Hassfeld Jorma, Farès Christophe, Steinmetz Heinrich, Carlomagno Teresa, Menche Dirk
Gesellschaft für Biotechnologische Forschung mbH, Medizinische Chemie and Umweltmikrobiologie, Mascheroder Weg 1, D-38124 Braunschweig, Germany.
Org Lett. 2006 Oct 12;8(21):4751-4. doi: 10.1021/ol061831y.
[structure: see text] The relative and absolute stereochemistry of the structurally unique 24-membered myxobacterial macrolides archazolid A and B, highly potent vacuolar-type ATPase (V-ATPase) inhibitors in vitro and in vivo, was determined on the basis of a combination of extensive high-field NMR studies, including J-based configuration analysis, molecular modeling, and chemical methods.
[结构:见正文] 结构独特的24元粘细菌大环内酯类化合物阿奇唑立德A和B的相对和绝对立体化学,它们在体外和体内都是高效的液泡型ATP酶(V-ATP酶)抑制剂,是基于广泛的高场核磁共振研究(包括基于J的构型分析、分子建模和化学方法)的组合来确定的。