Loading…
Revisiting the absolute chirality and polymorphism of (–)‐Istanbulin A
The terpenoid (−)‐Istanbulin A is a natural product isolated from Senecio filaginoides DC, one of the 270 species of Senecio (Asteraceae) which occurs in Argentina. The structure and absolute configuration of this compound [9a‐hydroxy‐3,4a,5‐trimethyl‐4a,6,7,8a,9,9a‐hexahydro‐4H,5H‐naphtho[2,3‐b]‐fu...
Saved in:
Published in: | Acta crystallographica. Section C, Crystal structure communications Crystal structure communications, 2020-09, Vol.76 (9), p.914-920 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
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-c3566-adbed64b9bb7ac017f2b9f7d8aa06e46afaa70c4c7c2e396884f83e23e1b91703 |
---|---|
cites | cdi_FETCH-LOGICAL-c3566-adbed64b9bb7ac017f2b9f7d8aa06e46afaa70c4c7c2e396884f83e23e1b91703 |
container_end_page | 920 |
container_issue | 9 |
container_start_page | 914 |
container_title | Acta crystallographica. Section C, Crystal structure communications |
container_volume | 76 |
creator | Arancibia, Luz Naspi, Mariana Pucci, Graciela Rodriguez, Maricel Di Salvo, Florencia |
description | The terpenoid (−)‐Istanbulin A is a natural product isolated from Senecio filaginoides DC, one of the 270 species of Senecio (Asteraceae) which occurs in Argentina. The structure and absolute configuration of this compound [9a‐hydroxy‐3,4a,5‐trimethyl‐4a,6,7,8a,9,9a‐hexahydro‐4H,5H‐naphtho[2,3‐b]‐furan‐2,8‐dione or (4S,5R,8R,10S)‐1‐oxo‐8β‐hydroxy‐10βH‐eremophil‐7(11)‐en‐12,8β‐olide, C15H20O4] were determined by single‐crystal X‐ray diffraction studies. It proved to be a sesquiterpene lactone showing an eremophilanolide skeleton whose chirality is described as 4S,5R,8R,10S. Structural results were also in agreement with the one‐ and two‐dimensional (1D and 2D) NMR and HR–ESI–MS data, and other complementary spectroscopic information. In addition, (−)‐Istanbulin A is a polymorph of the previously reported form of (−)‐Istanbulin A, form I; thus, the title compound is denoted form II or polymorph II. Structural data and a literature search allowed the chirality of Istanbulin A to be revisited. The antimicrobial and antifungal activities of (−)‐Istanbulin A, form II, were evaluated in order to establish a reference for future comparisons and applications related to specific crystal forms of Istanbulins.
The natural product (−)‐Istanbulin A was isolated from Senecio filaginoides DC and the chirality is described as 4S,5R,8R,10S based on single‐crystal X‐ray diffraction studies. (−)‐Istanbulin A corresponds to a polymorph of a previously reported form of (−)‐Istanbulin A (form I) and this is the first time that polymorphism has been reported in the Istanbulin family. |
doi_str_mv | 10.1107/S2053229620011493 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2440465543</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2440244824</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3566-adbed64b9bb7ac017f2b9f7d8aa06e46afaa70c4c7c2e396884f83e23e1b91703</originalsourceid><addsrcrecordid>eNqFkM1Kw0AUhQdRsNQ-gLsBN3VRnb_MJMtS_KkUFH8WXYXJZGKnTDIxkyjZ9REE37BPYmJdiC5cXO7l8J3L4QBwjNEZxkicPxAUUEIiThDCmEV0Dwx6adJr-z_uQzDyfo16igRC4AG4udevxpvaFM-wXmkoE-9sU2uoVqaS1tQtlEUKS2fb3FXlyvgcugyOt5uP0-3mfe5rWSSNNQWcHoGDTFqvR997CJ4uLx5n15PF7dV8Nl1MFA04n8g00SlnSZQkQiqERUaSKBNpKCXimnGZSSmQYkooomnEw5BlIdWEapxEWCA6BOPd37JyL432dZwbr7S1stCu8TFhDDEeBIx26MkvdO2aqujSfVHdhIR1FN5RqnLeVzqLy8rksmpjjOK-4PhPwZ0n2nnejNXt_4Z4upyR5R0liNNPpR1-gQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2440244824</pqid></control><display><type>article</type><title>Revisiting the absolute chirality and polymorphism of (–)‐Istanbulin A</title><source>Wiley-Blackwell Read & Publish Collection</source><source>Alma/SFX Local Collection</source><creator>Arancibia, Luz ; Naspi, Mariana ; Pucci, Graciela ; Rodriguez, Maricel ; Di Salvo, Florencia</creator><creatorcontrib>Arancibia, Luz ; Naspi, Mariana ; Pucci, Graciela ; Rodriguez, Maricel ; Di Salvo, Florencia</creatorcontrib><description>The terpenoid (−)‐Istanbulin A is a natural product isolated from Senecio filaginoides DC, one of the 270 species of Senecio (Asteraceae) which occurs in Argentina. The structure and absolute configuration of this compound [9a‐hydroxy‐3,4a,5‐trimethyl‐4a,6,7,8a,9,9a‐hexahydro‐4H,5H‐naphtho[2,3‐b]‐furan‐2,8‐dione or (4S,5R,8R,10S)‐1‐oxo‐8β‐hydroxy‐10βH‐eremophil‐7(11)‐en‐12,8β‐olide, C15H20O4] were determined by single‐crystal X‐ray diffraction studies. It proved to be a sesquiterpene lactone showing an eremophilanolide skeleton whose chirality is described as 4S,5R,8R,10S. Structural results were also in agreement with the one‐ and two‐dimensional (1D and 2D) NMR and HR–ESI–MS data, and other complementary spectroscopic information. In addition, (−)‐Istanbulin A is a polymorph of the previously reported form of (−)‐Istanbulin A, form I; thus, the title compound is denoted form II or polymorph II. Structural data and a literature search allowed the chirality of Istanbulin A to be revisited. The antimicrobial and antifungal activities of (−)‐Istanbulin A, form II, were evaluated in order to establish a reference for future comparisons and applications related to specific crystal forms of Istanbulins.
The natural product (−)‐Istanbulin A was isolated from Senecio filaginoides DC and the chirality is described as 4S,5R,8R,10S based on single‐crystal X‐ray diffraction studies. (−)‐Istanbulin A corresponds to a polymorph of a previously reported form of (−)‐Istanbulin A (form I) and this is the first time that polymorphism has been reported in the Istanbulin family.</description><identifier>ISSN: 2053-2296</identifier><identifier>ISSN: 0108-2701</identifier><identifier>EISSN: 2053-2296</identifier><identifier>EISSN: 1600-5759</identifier><identifier>DOI: 10.1107/S2053229620011493</identifier><language>eng</language><publisher>5 Abbey Square, Chester, Cheshire CH1 2HU, England: International Union of Crystallography</publisher><subject>absolute configuration ; Antiinfectives and antibacterials ; antimicrobial activity ; Chirality ; crystal structure ; Fungicides ; Istanbulin ; natural product ; Natural products ; NMR ; Nuclear magnetic resonance ; Polymorphism ; Senecio filaginoides ; terpenoid</subject><ispartof>Acta crystallographica. Section C, Crystal structure communications, 2020-09, Vol.76 (9), p.914-920</ispartof><rights>International Union of Crystallography, 2020</rights><rights>Copyright Wiley Subscription Services, Inc. Sep 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3566-adbed64b9bb7ac017f2b9f7d8aa06e46afaa70c4c7c2e396884f83e23e1b91703</citedby><cites>FETCH-LOGICAL-c3566-adbed64b9bb7ac017f2b9f7d8aa06e46afaa70c4c7c2e396884f83e23e1b91703</cites><orcidid>0000-0001-7295-2471</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Arancibia, Luz</creatorcontrib><creatorcontrib>Naspi, Mariana</creatorcontrib><creatorcontrib>Pucci, Graciela</creatorcontrib><creatorcontrib>Rodriguez, Maricel</creatorcontrib><creatorcontrib>Di Salvo, Florencia</creatorcontrib><title>Revisiting the absolute chirality and polymorphism of (–)‐Istanbulin A</title><title>Acta crystallographica. Section C, Crystal structure communications</title><description>The terpenoid (−)‐Istanbulin A is a natural product isolated from Senecio filaginoides DC, one of the 270 species of Senecio (Asteraceae) which occurs in Argentina. The structure and absolute configuration of this compound [9a‐hydroxy‐3,4a,5‐trimethyl‐4a,6,7,8a,9,9a‐hexahydro‐4H,5H‐naphtho[2,3‐b]‐furan‐2,8‐dione or (4S,5R,8R,10S)‐1‐oxo‐8β‐hydroxy‐10βH‐eremophil‐7(11)‐en‐12,8β‐olide, C15H20O4] were determined by single‐crystal X‐ray diffraction studies. It proved to be a sesquiterpene lactone showing an eremophilanolide skeleton whose chirality is described as 4S,5R,8R,10S. Structural results were also in agreement with the one‐ and two‐dimensional (1D and 2D) NMR and HR–ESI–MS data, and other complementary spectroscopic information. In addition, (−)‐Istanbulin A is a polymorph of the previously reported form of (−)‐Istanbulin A, form I; thus, the title compound is denoted form II or polymorph II. Structural data and a literature search allowed the chirality of Istanbulin A to be revisited. The antimicrobial and antifungal activities of (−)‐Istanbulin A, form II, were evaluated in order to establish a reference for future comparisons and applications related to specific crystal forms of Istanbulins.
The natural product (−)‐Istanbulin A was isolated from Senecio filaginoides DC and the chirality is described as 4S,5R,8R,10S based on single‐crystal X‐ray diffraction studies. (−)‐Istanbulin A corresponds to a polymorph of a previously reported form of (−)‐Istanbulin A (form I) and this is the first time that polymorphism has been reported in the Istanbulin family.</description><subject>absolute configuration</subject><subject>Antiinfectives and antibacterials</subject><subject>antimicrobial activity</subject><subject>Chirality</subject><subject>crystal structure</subject><subject>Fungicides</subject><subject>Istanbulin</subject><subject>natural product</subject><subject>Natural products</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Polymorphism</subject><subject>Senecio filaginoides</subject><subject>terpenoid</subject><issn>2053-2296</issn><issn>0108-2701</issn><issn>2053-2296</issn><issn>1600-5759</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkM1Kw0AUhQdRsNQ-gLsBN3VRnb_MJMtS_KkUFH8WXYXJZGKnTDIxkyjZ9REE37BPYmJdiC5cXO7l8J3L4QBwjNEZxkicPxAUUEIiThDCmEV0Dwx6adJr-z_uQzDyfo16igRC4AG4udevxpvaFM-wXmkoE-9sU2uoVqaS1tQtlEUKS2fb3FXlyvgcugyOt5uP0-3mfe5rWSSNNQWcHoGDTFqvR997CJ4uLx5n15PF7dV8Nl1MFA04n8g00SlnSZQkQiqERUaSKBNpKCXimnGZSSmQYkooomnEw5BlIdWEapxEWCA6BOPd37JyL432dZwbr7S1stCu8TFhDDEeBIx26MkvdO2aqujSfVHdhIR1FN5RqnLeVzqLy8rksmpjjOK-4PhPwZ0n2nnejNXt_4Z4upyR5R0liNNPpR1-gQ</recordid><startdate>202009</startdate><enddate>202009</enddate><creator>Arancibia, Luz</creator><creator>Naspi, Mariana</creator><creator>Pucci, Graciela</creator><creator>Rodriguez, Maricel</creator><creator>Di Salvo, Florencia</creator><general>International Union of Crystallography</general><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7295-2471</orcidid></search><sort><creationdate>202009</creationdate><title>Revisiting the absolute chirality and polymorphism of (–)‐Istanbulin A</title><author>Arancibia, Luz ; Naspi, Mariana ; Pucci, Graciela ; Rodriguez, Maricel ; Di Salvo, Florencia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3566-adbed64b9bb7ac017f2b9f7d8aa06e46afaa70c4c7c2e396884f83e23e1b91703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>absolute configuration</topic><topic>Antiinfectives and antibacterials</topic><topic>antimicrobial activity</topic><topic>Chirality</topic><topic>crystal structure</topic><topic>Fungicides</topic><topic>Istanbulin</topic><topic>natural product</topic><topic>Natural products</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Polymorphism</topic><topic>Senecio filaginoides</topic><topic>terpenoid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arancibia, Luz</creatorcontrib><creatorcontrib>Naspi, Mariana</creatorcontrib><creatorcontrib>Pucci, Graciela</creatorcontrib><creatorcontrib>Rodriguez, Maricel</creatorcontrib><creatorcontrib>Di Salvo, Florencia</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Acta crystallographica. Section C, Crystal structure communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arancibia, Luz</au><au>Naspi, Mariana</au><au>Pucci, Graciela</au><au>Rodriguez, Maricel</au><au>Di Salvo, Florencia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Revisiting the absolute chirality and polymorphism of (–)‐Istanbulin A</atitle><jtitle>Acta crystallographica. Section C, Crystal structure communications</jtitle><date>2020-09</date><risdate>2020</risdate><volume>76</volume><issue>9</issue><spage>914</spage><epage>920</epage><pages>914-920</pages><issn>2053-2296</issn><issn>0108-2701</issn><eissn>2053-2296</eissn><eissn>1600-5759</eissn><abstract>The terpenoid (−)‐Istanbulin A is a natural product isolated from Senecio filaginoides DC, one of the 270 species of Senecio (Asteraceae) which occurs in Argentina. The structure and absolute configuration of this compound [9a‐hydroxy‐3,4a,5‐trimethyl‐4a,6,7,8a,9,9a‐hexahydro‐4H,5H‐naphtho[2,3‐b]‐furan‐2,8‐dione or (4S,5R,8R,10S)‐1‐oxo‐8β‐hydroxy‐10βH‐eremophil‐7(11)‐en‐12,8β‐olide, C15H20O4] were determined by single‐crystal X‐ray diffraction studies. It proved to be a sesquiterpene lactone showing an eremophilanolide skeleton whose chirality is described as 4S,5R,8R,10S. Structural results were also in agreement with the one‐ and two‐dimensional (1D and 2D) NMR and HR–ESI–MS data, and other complementary spectroscopic information. In addition, (−)‐Istanbulin A is a polymorph of the previously reported form of (−)‐Istanbulin A, form I; thus, the title compound is denoted form II or polymorph II. Structural data and a literature search allowed the chirality of Istanbulin A to be revisited. The antimicrobial and antifungal activities of (−)‐Istanbulin A, form II, were evaluated in order to establish a reference for future comparisons and applications related to specific crystal forms of Istanbulins.
The natural product (−)‐Istanbulin A was isolated from Senecio filaginoides DC and the chirality is described as 4S,5R,8R,10S based on single‐crystal X‐ray diffraction studies. (−)‐Istanbulin A corresponds to a polymorph of a previously reported form of (−)‐Istanbulin A (form I) and this is the first time that polymorphism has been reported in the Istanbulin family.</abstract><cop>5 Abbey Square, Chester, Cheshire CH1 2HU, England</cop><pub>International Union of Crystallography</pub><doi>10.1107/S2053229620011493</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0001-7295-2471</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2053-2296 |
ispartof | Acta crystallographica. Section C, Crystal structure communications, 2020-09, Vol.76 (9), p.914-920 |
issn | 2053-2296 0108-2701 2053-2296 1600-5759 |
language | eng |
recordid | cdi_proquest_miscellaneous_2440465543 |
source | Wiley-Blackwell Read & Publish Collection; Alma/SFX Local Collection |
subjects | absolute configuration Antiinfectives and antibacterials antimicrobial activity Chirality crystal structure Fungicides Istanbulin natural product Natural products NMR Nuclear magnetic resonance Polymorphism Senecio filaginoides terpenoid |
title | Revisiting the absolute chirality and polymorphism of (–)‐Istanbulin A |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T03%3A52%3A50IST&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=Revisiting%20the%20absolute%20chirality%20and%20polymorphism%20of%20(%E2%80%93)%E2%80%90Istanbulin%20A&rft.jtitle=Acta%20crystallographica.%20Section%20C,%20Crystal%20structure%20communications&rft.au=Arancibia,%20Luz&rft.date=2020-09&rft.volume=76&rft.issue=9&rft.spage=914&rft.epage=920&rft.pages=914-920&rft.issn=2053-2296&rft.eissn=2053-2296&rft_id=info:doi/10.1107/S2053229620011493&rft_dat=%3Cproquest_cross%3E2440244824%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3566-adbed64b9bb7ac017f2b9f7d8aa06e46afaa70c4c7c2e396884f83e23e1b91703%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2440244824&rft_id=info:pmid/&rfr_iscdi=true |