CSAKD: Determining Absolute Ligand Affinities From <sup>19</sup> F NMR Chemical Shift Anisotropy

ABSTRACT Small‐molecule drug discovery typically begins with the screening of compound libraries to identify initial hits, which are subsequently optimized into lead compounds and, ultimately, drug candidates. Diverse screening methodologies are employed, including DNA‐encoded library technology, high‐throughput screening, and fragment‐based drug discovery (FBDD). Among these, FBDD is particularly powerful when integrated with structure‐guided drug design and biophysical affinity measurements. However, accurately quantifying the weak binding affinities of fragments remains a significant challenge. To address this, we introduce chemical shift anisotropy (CSAKD), a novel method for determining absolute fragment affinities using NMR relaxation. The CSAKD approach eliminates the need for titration experiments and isotopic labeling. Furthermore, we complement this method with a machine learning model for the rapid and accurate prediction of chemical shielding tensors. In summary, CSAKD allows fast and efficient affinity determination which seamlessly integrates into FBDD by NMR.

Authors

Institutions

Publication Details

Journal
Angewandte Chemie
Published
2026-06-12
DOI
https://doi.org/10.1002/ange.6036832
Primary Topic
Molecular spectroscopy and chirality
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

CSAKD: Determining Absolute Ligand Affinities From 19 F NMR Chemical Shift Anisotropy

Gabriela R. Stadler, Simon Rüdisser, Alvar D. Gossert
Angewandte Chemie
Molecular spectroscopy and chirality
article

CSAKD: Determining Absolute Ligand Affinities From 19 F NMR Chemical Shift Anisotropy

Gabriela R. Stadler, Simon Rüdisser, Alvar D. Gossert
article en

Abstract

ABSTRACT Small‐molecule drug discovery typically begins with the screening of compound libraries to identify initial hits, which are subsequently optimized into lead compounds and, ultimately, drug candidates. Diverse screening methodologies are employed, including DNA‐encoded library technology, high‐throughput screening, and fragment‐based drug discovery (FBDD). Among these, FBDD is particularly powerful when integrated with structure‐guided drug design and biophysical affinity measurements. However, accurately quantifying the weak binding affinities of fragments remains a significant challenge. To address this, we introduce chemical shift anisotropy (CSAKD), a novel method for determining absolute fragment affinities using NMR relaxation. The CSAKD approach eliminates the need for titration experiments and isotopic labeling. Furthermore, we complement this method with a machine learning model for the rapid and accurate prediction of chemical shielding tensors. In summary, CSAKD allows fast and efficient affinity determination which seamlessly integrates into FBDD by NMR.

Angewandte Chemie
ETH Zurich (CH)
Openalex Percentile: Top 11%
Molecular spectroscopy and chirality
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

CSAKD: Determining Absolute Ligand Affinities From <sup>19</sup> F NMR Chemical Shift Anisotropy — Gabriela R. Stadler, Simon Rüdisser, et al. · Angewandte Chemie (2026) | TGRS Research Map | TGRS