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首页> 外文期刊>Mass Spectrometry & Purification Techniques >Drug discovery From Simple Multicomponent into a Promising Drug-Drug Multicomponent Forms, Crystal Engineering is Taking Drug Search toanother Level
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Drug discovery From Simple Multicomponent into a Promising Drug-Drug Multicomponent Forms, Crystal Engineering is Taking Drug Search toanother Level

机译:药物发现从简单的多组分进入有前途的药物 - 药物多组分形式,水晶工程正在服用毒品搜索的特色水平

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摘要

In the fields of medication, biotechnology and pharmacology, drug revelation is the interaction by which new up-and-comer meds are found. All the more as of late, compound libraries of engineered little atoms, regular items or concentrates were screened in unblemished cells or entire creatures to distinguish substances that had an alluring restorative impact in an interaction known as traditional pharmacology. In the wake of sequencing of the human genome permitted fast cloning and union of enormous amounts of purged proteins, it has become normal practice to utilize high throughput screening of huge mixes libraries against detached organic targets which are theorized to be infection adjusting in a cycle known as converse pharmacology.
机译:在药物,生物技术和药理学领域,药物启示是发现新的上脱胶药物的相互作用。更晚的较晚,在无瑕疵的细胞或整个生物中筛选了设计的小原子,规则物品或浓缩物的复合文库,以区分在称为传统药理学的相互作用中具有吸引恢复冲击的物质。在对人类基因组的测序后允许的快速克隆和巨大量吹扫蛋白的联合,它已成为利用巨大混合文库的正常实践,该巨大混合文库对被理论为在已知循环中的感染调节的脱离的有机靶标的巨大混合物文库作为逆剂药理学。

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