KinITC-One Method Supports both Thermodynamic and Kinetic SARs as Exemplified on FimH Antagonists
作者:Pascal Zihlmann、Marleen Silbermann、Timothy Sharpe、Xiaohua Jiang、Tobias Mühlethaler、Roman P. Jakob、Said Rabbani、Christoph P. Sager、Priska Frei、Lijuan Pang、Timm Maier、Beat Ernst
DOI:10.1002/chem.201802599
日期:2018.9.3
thermodynamic but also kinetic information of the binding process can be deduced from isothermal titration calorimetry (ITC) experiments. Using kinITC, ITC data of 29 mannosides binding to the bacterial adhesin FimH were re‐analyzed to make their binding kinetics accessible. To validate these kinetic data, surface plasmon resonance (SPR) experiments were conducted. The kinetic analysis by kinITC revealed
[EN] MANNOSE 6-PHOSPHATE OR ASGPR RECEPTOR BINDING COMPOUNDS FOR THE DEGRADATION OF EXTRACELLULAR PROTEINS<br/>[FR] COMPOSÉS DE LIAISON AU RÉCEPTEUR MANNOSE-6-PHOSPHATE OU ASGPR POUR LA DÉGRADATION DE PROTÉINES EXTRACELLULAIRES
申请人:[en]AVILAR THERAPEUTICS, INC.
公开号:WO2023028338A2
公开(公告)日:2023-03-02
Compounds and compositions that have a mannose 6-phosphate receptor or ASGPR binding ligand bound to an extracellular protein binding ligand are provided for the selective degradation of a target extracellular protein in vivo to treat disorders mediated by the extracellular protein.
Cerny, Miloslav; Dolezalova, Jitka; Macova, Jindra, Collection of Czechoslovak Chemical Communications, 1983, vol. 48, # 9, p. 2693 - 2700