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[博来霉素衍生的凋亡诱导剂的分子设计]

[Molecular design of apoptosis inducing agents derived from bleomycin].

作者信息

Umezawa K, Otsuka M

机构信息

Faculty of Science and Technology, Keio University.

出版信息

Gan To Kagaku Ryoho. 1997 Feb;24(4):412-7.

PMID:9063477
Abstract

Reactive oxygen species (ROS) are often involved in the mechanism of apoptosis. Bleomycin consists of an oxygen activating domain and a DNA binding domain, and is an antitumour agent that induces double-strand scission in DNA by oxygen activation. However, bleomycin only weakly induces apoptosis in limited conditions. Previously we have reported efficient oxygen activation by iron complexes of synthetic models of bleomycin namely PYML designed by the direct analogy to the BLM metal core. Recently, novel ligands having symmetrized coordination environment consisting of two histidine units and a pyridine (HPH) were prepared. Oxygen activating efficiency of the iron complexes of the synthetic ligands increased by introducing electron donating substituent into the pyridine ring. HPH compounds have no DNA binding region which is present in bleomycin. HPH compounds but not bleomycin induced apoptosis in mouse leukemia L1210 cells.

摘要

活性氧(ROS)常参与细胞凋亡机制。博来霉素由一个氧活化结构域和一个DNA结合结构域组成,是一种通过氧活化诱导DNA双链断裂的抗肿瘤药物。然而,博来霉素仅在有限条件下微弱诱导细胞凋亡。此前我们报道了通过与博来霉素金属核心直接类比设计的博来霉素合成模型即PYML的铁配合物实现高效氧活化。最近,制备了具有由两个组氨酸单元和一个吡啶(HPH)组成的对称配位环境的新型配体。通过在吡啶环中引入供电子取代基,合成配体的铁配合物的氧活化效率提高。HPH化合物没有博来霉素中存在的DNA结合区域。HPH化合物而非博来霉素可诱导小鼠白血病L1210细胞凋亡。

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