1993
DOI: 10.1016/0969-8051(93)90143-i
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99mTc-DADT complexes substituted with heterocyclic amines: Effect of substitution on in vivo reactivity

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Cited by 9 publications
(3 citation statements)
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“…For instance [119], the alkaline hydrolysis of 2-amino-5-methyl-4-nitrobenzothiazole afforded 2-amino-5-methyl-3-nitrophenol. The ring opening of 3,3,6,6,10,10-hexamethyl-1,2-dithia-5,8-diazacyclodecane under the action of monochloroacetic anhydride was described [120]. The arising intermediate product was reduced into a dithiol by LiAlH 4 .…”
Section: Thiol Synthesis By Reduction Of Organosulfur Compoundsmentioning
confidence: 99%
“…For instance [119], the alkaline hydrolysis of 2-amino-5-methyl-4-nitrobenzothiazole afforded 2-amino-5-methyl-3-nitrophenol. The ring opening of 3,3,6,6,10,10-hexamethyl-1,2-dithia-5,8-diazacyclodecane under the action of monochloroacetic anhydride was described [120]. The arising intermediate product was reduced into a dithiol by LiAlH 4 .…”
Section: Thiol Synthesis By Reduction Of Organosulfur Compoundsmentioning
confidence: 99%
“…Various BFCs (Figure 2), including MAG 2 /MAG 3 [23], HYNIC (6‐hydrazinonicotinic acid) [24], DADT [25], EC [26], and N 3 S [27], have been developed for peptide radiolabeling. Another approach is the use of organometallic 99m Tc tricarbonyl complexes, which offer high stability and specific activity [28].…”
Section: Technetium‐99m and Radiolabelingmentioning
confidence: 99%
“…A previous study [14] showed that this type of substitution led to pharmacologically active 99mTc complexes. Animal studies of the investigated aminothiols (compounds 7 10) revealed that the sustituents introduced in DADT backbone also influenced, greatly the in vivo behaviour of the respective indium chelates.…”
Section: Fig 1 Ligands Investigated In the Present Study Synthesismentioning
confidence: 99%