Kinetic Studies Guide to Effective Administration of Tyrosinase Inhibitor

来源 :中国上海第七届国际新药发明科技年会 | 被引量 : 0次 | 上传用户:jerrykfczz
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
  Competitive enzyme inhibitors are of interest mainly for medicinal applications.Structure of inhibitor,the extent of its interaction with the enzyme,and the way the enzyme responds to the inhibitor are among the major factors determining the effectiveness of the medicine.Tyrosinase inhibitors have come to attention in recent decades for medical,nutritional,and cosmetic purposes.However,the side effect and the effectiveness of the introduced formulations which contain,at least,one of the tyrosinase inhibitors are matter of controversy.Considering the fact that tyrosinase is a tetrameric allosteric enzyme [1],we paid attention to the way it responds to the inhibitor.Therefore,during our recent works on tyrosinase [2-4],inhibition of both cresolase and catecholase activities of mushroom tyrosinase were studied in the presence of various linear,non-linear,and aromatic inhibitors (Following Figure).
其他文献
We developed a protocol in which a mix of different molecular modeling techniques was used in an attempt to identify and predict the mechanism of allosteric inhibition of human peroxiredoxin (Prx).Ins
会议
While many regard computer-aided drug design (CADD) as synonymous with structure-based design,its use in modern drug discovery research is much broader.In this talk,examples of real-world successes of
会议
The Aurora family of serine/threonine kinases are mitotic regulators involved in centrosome duplication,formation of the bipolar mitotic spindle and the alignment of the chromosomes alongthe spindle.T
会议
A detailed description of the molecular mechanism for the interactions between enzyme and its ligands (catalytic substrate or inhibitors) is of central importance for structure-based inhibitor design
会议
Adenosine receptors (ARs) belong to the G-protein-coupled receptor (GPCR) superfamily and consist of four subtypes referred to as A1,A2A,A2B,and A3.Adenosine receptors have very high sequence similari
会议
Microtubules have a major role in maintaining the growth,division,and functioning of both normal and cancer cells as well as being implicated in motility,shape maintenance,and intracellular transport.
会议
Examples,from our group,will highlight the use of microwave based technology in enabling the rapid,efficient synthesis of libraries of molecules of relevance to the pharmaceutical sector.For example,w
会议
As a method of searching for ligands capable of binding a target bioamacromolecule using a computer,a computational method is known,in which,based on three-dimensional data concerning a ligand-binding
会议
High throughput screening is the source of chemical starting points for a majority of drug discovery programs in the pharmaceutical industry.In most cases,the resulting hit list from the screening cam
会议
Several natural antimicrobial peptides including cecropins,magainins and melittins have been found to kill cancer cells.However,their efficacy may not be adequate for their development as anticancer a
会议