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Sesquiterpene Phenylpropanoids from Ferula f ukanensis and Their Nitric Oxide Production Inhibitory Effects
Five new sesquiterpene phenylpropanoid derivatives, fukanedone A (1), fukanedone B (2), fukanedone C (3), fukanedone D (4), and fukanedone E (5), and a novel phenyl-oxo-acetate ester, fukaneketoester A (6), were isolated from a 80% aqueous methanol extract of the roots of Ferula fukanensis. The stru...
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Published in: | Journal of natural products (Washington, D.C.) D.C.), 2005-03, Vol.68 (3), p.365-368 |
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Language: | English |
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cites | cdi_FETCH-LOGICAL-a104c-6be5dd5edd906d7259c4e1990c54c6e05794819971331966bdbab1d0f0525bcd3 |
container_end_page | 368 |
container_issue | 3 |
container_start_page | 365 |
container_title | Journal of natural products (Washington, D.C.) |
container_volume | 68 |
creator | Motai, Tsunetake Kitanaka, Susumu |
description | Five new sesquiterpene phenylpropanoid derivatives, fukanedone A (1), fukanedone B (2), fukanedone C (3), fukanedone D (4), and fukanedone E (5), and a novel phenyl-oxo-acetate ester, fukaneketoester A (6), were isolated from a 80% aqueous methanol extract of the roots of Ferula fukanensis. The structures were elucidated on the basis of spectroscorpic evidence, especially heteronuclear multiple-bond connectivity (HMBC) and high-resolution MS. The sesquiterpene phenylpropanoid derivatives inhibited nitric oxide (NO) production and inducible NO synthase (iNOS) gene expression by a murine macrophage-like cell line (RAW 264.7), which was activated by lipopolysaccharide (LPS) and recombinant mouse interferon-γ (IFN-γ). |
doi_str_mv | 10.1021/np040215c |
format | article |
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The structures were elucidated on the basis of spectroscorpic evidence, especially heteronuclear multiple-bond connectivity (HMBC) and high-resolution MS. The sesquiterpene phenylpropanoid derivatives inhibited nitric oxide (NO) production and inducible NO synthase (iNOS) gene expression by a murine macrophage-like cell line (RAW 264.7), which was activated by lipopolysaccharide (LPS) and recombinant mouse interferon-γ (IFN-γ).</description><identifier>ISSN: 0163-3864</identifier><identifier>EISSN: 1520-6025</identifier><identifier>DOI: 10.1021/np040215c</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Journal of natural products (Washington, D.C.), 2005-03, Vol.68 (3), p.365-368</ispartof><rights>Copyright © 2005 American Chemical Society and American Society of Pharmacognosy</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a104c-6be5dd5edd906d7259c4e1990c54c6e05794819971331966bdbab1d0f0525bcd3</citedby><cites>FETCH-LOGICAL-a104c-6be5dd5edd906d7259c4e1990c54c6e05794819971331966bdbab1d0f0525bcd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Motai, Tsunetake</creatorcontrib><creatorcontrib>Kitanaka, Susumu</creatorcontrib><title>Sesquiterpene Phenylpropanoids from Ferula f ukanensis and Their Nitric Oxide Production Inhibitory Effects</title><title>Journal of natural products (Washington, D.C.)</title><addtitle>J. Nat. Prod</addtitle><description>Five new sesquiterpene phenylpropanoid derivatives, fukanedone A (1), fukanedone B (2), fukanedone C (3), fukanedone D (4), and fukanedone E (5), and a novel phenyl-oxo-acetate ester, fukaneketoester A (6), were isolated from a 80% aqueous methanol extract of the roots of Ferula fukanensis. The structures were elucidated on the basis of spectroscorpic evidence, especially heteronuclear multiple-bond connectivity (HMBC) and high-resolution MS. The sesquiterpene phenylpropanoid derivatives inhibited nitric oxide (NO) production and inducible NO synthase (iNOS) gene expression by a murine macrophage-like cell line (RAW 264.7), which was activated by lipopolysaccharide (LPS) and recombinant mouse interferon-γ (IFN-γ).</description><issn>0163-3864</issn><issn>1520-6025</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNptkE1LAzEYhIMoWKsH_0EuHjysvtndpM1RSquFYgXreckmb2j6kazJLrj_3pWKJ0_DwDPDMITcMnhgkLNH30A5KNdnZMR4DpmAnJ-TETBRZMVUlJfkKqUdABQg-Yjs3zF9dq7F2KBH-rZF3x-aGBrlgzOJ2hiOdIGxOyhqabdXHn1yiSpv6GaLLtJX10an6frLmSEfg-l064KnS791tWtD7OncWtRtuiYXVh0S3vzqmHws5pvZS7ZaPy9nT6tMMSh1JmrkxnA0RoIwk5xLXSKTEjQvtUDgE1lOBz9hRcGkELWpVc0MWOA5r7UpxuT-1KtjSCmirZrojir2FYPq56Xq76WBvTuxSqdqF7roh2X_cN_x5Gf0</recordid><startdate>20050324</startdate><enddate>20050324</enddate><creator>Motai, Tsunetake</creator><creator>Kitanaka, Susumu</creator><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20050324</creationdate><title>Sesquiterpene Phenylpropanoids from Ferula f ukanensis and Their Nitric Oxide Production Inhibitory Effects</title><author>Motai, Tsunetake ; Kitanaka, Susumu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a104c-6be5dd5edd906d7259c4e1990c54c6e05794819971331966bdbab1d0f0525bcd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Motai, Tsunetake</creatorcontrib><creatorcontrib>Kitanaka, Susumu</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of natural products (Washington, D.C.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Motai, Tsunetake</au><au>Kitanaka, Susumu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sesquiterpene Phenylpropanoids from Ferula f ukanensis and Their Nitric Oxide Production Inhibitory Effects</atitle><jtitle>Journal of natural products (Washington, D.C.)</jtitle><addtitle>J. Nat. Prod</addtitle><date>2005-03-24</date><risdate>2005</risdate><volume>68</volume><issue>3</issue><spage>365</spage><epage>368</epage><pages>365-368</pages><issn>0163-3864</issn><eissn>1520-6025</eissn><abstract>Five new sesquiterpene phenylpropanoid derivatives, fukanedone A (1), fukanedone B (2), fukanedone C (3), fukanedone D (4), and fukanedone E (5), and a novel phenyl-oxo-acetate ester, fukaneketoester A (6), were isolated from a 80% aqueous methanol extract of the roots of Ferula fukanensis. The structures were elucidated on the basis of spectroscorpic evidence, especially heteronuclear multiple-bond connectivity (HMBC) and high-resolution MS. The sesquiterpene phenylpropanoid derivatives inhibited nitric oxide (NO) production and inducible NO synthase (iNOS) gene expression by a murine macrophage-like cell line (RAW 264.7), which was activated by lipopolysaccharide (LPS) and recombinant mouse interferon-γ (IFN-γ).</abstract><pub>American Chemical Society</pub><doi>10.1021/np040215c</doi><tpages>4</tpages></addata></record> |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
title | Sesquiterpene Phenylpropanoids from Ferula f ukanensis and Their Nitric Oxide Production Inhibitory Effects |
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