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A solution conformation analysis of forocidins I and isoforocidins I using NMR and molecular modeling. 1995

K Ramu, and S Shringarpure, and J S Williamson
Department of Medicinal Chemistry, University of Mississippi, University, Massachusetts 38677, USA.

UI MeSH Term Description Entries
D008958 Models, Molecular Models used experimentally or theoretically to study molecular shape, electronic properties, or interactions; includes analogous molecules, computer-generated graphics, and mechanical structures. Molecular Models,Model, Molecular,Molecular Model
D008968 Molecular Conformation The characteristic three-dimensional shape of a molecule. Molecular Configuration,3D Molecular Structure,Configuration, Molecular,Molecular Structure, Three Dimensional,Three Dimensional Molecular Structure,3D Molecular Structures,Configurations, Molecular,Conformation, Molecular,Conformations, Molecular,Molecular Configurations,Molecular Conformations,Molecular Structure, 3D,Molecular Structures, 3D,Structure, 3D Molecular,Structures, 3D Molecular
D006868 Hydrolysis The process of cleaving a chemical compound by the addition of a molecule of water.
D012996 Solutions The homogeneous mixtures formed by the mixing of a solid, liquid, or gaseous substance (solute) with a liquid (the solvent), from which the dissolved substances can be recovered by physical processes. (From Grant & Hackh's Chemical Dictionary, 5th ed) Solution
D015572 Spiramycin A macrolide antibiotic produced by Streptomyces ambofaciens. The drug is effective against gram-positive aerobic pathogens, N. gonorrhoeae, and staphylococci. It is used to treat infections caused by bacteria and Toxoplasma gondii. Spiramycin Adipate,Antibiotic 799,IL-5902,NSC-55926,NSC-64393,Rovamycin,Rovamycine,Selectomycin,Spiramycine,IL 5902,IL5902,NSC 55926,NSC 64393,NSC55926,NSC64393

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