Synthesis of radiolabeled biphenylsulfonamide matrix metalloproteinase inhibitors as new potential PET cancer imaging agents

Novel matrix metalloproteinase (MMP) inhibitor radiotracers, ( S)-3-methyl-2-(2′,3′,4′-methoxybiphenyl-4-sulfonylamino)-butyric acid [ 11C]methyl ester ( 1a– c), ( S)-3-methyl-2-(2′,3′,4′-fluorobiphenyl-4-sulfonylamino)-butyric acid [ 11C]methyl ester ( 1d– f), and ( S)-3-methyl-2-(4′-nitrobiphenyl-...

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Veröffentlicht in:Bioorganic & medicinal chemistry letters 2003-07, Vol.13 (13), p.2217-2222
Hauptverfasser: Fei, Xiangshu, Zheng, Qi-Huang, Liu, Xuan, Wang, Ji-Quan, Sun, Hui Bin, Mock, Bruce H., Stone, K.Lee, Miller, Kathy D., Sledge, George W., Hutchins, Gary D.
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Sprache:eng
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Zusammenfassung:Novel matrix metalloproteinase (MMP) inhibitor radiotracers, ( S)-3-methyl-2-(2′,3′,4′-methoxybiphenyl-4-sulfonylamino)-butyric acid [ 11C]methyl ester ( 1a– c), ( S)-3-methyl-2-(2′,3′,4′-fluorobiphenyl-4-sulfonylamino)-butyric acid [ 11C]methyl ester ( 1d– f), and ( S)-3-methyl-2-(4′-nitrobiphenyl-4-sulfonylamino)-butyric acid [ 11C]methyl ester ( 1g), a series of substituted biphenylsulfonamide derivatives, have been synthesized for evaluation as new potential positron emission tomography (PET) cancer imaging agents. Graphic
ISSN:0960-894X
1464-3405
DOI:10.1016/S0960-894X(03)00382-2