化学药物制剂
共收录 60 篇相关论文
-
PROTACs in targeted protein degradation: Advances in development and AI-enhanced drug discoveryPROTACs在靶向蛋白降解中的应用:开发进展与AI增强药物发现
-
Recent Advances in Multi-target Drugs Targeting Protein Kinases and Histone Deacetylases in Cancer Therapy靶向蛋白激酶和组蛋白去乙酰化酶的多靶点药物在癌症治疗中的最新进展
-
Pen-866, a miniature drug conjugate of a heat shock protein 90 (HSP90) ligand linked to SN38 for patients with advanced solid malignancies: Phase I and expansion cohort results.Pen-866,一种与SN38连接的热休克蛋白90(HSP90)配体的小型药物结合物,适用于晚期实体恶性肿瘤患者:I期和扩展队列结果
-
Membrane Proteins as Targets for Biological Drugs膜蛋白作为生物药物的靶点
-
Medicinal Research Reviews医学研究评论
-
A Review on the Novel Coronavirus Disease based on In-silico Analysis of Various Drugs and Target Proteins基于对各种药物和靶蛋白的计算分析的新型冠状病毒疾病综述
-
Interaction of Platinum-based Drugs with Proteins: An Overview of Representative Crystallographic Studies铂基药物与蛋白质的相互作用:代表性晶体学研究的概述
-
The Right Tool for the Job: An Overview of Hsp90 Inhibitors.合适的工具:Hsp90抑制剂的概述
-
Therapeutic Drug Monitoring of Targeted Anticancer Protein Kinase Inhibitors in Routine Clinical Use: A Critical Review靶向抗癌蛋白激酶抑制剂在常规临床使用中的治疗药物监测:一项批判性综述
-
The Right Tool for the Job: An Overview of Hsp90 Inhibitors.合适的工具:Hsp90抑制剂的概述
-
CETSA beyond Soluble Targets: a Broad Application to Multipass Transmembrane ProteinsCETSA在可溶性靶点之外的应用:在多次跨膜蛋白中的广泛应用
-
Recent advances in the determination of unbound concentration and plasma protein binding of drugs: Analytical methods.药物游离浓度和血浆蛋白结合的最新测定进展:分析方法
-
New horizons in drug discovery of lymphocyte-specific protein tyrosine kinase (Lck) inhibitors: a decade review (2011–2021) focussing on structure–activity relationship (SAR) and docking insights淋巴细胞特异性蛋白酪氨酸激酶(Lck)抑制剂药物研发新进展:十年回顾(2011–2021)——聚焦构效关系(SAR)与分子对接研究
-
Recent advances in identifying protein targets in drug discovery.药物发现中识别蛋白靶标的最新进展
-
鉴定小分子药物的靶蛋白对于理解药物的作用机理以及药物副作用至关重要。传统方法需要对药物进行化学修饰共价交联,可能会导致药物活性的改变。目前已经发展多种无需化学修饰便可以对药物靶蛋白鉴定的方法,包括药物亲和力反应靶标稳定性技术 (Drug affinity responsive target stability,DARTS)、蛋白质氧化速率稳定性技术 (Stability of proteins from rates of oxidation,SPROX)、细胞热移位分析...鉴定小分子药物的靶蛋白对于理解药物的作用机理以及药物副作用至关重要。传统方法需要对药物进行化学修饰共价交联,可能会导致药物活性的改变。目前已经发展多种无需化学修饰便可以对药物靶蛋白鉴定的方法,包括药物亲和力反应靶标稳定性技术 (Drug affinity responsive target stability,DARTS)、蛋白质氧化速率稳定性技术 (Stability of proteins from rates of oxidation,SPROX)、细胞热移位分析...
-
[Identification techniques of small molecule drug target proteins without chemical modification and its applications: a review].[无化学修饰的小分子药物靶蛋白的识别技术及其应用:综述]
-
Latest trends in structure based drug design with protein targets.基于结构的蛋白质靶点药物设计最新趋势
-
Role of protein-protein interactions in allosteric drug design for DNA methyltransferases.蛋白质-蛋白质相互作用在DNA甲基转移酶的别构药物设计中的作用
-
Protein-protein complexes as targets for drug discovery against infectious diseases.蛋白质-蛋白质复合物作为抗感染性疾病药物发现的靶点
-
Chagas disease is a serious parasitic infection caused by Trypanosoma cruzi. Unfortunately, the current chemotherapeutic tools are not enough to combat the infection. The aim of this study was to evaluate the trypanocidal activity of ben...恰加斯病是由克氏锥虫引起的一种严重寄生虫感染。不幸的是,目前的化疗工具不足以对抗感染。本研究旨在评估苯并咪唑的杀锥虫活性...