Inhibitor Synthesis and Biophysical Characterization of Protein–Ligand–Solvent Interactions An Analysis of the Thermodynamics and Kinetics of Ligand Binding to Thermolysin
In the pre-clinical development stages of most drug design campaigns, the equilibrium binding affinity of a prospective lead candidate, in the form of an IC50, Kd or ΔG° value, is the most commonly employed benchmark parameter for its effectiveness as a putative drug. Hydrogen bonding, van der Waals...
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Format: | Dissertation |
Idioma: | anglès |
Publicat: |
Philipps-Universität Marburg
2017
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Accés en línia: | PDF a text complet |
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Internet
PDF a text completSignatura: |
urn:nbn:de:hebis:04-z2017-04658 |
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Data de publicació: |
2018-08-08 |
Datum der Annahme: |
2017-06-09 |
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97 (2024), 99 (2023), 58 (2022), 37 (2021), 24 (2020), 36 (2019), 11 (2018) |
Lizenz: |
https://rightsstatements.org/vocab/InC-NC/1.0/ |
URL d'accés: |
https://archiv.ub.uni-marburg.de/diss/z2017/0465 https://doi.org/10.17192/z2017.0465 |