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Abstract

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
*
Author to whom correspondence should be addressed.
Sci. Pharm. 2009, 77(7), 222; https://doi.org/10.3797/scipharm.oephg.21.PO-23
Submission received: 16 April 2009 / Accepted: 16 April 2009 / 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 Style

GÖßNITZER, 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

APA Style

GÖßNITZER, E., PÖLZL, A., & WENDELIN, W. (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

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