Microscale purification in support of high-throughput medicinal chemistry

被引:12
|
作者
Barhate, Chandan L. [1 ]
Donnell, Andrew F. [2 ]
Davies, Merrill [1 ]
Li, Ling [2 ]
Zhang, Yong [3 ]
Yang, Fukang [3 ]
Black, Regina [4 ]
Zipp, Greg [1 ]
Zhang, Yingru [1 ]
Cavallaro, Cullen L. [2 ]
Priestley, E. Scott [2 ]
Weller, Harold N. [1 ]
机构
[1] Bristol Myers Squibb, Separat & Anal Technol Team, Lawrenceville, NJ 08648 USA
[2] Bristol Myers Squibb, Chemotype Discovery & Optimizat, Lawrenceville, NJ USA
[3] Bristol Myers Squibb, Novel Drug Modal, Lawrenceville, NJ USA
[4] Agilent Technol, Wilmington, DE 19808 USA
关键词
DRUG DISCOVERY; EXPERIMENTATION; CHROMATOGRAPHY; ANTAGONISTS;
D O I
10.1039/d1cc03791a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In recent years, successful assay miniaturization has enabled the exploration of synthesis scale reduction in pharmaceutical discovery. Miniaturization of pharmaceutical synthesis and purification allows a reduction in material consumption and shortens timelines, which ultimately reduces the cost per experiment without compromising data quality. Isolating and purifying the compounds of interest is a key step in the library synthesis process. In this manuscript we describe a high-throughput purification workflow in support of microscale (1-5 mu mol or 0.5-2 mg) library synthesis. The optimized microscale purification system can routinely purify 384-well reaction plates with an analysis time of 4 min per sample. Instrument optimization, critical parameters such as column loading, delay time calibration, ultrafast pre- and post-purification analysis and library purification examples are provided.
引用
收藏
页码:11037 / 11040
页数:4
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