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Metabolomics Tools for Natural Product Discovery

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Cover of 'Metabolomics Tools for Natural Product Discovery'

Table of Contents

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    Book Overview
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    Chapter 1 Bryophytes: liverworts, mosses, and hornworts: extraction and isolation procedures.
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    Chapter 2 Plant Tissue Extraction for Metabolomics
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    Chapter 3 Detection of polar metabolites through the use of gas chromatography-mass spectrometry.
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    Chapter 4 A Robust GC-MS Method for the Quantitation of Fatty Acids in Biological Systems
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    Chapter 5 A Workflow from Untargeted LC-MS Profiling to Targeted Natural Product Isolation
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    Chapter 6 Lipidomics: extraction protocols for biological matrices.
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    Chapter 7 Metabolite Analysis of Biological Fluids and Tissues by Proton Nuclear Magnetic Resonance Spectroscopy
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    Chapter 8 NMR Spectroscopy: Structure Elucidation of Cycloelatanene A: A Natural Product Case Study
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    Chapter 9 NMR-Based Metabolomics: A Probe to Utilize Biodiversity.
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    Chapter 10 Extraction Protocol for Nontargeted NMR and LC-MS Metabolomics-Based Analysis of Hard Coral and Their Algal Symbionts.
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    Chapter 11 Determination of absolute configuration using single crystal X-ray diffraction.
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    Chapter 12 Natural product chemistry in action: the synthesis of melatonin metabolites k1 and k 2.
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    Chapter 13 Discovery, biosynthesis, and rational engineering of novel enterocin and wailupemycin polyketide analogues.
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    Chapter 14 Bioassays for anticancer activities.
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    Chapter 15 Screening for antidiabetic activities.
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    Chapter 16 Screening for Antibacterial, Antifungal, and Anti quorum Sensing Activity.
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    Chapter 17 Metabolomics Tools for Natural Product Discovery
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    Chapter 18 Bridging the gap: basic metabolomics methods for natural product chemistry.
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    Chapter 19 Strategies in Biomarker Discovery. Peak Annotation by MS and Targeted LC-MS Micro-Fractionation for De Novo Structure Identification by Micro-NMR.
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    Chapter 20 Metabolomics Tools for Natural Product Discovery
Attention for Chapter 8: NMR Spectroscopy: Structure Elucidation of Cycloelatanene A: A Natural Product Case Study
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Chapter title
NMR Spectroscopy: Structure Elucidation of Cycloelatanene A: A Natural Product Case Study
Chapter number 8
Book title
Metabolomics Tools for Natural Product Discovery
Published in
Methods in molecular biology, January 2013
DOI 10.1007/978-1-62703-577-4_8
Pubmed ID
Book ISBNs
978-1-62703-576-7, 978-1-62703-577-4
Authors

Sylvia Urban, Daniel Anthony Dias

Editors

Ute Roessner, Daniel Anthony Dias

Abstract

The structure elucidation of new secondary metabolites derived from marine and terrestrial sources is frequently a challenging task. The hurdles include the ability to isolate stable secondary metabolites of sufficient purity that are often present in <0.5 % of the dry weight of the sample. This usually involves a minimum of several chromatographic purification steps. The second issue is the stability of the compound isolated. It must always be assumed when dealing with the isolation of natural products that the compound may rapidly degrade during and/or after the isolation, due to sensitivity to light, air oxidation, and/or temperature. In this way, precautions need to be taken, as much as possible to avoid any such chemical inter-conversions and/or degradations. Immediately after purification, the next step is to rapidly acquire all analytical spectroscopic data in order to complete the characterization of the isolated secondary metabolite(s), prior to any possible decomposition. The final hurdle in this multiple step process, especially in the acquisition of the NMR spectroscopic and other analytical data (mass spectra, infrared and ultra-violet spectra, optical rotation, etc.), is to assemble the structural moieties/units in an effort to complete the structure elucidation. Often ambiguity with the elucidation of the final structure remains when structural fragments identified are difficult to piece together on the basis of the HMBC NMR correlations or when the relative configuration cannot be unequivocally identified on the basis of NOE NMR enhancements observed. Herein, we describe the methodology used to carry out the structure elucidation of a new C16 chamigrene, cycloelatanene A (5) which was isolated from the southern Australian marine alga Laurencia elata (Rhodomelaceae). The general approach and principles used in the structure determination of this compound can be applied to the structure elucidation of other small molecular weight compounds derived from either natural or synthetic sources.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 9 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 9 100%

Demographic breakdown

Readers by professional status Count As %
Other 2 22%
Student > Ph. D. Student 2 22%
Lecturer 1 11%
Student > Bachelor 1 11%
Student > Master 1 11%
Other 2 22%
Readers by discipline Count As %
Chemistry 5 56%
Biochemistry, Genetics and Molecular Biology 2 22%
Pharmacology, Toxicology and Pharmaceutical Science 2 22%