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Published in 2020 at "Chemical communications"
DOI: 10.1039/c9cc09666c
Abstract: 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)…
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Keywords:
asymmetric rhodamine;
protease activated;
activated nir;
nir probes ... See more keywords