Aspterpenacids A and B, Two Sesterterpenoids from a Mangrove Endophytic Fungus Aspergillus terreus H010
Two new sesterterpenoids, aspterpenacids A (1) and B (2), with an unusual carbon skeleton of a 5/3/7/6/5 ring system were isolated from the mangrove endophytic fungus Aspergillus terreus H010. Their structures were elucidated on the basis of spectroscopic methods, single-crystal X-ray diffraction an...
Saved in:
| Published in | Organic letters Vol. 18; no. 6; pp. 1406 - 1409 |
|---|---|
| Main Authors | , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
WASHINGTON
American Chemical Society
18.03.2016
Amer Chemical Soc |
| Subjects | |
| Online Access | Get full text |
Cover
Loading…
| Abstract | Two new sesterterpenoids, aspterpenacids A (1) and B (2), with an unusual carbon skeleton of a 5/3/7/6/5 ring system were isolated from the mangrove endophytic fungus Aspergillus terreus H010. Their structures were elucidated on the basis of spectroscopic methods, single-crystal X-ray diffraction analysis, and electronic circular dichroism calculations. A biogenetic pathway for 1 and 2 is proposed. Both 1 and 2 showed no significant antibacterial activity or cytotoxicity at 50 μM. |
|---|---|
| AbstractList | Two new sesterterpenoids, aspterpenacids A (1) and B (2), with an unusual carbon skeleton of a 5/3/7/6/5 ring system were isolated from the mangrove endophytic fungus Aspergillus terreus H010. Their structures were elucidated on the basis of spectroscopic methods, single-crystal X-ray diffraction analysis, and electronic circular dichroism calculations. A biogenetic pathway for 1 and 2 is proposed. Both 1 and 2 showed no significant antibacterial activity or cytotoxicity at 50 μM. Two new sesterterpenoids, aspterpenacids A (1) and B (2), with an unusual carbon skeleton of a 5/3/7/6/5 ring system were isolated from the mangrove endophytic fungus Aspergillus terreus H010. Their structures were elucidated on the basis of spectroscopic methods, single-crystal X-ray diffraction analysis, and electronic circular dichroism calculations. A biogenetic pathway for 1 and 2 is proposed. Both 1 and 2 showed no significant antibacterial activity or cytotoxicity at 50 μM.Two new sesterterpenoids, aspterpenacids A (1) and B (2), with an unusual carbon skeleton of a 5/3/7/6/5 ring system were isolated from the mangrove endophytic fungus Aspergillus terreus H010. Their structures were elucidated on the basis of spectroscopic methods, single-crystal X-ray diffraction analysis, and electronic circular dichroism calculations. A biogenetic pathway for 1 and 2 is proposed. Both 1 and 2 showed no significant antibacterial activity or cytotoxicity at 50 μM. Two new sesterterpenoids, aspterpenacids A (1) and B (2), with an unusual carbon skeleton of a 5/3/7/6/5 ring system were isolated from the mangrove endophytic fungus Aspergillus terreus H010. Their structures were elucidated on the basis of spectroscopic methods, single crystal X-ray diffraction analysis, and electronic circular dichroism calculations. A biogenetic pathway for 1 and 2 is proposed. Both 1 and 2 showed no significant antibacterial activity or cytotoxicity at 50 mu M. |
| Author | Liu, Zhaoming Chen, Senhua Lu, Yongjun Huang, Xishan Liu, Yayue Lin, Yongcheng Chen, Yan Chen, Dongni She, Zhigang |
| AuthorAffiliation | School of Life Sciences and Biomedical Center Key Laboratory of Functional Molecules from Oceanic Microorganism, Department of Education of Guangdong Province School of Chemistry and Chemical Engineering Sun Yat-Sen University |
| AuthorAffiliation_xml | – name: School of Chemistry and Chemical Engineering – name: Key Laboratory of Functional Molecules from Oceanic Microorganism, Department of Education of Guangdong Province – name: Sun Yat-Sen University – name: School of Life Sciences and Biomedical Center |
| Author_xml | – sequence: 1 givenname: Zhaoming surname: Liu fullname: Liu, Zhaoming – sequence: 2 givenname: Yan surname: Chen fullname: Chen, Yan – sequence: 3 givenname: Senhua surname: Chen fullname: Chen, Senhua – sequence: 4 givenname: Yayue surname: Liu fullname: Liu, Yayue – sequence: 5 givenname: Yongjun surname: Lu fullname: Lu, Yongjun – sequence: 6 givenname: Dongni surname: Chen fullname: Chen, Dongni – sequence: 7 givenname: Yongcheng surname: Lin fullname: Lin, Yongcheng – sequence: 8 givenname: Xishan surname: Huang fullname: Huang, Xishan email: huangxishan13@foxmail.com – sequence: 9 givenname: Zhigang surname: She fullname: She, Zhigang email: cesshzhg@mail.sysu.edu.cn |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26938636$$D View this record in MEDLINE/PubMed |
| BookMark | eNqNkk1v1DAQhi1URD_oL0BCPiLBbsdx7MTH7aqlSK16oD1HjjMJqbJ2sB2q_nu8StgDB8rJI7_PY408c0qOrLNIyAcGawYZu9AmrJ3vBoxxLWsAzuUbcsJExlcFiOzoUEs4JqchPAGwdKPekeNMKl5KLk9ItwljRD-i1aZvAt1QbRt6-YU-PDv6HUPK5tjt09a7HdX0TtvOu19Ir2zjxh8vsTf0erLdlPwwou_6YUh1Ej2m8wYYvCdvWz0EPF_OM_J4ffWwvVnd3n_9tt3crjQvyrgSiLrVArQqVCMZ421ppMhB6KYwIJHxzDSNglbXQjAwslbMCJA5RwVlDfyMfJrfHb37OaX-q10fDA6DtuimUGWQQVkIztWrKCuKXHAQIBL6cUGneodNNfp-p_1L9ecfE1DOwDPWrg2mR2vwgEEaTpFJmctU5eW2jzr2zm7dZGNSP_-_mmg-08a7EDy2B5JBtV-LKq1FtaxFtaxFstRflll6iF73wyvuxezuwyc3eZvm90_jN8flzq8 |
| CitedBy_id | crossref_primary_10_1016_j_margen_2024_101162 crossref_primary_10_1039_C8NP00026C crossref_primary_10_1021_acs_joc_8b02263 crossref_primary_10_1002_cbdv_202200998 crossref_primary_10_1039_D0NP00070A crossref_primary_10_1021_acs_jnatprod_8b00448 crossref_primary_10_1021_acs_jnatprod_9b00183 crossref_primary_10_1002_anie_202421497 crossref_primary_10_1002_cjoc_201700375 crossref_primary_10_1021_acs_jnatprod_9b00462 crossref_primary_10_1039_C7NP00052A crossref_primary_10_3390_md18060321 crossref_primary_10_1007_s12272_018_1019_1 crossref_primary_10_1016_j_phytol_2017_05_010 crossref_primary_10_3390_md16090307 crossref_primary_10_3390_molecules22101675 crossref_primary_10_1016_j_tetlet_2020_152578 crossref_primary_10_1016_j_bmcl_2017_12_049 crossref_primary_10_1080_14786419_2019_1700504 crossref_primary_10_1039_C8NP00050F crossref_primary_10_1002_anie_201807139 crossref_primary_10_1080_10286020_2017_1391229 crossref_primary_10_1080_14786419_2024_2438268 crossref_primary_10_1039_C7OB02707A crossref_primary_10_1021_acs_jafc_3c08134 crossref_primary_10_1016_j_phytochem_2017_11_011 crossref_primary_10_1021_acs_orglett_1c01361 crossref_primary_10_1021_jacs_6b05799 crossref_primary_10_1007_s00294_021_01218_8 crossref_primary_10_1021_acs_orglett_9b03796 crossref_primary_10_1080_14786419_2019_1569658 crossref_primary_10_3390_molecules23030646 crossref_primary_10_1016_j_phytochem_2021_113015 crossref_primary_10_1016_j_bioorg_2022_106027 crossref_primary_10_1038_s41598_018_20916_x crossref_primary_10_1016_j_phytochem_2021_113011 crossref_primary_10_1039_D4NP00041B crossref_primary_10_1080_14786419_2020_1824225 crossref_primary_10_3390_md20080535 crossref_primary_10_3390_microbiolres15010005 crossref_primary_10_1016_j_steroids_2018_10_006 crossref_primary_10_1186_s40694_023_00153_2 crossref_primary_10_1039_C8QO00070K crossref_primary_10_1002_cbdv_202300735 crossref_primary_10_1002_ange_201807139 crossref_primary_10_1039_C9QO00384C crossref_primary_10_1016_j_sajb_2019_12_016 crossref_primary_10_1021_acs_jnatprod_6b00403 crossref_primary_10_1007_s00253_024_13299_9 crossref_primary_10_1016_j_phytol_2017_04_023 crossref_primary_10_1016_j_phytochem_2024_114377 crossref_primary_10_3389_fchem_2022_842405 crossref_primary_10_1017_S0025315424000286 crossref_primary_10_1080_10286020_2018_1488833 crossref_primary_10_1016_j_tetlet_2023_154613 crossref_primary_10_1038_ja_2016_169 crossref_primary_10_1021_acs_orglett_7b02748 crossref_primary_10_1021_acs_orglett_5c00038 crossref_primary_10_1002_cbdv_202200491 crossref_primary_10_1016_j_fitote_2020_104561 crossref_primary_10_1021_acs_jnatprod_4c00385 crossref_primary_10_1248_cpb_c18_00200 crossref_primary_10_1002_chin_201631215 crossref_primary_10_1016_j_steroids_2018_08_009 crossref_primary_10_1080_14786419_2017_1375924 crossref_primary_10_3762_bjoc_12_196 crossref_primary_10_1016_S1875_5364_19_30017_2 crossref_primary_10_3390_md18030134 crossref_primary_10_1021_acs_jnatprod_3c00893 crossref_primary_10_1039_D4NJ02991G crossref_primary_10_1080_14786419_2016_1214833 crossref_primary_10_1002_anie_201800167 crossref_primary_10_1038_srep36609 crossref_primary_10_1016_S1875_5364_20_30031_5 crossref_primary_10_1016_j_phytol_2017_06_020 crossref_primary_10_1016_j_tet_2017_12_057 crossref_primary_10_1021_acs_jnatprod_6b00639 crossref_primary_10_1039_C7OB01657C crossref_primary_10_1002_cbdv_202000192 crossref_primary_10_1002_ange_202421497 crossref_primary_10_1016_S1875_5364_18_30131_6 crossref_primary_10_1021_acs_orglett_9b00581 crossref_primary_10_3390_md14120217 crossref_primary_10_1039_C7RA03032K crossref_primary_10_1021_acs_jnatprod_8b01066 crossref_primary_10_3389_fchem_2018_00045 crossref_primary_10_3390_molecules27092691 crossref_primary_10_1039_D1NP00041A crossref_primary_10_1016_j_bmcl_2017_01_029 crossref_primary_10_3389_fntpr_2022_1086897 crossref_primary_10_1021_acs_orglett_4c01272 crossref_primary_10_1039_C6NP90022D crossref_primary_10_1039_D3QO01917A crossref_primary_10_1002_ange_201800167 crossref_primary_10_1039_C7NJ00059F crossref_primary_10_3390_jof7070570 |
| Cites_doi | 10.1039/c3np20089b 10.1021/np500885f 10.1021/np400880w 10.1080/10286020.2011.591386 10.1016/j.tetlet.2011.09.079 10.1007/s11101-005-5464-3 10.2174/156802609789909803 10.1007/s12263-011-0231-0 10.1016/j.bmcl.2014.07.066 10.1021/ol500868s 10.1016/j.tetlet.2012.01.052 10.1021/np060240d 10.1021/ol3019874 10.1021/np4002042 10.1021/jo2008127 10.1021/ol303549c 10.1021/ol401005j |
| ContentType | Journal Article |
| Copyright | Copyright © 2016 American Chemical Society |
| Copyright_xml | – notice: Copyright © 2016 American Chemical Society |
| DBID | AAYXX CITATION 17B 1KM BLEPL DTL EGQ GYFQL CGR CUY CVF ECM EIF NPM 7X8 7S9 L.6 |
| DOI | 10.1021/acs.orglett.6b00336 |
| DatabaseName | CrossRef Web of Knowledge Index Chemicus Web of Science Core Collection Science Citation Index Expanded Web of Science Primary (SCIE, SSCI & AHCI) Web of Science - Science Citation Index Expanded - 2016 Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic AGRICOLA AGRICOLA - Academic |
| DatabaseTitle | CrossRef Web of Science MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic AGRICOLA AGRICOLA - Academic |
| DatabaseTitleList | AGRICOLA MEDLINE MEDLINE - Academic Web of Science |
| Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: 1KM name: Index Chemicus url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/woscc/search-with-editions?editions=WOS.IC sourceTypes: Enrichment Source Index Database |
| DeliveryMethod | fulltext_linktorsrc |
| Discipline | Chemistry |
| EISSN | 1523-7052 |
| EndPage | 1409 |
| ExternalDocumentID | 26938636 000372664600048 10_1021_acs_orglett_6b00336 a595040347 |
| Genre | Research Support, Non-U.S. Gov't Journal Article |
| GrantInformation_xml | – fundername: Special Financial Fund of Innovative Development of Marine Economic Demonstration Project grantid: GD2012-D01-001 – fundername: Science & Technology Plan Project of Guangdong Province of China grantid: 2013B021100011 – fundername: Fundamental Research Funds for the Central Universities grantid: 141gjc16 – fundername: National Natural Science Foundation of China; National Natural Science Foundation of China (NSFC) grantid: 21472251; 41276146; 41404134 – fundername: China's Marine Commonweal Research Project grantid: 201305017 |
| GroupedDBID | - .K2 123 53G 55A 5VS 7~N AABXI ABFLS ABMVS ABPTK ABUCX ACGFS ACS AEESW AENEX AFEFF ALMA_UNASSIGNED_HOLDINGS AQSVZ BAANH CS3 DU5 DZ EBS ED ED~ F5P GNL IH9 IHE JG JG~ K2 P2P RNS ROL TN5 UI2 VF5 VG9 W1F X YNT --- -DZ -~X 4.4 6P2 AAHBH AAYXX ABBLG ABJNI ABLBI ABQRX ADHLV AHGAQ CITATION CUPRZ GGK 17B 1KM BLEPL DTL GROUPED_WOS_SCIENCE_CITATION_INDEX_EXPANDED GROUPED_WOS_WEB_OF_SCIENCE CGR CUY CVF ECM EIF NPM 7X8 7S9 L.6 |
| ID | FETCH-LOGICAL-a378t-5eeafa50a979d6113f8c65405ad7c06e132cdd90fab5510c6b91c50643e908b03 |
| IEDL.DBID | ACS |
| ISICitedReferencesCount | 94 |
| ISICitedReferencesURI | https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=CitingArticles&UT=000372664600048 |
| ISSN | 1523-7060 1523-7052 |
| IngestDate | Fri Jul 11 08:33:46 EDT 2025 Thu Jul 10 18:45:19 EDT 2025 Mon Jul 21 05:48:41 EDT 2025 Fri Aug 29 16:15:19 EDT 2025 Wed Jul 09 07:12:52 EDT 2025 Tue Jul 01 03:08:03 EDT 2025 Thu Apr 24 22:56:21 EDT 2025 Thu Aug 27 13:42:38 EDT 2020 |
| IsPeerReviewed | true |
| IsScholarly | true |
| Issue | 6 |
| Keywords | SPONGE MARINE ORGANISMS PHORBAS |
| Language | English |
| LinkModel | DirectLink |
| LogoURL | https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg |
| MergedId | FETCHMERGED-LOGICAL-a378t-5eeafa50a979d6113f8c65405ad7c06e132cdd90fab5510c6b91c50643e908b03 |
| Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
| PMID | 26938636 |
| PQID | 1774530505 |
| PQPubID | 23479 |
| PageCount | 4 |
| ParticipantIDs | crossref_primary_10_1021_acs_orglett_6b00336 proquest_miscellaneous_2020875339 proquest_miscellaneous_1774530505 pubmed_primary_26938636 webofscience_primary_000372664600048CitationCount crossref_citationtrail_10_1021_acs_orglett_6b00336 acs_journals_10_1021_acs_orglett_6b00336 webofscience_primary_000372664600048 |
| ProviderPackageCode | JG~ 55A AABXI GNL VF5 7~N VG9 W1F ACS AEESW AFEFF .K2 ABMVS ABUCX IH9 BAANH AQSVZ ED~ UI2 CITATION AAYXX |
| PublicationCentury | 2000 |
| PublicationDate | 20160318 2016-03-18 2016-Mar-18 |
| PublicationDateYYYYMMDD | 2016-03-18 |
| PublicationDate_xml | – month: 03 year: 2016 text: 20160318 day: 18 |
| PublicationDecade | 2010 |
| PublicationPlace | WASHINGTON |
| PublicationPlace_xml | – name: WASHINGTON – name: United States |
| PublicationTitle | Organic letters |
| PublicationTitleAbbrev | ORG LETT |
| PublicationTitleAlternate | Org. Lett |
| PublicationYear | 2016 |
| Publisher | American Chemical Society Amer Chemical Soc |
| Publisher_xml | – name: American Chemical Society – name: Amer Chemical Soc |
| References | ref9/cit9 ref17/cit17 ref6/cit6 ref10/cit10 ref3/cit3 ref11/cit11 ref12/cit12 ref15/cit15 ref16/cit16 ref13/cit13 ref14/cit14 ref8/cit8 ref5/cit5 ref2/cit2 ref4/cit4 ref1/cit1 ref7/cit7 Shao, CL (WOS:000318264700046) 2013; 76 Chakraborty, C (WOS:000272785100004) 2009; 9 Woo, JK (WOS:000337074300011) 2014; 16 Pedpradab, P (WOS:000294802400014) 2011; 13 Wang, W (WOS:000308390000048) 2012; 14 Lee, Y (WOS:000341339300005) 2014; 24 Gross, Harald (BCI:BCI200600547963) 2006; 5 Schumacher, M (WOS:000290540300001) 2011; 6 Liangsakul, J (WOS:000297523700030) 2011; 52 Wang, LS (WOS:000314846900004) 2013; 30 Li, HX (WOS:000335127200010) 2014; 77 Liu, YY (WOS:000360773700003) 2015; 78 Ettinger-Epstein, P (WOS:000246007200029) 2007; 70 Xiao, ZE (WOS:000319720900050) 2013; 15 Chen, XB (WOS:000294242900027) 2011; 76 Huang, XS (WOS:000315254500001) 2013; 15 Tanaka, N (WOS:000301563300020) 2012; 53 |
| References_xml | – ident: ref1/cit1 doi: 10.1039/c3np20089b – ident: ref15/cit15 doi: 10.1021/np500885f – ident: ref16/cit16 doi: 10.1021/np400880w – ident: ref3/cit3 doi: 10.1080/10286020.2011.591386 – ident: ref7/cit7 doi: 10.1016/j.tetlet.2011.09.079 – ident: ref2/cit2 doi: 10.1007/s11101-005-5464-3 – ident: ref10/cit10 doi: 10.2174/156802609789909803 – ident: ref11/cit11 doi: 10.1007/s12263-011-0231-0 – ident: ref9/cit9 doi: 10.1016/j.bmcl.2014.07.066 – ident: ref8/cit8 doi: 10.1021/ol500868s – ident: ref5/cit5 doi: 10.1016/j.tetlet.2012.01.052 – ident: ref4/cit4 doi: 10.1021/np060240d – ident: ref12/cit12 doi: 10.1021/ol3019874 – ident: ref17/cit17 doi: 10.1021/np4002042 – ident: ref6/cit6 doi: 10.1021/jo2008127 – ident: ref13/cit13 doi: 10.1021/ol303549c – ident: ref14/cit14 doi: 10.1021/ol401005j – volume: 30 start-page: 455 year: 2013 ident: WOS:000314846900004 article-title: Sesterterpenoids publication-title: NATURAL PRODUCT REPORTS doi: 10.1039/c3np20089b – volume: 15 start-page: 721 year: 2013 ident: WOS:000315254500001 article-title: Asperterpenoid A, a New Sesterterpenoid as an Inhibitor of Mycobacterium tuberculosis Protein Tyrosine Phosphatase B from the Culture of Aspergillus sp 16-5c publication-title: ORGANIC LETTERS doi: 10.1021/ol303549c – volume: 16 start-page: 2826 year: 2014 ident: WOS:000337074300011 article-title: Gombaspiroketals A-C, Sesterterpenes from the Sponge Clathria gombawuiensis publication-title: ORGANIC LETTERS doi: 10.1021/ol500868s – volume: 13 start-page: 879 year: 2011 ident: WOS:000294802400014 article-title: A new acyclic thiophene sesterterpene from the Sikao Bay sponge, Xestospongia sp. publication-title: JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH doi: 10.1080/10286020.2011.591386 – volume: 70 start-page: 648 year: 2007 ident: WOS:000246007200029 article-title: Acetylated sesterterpenes from the Great Barrier Reef sponge Luffariella variabilis publication-title: JOURNAL OF NATURAL PRODUCTS doi: 10.1021/np060240d – volume: 15 start-page: 2522 year: 2013 ident: WOS:000319720900050 article-title: Asperterpenols A and B, New Sesterterpenoids Isolated from a Mangrove Endophytic Fungus Aspergillus sp 085242 publication-title: ORGANIC LETTERS doi: 10.1021/ol401005j – volume: 9 start-page: 1536 year: 2009 ident: WOS:000272785100004 article-title: Anticancer Drugs Discovery and Development from Marine Organisms publication-title: CURRENT TOPICS IN MEDICINAL CHEMISTRY – volume: 76 start-page: 779 year: 2013 ident: WOS:000318264700046 article-title: Structure and Absolute Configuration of Fumiquinazoline L, an Alkaloid from a Gorgonian-Derived Scopulariopsis sp Fungus publication-title: JOURNAL OF NATURAL PRODUCTS doi: 10.1021/np4002042 – volume: 14 start-page: 4486 year: 2012 ident: WOS:000308390000048 article-title: Phorone A and Isophorbasone A, Sesterterpenoids Isolated from the Marine Sponge Phorbas sp. publication-title: ORGANIC LETTERS doi: 10.1021/ol3019874 – volume: 53 start-page: 1507 year: 2012 ident: WOS:000301563300020 article-title: Biyoulactones D and E, meroterpenoids from Hypericum chinense publication-title: TETRAHEDRON LETTERS doi: 10.1016/j.tetlet.2012.01.052 – volume: 24 start-page: 4095 year: 2014 ident: WOS:000341339300005 article-title: Phorbaketals L-N, cytotoxic sesterterpenoids isolated from the marine sponge of the genus Phorbas publication-title: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS doi: 10.1016/j.bmcl.2014.07.066 – volume: 6 start-page: 89 year: 2011 ident: WOS:000290540300001 article-title: Natural compounds as inflammation inhibitors publication-title: GENES AND NUTRITION doi: 10.1007/s12263-011-0231-0 – volume: 76 start-page: 7216 year: 2011 ident: WOS:000294242900027 article-title: Synthesis of the Scalarane Sesterterpenoid 16-deacetoxy-12-epi-scalarafuranacetate publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/jo2008127 – volume: 77 start-page: 800 year: 2014 ident: WOS:000335127200010 article-title: Peniphenones A-D from the Mangrove Fungus Penicillium dipodomyicola HN4-3A as Inhibitors of Mycobacterium tuberculosis Phosphatase MptpB publication-title: JOURNAL OF NATURAL PRODUCTS doi: 10.1021/np400880w – volume: 78 start-page: 1816 year: 2015 ident: WOS:000360773700003 article-title: Polyketides with alpha-Glucosidase Inhibitory Activity from a Mangrove Endophytic Fungus, Penicillium sp HN29-3B1 publication-title: JOURNAL OF NATURAL PRODUCTS doi: 10.1021/np500885f – volume: 52 start-page: 6427 year: 2011 ident: WOS:000297523700030 article-title: Emervaridione and varioxiranediol, two new metabolites from the endophytic fungus, Emericella variecolor publication-title: TETRAHEDRON LETTERS doi: 10.1016/j.tetlet.2011.09.079 – volume: 5 start-page: 115 year: 2006 ident: BCI:BCI200600547963 article-title: Terpenoids from marine organisms: unique structures and their pharmacological potential publication-title: Phytochemistry Reviews doi: 10.1007/s11101-005-5464-3 |
| SSID | ssj0011529 |
| Score | 2.489442 |
| Snippet | Two new sesterterpenoids, aspterpenacids A (1) and B (2), with an unusual carbon skeleton of a 5/3/7/6/5 ring system were isolated from the mangrove endophytic... |
| Source | Web of Science |
| SourceID | proquest pubmed webofscience crossref acs |
| SourceType | Aggregation Database Index Database Enrichment Source Publisher |
| StartPage | 1406 |
| SubjectTerms | Anti-Bacterial Agents - chemistry Anti-Bacterial Agents - isolation & purification Anti-Bacterial Agents - pharmacology antibacterial properties Aspergillus - chemistry Aspergillus terreus carbon chemical reactions chemical structure Chemistry Chemistry, Organic Circular Dichroism circular dichroism spectroscopy Crystallography, X-Ray cytotoxicity endophytes fungi Molecular Structure organic compounds Physical Sciences Rhizophoraceae - microbiology Science & Technology Sesterterpenes - chemistry Sesterterpenes - isolation & purification Sesterterpenes - pharmacology X-ray diffraction |
| Title | Aspterpenacids A and B, Two Sesterterpenoids from a Mangrove Endophytic Fungus Aspergillus terreus H010 |
| URI | http://dx.doi.org/10.1021/acs.orglett.6b00336 http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000372664600048 https://www.ncbi.nlm.nih.gov/pubmed/26938636 https://www.proquest.com/docview/1774530505 https://www.proquest.com/docview/2020875339 |
| Volume | 18 |
| WOS | 000372664600048 |
| WOSCitedRecordID | wos000372664600048 |
| hasFullText | 1 |
| inHoldings | 1 |
| isFullTextHit | |
| isPrint | |
| link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1LT9tAEB619NBeoE9IaautxKEHnK698Wb3mEZEERJcAImbta9EiMhGsQMSv74zfkQUKMrJj33Zs7Oeb7y73wAcBJsKrYKNEh-LaGC1iXAUoauiUquVsFo7-g95ciqnF4Pjy_TywWb1RzP4SfzbuJKu8S2qviQlFPI1vEmkGpKvNRqfrScN0BTpmh41ERGRwnQkQ89XQubIlf-aoycY81lzVJueyQ6cdht4mhUn1_1VZfvu_imf42Zv9R62WxDKRo3WfIBXIf8Ib8dd7LdPMB-VN7QYMeTGXfmSjZjJPftzyM7vCnZWkys0yQWl0hYVZtiJyefL4jawo9wX2HtYOZvgt2SF5YmPfH61WOA5FlwGPE7RR_sMF5Oj8_E0akMyREYMVRWlIZiZSbnRQ-1lHIuZcpJAn_FDx2VA39Z5r_nMWIRi3EmrY0eceCJoriwXX2ArL_KwByxYJXiYKYkAaeBFMEGjh8yxFo41c9mDXyikrB1SZVbPlidxRjdbyWWt5HqQdJ2YuZbanCJsLF4udLgudNMwe7yc_WenHRl2Bk2rmDwUK3wwRNCpoIiA_8-TUCxU9AyF7sFuo1rrRhOUgJLUwsFDXVun1xxBiKMGsmYA6EG8SbZxKweiNqi-bi7LfXiHmFDSMrtYfYOtarkK3xF3VfZHPdr-ArRaKLA |
| linkProvider | American Chemical Society |
| linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwzV1Lb9swDCa67tBd9n6ke2lAB-xQZ7JkK9JhhyxrkK5NL02B3jxJVoKigV3Ezort9-yv7H-Ncmzv1RW9FNjJhiXRMkmZpEV_BNhyJuZKOhOwNORBZJQOcBVhqCJjoyQ3Sln_HXJ8IEZH0cfj-HgNvjX_wuAkCqRUVJv4P9EFwrf1NXyYsiu8LnJRp1LuuS_nGKgV73Y_oFRfMzbcmQxGQV1LINC8J8sgdk5PdUy16qlUhCGfSiu8t6LTnqXCYVBm01TRqTboQ1ArjAqtB3PjTlFpKEe6N-Amuj_Mh3j9wWG7V4EWUFWorIwHHoumwTa6eNLeCtridyv4l2t7oRWsLN7wDnxveVUlupx2l6Xp2q9_wEj-78y8C7drl5v0V2vkHqy57D5sDJpKdw9g1i_OfOqly7Q9SQvSJzpLyfttMjnPyWEFJbFqzn2r_yGHaDLW2WyRf3ZkJ0tz1FUkTob45lzieI--PjuZz_EcBy4cHkcYkT6Eo2t5zkewnuWZewLEGcmpm0qB7mCUcqedYr2IIhWKlKnowBsUSlK_QIqkyg1gYeIv1pJKakl1gDW6k9gayN3XE5lfPmi7HXS2wjG5vPurRikTFIbfRNKZy5c4MYwXYu7rH_67D_OVXzEO5qoDj1ca3d6UIQek8HfY-lXF2_YKEQm9xkhUeAcdCK_SbVDzwQM5lJtX5-VL2BhNxvvJ_u7B3lO4hd6w8AmGoXwG6-Vi6Z6jx1maF9WCJ_DpuhfFD5wpiss |
| linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMw1V1Lb9QwELZKkYAL78fyNFKRODSLEyde-8Bh2Xa1pbRCaiv1FvzKqmKVrDZZKvhF_BX-FTPZJOJRql564JQotifOPOKZePINIRveJFxJb4LIhTyIjdIBWBGEKjIxSnKjlMXvkHv7YnIUvz9OjtfI9_ZfGJhECZTKehMfrXrusgZhIHzTXIcHqvoC9ZGLJp1y1389hWCtfLuzBZJ9FUXj7cPRJGjqCQSaD2QVJN7rTCdMq4FyIgx5Jq1Aj0W7gWXCQ2BmnVMs0wb8CGaFUaFFQDfuFZOGcaB7hVzFjUIM84ajg26_AlZBVSOzRjxAPJoW3-jsSeNKaMvfV8K_3NszV8J61RvfIj86ftXJLp_7y8r07bc_oCT_B4beJjcb15sOV7Zyh6z5_C65Pmor3t0j02E5xxRMn2t74ko6pDp39N0mPTwt6EENKbFqLrAVf8yhmu7pfLoovni6nbsCdBaI0zG8QZcwHlHYpyezGZzDwIWH4wQi0_vk6FKe8wFZz4vcPyLUG8mZz6QAtzB23GuvokHMgAoDykz0yGsQStq8SMq0zhGIwhQvNpJKG0n1SNTqT2obQHesKzI7f9BmN2i-wjM5v_vLVjFTEAZuJuncF0uYGMQNCcc6iP_uE2EFWIiHueqRhyut7m4aAQekwDts_KrmXXuNjATeYyxq3IMeCS_SbdTwAQEdqscX5-ULcu3j1jj9sLO_-4TcAKdYYJ5hKJ-S9Wqx9M_A8azM89rmKfl02TbxE3m3jU4 |
| openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Aspterpenacids+A+and+B%2C+Two+Sesterterpenoids+from+a+Mangrove+Endophytic+Fungus+Aspergillus+terreus+H010&rft.jtitle=Organic+letters&rft.au=Liu%2C+Zhaoming&rft.au=Chen%2C+Yan&rft.au=Chen%2C+Senhua&rft.au=Liu%2C+Yayue&rft.date=2016-03-18&rft.issn=1523-7052&rft.volume=18&rft.issue=6+p.1406-1409&rft.spage=1406&rft.epage=1409&rft_id=info:doi/10.1021%2Facs.orglett.6b00336&rft.externalDBID=NO_FULL_TEXT |
| thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1523-7060&client=summon |
| thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1523-7060&client=summon |
| thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1523-7060&client=summon |