Loading…

Dispolongiosides A and B, Two New Fucose Containing Spirostanol Glycosides From the Rhizomes of Disporopsis longifolia Craib., and Their Nitric Oxide Production Inhibitory Activities

Two new fucose containing spirostanol glycosides, (25R)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-fucopyranoside (1) and (25S)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-fucopyranoside (2), together with five known spirostan glycosides, (25R)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1...

Full description

Saved in:
Bibliographic Details
Published in:Natural product communications 2021-10, Vol.16 (10)
Main Authors: Thu Ha, Tran Thi, Vui, Dang Kim, Hoang, Nguyen Huy, Tai, Bui Huu, Van Kiem, Phan
Format: Article
Language:English
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c327t-3e3df9a8ab633cade132c93769ea44a915c9dff8438030c2f404f7db001485243
cites cdi_FETCH-LOGICAL-c327t-3e3df9a8ab633cade132c93769ea44a915c9dff8438030c2f404f7db001485243
container_end_page
container_issue 10
container_start_page
container_title Natural product communications
container_volume 16
creator Thu Ha, Tran Thi
Vui, Dang Kim
Hoang, Nguyen Huy
Tai, Bui Huu
Van Kiem, Phan
description Two new fucose containing spirostanol glycosides, (25R)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-fucopyranoside (1) and (25S)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-fucopyranoside (2), together with five known spirostan glycosides, (25R)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (3), (25S)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (4), (25R)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (5), (25R)-26-[(β-D-glucopyranosyl)oxy]-22α-methoxyfurost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (6), and (25R)-26-[(β-D-glucopyranosyl)oxy]-22α-hydroxyfurost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (7) were isolated from the rhizomes of Disporopsis longifolia Craib. Their structures were determined by extensive analysis of HRESIMS and NMR spectral data, as well as by comparison of the spectral data with those reported in the literature. Compounds 1 to 7 inhibited NO production in LPS-activated RAW264.7 cells with IC50 values in the range from 24.5 ± 2.5 μM to 81.3 ± 4.2 μM. The NO production inhibitory activities of compounds 1 and 2 with IC50 values of 26.6 ± 1.9 μM and 24.5 ± 2.5 μM are as potent as that of the positive control of NG-monomethyl-L-arginine acetate (L-NMMA) with an IC50 value of 23.8 ± 2.1 μM.
doi_str_mv 10.1177/1934578X211055013
format article
fullrecord <record><control><sourceid>sage_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1177_1934578X211055013</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_1934578X211055013</sage_id><sourcerecordid>10.1177_1934578X211055013</sourcerecordid><originalsourceid>FETCH-LOGICAL-c327t-3e3df9a8ab633cade132c93769ea44a915c9dff8438030c2f404f7db001485243</originalsourceid><addsrcrecordid>eNp9UMFOwzAMrRBIIOADuPkD6EiahLbHMRggIUAwJG5VliabURdPSQeMD-P7CIMbEr7Ysv3es1-WHXE24LwsT3gtpCqr54JzphTjYivb40qpvJal2k51muffC7vZYYwvLEVVSSbrvezzHOOSOvIzpIitjTAE7Vs4O4bJG8GtfYPxylC0MCLfa_ToZ_C4xECx1546uOzW5hc5DrSAfm7hYY4ftEgdcrDhD7SMGGEj46hDDaOgcTo43mhN5hYD3GIf0MDde-KC-0DtyvRIHq79HKfYU1jDMHVesUcbD7Idp7toD3_zfvY0vpiMrvKbu8vr0fAmN6Io-1xY0bpaV3p6KoTRreWiMLUoT2urpdQ1V6ZunaukqJhgpnDJFFe2U8a4rFQhxX7Gf3hNejgG65plwIUO64az5tv75o_3CTP4wUQ9s80LrYJPJ_4D-AJJGIeI</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Dispolongiosides A and B, Two New Fucose Containing Spirostanol Glycosides From the Rhizomes of Disporopsis longifolia Craib., and Their Nitric Oxide Production Inhibitory Activities</title><source>SAGE Journals Open Access</source><creator>Thu Ha, Tran Thi ; Vui, Dang Kim ; Hoang, Nguyen Huy ; Tai, Bui Huu ; Van Kiem, Phan</creator><creatorcontrib>Thu Ha, Tran Thi ; Vui, Dang Kim ; Hoang, Nguyen Huy ; Tai, Bui Huu ; Van Kiem, Phan</creatorcontrib><description>Two new fucose containing spirostanol glycosides, (25R)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-fucopyranoside (1) and (25S)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-fucopyranoside (2), together with five known spirostan glycosides, (25R)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (3), (25S)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (4), (25R)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (5), (25R)-26-[(β-D-glucopyranosyl)oxy]-22α-methoxyfurost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (6), and (25R)-26-[(β-D-glucopyranosyl)oxy]-22α-hydroxyfurost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (7) were isolated from the rhizomes of Disporopsis longifolia Craib. Their structures were determined by extensive analysis of HRESIMS and NMR spectral data, as well as by comparison of the spectral data with those reported in the literature. Compounds 1 to 7 inhibited NO production in LPS-activated RAW264.7 cells with IC50 values in the range from 24.5 ± 2.5 μM to 81.3 ± 4.2 μM. The NO production inhibitory activities of compounds 1 and 2 with IC50 values of 26.6 ± 1.9 μM and 24.5 ± 2.5 μM are as potent as that of the positive control of NG-monomethyl-L-arginine acetate (L-NMMA) with an IC50 value of 23.8 ± 2.1 μM.</description><identifier>ISSN: 1934-578X</identifier><identifier>EISSN: 1555-9475</identifier><identifier>DOI: 10.1177/1934578X211055013</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><ispartof>Natural product communications, 2021-10, Vol.16 (10)</ispartof><rights>The Author(s) 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c327t-3e3df9a8ab633cade132c93769ea44a915c9dff8438030c2f404f7db001485243</citedby><cites>FETCH-LOGICAL-c327t-3e3df9a8ab633cade132c93769ea44a915c9dff8438030c2f404f7db001485243</cites><orcidid>0000-0003-0756-6990</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/1934578X211055013$$EPDF$$P50$$Gsage$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/1934578X211055013$$EHTML$$P50$$Gsage$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,21945,27830,27901,27902,44921,45309</link.rule.ids></links><search><creatorcontrib>Thu Ha, Tran Thi</creatorcontrib><creatorcontrib>Vui, Dang Kim</creatorcontrib><creatorcontrib>Hoang, Nguyen Huy</creatorcontrib><creatorcontrib>Tai, Bui Huu</creatorcontrib><creatorcontrib>Van Kiem, Phan</creatorcontrib><title>Dispolongiosides A and B, Two New Fucose Containing Spirostanol Glycosides From the Rhizomes of Disporopsis longifolia Craib., and Their Nitric Oxide Production Inhibitory Activities</title><title>Natural product communications</title><description>Two new fucose containing spirostanol glycosides, (25R)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-fucopyranoside (1) and (25S)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-fucopyranoside (2), together with five known spirostan glycosides, (25R)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (3), (25S)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (4), (25R)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (5), (25R)-26-[(β-D-glucopyranosyl)oxy]-22α-methoxyfurost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (6), and (25R)-26-[(β-D-glucopyranosyl)oxy]-22α-hydroxyfurost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (7) were isolated from the rhizomes of Disporopsis longifolia Craib. Their structures were determined by extensive analysis of HRESIMS and NMR spectral data, as well as by comparison of the spectral data with those reported in the literature. Compounds 1 to 7 inhibited NO production in LPS-activated RAW264.7 cells with IC50 values in the range from 24.5 ± 2.5 μM to 81.3 ± 4.2 μM. The NO production inhibitory activities of compounds 1 and 2 with IC50 values of 26.6 ± 1.9 μM and 24.5 ± 2.5 μM are as potent as that of the positive control of NG-monomethyl-L-arginine acetate (L-NMMA) with an IC50 value of 23.8 ± 2.1 μM.</description><issn>1934-578X</issn><issn>1555-9475</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><recordid>eNp9UMFOwzAMrRBIIOADuPkD6EiahLbHMRggIUAwJG5VliabURdPSQeMD-P7CIMbEr7Ysv3es1-WHXE24LwsT3gtpCqr54JzphTjYivb40qpvJal2k51muffC7vZYYwvLEVVSSbrvezzHOOSOvIzpIitjTAE7Vs4O4bJG8GtfYPxylC0MCLfa_ToZ_C4xECx1546uOzW5hc5DrSAfm7hYY4ftEgdcrDhD7SMGGEj46hDDaOgcTo43mhN5hYD3GIf0MDde-KC-0DtyvRIHq79HKfYU1jDMHVesUcbD7Idp7toD3_zfvY0vpiMrvKbu8vr0fAmN6Io-1xY0bpaV3p6KoTRreWiMLUoT2urpdQ1V6ZunaukqJhgpnDJFFe2U8a4rFQhxX7Gf3hNejgG65plwIUO64az5tv75o_3CTP4wUQ9s80LrYJPJ_4D-AJJGIeI</recordid><startdate>20211001</startdate><enddate>20211001</enddate><creator>Thu Ha, Tran Thi</creator><creator>Vui, Dang Kim</creator><creator>Hoang, Nguyen Huy</creator><creator>Tai, Bui Huu</creator><creator>Van Kiem, Phan</creator><general>SAGE Publications</general><scope>AFRWT</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0003-0756-6990</orcidid></search><sort><creationdate>20211001</creationdate><title>Dispolongiosides A and B, Two New Fucose Containing Spirostanol Glycosides From the Rhizomes of Disporopsis longifolia Craib., and Their Nitric Oxide Production Inhibitory Activities</title><author>Thu Ha, Tran Thi ; Vui, Dang Kim ; Hoang, Nguyen Huy ; Tai, Bui Huu ; Van Kiem, Phan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c327t-3e3df9a8ab633cade132c93769ea44a915c9dff8438030c2f404f7db001485243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thu Ha, Tran Thi</creatorcontrib><creatorcontrib>Vui, Dang Kim</creatorcontrib><creatorcontrib>Hoang, Nguyen Huy</creatorcontrib><creatorcontrib>Tai, Bui Huu</creatorcontrib><creatorcontrib>Van Kiem, Phan</creatorcontrib><collection>SAGE Journals Open Access</collection><collection>CrossRef</collection><jtitle>Natural product communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thu Ha, Tran Thi</au><au>Vui, Dang Kim</au><au>Hoang, Nguyen Huy</au><au>Tai, Bui Huu</au><au>Van Kiem, Phan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dispolongiosides A and B, Two New Fucose Containing Spirostanol Glycosides From the Rhizomes of Disporopsis longifolia Craib., and Their Nitric Oxide Production Inhibitory Activities</atitle><jtitle>Natural product communications</jtitle><date>2021-10-01</date><risdate>2021</risdate><volume>16</volume><issue>10</issue><issn>1934-578X</issn><eissn>1555-9475</eissn><abstract>Two new fucose containing spirostanol glycosides, (25R)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-fucopyranoside (1) and (25S)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-fucopyranoside (2), together with five known spirostan glycosides, (25R)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (3), (25S)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (4), (25R)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (5), (25R)-26-[(β-D-glucopyranosyl)oxy]-22α-methoxyfurost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (6), and (25R)-26-[(β-D-glucopyranosyl)oxy]-22α-hydroxyfurost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (7) were isolated from the rhizomes of Disporopsis longifolia Craib. Their structures were determined by extensive analysis of HRESIMS and NMR spectral data, as well as by comparison of the spectral data with those reported in the literature. Compounds 1 to 7 inhibited NO production in LPS-activated RAW264.7 cells with IC50 values in the range from 24.5 ± 2.5 μM to 81.3 ± 4.2 μM. The NO production inhibitory activities of compounds 1 and 2 with IC50 values of 26.6 ± 1.9 μM and 24.5 ± 2.5 μM are as potent as that of the positive control of NG-monomethyl-L-arginine acetate (L-NMMA) with an IC50 value of 23.8 ± 2.1 μM.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><doi>10.1177/1934578X211055013</doi><orcidid>https://orcid.org/0000-0003-0756-6990</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1934-578X
ispartof Natural product communications, 2021-10, Vol.16 (10)
issn 1934-578X
1555-9475
language eng
recordid cdi_crossref_primary_10_1177_1934578X211055013
source SAGE Journals Open Access
title Dispolongiosides A and B, Two New Fucose Containing Spirostanol Glycosides From the Rhizomes of Disporopsis longifolia Craib., and Their Nitric Oxide Production Inhibitory Activities
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-31T08%3A19%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-sage_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Dispolongiosides%20A%20and%20B,%20Two%20New%20Fucose%20Containing%20Spirostanol%20Glycosides%20From%20the%20Rhizomes%20of%20Disporopsis%20longifolia%20Craib.,%20and%20Their%20Nitric%20Oxide%20Production%20Inhibitory%20Activities&rft.jtitle=Natural%20product%20communications&rft.au=Thu%20Ha,%20Tran%20Thi&rft.date=2021-10-01&rft.volume=16&rft.issue=10&rft.issn=1934-578X&rft.eissn=1555-9475&rft_id=info:doi/10.1177/1934578X211055013&rft_dat=%3Csage_cross%3E10.1177_1934578X211055013%3C/sage_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c327t-3e3df9a8ab633cade132c93769ea44a915c9dff8438030c2f404f7db001485243%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rft_sage_id=10.1177_1934578X211055013&rfr_iscdi=true