18O/16O‐Encoding Strategy for Microscale Stereochemical Determination of Peptidic Natural Products
The demand for more efficient methods of establishing the undetermined stereochemistries of peptidic natural products continues unabated. A new method for microscale stereochemical determination was devised by integrating solid‐phase synthesis, split‐and‐mix randomization, 18O/16O‐encoding of d/l‐co...
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Veröffentlicht in: | Chemistry, an Asian journal an Asian journal, 2021-09, Vol.16 (17), p.2447-2452 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The demand for more efficient methods of establishing the undetermined stereochemistries of peptidic natural products continues unabated. A new method for microscale stereochemical determination was devised by integrating solid‐phase synthesis, split‐and‐mix randomization, 18O/16O‐encoding of d/l‐configurations, tandem mass spectrometry, and biological evaluation. Here we applied gramicidin A as the molecule for a blind test. Gramicidin A and its 31 diastereomers were randomly prepared in microgram scale with 18O/16O‐stereochemical encoding and subjected to MS/MS‐structural determination and cytotoxicity assay. Only the parent gramicidin A was selected from among the 32 stereoisomers, validating the high reliability of the present strategy.
A novel 18O/16O‐encoding strategy for microscale stereochemical determination of peptidic natural products has been devised. The strategy integrates the one‐bead‐one‐compound (OBOC) strategy, 18O/16O‐stereochemical encoding, tandem mass (MS/MS) spectrometry, and biological evaluation. Its application enabled the correct identification of gramicidin A from 32 stereoisomers randomly prepared in microgram scale, thereby validating the high reliability. |
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ISSN: | 1861-4728 1861-471X |
DOI: | 10.1002/asia.202100674 |