Related ArticlesSubtle Chemical Shifts Explain the NMR Fingerprints of Oligomeric Proanthocyanidins with High Dentin Biomodification Potency.
J Org Chem. 2015 Jul 27;
Authors: Nam JW, Phansalkar RS, Lankin DC, Bisson J, McAlpine JB, Leme AA, Vidal CM, Ramirez B, Niemitz M, Bedran-Russo A, Chen SN, Pauli GF
Abstract
The ability of certain oligomeric proanthocyanidins (OPACs) to enhance the biomechanical properties of dentin involves collagen cross-linking of the 1.3-4.5 nm wide space via protein-polyphenol interactions. A systematic interdisciplinary search for the bioactive principles of pine bark has yielded the trimeric PAC, ent-epicatechin-(4?->8)-epicatechin-(2?->O->7,4?->8)-catechin (3), representing the hitherto most potent single chemical entity capable of enhancing dentin stiffness. Building the case from two congeneric PAC dimers, a detailed structural analysis decoded the stereochemistry, spatial arrangement, and chemical properties of three dentin biomodifiers. Quantum-mechanics-driven (1)H iterative full spin analysis (QM-HiFSA) of NMR spectra distinguished previously unrecognized details such as higher order J coupling and provided valuable information about 3D structure. Detection and quantification of H/D-exchange effects by QM-HiFSA identified C-8 and C-6 as (re)active sites, explain preferences in biosynthetic linkage, and suggest their involvement in dentin cross-linking activity. Mapping of these molecular properties underscored the significance of high ? precision in both (1)H and (13)C NMR spectroscopy. Occurring at low- to subppb levels, these newly characterized chemical shift differences in ppb are small but diagnostic measures of dynamic processes inherent to the OPAC pharmacophores and can help augment our understanding of nanometer-scale intermolecular interactions in biomodified dentin macromolecules.
PMID: 26214362 [PubMed - as supplied by publisher]
19F NMR Fingerprints: Identification ofNeutral Organic Compounds in a Molecular Container
19F NMR Fingerprints: Identification ofNeutral Organic Compounds in a Molecular Container
Yanchuan Zhao, Georgios Markopoulos and Timothy M. Swager
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/ja504110f/aop/images/medium/ja-2014-04110f_0017.gif
Journal of the American Chemical Society
DOI: 10.1021/ja504110f
http://feeds.feedburner.com/~ff/acs/jacsat?d=yIl2AUoC8zA
http://feeds.feedburner.com/~r/acs/jacsat/~4/O48hPTaD2jE
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07-22-2014 09:19 PM
Dating fingerprints
Dating fingerprints
http://www.spectroscopynow.com/common/images/thumbnails/14632f55c59.jpgThe focus on fingermarks continues with news that their age can now be estimated by measuring the degree of oxidation of the lipids which form fluorescent products with the proteins present.
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05-25-2014 06:31 PM
Lecture 9. Chemical Shift. 1H NMR Chemical Shifts.
Lecture 9. Chemical Shift. 1H NMR Chemical Shifts.
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Lecture 9. Chemical Shift. 1H NMR Chemical Shifts.
This video is part of a 28-lecture graduate-level course titled "Organic Spectroscopy" taught at UC Irvine by Professor James S. Nowick. The course covers in...
From:UCITLTC
Views:7351
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NMR educational videos
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03-22-2013 05:19 AM
[NMR paper] An NMR comparison of the light-harvesting complex II (LHCII) in active and photoprotective states reveals subtle changes in the chlorophyll a ground-state electronic structures.
An NMR comparison of the light-harvesting complex II (LHCII) in active and photoprotective states reveals subtle changes in the chlorophyll a ground-state electronic structures.
Related Articles An NMR comparison of the light-harvesting complex II (LHCII) in active and photoprotective states reveals subtle changes in the chlorophyll a ground-state electronic structures.
Biochim Biophys Acta. 2013 Mar 4;
Authors: Pandit A, Reus M, Morosinotto T, Bassi R, Holzwarth AR, de Groot HJ
Abstract
To protect the photosynthetic apparatus against...
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Journal club
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03-08-2013 10:35 PM
Lecture 10. 13C NMR Chemical Shifts. Chemical Equivalence and Spin-Spin Coupling.
Lecture 10. 13C NMR Chemical Shifts. Chemical Equivalence and Spin-Spin Coupling.
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Lecture 10. 13C NMR Chemical Shifts. Chemical Equivalence and Spin-Spin Coupling.
This video is part of a 28-lecture graduate-level course titled "Organic Spectroscopy" taught at UC Irvine by Professor James S. Nowick. The course covers in...
From:UCITLTC
Views:12165
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03-07-2013 05:38 AM
[Question from NMRWiki Q&A forum] Are there ways to explain magnetic-field dependent chemical shift?
Are there ways to explain magnetic-field dependent chemical shift?
Hi everyone,
I was wondering whether anyone could help me to explain why the chemical shifts in my proton and carbon NMR results do not exactly match with those reported in the literature?The solvent used in my experiment is exactly the same as the one used in the literature of reference (CD3OD), however the frequency applied in my experiment was 500MHz as opposed to 400MHz by the study i am comparing my results with.
For example, in my proton NMR spectra, my results are usually 0.08 to 0.26 ppm higher than that in...
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08-05-2012 03:59 PM
19F chemical shifts.jpg
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Uploaded by user "Artb33" on Sun, 06 Mar 2011 14:16:00 UTC
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NMR pictures
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03-06-2011 03:35 PM
[NMR paper] Proton NMR spin grouping and exchange in dentin.
Proton NMR spin grouping and exchange in dentin.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--linkinghub.elsevier.com-ihub-images-cellhub.gif http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--www.pubmedcentral.nih.gov-corehtml-pmc-pmcgifs-pubmed-pmc.gif Related Articles Proton NMR spin grouping and exchange in dentin.
Biophys J. 1991 Mar;59(3):629-39
Authors: Schreiner LJ, Cameron IG, Funduk N, MiljkoviÄ? L, Pintar MM, Kydon DN
The nuclear magnetic resonance spin-grouping technique has been applied to dentin from human donors...