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Hydrogen Bonding Parameters by Rapid Colorimetric Assessment: Evaluation of Structural Components Found in Biological Ligands and Organocatalysts.


ABSTRACT: Hydrogen bonding is a key molecular interaction in biological processes, drug delivery, and catalysis. This report describes a high throughput UV-Vis spectroscopic method to measure hydrogen bonding capacity using a pyrazinone sensor. This colormetric sensor reversibly binds to a hydrogen bond donor, resulting in a blue shift as additional equivalents of donor are added. Titration with excess equivalents of donor is used to determine the binding coefficient, ln(Keq ). Over 100 titrations were performed for a variety of biologically relevant compounds. This data enabled development a multiple linear regression model that is capable of predicting 95 % of ln(Keq ) values within 1 unit, allowing for the estimation of hydrogen bonding affinity from a single measurement. To show the effectiveness of the single point measurements, hydrogen bond strengths were obtained for a set of carboxylic acid bioisosteres. The values from the single point measurements were validated with full titrations.

SUBMITTER: Roenfanz HF 

PROVIDER: S-EPMC10363249 | biostudies-literature | 2023 Jul

REPOSITORIES: biostudies-literature

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Hydrogen Bonding Parameters by Rapid Colorimetric Assessment: Evaluation of Structural Components Found in Biological Ligands and Organocatalysts.

Roenfanz Hanna F HF   Paniak Thomas J TJ   Berlin Cameron B CB   Tran Van V   Francisco Karol R KR   Lassalas Pierrik P   Devas Anisha A   Landes Olivia O   Rosenberger Avalon A   Rotella Madeline E ME   Ballatore Carlo C   Kozlowski Marisa C MC  

Chemistry (Weinheim an der Bergstrasse, Germany) 20230526 40


Hydrogen bonding is a key molecular interaction in biological processes, drug delivery, and catalysis. This report describes a high throughput UV-Vis spectroscopic method to measure hydrogen bonding capacity using a pyrazinone sensor. This colormetric sensor reversibly binds to a hydrogen bond donor, resulting in a blue shift as additional equivalents of donor are added. Titration with excess equivalents of donor is used to determine the binding coefficient, ln(K<sub>eq</sub> ). Over 100 titrati  ...[more]

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