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Structure elucidation and complete NMR spectral assignment of an unusual aromatic monacolin analog from Monascus purpureus-fermented rice
One unusual aromatic monacolin analog, monacophenyl, was isolated from the ethanolic extract of Monascus purpureus‐fermented rice. Its structure was completely and unambiguously assigned by one‐ and two‐dimensional NMR techniques (1H NMR, 13C NMR, HSQC, HMBC and NOESY) and high‐resolution ESI‐MS spe...
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| Published in: | Magnetic resonance in chemistry 2011-03, Vol.49 (3), p.129-131 |
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| Main Authors: | , , , , , , |
| Format: | Article |
| Language: | English |
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| cited_by | cdi_FETCH-LOGICAL-c3914-ec403e970a8fa9d20f453da5a21a0d924650fd2bf77bda6e9a9e89d6f1cb26773 |
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| cites | cdi_FETCH-LOGICAL-c3914-ec403e970a8fa9d20f453da5a21a0d924650fd2bf77bda6e9a9e89d6f1cb26773 |
| container_end_page | 131 |
| container_issue | 3 |
| container_start_page | 129 |
| container_title | Magnetic resonance in chemistry |
| container_volume | 49 |
| creator | Liu, Ming-Tao Li, Jin-Jie Shang, Xiao-Ya Li, Shuai Li, Ling-Ling Luan, Na Jin, Zong-Lian |
| description | One unusual aromatic monacolin analog, monacophenyl, was isolated from the ethanolic extract of Monascus purpureus‐fermented rice. Its structure was completely and unambiguously assigned by one‐ and two‐dimensional NMR techniques (1H NMR, 13C NMR, HSQC, HMBC and NOESY) and high‐resolution ESI‐MS spectrometry. Copyright © 2011 John Wiley & Sons, Ltd.
One unusual aromatic monacolin analog, monacophenyl, was isolated from the ethanolic extract of Monascus purpureus‐fermented rice. Its structure was completely and unambiguously assigned by one‐ and two‐dimensional NMR techniques (1H NMR, 13C NMR, HSQC, HMBC and NOESY) and high‐resolution ESI‐MS spectrometry. |
| doi_str_mv | 10.1002/mrc.2714 |
| format | article |
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One unusual aromatic monacolin analog, monacophenyl, was isolated from the ethanolic extract of Monascus purpureus‐fermented rice. Its structure was completely and unambiguously assigned by one‐ and two‐dimensional NMR techniques (1H NMR, 13C NMR, HSQC, HMBC and NOESY) and high‐resolution ESI‐MS spectrometry.</description><identifier>ISSN: 0749-1581</identifier><identifier>ISSN: 1097-458X</identifier><identifier>EISSN: 1097-458X</identifier><identifier>DOI: 10.1002/mrc.2714</identifier><identifier>PMID: 21322007</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>13C ; 2D NMR ; Anticholesteremic Agents - chemistry ; Lovastatin - analogs & derivatives ; Lovastatin - chemistry ; Magnetic Resonance Spectroscopy ; Molecular Structure ; monacolin analog ; Monascus ; Monascus - chemistry ; Monascus purpureus-fermented rice ; NMR ; Oryza - chemistry ; Oryza sativa ; Pyrones - chemistry ; Tetrahydronaphthalenes - chemistry</subject><ispartof>Magnetic resonance in chemistry, 2011-03, Vol.49 (3), p.129-131</ispartof><rights>Copyright © 2011 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3914-ec403e970a8fa9d20f453da5a21a0d924650fd2bf77bda6e9a9e89d6f1cb26773</citedby><cites>FETCH-LOGICAL-c3914-ec403e970a8fa9d20f453da5a21a0d924650fd2bf77bda6e9a9e89d6f1cb26773</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21322007$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Ming-Tao</creatorcontrib><creatorcontrib>Li, Jin-Jie</creatorcontrib><creatorcontrib>Shang, Xiao-Ya</creatorcontrib><creatorcontrib>Li, Shuai</creatorcontrib><creatorcontrib>Li, Ling-Ling</creatorcontrib><creatorcontrib>Luan, Na</creatorcontrib><creatorcontrib>Jin, Zong-Lian</creatorcontrib><title>Structure elucidation and complete NMR spectral assignment of an unusual aromatic monacolin analog from Monascus purpureus-fermented rice</title><title>Magnetic resonance in chemistry</title><addtitle>Magn. Reson. Chem</addtitle><description>One unusual aromatic monacolin analog, monacophenyl, was isolated from the ethanolic extract of Monascus purpureus‐fermented rice. Its structure was completely and unambiguously assigned by one‐ and two‐dimensional NMR techniques (1H NMR, 13C NMR, HSQC, HMBC and NOESY) and high‐resolution ESI‐MS spectrometry. Copyright © 2011 John Wiley & Sons, Ltd.
One unusual aromatic monacolin analog, monacophenyl, was isolated from the ethanolic extract of Monascus purpureus‐fermented rice. Its structure was completely and unambiguously assigned by one‐ and two‐dimensional NMR techniques (1H NMR, 13C NMR, HSQC, HMBC and NOESY) and high‐resolution ESI‐MS spectrometry.</description><subject>13C</subject><subject>2D NMR</subject><subject>Anticholesteremic Agents - chemistry</subject><subject>Lovastatin - analogs & derivatives</subject><subject>Lovastatin - chemistry</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Molecular Structure</subject><subject>monacolin analog</subject><subject>Monascus</subject><subject>Monascus - chemistry</subject><subject>Monascus purpureus-fermented rice</subject><subject>NMR</subject><subject>Oryza - chemistry</subject><subject>Oryza sativa</subject><subject>Pyrones - chemistry</subject><subject>Tetrahydronaphthalenes - chemistry</subject><issn>0749-1581</issn><issn>1097-458X</issn><issn>1097-458X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp90c1qFTEUwPEgFnutgk8g2elm2nzMTCZLudgq9Lb2qtRdyE1OymhmMk0maB_BtzZDr3VlIRDI-eW_OQi9ouSYEsJOhmiOmaD1E7SiRIqqbrpvT9GKiFpWtOnoIXqe0ndCiJSCP0OHjHLGCBEr9PvzHLOZcwQMPpve6rkPI9ajxSYMk4cZ8MVmi9MEZo7aY51SfzMOMM44uOJwHnPKyyCGoXw2eAijNsH3S0X7cINdmeBNeU0mJzzlWA7kVDmISwcsjr2BF-jAaZ_g5f4-Ql9P339Zf6jOL88-rt-dV4ZLWldgasJBCqI7p6VlxNUNt7rRjGpiJavbhjjLdk6IndUtSC2hk7Z11OxYKwQ_Qm_uu1MMtxnSrIY-GfBejxByUl1DJS-Rrsi3j0pKGGtaTgj9R00MKUVwaor9oONdQWpZkSorUsuKCn29r-bdAPYB_t1JAdU9-Nl7uPtvSG22631w7_s0w68Hr-MP1QouGnV9caZOr8R1xz5dqS3_A1_2rL4</recordid><startdate>201103</startdate><enddate>201103</enddate><creator>Liu, Ming-Tao</creator><creator>Li, Jin-Jie</creator><creator>Shang, Xiao-Ya</creator><creator>Li, Shuai</creator><creator>Li, Ling-Ling</creator><creator>Luan, Na</creator><creator>Jin, Zong-Lian</creator><general>John Wiley & Sons, Ltd</general><scope>BSCLL</scope><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201103</creationdate><title>Structure elucidation and complete NMR spectral assignment of an unusual aromatic monacolin analog from Monascus purpureus-fermented rice</title><author>Liu, Ming-Tao ; Li, Jin-Jie ; Shang, Xiao-Ya ; Li, Shuai ; Li, Ling-Ling ; Luan, Na ; Jin, Zong-Lian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3914-ec403e970a8fa9d20f453da5a21a0d924650fd2bf77bda6e9a9e89d6f1cb26773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>13C</topic><topic>2D NMR</topic><topic>Anticholesteremic Agents - chemistry</topic><topic>Lovastatin - analogs & derivatives</topic><topic>Lovastatin - chemistry</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Molecular Structure</topic><topic>monacolin analog</topic><topic>Monascus</topic><topic>Monascus - chemistry</topic><topic>Monascus purpureus-fermented rice</topic><topic>NMR</topic><topic>Oryza - chemistry</topic><topic>Oryza sativa</topic><topic>Pyrones - chemistry</topic><topic>Tetrahydronaphthalenes - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Ming-Tao</creatorcontrib><creatorcontrib>Li, Jin-Jie</creatorcontrib><creatorcontrib>Shang, Xiao-Ya</creatorcontrib><creatorcontrib>Li, Shuai</creatorcontrib><creatorcontrib>Li, Ling-Ling</creatorcontrib><creatorcontrib>Luan, Na</creatorcontrib><creatorcontrib>Jin, Zong-Lian</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Magnetic resonance in chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Ming-Tao</au><au>Li, Jin-Jie</au><au>Shang, Xiao-Ya</au><au>Li, Shuai</au><au>Li, Ling-Ling</au><au>Luan, Na</au><au>Jin, Zong-Lian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structure elucidation and complete NMR spectral assignment of an unusual aromatic monacolin analog from Monascus purpureus-fermented rice</atitle><jtitle>Magnetic resonance in chemistry</jtitle><addtitle>Magn. Reson. Chem</addtitle><date>2011-03</date><risdate>2011</risdate><volume>49</volume><issue>3</issue><spage>129</spage><epage>131</epage><pages>129-131</pages><issn>0749-1581</issn><issn>1097-458X</issn><eissn>1097-458X</eissn><abstract>One unusual aromatic monacolin analog, monacophenyl, was isolated from the ethanolic extract of Monascus purpureus‐fermented rice. Its structure was completely and unambiguously assigned by one‐ and two‐dimensional NMR techniques (1H NMR, 13C NMR, HSQC, HMBC and NOESY) and high‐resolution ESI‐MS spectrometry. Copyright © 2011 John Wiley & Sons, Ltd.
One unusual aromatic monacolin analog, monacophenyl, was isolated from the ethanolic extract of Monascus purpureus‐fermented rice. Its structure was completely and unambiguously assigned by one‐ and two‐dimensional NMR techniques (1H NMR, 13C NMR, HSQC, HMBC and NOESY) and high‐resolution ESI‐MS spectrometry.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>21322007</pmid><doi>10.1002/mrc.2714</doi><tpages>3</tpages></addata></record> |
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| ispartof | Magnetic resonance in chemistry, 2011-03, Vol.49 (3), p.129-131 |
| issn | 0749-1581 1097-458X 1097-458X |
| language | eng |
| recordid | cdi_proquest_miscellaneous_851936508 |
| source | Wiley:Jisc Collections:Wiley Read and Publish Open Access 2024-2025 (reading list) |
| subjects | 13C 2D NMR Anticholesteremic Agents - chemistry Lovastatin - analogs & derivatives Lovastatin - chemistry Magnetic Resonance Spectroscopy Molecular Structure monacolin analog Monascus Monascus - chemistry Monascus purpureus-fermented rice NMR Oryza - chemistry Oryza sativa Pyrones - chemistry Tetrahydronaphthalenes - chemistry |
| title | Structure elucidation and complete NMR spectral assignment of an unusual aromatic monacolin analog from Monascus purpureus-fermented rice |
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