ArticleInorganic chemistry2011
Design and synthesis of a bombesin peptide-conjugated tripodal phosphino dithioether ligand topology for the stabilization of the fac-[M(CO)3]+ core (M=(99 m)Tc or Re).
Article in Inorganic chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Versatile Diphosphine Chelators for Radiolabeling Peptides withInorganic chemistry · 2023Article
- N-Centered Tripodal Phosphine Re(V) and Tc(V) Oxo Complexes: Revisiting a [3 + 2] Mixed-Ligand Approach.Inorganic chemistry · 2022Article
- One-step, kit-based radiopharmaceuticals for molecular SPECT imaging: a versatile diphosphine chelator forDalton transactions (Cambridge, England : 2003) · 2021Article
- Optimal His-Tag Design for Efficient [Bioconjugate chemistry · 2021Article
- Silica: An efficient catalyst for one-pot regioselective synthesis of dithioethers.Beilstein journal of organic chemistry · 2014Article
Corrections and comments
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Authors and funding
8 authors.
Funding
Abstract
A new tumor-seeking tridentate topology consisting of a phosphino dithioether ((HOCH(2))(2)PCH(2)CH(2)S(CH(2))(n)CH(2)SR; PS(2)) ligand framework for the production of kinetically inert and in vivo stable facial [(99m)Tc(CO)(3)(PS(2))](+) or [Re(CO)(3)(PS(2))](+) is described. The X-ray crystal structure of fac-Re(CO)(3)(PS(2))PF(6) is reported. The bioconjugation strategies for incorporating bombesin (BBN) peptides on to the PS(2) tripodal framework and, thereby, de novo designing of GRP receptor-seeking Tc(PS(2)-BBN)(CO)(3) are developed.
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Registered trials
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