FK506-binding protein 51 (FKBP51 or FKBP5) serves as a crucial stress modulator implicated in mental disorders, presenting a potential target for intervention. Inhibitors like SAFit2, rapamycin, and t

Figshare2025-03-17 更新40

QSAR-DATASET-FOR-DRUG-TARGET-CHEMBL6194

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This dataset contains QSAR data (from ChEMBL version 17) showing activity values (unit is pseudo-pCI50) of several compounds on drug target ChEMBL_ID: CHEMBL6194 (TID: 102805), and it has 39 rows and

OpenML2016-07-15 更新40

Expansion of UBTR012574 Chemical Series

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Expansion of the chemical series of UBTR012574 (KD= 10 ± 0.1 µM) by docking analogue compounds from the Enamine REAL database and SciFinder against the USP5 zinc finger ubiquitin-binding domain (ZnF-U

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Kinetically Selective Inhibitors of Human Carbonic Anhydrase Isozymes I, II, VII, IX, XII, and XIII

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To get a better understanding of the possibility of developing selective carbonic anhydrase (CA) inhibitors, interactions between 17 benzenesulphonamide ligands and 6 human CAs (full-length CA I, II,

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Pyruvate kinase (PYK) from Trypanosoma brucei in the presence of Magnesium, PEP and F26BP

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