Asymmetric Si-rhodamine scaffolds: rational design of pH-durable protease-activated NIR probes
A group of asymmetric Si-rhodamine scaffolds was designed for protease-activated NIR probes. Dual pH-inertia for both spirocyclized fluorescent probes and fluorescent products of zwitterions form over a wide range of pH (4.0-11.0). Leucine aminopeptidase (LAP) and γ-glutamyl transpeptidase (GGT) wer...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2020-02, Vol.56 (16), p.2455-2458 |
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Zusammenfassung: | A group of asymmetric Si-rhodamine scaffolds was designed for protease-activated NIR probes. Dual pH-inertia for both spirocyclized fluorescent probes and fluorescent products of zwitterions form over a wide range of pH (4.0-11.0). Leucine aminopeptidase (LAP) and γ-glutamyl transpeptidase (GGT) were monitored by fluorescent imaging
in vivo
.
A group of asymmetric Si-rhodamine scaffolds was designed for protease-activated NIR probes. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c9cc09666c |