New inhibitors of matrix metalloproteinases 9 (MMP-9): Lignans from Selaginella moellendorffii

Matrix metalloproteinase 9 (MMP-9) is one of the structurally related zinc-dependent endopeptidases families and provides a new target for cancer therapy owing to its pivotal role in metastatic tumors. In this paper, fourteen lignans, including three novel lignans, named selamoellenin B–D (1–3), and...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Fitoterapia 2018-10, Vol.130, p.281-289
Hauptverfasser: Zhu, Yuan, Huang, Ri-Zhen, Wang, Chun-Gu, Ouyang, Xi-Lin, Jing, Xiao-Teng, Liang, Dong, Wang, Heng-Shan
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 289
container_issue
container_start_page 281
container_title Fitoterapia
container_volume 130
creator Zhu, Yuan
Huang, Ri-Zhen
Wang, Chun-Gu
Ouyang, Xi-Lin
Jing, Xiao-Teng
Liang, Dong
Wang, Heng-Shan
description Matrix metalloproteinase 9 (MMP-9) is one of the structurally related zinc-dependent endopeptidases families and provides a new target for cancer therapy owing to its pivotal role in metastatic tumors. In this paper, fourteen lignans, including three novel lignans, named selamoellenin B–D (1–3), and eleven known lignan derivatives (4–14) were isolated from the plant of Selaginella moellendorffii. Among them, compound 3 is optically active, which was enantiomerically seperated to afford a pair of enantiomers, (−)-3 and (+)-3. Their structures were elucidated by extensive spectroscopic analyses. Their cytotoxic activities were evaluated against four human cancer cell lines. Among them, five compounds (4, 5, 6, 11 and 13) exhibited great potent cytotoxicity and their structure-activity relationships were also discussed. All compounds except for 3 lignan analogues with low cytotoxicity were selected for further in vitro enzyme inhibition, surface plasmon resonance (SPR), and molecular docking assays based on the MMPs target. The results shown that, compound 11 have the best inhibitory effect and can be considered as a potential drug candidate targeting at MMP-9 for cancer therapy. [Display omitted]
doi_str_mv 10.1016/j.fitote.2018.09.008
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2131838732</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0367326X18310803</els_id><sourcerecordid>2131838732</sourcerecordid><originalsourceid>FETCH-LOGICAL-c456t-69ae937e8deecb61743ec712faed32759bc2526cf5b4f9b04ab00dc8ba76038f3</originalsourceid><addsrcrecordid>eNp9kMlKLDEUhoNc0XZ4A7kE7kYXVZ4kNboQRJygHUAFV4ZU6kTTVFXapNrh7Y2016Wrs_mn8xGywyBlwIr9WWrs6EZMObAqhToFqFbIhFWlSIq6ZH_IBERRJoIXD-tkI4QZAMtFxtbIugCeQZXxCXm8wjdqh2fbxDAfqDO0V6O377THUXWdm_vYYQcVMNCa7l5e3iT13gGd2qdBDYEa73p6i516sgN2naK9iweH1nljrN0iq0Z1Abe_7ya5Pz25Oz5PptdnF8dH00RneTHGvQprUWLVIuqmYGUmUJeMG4Wt4GVeN5rnvNAmbzJTN5CpBqDVVaPKAkRlxCb5t8yNc18WGEY5cws_xErJmWCViFR4VGVLlfYuBI9Gzr3tlf-QDOQXVDmTS6jyC6qEWkao0fb3O3zR9Nj-mP5TjILDpQDji68WvQza4qCxtR71KFtnf2_4BAjjir0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2131838732</pqid></control><display><type>article</type><title>New inhibitors of matrix metalloproteinases 9 (MMP-9): Lignans from Selaginella moellendorffii</title><source>ScienceDirect Journals (5 years ago - present)</source><creator>Zhu, Yuan ; Huang, Ri-Zhen ; Wang, Chun-Gu ; Ouyang, Xi-Lin ; Jing, Xiao-Teng ; Liang, Dong ; Wang, Heng-Shan</creator><creatorcontrib>Zhu, Yuan ; Huang, Ri-Zhen ; Wang, Chun-Gu ; Ouyang, Xi-Lin ; Jing, Xiao-Teng ; Liang, Dong ; Wang, Heng-Shan</creatorcontrib><description>Matrix metalloproteinase 9 (MMP-9) is one of the structurally related zinc-dependent endopeptidases families and provides a new target for cancer therapy owing to its pivotal role in metastatic tumors. In this paper, fourteen lignans, including three novel lignans, named selamoellenin B–D (1–3), and eleven known lignan derivatives (4–14) were isolated from the plant of Selaginella moellendorffii. Among them, compound 3 is optically active, which was enantiomerically seperated to afford a pair of enantiomers, (−)-3 and (+)-3. Their structures were elucidated by extensive spectroscopic analyses. Their cytotoxic activities were evaluated against four human cancer cell lines. Among them, five compounds (4, 5, 6, 11 and 13) exhibited great potent cytotoxicity and their structure-activity relationships were also discussed. All compounds except for 3 lignan analogues with low cytotoxicity were selected for further in vitro enzyme inhibition, surface plasmon resonance (SPR), and molecular docking assays based on the MMPs target. The results shown that, compound 11 have the best inhibitory effect and can be considered as a potential drug candidate targeting at MMP-9 for cancer therapy. [Display omitted]</description><identifier>ISSN: 0367-326X</identifier><identifier>EISSN: 1873-6971</identifier><identifier>DOI: 10.1016/j.fitote.2018.09.008</identifier><identifier>PMID: 30240842</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Anticancer activity ; Cancer ; Cancer therapies ; Cytotoxicity ; Enantiomers ; Gelatinase B ; Lignans ; Matrix metalloproteinase ; Matrix metalloproteinases ; Metalloproteinase ; Metastases ; Metastasis ; Migration ; Molecular docking ; Optical activity ; Selaginella moellendorffii ; Structure-activity relationships ; Surface plasmon resonance ; Therapy ; Toxicity ; Tumor cell lines ; Tumors ; Zinc</subject><ispartof>Fitoterapia, 2018-10, Vol.130, p.281-289</ispartof><rights>2018 Elsevier B.V.</rights><rights>Copyright © 2018 Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier Science Ltd. Oct 2018</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456t-69ae937e8deecb61743ec712faed32759bc2526cf5b4f9b04ab00dc8ba76038f3</citedby><cites>FETCH-LOGICAL-c456t-69ae937e8deecb61743ec712faed32759bc2526cf5b4f9b04ab00dc8ba76038f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.fitote.2018.09.008$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30240842$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhu, Yuan</creatorcontrib><creatorcontrib>Huang, Ri-Zhen</creatorcontrib><creatorcontrib>Wang, Chun-Gu</creatorcontrib><creatorcontrib>Ouyang, Xi-Lin</creatorcontrib><creatorcontrib>Jing, Xiao-Teng</creatorcontrib><creatorcontrib>Liang, Dong</creatorcontrib><creatorcontrib>Wang, Heng-Shan</creatorcontrib><title>New inhibitors of matrix metalloproteinases 9 (MMP-9): Lignans from Selaginella moellendorffii</title><title>Fitoterapia</title><addtitle>Fitoterapia</addtitle><description>Matrix metalloproteinase 9 (MMP-9) is one of the structurally related zinc-dependent endopeptidases families and provides a new target for cancer therapy owing to its pivotal role in metastatic tumors. In this paper, fourteen lignans, including three novel lignans, named selamoellenin B–D (1–3), and eleven known lignan derivatives (4–14) were isolated from the plant of Selaginella moellendorffii. Among them, compound 3 is optically active, which was enantiomerically seperated to afford a pair of enantiomers, (−)-3 and (+)-3. Their structures were elucidated by extensive spectroscopic analyses. Their cytotoxic activities were evaluated against four human cancer cell lines. Among them, five compounds (4, 5, 6, 11 and 13) exhibited great potent cytotoxicity and their structure-activity relationships were also discussed. All compounds except for 3 lignan analogues with low cytotoxicity were selected for further in vitro enzyme inhibition, surface plasmon resonance (SPR), and molecular docking assays based on the MMPs target. The results shown that, compound 11 have the best inhibitory effect and can be considered as a potential drug candidate targeting at MMP-9 for cancer therapy. [Display omitted]</description><subject>Anticancer activity</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Cytotoxicity</subject><subject>Enantiomers</subject><subject>Gelatinase B</subject><subject>Lignans</subject><subject>Matrix metalloproteinase</subject><subject>Matrix metalloproteinases</subject><subject>Metalloproteinase</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Migration</subject><subject>Molecular docking</subject><subject>Optical activity</subject><subject>Selaginella moellendorffii</subject><subject>Structure-activity relationships</subject><subject>Surface plasmon resonance</subject><subject>Therapy</subject><subject>Toxicity</subject><subject>Tumor cell lines</subject><subject>Tumors</subject><subject>Zinc</subject><issn>0367-326X</issn><issn>1873-6971</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kMlKLDEUhoNc0XZ4A7kE7kYXVZ4kNboQRJygHUAFV4ZU6kTTVFXapNrh7Y2016Wrs_mn8xGywyBlwIr9WWrs6EZMObAqhToFqFbIhFWlSIq6ZH_IBERRJoIXD-tkI4QZAMtFxtbIugCeQZXxCXm8wjdqh2fbxDAfqDO0V6O377THUXWdm_vYYQcVMNCa7l5e3iT13gGd2qdBDYEa73p6i516sgN2naK9iweH1nljrN0iq0Z1Abe_7ya5Pz25Oz5PptdnF8dH00RneTHGvQprUWLVIuqmYGUmUJeMG4Wt4GVeN5rnvNAmbzJTN5CpBqDVVaPKAkRlxCb5t8yNc18WGEY5cws_xErJmWCViFR4VGVLlfYuBI9Gzr3tlf-QDOQXVDmTS6jyC6qEWkao0fb3O3zR9Nj-mP5TjILDpQDji68WvQza4qCxtR71KFtnf2_4BAjjir0</recordid><startdate>20181001</startdate><enddate>20181001</enddate><creator>Zhu, Yuan</creator><creator>Huang, Ri-Zhen</creator><creator>Wang, Chun-Gu</creator><creator>Ouyang, Xi-Lin</creator><creator>Jing, Xiao-Teng</creator><creator>Liang, Dong</creator><creator>Wang, Heng-Shan</creator><general>Elsevier B.V</general><general>Elsevier Science Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope></search><sort><creationdate>20181001</creationdate><title>New inhibitors of matrix metalloproteinases 9 (MMP-9): Lignans from Selaginella moellendorffii</title><author>Zhu, Yuan ; Huang, Ri-Zhen ; Wang, Chun-Gu ; Ouyang, Xi-Lin ; Jing, Xiao-Teng ; Liang, Dong ; Wang, Heng-Shan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456t-69ae937e8deecb61743ec712faed32759bc2526cf5b4f9b04ab00dc8ba76038f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Anticancer activity</topic><topic>Cancer</topic><topic>Cancer therapies</topic><topic>Cytotoxicity</topic><topic>Enantiomers</topic><topic>Gelatinase B</topic><topic>Lignans</topic><topic>Matrix metalloproteinase</topic><topic>Matrix metalloproteinases</topic><topic>Metalloproteinase</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Migration</topic><topic>Molecular docking</topic><topic>Optical activity</topic><topic>Selaginella moellendorffii</topic><topic>Structure-activity relationships</topic><topic>Surface plasmon resonance</topic><topic>Therapy</topic><topic>Toxicity</topic><topic>Tumor cell lines</topic><topic>Tumors</topic><topic>Zinc</topic><toplevel>online_resources</toplevel><creatorcontrib>Zhu, Yuan</creatorcontrib><creatorcontrib>Huang, Ri-Zhen</creatorcontrib><creatorcontrib>Wang, Chun-Gu</creatorcontrib><creatorcontrib>Ouyang, Xi-Lin</creatorcontrib><creatorcontrib>Jing, Xiao-Teng</creatorcontrib><creatorcontrib>Liang, Dong</creatorcontrib><creatorcontrib>Wang, Heng-Shan</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Fitoterapia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhu, Yuan</au><au>Huang, Ri-Zhen</au><au>Wang, Chun-Gu</au><au>Ouyang, Xi-Lin</au><au>Jing, Xiao-Teng</au><au>Liang, Dong</au><au>Wang, Heng-Shan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New inhibitors of matrix metalloproteinases 9 (MMP-9): Lignans from Selaginella moellendorffii</atitle><jtitle>Fitoterapia</jtitle><addtitle>Fitoterapia</addtitle><date>2018-10-01</date><risdate>2018</risdate><volume>130</volume><spage>281</spage><epage>289</epage><pages>281-289</pages><issn>0367-326X</issn><eissn>1873-6971</eissn><abstract>Matrix metalloproteinase 9 (MMP-9) is one of the structurally related zinc-dependent endopeptidases families and provides a new target for cancer therapy owing to its pivotal role in metastatic tumors. In this paper, fourteen lignans, including three novel lignans, named selamoellenin B–D (1–3), and eleven known lignan derivatives (4–14) were isolated from the plant of Selaginella moellendorffii. Among them, compound 3 is optically active, which was enantiomerically seperated to afford a pair of enantiomers, (−)-3 and (+)-3. Their structures were elucidated by extensive spectroscopic analyses. Their cytotoxic activities were evaluated against four human cancer cell lines. Among them, five compounds (4, 5, 6, 11 and 13) exhibited great potent cytotoxicity and their structure-activity relationships were also discussed. All compounds except for 3 lignan analogues with low cytotoxicity were selected for further in vitro enzyme inhibition, surface plasmon resonance (SPR), and molecular docking assays based on the MMPs target. The results shown that, compound 11 have the best inhibitory effect and can be considered as a potential drug candidate targeting at MMP-9 for cancer therapy. [Display omitted]</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>30240842</pmid><doi>10.1016/j.fitote.2018.09.008</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0367-326X
ispartof Fitoterapia, 2018-10, Vol.130, p.281-289
issn 0367-326X
1873-6971
language eng
recordid cdi_proquest_journals_2131838732
source ScienceDirect Journals (5 years ago - present)
subjects Anticancer activity
Cancer
Cancer therapies
Cytotoxicity
Enantiomers
Gelatinase B
Lignans
Matrix metalloproteinase
Matrix metalloproteinases
Metalloproteinase
Metastases
Metastasis
Migration
Molecular docking
Optical activity
Selaginella moellendorffii
Structure-activity relationships
Surface plasmon resonance
Therapy
Toxicity
Tumor cell lines
Tumors
Zinc
title New inhibitors of matrix metalloproteinases 9 (MMP-9): Lignans from Selaginella moellendorffii
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T20%3A15%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=New%20inhibitors%20of%20matrix%20metalloproteinases%209%20(MMP-9):%20Lignans%20from%20Selaginella%20moellendorffii&rft.jtitle=Fitoterapia&rft.au=Zhu,%20Yuan&rft.date=2018-10-01&rft.volume=130&rft.spage=281&rft.epage=289&rft.pages=281-289&rft.issn=0367-326X&rft.eissn=1873-6971&rft_id=info:doi/10.1016/j.fitote.2018.09.008&rft_dat=%3Cproquest_cross%3E2131838732%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2131838732&rft_id=info:pmid/30240842&rft_els_id=S0367326X18310803&rfr_iscdi=true