کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1379566 | 982032 | 2005 | 4 صفحه PDF | دانلود رایگان |

N-(2-Mercapto-propyl)-1,2-phenylenediamine (MPPDA) and N-β-aminoethylglycine (AEG) were labelled with 99mTc(CO)3+ to form the neutral complexes [99mTc(CO)3(MPPDA)] and [99mTc(CO)3(AEG)]. Both complexes were formed in excellent yields and their identity was confirmed by LC–MS. In mice, none of the new tracer agents showed brain uptake. [99mTc(CO)3(MPPDA)] was trapped mainly in the liver and excreted via the hepatobiliary system, whereas [99mTc(CO)3(AEG)] was excreted rapidly via the kidneys to the urine.
N-(2-Mercapto-propyl)-1,2-phenylenediamine (MPPDA) and N-β-aminoethylglycine (AEG) were labelled with 99mTc(CO)3+ to form the neutral complexes [99mTc(CO)3(MPPDA)] (1) and [99mTc(CO)3(AEG)], which were analysed by LC–MS. Their biodistribution in mice was studied.Figure optionsDownload as PowerPoint slide
Journal: Bioorganic & Medicinal Chemistry Letters - Volume 15, Issue 19, 1 October 2005, Pages 4192–4195