基于虚拟筛选的新型PTP1B抑制剂的发现

来源 :2015年全国药物化学学术会议暨第五届中英药物化学学术会议 | 被引量 : 0次 | 上传用户:chenbin198718
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
  蛋白酪氨酸磷酸酯酶1B(protein tyrosine phosphatase 1B,PTP1B)在胰岛素和瘦素信号通路中起着重要的双重负调控作用,是治疗2型糖尿病及其综合征的潜在靶标。虽然PTP1B抑制剂的研究成为热点,但是至今没有成功上市的药物。
其他文献
The synthesis of 4-isochromanones via Parham-type cyclization with Weinreb amide as the internal electrophilic group,t-BuLi as the lithium reagent was described.The reaction was very efficient and cou
酸性神经鞘磷脂酶(ASM)水解鞘磷脂生成神经酰胺和磷酰胆碱,调节体内神经鞘磷脂的动态平衡及神经酰胺参与的信号转导,在动脉粥样硬化,抑郁症,肺泡组织损伤,肝损伤等多种疾病的发生发展过程中起着重要的作用[1]。
Heat shock protein 90(Hsp90)is highly expressed in many tumor cells and is associated with the maintenance of malignant phenotypes.Targeting Hsp90 has shown some therapeutic success in solid and hemat
会议
会议
Brutions tyrosine kinase(BTK)is a key component of the B-cell receptor signaling pathway which plays a critical role in B-cell development.Ample evidence indicates that the dysregulation of BTK is ass
钩吻(Gelsemium elegans Benth.)为马钱科(Loganiaceae)胡蔓藤属(Gelsemium)植物.钩吻全草有毒,民间一直以外用为主,治疗皮肤病.吲哚类生物碱钩吻素子是其主要化学成分,钩吻素子具有良好的抗肿瘤作用,但其作用机制尚不明确[1-3].
The design,synthesis,and biological activity evaluation of the potency of new inhibitors of sphingosine kinases 1 and 2(SphK1 and SphK2),the enzyme that catalyzes the phosphorylation of D-erythro-sphi
The overexpressed GSTπ isozyme in tumor cells was regarded as targets for the design of anti-cancer agents.Herein,a group of GSTπ-based nitric oxide(NO)-releasing derivatives of oleanolic acid(OA)(1–9
Lorcaserin was approved in June 2012 by the FDA for the treatment of obesity.1 Several methods for the synthesis of lorcaserin have been reported,but these methods are unsuitable for industrial-scale
硫化氢(hydrogen sulfide,H2S)作为新型的气体信号分子,广泛参与人体生理和病理过程,尤其在高血压、肺动脉高压、帕金森、阿尔兹海默等疾病的发病过程中发挥着重要作用.H2S供体可用来模拟体内H2S的释放过程,对H2S气体的活性研究至关重要,也是潜在的治疗型药物.