An Optimized Two-Dimensional Quantitative Nuclear Magnetic Resonance Strategy for the Rapid Quantitation of Diester-Type C19-Diterpenoid Alkaloids from Aconitum carmichaelii

Analytical Chemistry
2023.0

Abstract

With the development of nuclear magnetic resonance (NMR) spectrometers and probes, two-dimensional quantitative nuclear magnetic resonance (2D qNMR) technology with a high signal resolution and great application potential has become increasingly accessible for the quantitation of complex mixtures. However, the requirement that the relaxation recovery time be equal to at least five times T(1) (longitudinal relaxation time) makes it difficult for 2D qNMR to simultaneously achieve high quantitative accuracy and high data acquisition efficiency. By comprehensively using relaxation optimization and nonuniform sampling, we successfully established an optimized 2D qNMR strategy for HSQC experiments at the half-hour level and then accurately quantified the diester-type C(19)-diterpenoid alkaloids in Aconitum carmichaelii. The optimized strategy had the advantages of high efficiency, high accuracy, good reproducibility, and low cost and thus could serve as a reference to optimize 2D qNMR experiments for quantitative analysis of natural products, metabolites, and other complex mixtures.

Knowledge Graph

Similar Paper

An Optimized Two-Dimensional Quantitative Nuclear Magnetic Resonance Strategy for the Rapid Quantitation of Diester-Type C<sub>19</sub>-Diterpenoid Alkaloids from Aconitum carmichaelii
Analytical Chemistry 2023.0
<sup>13</sup>C Nuclear magnetic resonance spectroscopy in the elucidation of structures of diterpenoid alkaloids
Canadian Journal of Chemistry 1987.0
<scp>2D NMR</scp>‐based <scp>MatchNat</scp> Dereplication Strategy Enables Explosive Discovery of Novel Diterpenoid Alkaloids<sup>†</sup>
Chinese Journal of Chemistry 2022.0
Differential Analysis of 2D NMR Spectra: New Natural Products from a Pilot‐Scale Fungal Extract Library
Angewandte Chemie International Edition 2007.0
Quindolinocryptotackieine: the elucidation of a novel indoloquinoline alkaloid structure through the use of computer‐assisted structure elucidation and 2D NMR
Magnetic Resonance in Chemistry 2003.0
Application of Two-Dimensional Nmr Spectroscopy in the Structural Determination of Marine Natural Products. Isolation and Total Structural Assignment of 4-Deoxyasbestinin Diterpenes from the Caribbean Gorgonian Briareum asbestinum
Journal of Natural Products 1991.0
Quantification of sesquiterpene pyridine alkaloids from genus Tripterygium by band-selective HSQC NMR
Analytica Chimica Acta 2023.0
Quindolinocryptotackieine: the elucidation of a novel indoloquinoline alkaloid structure through the use of computer‐assisted structure elucidation and 2D NMR
Magnetic Resonance in Chemistry 2003.0
A Study of Stemona Alkaloids, III. Application of 2D-nmr Spectroscopy in the Structure Determination of Stemoninine
Journal of Natural Products 1988.0
Neutral Fragment Filtering for Rapid Identification of New Diester-Diterpenoid Alkaloids in Roots of Aconitum carmichaeli by Ultra-High-Pressure Liquid Chromatography Coupled with Linear Ion Trap-Orbitrap Mass Spectrometry
PLoS ONE 2012.0