Synthesis of 3-Farnesyl Salicylic Acid a Novel Antimicrobial from Piper multiplinervium
Both 3-farnesyl salicylic acid and 3-geranyl salicylic acid were synthesized from 2,6-dibromophenol and showed low levels of antimicrobial activity against E. coli strains.
Gespeichert in:
| Veröffentlicht in: | Natural product communications 2013-07, Vol.8 (7), p.911-913 |
|---|---|
| Hauptverfasser: | , , , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext bestellen |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 913 |
|---|---|
| container_issue | 7 |
| container_start_page | 911 |
| container_title | Natural product communications |
| container_volume | 8 |
| creator | Kraus, George A. Chaudhary, Divya Riley, Sean Liu, Feng Schlapkohl, Allison Weems, Megan Phillips, Gregory J. |
| description | Both 3-farnesyl salicylic acid and 3-geranyl salicylic acid were synthesized from 2,6-dibromophenol and showed low levels of antimicrobial activity against E. coli strains. |
| doi_str_mv | 10.1177/1934578X1300800714 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_AFRWT</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3891047</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_1934578X1300800714</sage_id><sourcerecordid>1428775654</sourcerecordid><originalsourceid>FETCH-LOGICAL-c393t-65e1494a26ed6855d45402d31d133777d34e82f5165177259dae914fd46420ac3</originalsourceid><addsrcrecordid>eNp9kV1rFTEQhoMottT-AS8kl96szcdkk9wIh2JVKCpU0buQbmbblOzmmOweOP_elFOLIjgQZiDPvJPJS8hLzt5wrvUZtxKUNj-4ZMwwpjk8IcdcKdVZ0OppqxvQ3RNH5LTWO9bCGGBgn5MjIa1hIMQx-X61n5dbrLHSPFLZXfgyY90neuVTHPbt0M0QA_X0U95hopt5iVMcSr6OPtGx5Il-iVssdFrTErcpzlh2cZ1ekGejTxVPH_IJ-Xbx7uv5h-7y8_uP55vLbpBWLl2vkIMFL3oMvVEqgAImguSBS6m1DhLQiFHxXrWlhbLBo-UwBuhBMD_IE_L2oLtdrycMA85L8cltS5x82bvso_v7Zo637ibvnDSWM9BN4PWDQMk_V6yLm2IdMCU_Y16r4yCM1qpX0FBxQNv6tRYcH8dw5u5Ncf-a0ppe_fnAx5bfFjTg7ABUf4PuLq9lbh_2P8lf2feU3g</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1428775654</pqid></control><display><type>article</type><title>Synthesis of 3-Farnesyl Salicylic Acid a Novel Antimicrobial from Piper multiplinervium</title><source>Sage Journals GOLD Open Access 2024</source><creator>Kraus, George A. ; Chaudhary, Divya ; Riley, Sean ; Liu, Feng ; Schlapkohl, Allison ; Weems, Megan ; Phillips, Gregory J.</creator><creatorcontrib>Kraus, George A. ; Chaudhary, Divya ; Riley, Sean ; Liu, Feng ; Schlapkohl, Allison ; Weems, Megan ; Phillips, Gregory J.</creatorcontrib><description>Both 3-farnesyl salicylic acid and 3-geranyl salicylic acid were synthesized from 2,6-dibromophenol and showed low levels of antimicrobial activity against E. coli strains.</description><identifier>ISSN: 1934-578X</identifier><identifier>EISSN: 1555-9475</identifier><identifier>DOI: 10.1177/1934578X1300800714</identifier><identifier>PMID: 23980422</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Anti-Infective Agents - chemical synthesis ; Piper - chemistry ; Salicylates - chemical synthesis ; Salicylates - pharmacology</subject><ispartof>Natural product communications, 2013-07, Vol.8 (7), p.911-913</ispartof><rights>2013 SAGE Publications Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c393t-65e1494a26ed6855d45402d31d133777d34e82f5165177259dae914fd46420ac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/1934578X1300800714$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/1934578X1300800714$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>230,314,776,780,881,21945,27830,27901,27902,44921,45309</link.rule.ids><linktorsrc>$$Uhttps://journals.sagepub.com/doi/full/10.1177/1934578X1300800714?utm_source=summon&utm_medium=discovery-provider$$EView_record_in_SAGE_Publications$$FView_record_in_$$GSAGE_Publications</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23980422$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kraus, George A.</creatorcontrib><creatorcontrib>Chaudhary, Divya</creatorcontrib><creatorcontrib>Riley, Sean</creatorcontrib><creatorcontrib>Liu, Feng</creatorcontrib><creatorcontrib>Schlapkohl, Allison</creatorcontrib><creatorcontrib>Weems, Megan</creatorcontrib><creatorcontrib>Phillips, Gregory J.</creatorcontrib><title>Synthesis of 3-Farnesyl Salicylic Acid a Novel Antimicrobial from Piper multiplinervium</title><title>Natural product communications</title><addtitle>Nat Prod Commun</addtitle><description>Both 3-farnesyl salicylic acid and 3-geranyl salicylic acid were synthesized from 2,6-dibromophenol and showed low levels of antimicrobial activity against E. coli strains.</description><subject>Anti-Infective Agents - chemical synthesis</subject><subject>Piper - chemistry</subject><subject>Salicylates - chemical synthesis</subject><subject>Salicylates - pharmacology</subject><issn>1934-578X</issn><issn>1555-9475</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kV1rFTEQhoMottT-AS8kl96szcdkk9wIh2JVKCpU0buQbmbblOzmmOweOP_elFOLIjgQZiDPvJPJS8hLzt5wrvUZtxKUNj-4ZMwwpjk8IcdcKdVZ0OppqxvQ3RNH5LTWO9bCGGBgn5MjIa1hIMQx-X61n5dbrLHSPFLZXfgyY90neuVTHPbt0M0QA_X0U95hopt5iVMcSr6OPtGx5Il-iVssdFrTErcpzlh2cZ1ekGejTxVPH_IJ-Xbx7uv5h-7y8_uP55vLbpBWLl2vkIMFL3oMvVEqgAImguSBS6m1DhLQiFHxXrWlhbLBo-UwBuhBMD_IE_L2oLtdrycMA85L8cltS5x82bvso_v7Zo637ibvnDSWM9BN4PWDQMk_V6yLm2IdMCU_Y16r4yCM1qpX0FBxQNv6tRYcH8dw5u5Ncf-a0ppe_fnAx5bfFjTg7ABUf4PuLq9lbh_2P8lf2feU3g</recordid><startdate>201307</startdate><enddate>201307</enddate><creator>Kraus, George A.</creator><creator>Chaudhary, Divya</creator><creator>Riley, Sean</creator><creator>Liu, Feng</creator><creator>Schlapkohl, Allison</creator><creator>Weems, Megan</creator><creator>Phillips, Gregory J.</creator><general>SAGE Publications</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201307</creationdate><title>Synthesis of 3-Farnesyl Salicylic Acid a Novel Antimicrobial from Piper multiplinervium</title><author>Kraus, George A. ; Chaudhary, Divya ; Riley, Sean ; Liu, Feng ; Schlapkohl, Allison ; Weems, Megan ; Phillips, Gregory J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c393t-65e1494a26ed6855d45402d31d133777d34e82f5165177259dae914fd46420ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Anti-Infective Agents - chemical synthesis</topic><topic>Piper - chemistry</topic><topic>Salicylates - chemical synthesis</topic><topic>Salicylates - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kraus, George A.</creatorcontrib><creatorcontrib>Chaudhary, Divya</creatorcontrib><creatorcontrib>Riley, Sean</creatorcontrib><creatorcontrib>Liu, Feng</creatorcontrib><creatorcontrib>Schlapkohl, Allison</creatorcontrib><creatorcontrib>Weems, Megan</creatorcontrib><creatorcontrib>Phillips, Gregory J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Natural product communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Kraus, George A.</au><au>Chaudhary, Divya</au><au>Riley, Sean</au><au>Liu, Feng</au><au>Schlapkohl, Allison</au><au>Weems, Megan</au><au>Phillips, Gregory J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of 3-Farnesyl Salicylic Acid a Novel Antimicrobial from Piper multiplinervium</atitle><jtitle>Natural product communications</jtitle><addtitle>Nat Prod Commun</addtitle><date>2013-07</date><risdate>2013</risdate><volume>8</volume><issue>7</issue><spage>911</spage><epage>913</epage><pages>911-913</pages><issn>1934-578X</issn><eissn>1555-9475</eissn><abstract>Both 3-farnesyl salicylic acid and 3-geranyl salicylic acid were synthesized from 2,6-dibromophenol and showed low levels of antimicrobial activity against E. coli strains.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>23980422</pmid><doi>10.1177/1934578X1300800714</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
| fulltext | fulltext_linktorsrc |
| identifier | ISSN: 1934-578X |
| ispartof | Natural product communications, 2013-07, Vol.8 (7), p.911-913 |
| issn | 1934-578X 1555-9475 |
| language | eng |
| recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3891047 |
| source | Sage Journals GOLD Open Access 2024 |
| subjects | Anti-Infective Agents - chemical synthesis Piper - chemistry Salicylates - chemical synthesis Salicylates - pharmacology |
| title | Synthesis of 3-Farnesyl Salicylic Acid a Novel Antimicrobial from Piper multiplinervium |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-03T12%3A46%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_AFRWT&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20of%203-Farnesyl%20Salicylic%20Acid%20a%20Novel%20Antimicrobial%20from%20Piper%20multiplinervium&rft.jtitle=Natural%20product%20communications&rft.au=Kraus,%20George%20A.&rft.date=2013-07&rft.volume=8&rft.issue=7&rft.spage=911&rft.epage=913&rft.pages=911-913&rft.issn=1934-578X&rft.eissn=1555-9475&rft_id=info:doi/10.1177/1934578X1300800714&rft_dat=%3Cproquest_AFRWT%3E1428775654%3C/proquest_AFRWT%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1428775654&rft_id=info:pmid/23980422&rft_sage_id=10.1177_1934578X1300800714&rfr_iscdi=true |