Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Biodegradation of Nitro-Substituted Explosives 2,4,6-Trinitrotoluene, Hexahydro-1,3,5-Trinitro-1,3,5-Triazine, and Octahydro-1,3,5,7-Tetranitro-1,3,5-Tetrazocine by a Phytosymbiotic Methylobacterium Sp. Associated With Poplar Tissues (Populus Deltoides X Nigra DN34)
Applied and Environmental Microbiology
Applied Microbiology
Biotechnology
Ecology
Food Science
Part 2: Efficient Strategies for the Construction of Variably Substituted Bicyclo[5.3.1]undecenones (AB-taxane Ring Systems) and Their Conversion to Tricyclo[9.3.1.03,8]pentadecenones (ABC Taxane Ring Systems) and Bicyclo[2.2.2]octanones
Canadian Journal of Chemistry
Organic Chemistry
Catalysis
Chemistry
A Computational Study on P and S Modes of Metal Ion Binding to Heteroaromatics (CH)5-mXm and (CH)6-mXm (X = N and P): Contrasting Preferences Between Nitrogen- And Phosphorous-Substituted Rings
Discovery of 5-Substituted Pyrrolo[2,3-D]pyrimidine Antifolates as Dual-Acting Inhibitors of Glycinamide Ribonucleotide Formyltransferase and 5-Aminoimidazole-4-Carboxamide Ribonucleotide Formyltransferase in De Novo Purine Nucleotide Biosynthesis: Implications of Inhibiting 5-Aminoimidazole-4-Carboxamide Ribonucleotide Formyltransferase to AMPK Activation and Antitumor Activity
Journal of Medicinal Chemistry
Drug Discovery
Molecular Medicine
Role of the Ligand and of the Size and Flexibility of the Palladium-Ancillary Ligand Cycle on the Reactivity of Substituted Alkynes Toward Palladium(0) Complexes Bearing Potentially Terdentate Nitrogen-Sulfur-Nitrogen or Nitrogen-Nitrogen-Nitrogen Ligands: Kinetic and Structural Study
Synthesis, Properties, and NAD+-NADH-Type Redox Ability of 14-Substituted 1, 3-Dimethyl-5, 10-Methanocycloundeca[4, 5]pyrrolo[2, 3-D]pyrimidine-2, 4(1, 3h)-Dionylium Tetrafluoroborates and Their Hydride Adducts
Discovery of [Cis-3-({(5r)5-[(7-Fluoro-1,1-Dimethyl-2,3-Dihydro1Hinden-5-Yl)carbamoyl]-2-Methoxy-7,8-Dihydro-1,6-Naphthyridin-6(5H)yl}carbonyl)cyclobutyl]acetic Acid (TAK-828F) as a Potent, Selective, and Orally Available Novel Retinoic Acid Receptor-Related Orphan Receptor T Inverse Agonist
The Studies on the Structure-Activity Relationship of Allyl Substituted Oxopyrimidines Searching for the Novel Antagonist or Agonist of Barbiturates to the Sleep Mechanism Based on the Uridine Receptor Theory &Mdash;Barbituric Acid to Uridine (Part I)1)—
Yakugaku Zasshi
Pharmacology
Pharmaceutical Science
Design and Synthesis of Novel Derivatives of the Muscarinic Agonist Tetra(ethylene Glycol)(3-Methoxy-1, 2, 5-Thiadiazol-4-Yl) [3-(1-Methyl-1, 2, 5, 6-Tetrahydropyrid-3-Yl)-1, 2, 5-Thiadiazol-4-Yl] Ether (CDD-0304): Effects of Structural Modifications on the Binding and Activity at Muscarinic Receptor Subtypes and Chimeras
Thermal and Metal-Catalyzed Cyclization of 1-Substituted 3, 5-Dien-1-Ynes via a [1, 7]-Hydrogen Shift: Development of a Tandem Aldol Condensation-Dehydration and Aromatization Catalysis Between 3-En-1-Yn-5-Al Units and Cyclic Ketones
‹
216
217
218
219
220
221
222
›