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Alkoxy Tetrazine Substitution at a Boron Center: A Strategy for Synthesizing Highly Fluorogenic Hydrophilic Probes
Authors:Dr Min Wu  Dr Xiaoai Wu  Yayue Wang  Lei Gu  Jiao You  Prof Haoxing Wu  Prof Ping Feng
Affiliation:1. Huaxi MR Research Center (HMRRC), Department of Radiology, West China Hospital, West China Medical School, Sichuan University, Chengdu, P.R. China;2. Department of Nuclear Medicine, West China Hospital, Sichuan University, Sichuan, P.R. China;3. Institute of Clinical Trials, West China Hospital, Sichuan University, Chengdu, Sichuan, P.R. China
Abstract:Strongly fluorogenic boron dipyrromethene (BODIPY)–tetrazine probes have been obtained by introducing an alkoxy tetrazine fragment at the boron center. The fluorescence signal from these probes strongly increases by up to 225‐fold after reaction with bioorthogonal coupling partners, and the hydrophilicity of probes is improved, such that they are suitable for live‐cell imaging.
Keywords:bioorthogonal chemistry  dyes/pigments  fluorescent probes  imaging agents  tetrazines
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