| Stereochemistry of ulapualides, a new family of tris-oxazole-containing macrolide ionophores from marine nudibranchs. A molecular mechanics study. | |
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MedLine Citation:
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PMID: 8294947 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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A molecular mechanics study of the marine metabolite ulapualide A, which is suggested to have ionophoric properties, has been carried out on various metal chelated complexes in order to predict the stereochemistry of the natural product. The results suggest a stereochemistry for ulapualide A which is closely similar to structurally related marine metabolites, whose stereochemistries have been established by X-ray crystallography and by partial synthesis. |
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Authors:
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J Maddock; G Pattenden; P G Wight |
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Publication Detail:
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Type: Journal Article; Research Support, Non-U.S. Gov't |
Journal Detail:
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Title: Journal of computer-aided molecular design Volume: 7 ISSN: 0920-654X ISO Abbreviation: J. Comput. Aided Mol. Des. Publication Date: 1993 Oct |
Date Detail:
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Created Date: 1994-02-28 Completed Date: 1994-02-28 Revised Date: 2006-11-15 |
Medline Journal Info:
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Nlm Unique ID: 8710425 Medline TA: J Comput Aided Mol Des Country: NETHERLANDS |
Other Details:
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Languages: eng Pagination: 573-86 Citation Subset: IM |
Affiliation:
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Chemistry Department, University, Nottingham, U.K. |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Animals Computer Simulation Ionophores / chemistry* Models, Molecular Molecular Conformation Molecular Structure Mollusca / chemistry* Oxazoles / chemistry* Stereoisomerism Thermodynamics |
| Chemical | |
Reg. No./Substance:
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0/Ionophores; 0/Oxazoles; 100045-73-6/ulapualide A |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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