Krojer Melanie, Keller Marco, Bracher Franz
Department of Pharmacy - Center for Drug Research, Ludwig-Maximilians University, Butenandtstr. 5-13, 81377 Munich, Germany.
Sci Pharm. 2013 Apr-Jun;81(2):329-38. doi: 10.3797/scipharm.1303-03. Epub 2013 Apr 14.
This paper describes a convenient approach to the 7-aza-des-A-steroid (6,6a,7,8,9,9a-hexahydro-5H-cyclopenta[h]quinoline) scaffold starting from Grundmann's ketone using two different pyridine annulation protocols. The biological evaluation of the pyridine and pyridinium products revealed that these compounds unexpectedly do not interfere with ergosterol and cholesterol biosynthesis. The pyridinium compound 6 showed significant antimicrobial and cytotoxic activities which are most likely due to its detergent-like structure.
本文描述了一种从格伦德曼酮出发,利用两种不同的吡啶环合方案制备7-氮杂-去-A-甾体(6,6a,7,8,9,9a-六氢-5H-环戊并[h]喹啉)骨架的简便方法。对吡啶和吡啶鎓产物的生物学评价表明,这些化合物出乎意料地不干扰麦角固醇和胆固醇的生物合成。吡啶鎓化合物6表现出显著的抗菌和细胞毒性活性,这很可能归因于其类似洗涤剂的结构。