicity was assessed daily over a 14 day period and the test was repeated. [Pg.237]

The search for new antifungal molecules for material protection is often linked to the research for new antifungal compounds in plant-protection and medicine. In all applications the intention is to kill or inhibit fungi to prevent damage caused by them. [Pg.25]

Shamsipur and Jalali described a simple and accurate pH metric method for the determination of two sparingly soluble (in water) antifungal agents miconazole and ketoconazole in micellar media [17]. Cetyltrimethylammonium bromide and sodium dodecyl sulfate micelles were used to solubilize these compounds. The application of this method to the analysis of pharmaceutical preparation of the related species gave satisfactory results. Simplicity and the absence of harmful organic solvents in this method make it possible to be used in the routine analyses. [Pg.38]

The facile conversion of carbonyl groups into lactones via cyclobutanones offers many opportunities for synthetic applications considering the importance of butanol-ides in natural products synthesis. The iridoids vividly illustrate this potential. Allamandin (163) 135 c) and its dehydrated relative plumericin (164) 135 d), compounds possessing antifungal, antibacterial, and antitumor activity, pack a great deal of... [Pg.72]

Over the past years, synthetic base-modified nucleosides and nucleotides have displayed important impact in diverse fields. Their biological properties have found application as antiviral tools against hepatitis virus (HBV), herpes virus (VZV) and human immunodeficiency (HIV).94,95,136 Many of those compounds exhibit antiproliferative, antibiotic and antifungal activities and some have been used as probes for DNA damages96,97,137 as well as in the anti-sense approach and DNA-probe technology with fluorescence properties.99... [Pg.162]

New applications of dithioles and dithiolanes include evaluation of compounds such as 69 and 70 as flavour components <98MI177>, 71 for antimycotic activity <99MIP33826>, 72 for antiviral activity <99CC1245>, 73 for antifungal and antibacterial activity <99MI6> and use of 74 in prevention and heatment of asthma complications <99EUP909758>. [Pg.209]

The active compounds used earliest were termed "mass action" compounds because they were applied at high rates (up to 100 lb per acre). Unfortunately at these levels, the chemicals damaged both the fruit and the tree. The first breakthrough came when the antifungal antibiotic 3-(2-C3,5-dimethyl-2-oxocyclohex-ylj -2-hydroxyethyl)glutarimide (cycloheximide or Upjohn s Acti-Aid) was found to loosen citrus fruits at application rates of less than 0.1 lb per acre (5). [Pg.267]


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See also in sourсe #XX -- [ Pg.341 , Pg.342 ]




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Potential applications of lactic acid bacteria as antifungal compounds

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