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An Investigation Into the Cytotoxicity and Mode of Action of Some Novel N-Alkyl-Substituted Isatins
Synthesis and Regioselective N- And O-Alkylation of 1h- Or 3h-[1,2,3]Triazolo[4,5-D]pyrimidine-5,7(4h,6h)-Diones (8-Azaxanthines) and Transformation of Their 3-Alkyl Derivatives Into 1-Alkyl Isomers.
ChemInform
Development of a Series of (1-Benzyl-3-(6-Methoxypyrimidin-3-Yl)-5-(Trifluoromethoxy)-1h-Indol-2-Yl)methanols as Selective Protease Activated Receptor 4 (PAR4) Antagonists With in Vivo Utility and Activity Against Γ-Thrombin
Journal of Medicinal Chemistry
Drug Discovery
Molecular Medicine
Targeting a Subpocket in Trypanosoma Brucei Phosphodiesterase B1 (TbrPDEB1) Enables the Structure-Based Discovery of Selective Inhibitors With Trypanocidal Activity
Structure-Activity Relationship of 3-O-Acylated Betulinic Acid Derivatives Obtained by Enzymatic Synthesis as Anticancer Agents
The Open Conference Proceedings Journal
4-Iodo-N-(O-Tolylsulfonyl)benzamide
IUCrData
Development of Inhibitors as Research Tools for Carbohydrate-Processing Enzymes
Biochemical Society Transactions
Biochemistry
Development of Peptide-Conjugated Morpholino Oligomers as Pan-Arenavirus Inhibitors
Antimicrobial Agents and Chemotherapy
Infectious Diseases
Pharmacology
Discovery of Inhibitors of Aurora/PLK Targets as Anticancer Agents
Figure 3: Body Fat, Protein and Body Water in Rats Fed a Control (C, N = 6), High Fat (HF, N = 6) or Cafeteria Diet (CAF, N = 6).
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