Synthesis of coumarin conjugates of biological thiols for fluorescent detection and estimation

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Abstract

Coumarin-labeled thioesters are efficiently prepared from biological thiols using N-coumarin-3-carbonyl benzotriazoles. Absorption (λabs) , fluorescence (λem) wavelength maxima and quantum yields (φ) for the thioesters are measured in buffer solution at physiological pH 7.4. Quantum yields (φ = 0.0318-0.1068) of four of the products are higher than their precursor 7-methoxy-3-(1H-benzotriazol-1-ylcarbonyl)-2H-chromen-2-one (φ = 0.0195), suggesting that derivatives of this type could be suitable for quantitative thiol assays. © Georg Thieme Verlag Stuttgart New York.

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Katritzky, A. R., Ibrahim, T. S., Tala, S. R., Abo-Dya, N. E., Abdel-Samii, Z. K., & El-Feky, S. A. (2011). Synthesis of coumarin conjugates of biological thiols for fluorescent detection and estimation. Synthesis, (9), 1494–1500. https://doi.org/10.1055/s-0030-1259991

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