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Author Correction: Tripterygium wilfordii cytochrome P450s catalyze the methyl shift and epoxidations in the biosynthesis of triptonide. [PDF]
Kongstad KT +7 more
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Editor's Choice JAAG: a JSON input file assembler for AlphaFold 3 with glycan integration. [PDF]
Huang C, Moremen KW.
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Caylobolide B: Structure Revision, Total Synthesis, Biological Characterization, and Discovery of New Analogues. [PDF]
George MRP +9 more
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DP5 without DFT: uncertainty-calibrated graph neural net accelerates structure confirmation <i>via</i> NMR. [PDF]
Kotlyarov R, Howarth A, Goodman JM.
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Inverse stable isotopic labeling for natural product characterization and discovery.
Robes JMD, Puri AW.
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STEREOCHEMISTRY IN ANAESTHESIA
Clinical and Experimental Pharmacology and Physiology, 1997SUMMARY1. Interest in the pharmacokinetic and pharmacodynamic properties of the enantiomers of chiral drugs has greatly increased in recent years. This is particularly so for agents used in anaesthesia.2. Chiral compounds are those that can exist in two nonâsuperimposable forms. Each form is termed an enantiomer or stereoisomer.
D A, Sidebotham, S A, Schug
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The stereochemistry of pinidine
Tetrahedron, 1965Abstract The stereochemistry of pinidine, a piperidine alkaloid from Pinus sabiniana, was established by chemical and spectroscopic methods as 2-(R)-methyl-6-(R)-(2-trans-propenyl)-piperidine (XXI). Some interesting rearrangements which occurred during degradative studies are discussed, and the configuration of pinidine is compared with that of ...
R K, Hill, T H, Chan, J A, Joule
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Stereochemistry and Bioequivalence
The Journal of Clinical Pharmacology, 1992Despite the fact that many important drugs are chiral, for a variety of reasons they are marketed as racemates (i.e., an equal proportion of two enantiomers). Although enantiomers of racemic drugs often differ from one another in their pharmacodynamic and pharmacokinetic properties, bioequivalence assessments are made using nonstereospecific assays ...
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