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首页> 外文期刊>Chemistry: A European journal >Nocardiopsins: New FKBP12-Binding Macrolide Polyketides from an Australian Marine-Derived Actinomycete, Nocardiopsis sp
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Nocardiopsins: New FKBP12-Binding Macrolide Polyketides from an Australian Marine-Derived Actinomycete, Nocardiopsis sp

机译:Nocardiopsins:从澳大利亚海洋衍生的放线菌,Nocardiopsis sp的新的结合FKBP12的大环内酯聚酮化合物

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摘要

A marine-derived actinomycete,Nocardiopsis sp. (CMB-M0232),obtained from a sediment sample collected at a depth of 55 m off the coast of Brisbane, Australia, yielded two new macrolide polyketides. Structures for nocardiopsins A and B were assigned by detailed spectroscopic analysis, degradation and chemical derivatization. A Marfeys analysis revealed an unexpected acid-mediated partial racemization of the l-pipecolic acid incorporated within the nocardiopsins. The scope of this racemization was assessed against a selection of natural and synthetic N-acyl pipecolic acids. While the nocardiopsins are not antibacterial, antifungal or cytotoxic, they do exhibit low-micromolar binding to the immunophilin FKBP12, consistent with their structural and biosynthetic relationship to the immunosuppressive agents FK506 and rapamycin. The nocardiopsins represent a new point of entry into what has been a valuable, exclusive and reclusive region of bioactive chemical space—that surrounding the FK506/rapamycin pharmacophore.
机译:海洋来源的放线菌,Nocardiopsis sp。 (CMB-M0232)是从澳大利亚布里斯班海岸附近55 m深度采集的沉积物样品中获得的,产生了两种新的大环内酯聚酮化合物。通过详细的光谱分析,降解和化学衍生化,确定了诺卡视菌素A和B的结构。 Marfeys分析显示,在诺卡视蛋白酶内掺入的L-哌酸具有意想不到的酸介导的部分消旋作用。该消旋作用的范围是根据对天然和合成的N-酰基胡椒酸的选择进行评估的。虽然诺卡视蛋白酶不是抗菌的,抗真菌的或无细胞毒性的,但它们确实表现出与免疫亲和素FKBP12的低微摩尔结合,这与它们与免疫抑制剂FK506和雷帕霉素的结构和生物合成关系一致。诺卡视视蛋白代表了进入生物活性化学空间的宝贵,专有和隐蔽区域的新切入点,该区域围绕FK506 /雷帕霉素药效团。

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