Modular One-Pot Strategy for the Synthesis of Heterobivalent Tracers

Bivalent ligands, i.e., molecules having two ligands covalently connected by a linker, have been gathering attention since the first description of their pharmacological potential in the early 80s. However, their synthesis, particularly of labeled heterobivalent ligands, can still be cumbersome and...

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Vydáno v:ACS medicinal chemistry letters Ročník 14; číslo 5; s. 636 - 644
Hlavní autoři: Bailly, Thibaud, Bodin, Sacha, Goncalves, Victor, Denat, Franck, Morgat, Clement, Prignon, Aurelie, Valverde, Ibai E.
Médium: Journal Article
Jazyk:angličtina
Vydáno: WASHINGTON Amer Chemical Soc 11.05.2023
Témata:
Chemistry, Medicinal
Life Sciences & Biomedicine
Pharmacology & Pharmacy
Science & Technology
PROSTATE
Heterobivalent ligands
AVIDITY
CXCR4
Drug delivery
PEPTIDE RECEPTORS
ANTAGONIST BIVALENT LIGANDS
IN-VITRO
AFFINITY
SPACER LENGTH
Bioconjugation
OPIOID AGONIST
Click chemistry
Radiopharmaceuticals
BINDING
ISSN:1948-5875, 1948-5875
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Popis
Shrnutí:Bivalent ligands, i.e., molecules having two ligands covalently connected by a linker, have been gathering attention since the first description of their pharmacological potential in the early 80s. However, their synthesis, particularly of labeled heterobivalent ligands, can still be cumbersome and time-consuming. We herein report a straightforward procedure for the modular synthesis of labeled heterobivalent ligands (HBLs) using dual reactive 3,6-dichloro-1,2,4,5-tetrazine as a starting material and suitable partners for sequential SNAr and inverse electron-demand Diels-Alder (IEDDA) reactions. This assembly method conducted in a stepwise or in a sequential one-pot manner provides quick access to multiple HBLs. A conjugate combining ligands toward the prostate-specific membrane antigen (PSMA) and the gastrin-releasing peptide receptor (GRPR) was radiolabeled, and its biological activity was assessed in vitro and in vivo (receptor binding affinity, biodistribution, imaging) as an illustration that the assembly methodology preserves the tumor targeting properties of the ligands.
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ISSN:1948-5875
1948-5875
DOI:10.1021/acsmedchemlett.3c00057