Literature DB >> 10902110

Mass spectrometry in combinatorial chemistry.

C Enjalbal1, J Martinez, J L Aubagnac.   

Abstract

In the fast expanding field of combinatorial chemistry, profiling libraries has always been a matter of concern--as illustrated by the buoyant literature over the past seven years. Spectroscopic methods, including especially mass spectrometry and to a lesser extent IR and NMR, have been applied at different levels of combinatorial library synthesis: in the rehearsal phase to optimize the chemistry prior to library generation, to confirm library composition, and to characterize after screening each structure that exhibits positive response. Most of the efforts have been concentrated on library composition assessment. The difficulties of such analyses have evolved from the infancy of the combinatorial concept, where large mixtures were prepared, to the recent parallel syntheses of collections of discrete compounds. Whereas the complexity of the analyses has diminished, an increased degree of automation was simultaneously required to achieve efficient library component identification and quantification. In this respect, mass spectrometry has been found to be the method of choice, providing rapid, sensitive, and informative analyses, especially when coupled to chromatographic separation. Fully automated workstations able to cope with several hundreds of compounds per day have been designed. After a brief introduction to describe the combinatorial approach, library characterization will be discussed in detail, considering first the solution-based methodologies and secondly the support-bound material analyses.

Mesh:

Year:  2000        PMID: 10902110     DOI: 10.1002/1098-2787(200005/06)19:3<139::AID-MAS2>3.0.CO;2-S

Source DB:  PubMed          Journal:  Mass Spectrom Rev        ISSN: 0277-7037            Impact factor:   10.946


  3 in total

1.  Occurrence of C-terminal residue exclusion in peptide fragmentation by ESI and MALDI tandem mass spectrometry.

Authors:  Mathieu Dupré; Sonia Cantel; Jean Martinez; Christine Enjalbal
Journal:  J Am Soc Mass Spectrom       Date:  2011-11-18       Impact factor: 3.109

2.  MALDI-TOF MS analysis of soluble PEG based multi-step synthetic reaction mixtures with automated detection of reaction failure.

Authors:  Christine Enjalbal; Patrice Ribière; Frédéric Lamaty; Neerja Yadav-Bhatnagar; Jean Martinez; Jean-Louis Aubagnac
Journal:  J Am Soc Mass Spectrom       Date:  2005-05       Impact factor: 3.109

3.  Static secondary ion mass spectrometry to monitor solid-phase peptide synthesis.

Authors:  D Maux; C Enjalbal; J Martinez; J L Aubagnac; R Combarieu
Journal:  J Am Soc Mass Spectrom       Date:  2001-10       Impact factor: 3.109

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.