Methods for the synthesis of tritium-labelled fatty acids and their derivatives, oxylipins and steroids
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- Type
- article
- Published
- 1999-10-31
- Cited by
- 16
- References
- 80
- OpenAlex
- https://openalex.org/W2070183097
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:84857853
Keywords
Chemistry, Tritium, Biochemistry, Organic chemistry
References
- Fatty acids and cell signal transduction.
- Anandamide Amidohydrolase Activity in Rat Brain Microsomes
- Substrate specificity of soybean lipoxidase.
- The pharmacological activity of anandamide, a putative endogenous cannabinoid, in mice.
- Labeling of steroids by activated tritium
- In vivo effect of free fatty acids on the specific binding of glucocorticosteroids to corticosteroid binding globulin and liver receptors in immature rats.
- Induction of apoptotic DNA fragmentation and cell death by natural ceramide
- Anandamide, a Brain Endogenous Compound, Interacts Specifically with Cannabinoid Receptors and Inhibits Adenylate Cyclase
- A Mediator Role of Ceramide in the Regulation of Neuroblastoma Neuro2a Cell Differentiation (*)
- Synthesis of tritium‐labelled natural prostaglandins of series 1,2,3
- CV-3988 - a specific antagonist of platelet activating factor (PAF).
- Synthesis of tritium‐labelled isocarbacyclin derivatives, radiolabelled prostaglandin I 1 analogs(1)
- Brain cannabinoids in chocolate
- Regulation of gene transcription by polyunsaturated fatty acids.
- Ceramide Inhibits Phospholipase D in a Cell-free System*
- Activation of the sphingomyelin cycle through the low-affinity neurotrophin receptor.
- Isolation and structure of a brain constituent that binds to the cannabinoid receptor.
- Synthesis of tritiated 1α,25-dihydroxy-22-oxavitamin D3
- Synthesis and biological evaluation of 14,15-dehydro-LTA4 analog
- Modulation of cell growth and differentiation by ceramide
Cited by
- Selective dehalogenation and hydrogenation of compounds in adsorption layers with tritium gas
- The efficiency of solvent‐free catalyst systems in the synthesis of tritium‐labelled biologically active compounds
- Synthesis of tritium labelled arachidonic acid amide and ester derivatives with dopamine, serotonin, vanillylamine, and ethyleneglycol moieties
- The synthesis of O-substituted 3-oximes of 6α -methyl-16α,17α-cyclohexanopregn-4-ene-3,20-diones tritium-labeled in the 1,2-position
- Tritium labeling of bioorganic compounds by isotope exchange
- Palladium-catalysed 3H-labelling of Neu5AcOMe and spacered 3'-sialyllactose
- 5-Substituted pyridylisoxazoles as effective inhibitors of platelet aggregation
- Selective Ru(0)-catalyzed deuteration of electron-rich and electron-poor nitrogen-containing heterocycles.
- Acid-catalyzed hydrogen-deuterium exchange in β-pyrrolic positions of calix[4]pyrrole at room temperature
- Structural study of the novel deuterated calix[4]pyrrole complex d12-meso-tetrakis(4-methoxyphenyl)-meso-tetramethylcalix[4]pyrrole-pyridine N-oxide-acetonitrile (1/1/1).
- Development of New Tritium Labelling Methods for Peptides & Investigation of Guest-Host Mediated Electrocyclization and Sigma-Tropic Rearrangement Reactions
- Heterogeneous Catalytic Synthesis of Organic Compounds Labeled with Hydrogen Isotopes without Using Solvents
- Synthesis and Testing of Abscisic Acid with Predominant Replacement of Protium Atoms by Tritium in the Cyclohexene Moiety
- Effect of Processes Occurring in the Presence of Metal Catalysts on the Main Characteristics of the Hydrogen Isotope Labeled Organic Compounds Obtained
- Methods for the Synthesis of Tritium‐Labeled Fatty Acids and Their Derivatives, Oxylipins and Steroids
- Comparative Study of the Abscisic Acid Metabolism Using Analogue Tritium-Labeled in the Cyclohexene or Side Moiety
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