Bioorganic & Medicinal Chemistry
ISSN: 0968-0896
Datasets associated with articles published in Bioorganic & Medicinal Chemistry
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- Data for: Synthesis and Biological Evaluation of 4-(Piperid-3-yl)amino Substituted 6-Pyridylquinazolines as Potent PI3Kδ InhibitorsSupplementary data to this article
- Data for: Identification of New Dual FABP4/5 Inhibitors Based on a Naphthalene-1-sulfonamide FABP4 InhibitorSupplementary Data
- Data for: Identification of New Dual FABP4/5 Inhibitors Based on a Naphthalene-1-sulfonamide FABP4 InhibitorSupplementary Material
- Data for: Evaluation of alpha-hydroxycinnamic acids as pyruvate carboxylase inhibitorsSupplementary Table S1. % Interference of FVB and MDH assay signals Supplementary Figure S1. Inhibition of S. aureus pyruvate carboxylase (Michaelis-Menten) Supplementary Figure S2. Lactate dehydrogenase (LDH) inhibition Supplementary Figure S3. The ability of LDH to accept the compounds as substrates 1H NMR spectrum of 7a (CDCl3) 13C NMR spectrum of 7a (CDCl3) 1H NMR spectrum of 6j (d6-DMSO) 13C NMR spectrum of 6j (d6-DMSO) 1H NMR spectrum of 6r (d6-DMSO) 13C NMR spectrum of 6r (d6-DMSO) 1H NMR spectrum of 6v (d6-DMSO) 13C NMR spectrum of 8j (d6-DMSO) 1H NMR spectrum of 8m (d6-DMSO) 13C NMR spectrum of 8m (d6-DMSO) 1H NMR spectrum of 8r (CD3OD) 13C NMR spectrum of 8r (d6-DMSO) 1H NMR spectrum of 8u (d6-DMSO) 13C NMR spectrum of 8u (d6-DMSO) 1H NMR spectrum of 8v (d6-DMSO)
- Data for: Design, synthesis, biological evaluation of benzoyl amide derivatives containing nitrogen heterocyclic ring as potential VEGFR-2 inhibitorsNMR spectrum of several representative compounds
- Data for: Identification and Characterization of the First Fragment Hits for SETDB1 Tudor DomainSupporting information containing Spectroscopic and chromatography data
- Data for: The Parmodulin NRD-21 is an Allosteric Inhibitor of PAR1 Gq Signaling with Improved Anti-Inflammatory Activity and StabilityAssay protocols, additional synthetic protocols, and compound characterization data (1H NMR, 13C NMR, and LC-MS chromatograms).
- Data for: Novel meriolin derivatives as rapid apoptosis inducersSupporting Information of preparative details, characterization, and NMR spectra
- Data for: Optimization of Novel Reversible Bruton's Tyrosine Kinase Inhibitors Identified using Tethering-Fragment-Based ScreensKinases selectivity data for compounds 43 and 50. Analytical data for the synthesis of compound 50. Cellular IC50 graphs.
- Data for: Identification and immunological evaluation of novel TLR2 agonists through structure optimization of Pam3CSK4 Supplementary material of manuscript which called identification and immunological evaluation of novel TLR2 agonists through structure optimization of Pam3CSK4
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