From retrospective assessment to prospective decisions in natural product isolation: HPLC-SPE-NMR analysis of Carthamus oxyacantha

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

From retrospective assessment to prospective decisions in natural product isolation : HPLC-SPE-NMR analysis of Carthamus oxyacantha. / Johansen, Kenneth T; Wubshet, Sileshi G; Nyberg, Nils T; Jaroszewski, Jerzy W.

In: Journal of Natural Products, Vol. 74, No. 11, 28.11.2011, p. 2454-2461.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Johansen, KT, Wubshet, SG, Nyberg, NT & Jaroszewski, JW 2011, 'From retrospective assessment to prospective decisions in natural product isolation: HPLC-SPE-NMR analysis of Carthamus oxyacantha', Journal of Natural Products, vol. 74, no. 11, pp. 2454-2461. https://doi.org/10.1021/np200780m

APA

Johansen, K. T., Wubshet, S. G., Nyberg, N. T., & Jaroszewski, J. W. (2011). From retrospective assessment to prospective decisions in natural product isolation: HPLC-SPE-NMR analysis of Carthamus oxyacantha. Journal of Natural Products, 74(11), 2454-2461. https://doi.org/10.1021/np200780m

Vancouver

Johansen KT, Wubshet SG, Nyberg NT, Jaroszewski JW. From retrospective assessment to prospective decisions in natural product isolation: HPLC-SPE-NMR analysis of Carthamus oxyacantha. Journal of Natural Products. 2011 Nov 28;74(11):2454-2461. https://doi.org/10.1021/np200780m

Author

Johansen, Kenneth T ; Wubshet, Sileshi G ; Nyberg, Nils T ; Jaroszewski, Jerzy W. / From retrospective assessment to prospective decisions in natural product isolation : HPLC-SPE-NMR analysis of Carthamus oxyacantha. In: Journal of Natural Products. 2011 ; Vol. 74, No. 11. pp. 2454-2461.

Bibtex

@article{52f4a791deab486c9cc0ca7b4a4fb15d,
title = "From retrospective assessment to prospective decisions in natural product isolation: HPLC-SPE-NMR analysis of Carthamus oxyacantha",
abstract = "An extract of Carthamus oxyacantha (wild safflower) was investigated using two approaches: a traditional, nontarget fractionation by VLC and HPLC, and the hyphenated technique HPLC-PDA-HRMS-SPE-NMR followed by targeted isolation of selected constituents for inclusion in a screening library of pure natural products. While the nontarget fractionation involved considerable time spent on pursuing fractions containing well-known or undesired compounds, the hyphenated analysis was considerably faster and required less solvent and other consumables. The results were used to design and execute an optimized, HPLC-HRMS-guided, targeted isolation scheme aiming exclusively at a series of identified spiro compounds. Thus, HPLC-PDA-HRMS-SPE-NMR is a dereplication technique of choice, allowing economical acquisition of comprehensive data about compounds in crude extracts, which can be used for rational, prospective decisions about further isolation efforts. A total of 15 compounds were identified in the extract. Six spiro compounds, of which four have not previously been characterized, and tracheloside (a lignin glucoside) are presented with assigned (1)H and (13)C chemical shifts.",
keywords = "Former Faculty of Pharmaceutical Sciences",
author = "Johansen, {Kenneth T} and Wubshet, {Sileshi G} and Nyberg, {Nils T} and Jaroszewski, {Jerzy W}",
year = "2011",
month = "11",
day = "28",
doi = "10.1021/np200780m",
language = "English",
volume = "74",
pages = "2454--2461",
journal = "Journal of Natural Products",
issn = "0163-3864",
publisher = "American Chemical Society",
number = "11",

}

RIS

TY - JOUR

T1 - From retrospective assessment to prospective decisions in natural product isolation

T2 - HPLC-SPE-NMR analysis of Carthamus oxyacantha

AU - Johansen, Kenneth T

AU - Wubshet, Sileshi G

AU - Nyberg, Nils T

AU - Jaroszewski, Jerzy W

PY - 2011/11/28

Y1 - 2011/11/28

N2 - An extract of Carthamus oxyacantha (wild safflower) was investigated using two approaches: a traditional, nontarget fractionation by VLC and HPLC, and the hyphenated technique HPLC-PDA-HRMS-SPE-NMR followed by targeted isolation of selected constituents for inclusion in a screening library of pure natural products. While the nontarget fractionation involved considerable time spent on pursuing fractions containing well-known or undesired compounds, the hyphenated analysis was considerably faster and required less solvent and other consumables. The results were used to design and execute an optimized, HPLC-HRMS-guided, targeted isolation scheme aiming exclusively at a series of identified spiro compounds. Thus, HPLC-PDA-HRMS-SPE-NMR is a dereplication technique of choice, allowing economical acquisition of comprehensive data about compounds in crude extracts, which can be used for rational, prospective decisions about further isolation efforts. A total of 15 compounds were identified in the extract. Six spiro compounds, of which four have not previously been characterized, and tracheloside (a lignin glucoside) are presented with assigned (1)H and (13)C chemical shifts.

AB - An extract of Carthamus oxyacantha (wild safflower) was investigated using two approaches: a traditional, nontarget fractionation by VLC and HPLC, and the hyphenated technique HPLC-PDA-HRMS-SPE-NMR followed by targeted isolation of selected constituents for inclusion in a screening library of pure natural products. While the nontarget fractionation involved considerable time spent on pursuing fractions containing well-known or undesired compounds, the hyphenated analysis was considerably faster and required less solvent and other consumables. The results were used to design and execute an optimized, HPLC-HRMS-guided, targeted isolation scheme aiming exclusively at a series of identified spiro compounds. Thus, HPLC-PDA-HRMS-SPE-NMR is a dereplication technique of choice, allowing economical acquisition of comprehensive data about compounds in crude extracts, which can be used for rational, prospective decisions about further isolation efforts. A total of 15 compounds were identified in the extract. Six spiro compounds, of which four have not previously been characterized, and tracheloside (a lignin glucoside) are presented with assigned (1)H and (13)C chemical shifts.

KW - Former Faculty of Pharmaceutical Sciences

U2 - 10.1021/np200780m

DO - 10.1021/np200780m

M3 - Journal article

C2 - 22060189

VL - 74

SP - 2454

EP - 2461

JO - Journal of Natural Products

JF - Journal of Natural Products

SN - 0163-3864

IS - 11

ER -

ID: 35457116