Coumarins from the roots of Prangos uloptera

Seyed M. Razavi; Hossein Nazemiyeh; Abbas Delazar; Rogaieh Hajiboland; M. Mukhlesur Rahman; Simon Gibbons; Lutfun Nahar; Satyajit D. Sarker

doi:10.1016/j.phytol.2008.07.009

Coumarins from the roots of Prangos uloptera

Seyed M. Razavi, Hossein Nazemiyeh, Abbas Delazar, Rogaieh Hajiboland, M. Mukhlesur Rahman, Simon Gibbons, Lutfun Nahar, Satyajit D. Sarker

Research output: Contribution to journal › Article › peer-review

34 Citations (Scopus)

Abstract

Three new coumarins, 6-O-[β-d-apiofuranosyl-(1 → 6)-β-d-glucopyranosyl]-prenyletin, 3″-O-[β-d-apiofuranosyl-(1 → 6)-β-d-glucopyranosyl]-oxypeucedanin hydrate and 2″-O-[β-d-apiofuranosyl-(1 → 6)-β-d-glucopyranosyl]-oxypeucedanin hydrate, together with six known coumarins, 3″-O-[β-d-apiofuranosyl-(1 → 6)-β-d-glucopyranosyl]-heraclenol, 3″-O-(β-d-glucopyranosyl)-heraclenol, tortuoside, 3″-O-(β-d-glucopyranosyl)-oxypeucedanin hydrate, heraclenol and oxypeucedanin hydrate, have been isolated from the roots of Prangos uloptera, and the structures of these coumarins were unequivocally determined by spectroscopic means, notably UV, HRESIMS, and 1D and 2D NMR spectroscopy.

Original language	English
Pages (from-to)	159-162
Number of pages	4
Journal	Phytochemistry Letters
Volume	1
Issue number	3
DOIs	https://doi.org/10.1016/j.phytol.2008.07.009
Publication status	Published - 1 Nov 2008

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10.1016/j.phytol.2008.07.009

https://linkinghub.elsevier.com/retrieve/pii/S1874390008000566

Cite this

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title = "Coumarins from the roots of Prangos uloptera",

abstract = "Three new coumarins, 6-O-[β-d-apiofuranosyl-(1 → 6)-β-d-glucopyranosyl]-prenyletin, 3″-O-[β-d-apiofuranosyl-(1 → 6)-β-d-glucopyranosyl]-oxypeucedanin hydrate and 2″-O-[β-d-apiofuranosyl-(1 → 6)-β-d-glucopyranosyl]-oxypeucedanin hydrate, together with six known coumarins, 3″-O-[β-d-apiofuranosyl-(1 → 6)-β-d-glucopyranosyl]-heraclenol, 3″-O-(β-d-glucopyranosyl)-heraclenol, tortuoside, 3″-O-(β-d-glucopyranosyl)-oxypeucedanin hydrate, heraclenol and oxypeucedanin hydrate, have been isolated from the roots of Prangos uloptera, and the structures of these coumarins were unequivocally determined by spectroscopic means, notably UV, HRESIMS, and 1D and 2D NMR spectroscopy.",

author = "Razavi, {Seyed M.} and Hossein Nazemiyeh and Abbas Delazar and Rogaieh Hajiboland and Rahman, {M. Mukhlesur} and Simon Gibbons and Lutfun Nahar and Sarker, {Satyajit D.}",

year = "2008",

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doi = "10.1016/j.phytol.2008.07.009",

language = "English",

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journal = "Phytochemistry Letters",

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T1 - Coumarins from the roots of Prangos uloptera

AU - Razavi, Seyed M.

AU - Nazemiyeh, Hossein

AU - Delazar, Abbas

AU - Hajiboland, Rogaieh

AU - Rahman, M. Mukhlesur

AU - Gibbons, Simon

AU - Nahar, Lutfun

AU - Sarker, Satyajit D.

PY - 2008/11/1

Y1 - 2008/11/1

N2 - Three new coumarins, 6-O-[β-d-apiofuranosyl-(1 → 6)-β-d-glucopyranosyl]-prenyletin, 3″-O-[β-d-apiofuranosyl-(1 → 6)-β-d-glucopyranosyl]-oxypeucedanin hydrate and 2″-O-[β-d-apiofuranosyl-(1 → 6)-β-d-glucopyranosyl]-oxypeucedanin hydrate, together with six known coumarins, 3″-O-[β-d-apiofuranosyl-(1 → 6)-β-d-glucopyranosyl]-heraclenol, 3″-O-(β-d-glucopyranosyl)-heraclenol, tortuoside, 3″-O-(β-d-glucopyranosyl)-oxypeucedanin hydrate, heraclenol and oxypeucedanin hydrate, have been isolated from the roots of Prangos uloptera, and the structures of these coumarins were unequivocally determined by spectroscopic means, notably UV, HRESIMS, and 1D and 2D NMR spectroscopy.

AB - Three new coumarins, 6-O-[β-d-apiofuranosyl-(1 → 6)-β-d-glucopyranosyl]-prenyletin, 3″-O-[β-d-apiofuranosyl-(1 → 6)-β-d-glucopyranosyl]-oxypeucedanin hydrate and 2″-O-[β-d-apiofuranosyl-(1 → 6)-β-d-glucopyranosyl]-oxypeucedanin hydrate, together with six known coumarins, 3″-O-[β-d-apiofuranosyl-(1 → 6)-β-d-glucopyranosyl]-heraclenol, 3″-O-(β-d-glucopyranosyl)-heraclenol, tortuoside, 3″-O-(β-d-glucopyranosyl)-oxypeucedanin hydrate, heraclenol and oxypeucedanin hydrate, have been isolated from the roots of Prangos uloptera, and the structures of these coumarins were unequivocally determined by spectroscopic means, notably UV, HRESIMS, and 1D and 2D NMR spectroscopy.

U2 - 10.1016/j.phytol.2008.07.009

DO - 10.1016/j.phytol.2008.07.009

M3 - Article

VL - 1

SP - 159

EP - 162

JO - Phytochemistry Letters

JF - Phytochemistry Letters

SN - 1874-3900

IS - 3

ER -