Ratiometric Fluorescent Probe for Homocysteine and Cysteine Based on the Aldehyde Functionalized Coumarin and Successful Bioimaging Application
- Corresponding author: Cheng Xiaohong, chengxiaohong0807@126.com
Citation:
Cheng Xiaohong, Xu Ke, Qu Shaohua, Ruan Zhijun. Ratiometric Fluorescent Probe for Homocysteine and Cysteine Based on the Aldehyde Functionalized Coumarin and Successful Bioimaging Application[J]. Chinese Journal of Organic Chemistry,
;2019, 39(10): 2835-2842.
doi:
10.6023/cjoc201904020
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Inset: structure of probe C1 and fluorescent photograph of C1 and C1+Hcy
[Hcy]/(10-5 mol/L): 0, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1.0, 1.2, 1.4, 1.6, 1.8, 2.0, 2.2, 2.5, 3.0. Inset: plot of emission intensity of probe C2 (10-5 mol•L-1) centered at 450/550 nm in the presence of different concentrations of Hcy; fluorescent photograph of C2 and C2+Hcy
Inset: Photograph of C2 in the presence of various amino acid. Hcy: 30 mol•L-1, Cys: 30 μmol/L, others: 300 μmol/L. a~v: C2+Ala, Arg, Asn, Asp, Val, Glu, Gln, Gly, His, Ile, Leu, Lys, Met, Phe, Pro, Ser, Trp, Thr, Tyr, GSH, Cys and Hcy
(a, d) fluorescence at the blue emission channel, (b, e) fluorescence at the green emission channel, and (c, f) bright field images. Scale bar: 20 μm