Design and Synthesis of 23-Amino- 24,25,26,27-tetrakisnorlanosterolacetate and Derivatives as New Antimycotic Agents
Institute of Pharmaceutical Sciences, Pharmaceutical Chemistry, Karl-Franzens-University Graz, Schubertstraße 1, A-8010 Graz
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Sci. Pharm. 2009, 77(7), 222; https://doi.org/10.3797/scipharm.oephg.21.PO-23
Submission received: 16 April 2009
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Accepted: 16 April 2009
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Published: 16 April 2009
Abstract
In search of new antimycotic agents acting as ergosterol biosynthesis inhibitors we investigated widely new and optimized reaction pathways for preparing different types of triazasteroids [1, 2]. The various mono-, bi-, tri- and tetracyclic triazasteroidal compounds are designed as stable aza-analogues of carbo-cationic high energy intermediates (HEIA) of fungal enzymes [1, 2].
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MDPI and ACS Style
GÖßNITZER, E.; PÖLZL, A.; WENDELIN, W. Design and Synthesis of 23-Amino- 24,25,26,27-tetrakisnorlanosterolacetate and Derivatives as New Antimycotic Agents. Sci. Pharm. 2009, 77, 222. https://doi.org/10.3797/scipharm.oephg.21.PO-23
AMA Style
GÖßNITZER E, PÖLZL A, WENDELIN W. Design and Synthesis of 23-Amino- 24,25,26,27-tetrakisnorlanosterolacetate and Derivatives as New Antimycotic Agents. Scientia Pharmaceutica. 2009; 77(Posters (PO)):222. https://doi.org/10.3797/scipharm.oephg.21.PO-23
Chicago/Turabian StyleGÖßNITZER, E., A. PÖLZL, and W. WENDELIN. 2009. "Design and Synthesis of 23-Amino- 24,25,26,27-tetrakisnorlanosterolacetate and Derivatives as New Antimycotic Agents" Scientia Pharmaceutica 77, Posters (PO): 222. https://doi.org/10.3797/scipharm.oephg.21.PO-23
