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GSK-3 Beta
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2024-10-05
相关数据集
BindingDB Entry 50018569: Discovery and Optimization of Potent and Orally Available CTP Synthetase Inhibitors for Use in Treatment of Diseases Driven by Aberrant Immune Cell Proliferation.
Small molecule binding data for protein CTP synthase 1 and CTP synthase 2, Uniprot P17812, P70303, P70698, Q5U2N0, and Q9NRF8
DataCite Commons2024-04-26 更新90
Selectivity of PF1367550.
Calculated IC50 values for PF1367550 against >50 kinases. Data are presented for the kinases that showed >50% inhibition at 1mM ATP or at the Km as indicated (Data from Coe et al., [25]). Selectivity
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Identification of New Fisetin Analogs as Kinase Inhibitors: Data on Synthesis and Anti-Skin Cancer Activities Evaluation
These data are supplementary raw data generated for the original figures and tables of the Data-In-Brief Article. all data collected were analyzed and only summary figure are included in the original
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Activity comparison for TBK1 and IKKε.
Number of active compounds (N) detected in each screen for total number detected (unfiltered), number after drug like filtering (filtered.drug-like), hits from the LOPAC and Kinase libraries, and the
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Text S1 - Select Small Core Structure Carbamates Exhibit High Contact Toxicity to “Carbamate-Resistant” Strain Malaria Mosquitoes, Anopheles gambiae (Akron)
Detailed methods and Additional Figures. This document contains detailed experimental protocols, additional figures, synthetic procedures and analytical characterization data for pyrazol-4-yl methylca
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