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Glaucatotones A−I: Guaiane-type sesquiterpenoids from the roots of Lindera glauca with anti-inflammatory activity

[Display omitted] •Nine new guaiane-type sesquiterpenoids were isolated from the roots of Lindera glauca.•Glaucatotone A (1) is a dihomosesquiterpenoid with an unprecedented 5/5/7/6 ring system.•(±)-Glaucatotone B (2a/2b) represent the first norsesquiterpenoids with a (cyclopentylmethyl)cyclohexane...

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Published in:Bioorganic chemistry 2024-03, Vol.144, p.107135-107135, Article 107135
Main Authors: Pan, Xinyuan, Cai, Jiayi, Liu, Kaohua, Guo, Jiaqi, Li, Siqi, Wang, Ling, Han, Lizhu, Zhou, Kexin, Meng, Xiongyu, Qin, Luping, Li, Huaqiang
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container_title Bioorganic chemistry
container_volume 144
creator Pan, Xinyuan
Cai, Jiayi
Liu, Kaohua
Guo, Jiaqi
Li, Siqi
Wang, Ling
Han, Lizhu
Zhou, Kexin
Meng, Xiongyu
Qin, Luping
Li, Huaqiang
description [Display omitted] •Nine new guaiane-type sesquiterpenoids were isolated from the roots of Lindera glauca.•Glaucatotone A (1) is a dihomosesquiterpenoid with an unprecedented 5/5/7/6 ring system.•(±)-Glaucatotone B (2a/2b) represent the first norsesquiterpenoids with a (cyclopentylmethyl)cyclohexane skeleton.•1, 2a, 2b and 7 exhibited potent inhibitory effects. Glaucatotones A − I, nine new guaiane-type sesquiterpenoids, along with two reported compounds, namely (1β,5β)-1-hydroxyguaia-4(15),11(13)-dieno-12,5-lactone (10) and pseudoguaianelactone C (11), were isolated from the roots of Lindera glauca. The structures and absolute configurations of these compounds were elucidated by extensive spectroscopic analyses, single-crystal X-ray diffraction, and comparison of experimental and calculated electronic circular dichroism (ECD) data. Structurally, glaucatotone A (1) is characterized as a dihomosesquiterpenoid with an unprecedented 5/5/7/6 ring system. A pair of enantiomers, (±)-glaucatotone B (2a/2b), represent the first rearranged norsesquiterpenoid with a (cyclopentylmethyl)cyclohexane skeleton. 3 is defined as a dinorsesquiterpenoid possessing a 5/7/5 ring system. 4–6 are three guaiane-type norsesquiterpenoids. In vitro bioactivity, 2a selectively inhibited Bcap-37 with IC50 value of 5.60 μM, and 9 selectively inhibited Du-145 with IC50 value of 5.52 μM. The anti-inflammatory activity of 1–9 were tested, and of these compounds, 1, 2a, 2b and 7 exhibited potent inhibitory effects.
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Glaucatotones A − I, nine new guaiane-type sesquiterpenoids, along with two reported compounds, namely (1β,5β)-1-hydroxyguaia-4(15),11(13)-dieno-12,5-lactone (10) and pseudoguaianelactone C (11), were isolated from the roots of Lindera glauca. The structures and absolute configurations of these compounds were elucidated by extensive spectroscopic analyses, single-crystal X-ray diffraction, and comparison of experimental and calculated electronic circular dichroism (ECD) data. Structurally, glaucatotone A (1) is characterized as a dihomosesquiterpenoid with an unprecedented 5/5/7/6 ring system. A pair of enantiomers, (±)-glaucatotone B (2a/2b), represent the first rearranged norsesquiterpenoid with a (cyclopentylmethyl)cyclohexane skeleton. 3 is defined as a dinorsesquiterpenoid possessing a 5/7/5 ring system. 4–6 are three guaiane-type norsesquiterpenoids. In vitro bioactivity, 2a selectively inhibited Bcap-37 with IC50 value of 5.60 μM, and 9 selectively inhibited Du-145 with IC50 value of 5.52 μM. The anti-inflammatory activity of 1–9 were tested, and of these compounds, 1, 2a, 2b and 7 exhibited potent inhibitory effects.</description><identifier>ISSN: 0045-2068</identifier><identifier>EISSN: 1090-2120</identifier><identifier>DOI: 10.1016/j.bioorg.2024.107135</identifier><identifier>PMID: 38281383</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Anti-inflammatory ; Cytotoxicity ; Lindera glauca ; Norsesquiterpenoids ; Sesquiterpenoids</subject><ispartof>Bioorganic chemistry, 2024-03, Vol.144, p.107135-107135, Article 107135</ispartof><rights>2024 Elsevier Inc.</rights><rights>Copyright © 2024 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c362t-13d2176332881f457f49a2eb698c8dec021cc064e98b3086fe7bd4b2865024643</citedby><cites>FETCH-LOGICAL-c362t-13d2176332881f457f49a2eb698c8dec021cc064e98b3086fe7bd4b2865024643</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/38281383$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pan, Xinyuan</creatorcontrib><creatorcontrib>Cai, Jiayi</creatorcontrib><creatorcontrib>Liu, Kaohua</creatorcontrib><creatorcontrib>Guo, Jiaqi</creatorcontrib><creatorcontrib>Li, Siqi</creatorcontrib><creatorcontrib>Wang, Ling</creatorcontrib><creatorcontrib>Han, Lizhu</creatorcontrib><creatorcontrib>Zhou, Kexin</creatorcontrib><creatorcontrib>Meng, Xiongyu</creatorcontrib><creatorcontrib>Qin, Luping</creatorcontrib><creatorcontrib>Li, Huaqiang</creatorcontrib><title>Glaucatotones A−I: Guaiane-type sesquiterpenoids from the roots of Lindera glauca with anti-inflammatory activity</title><title>Bioorganic chemistry</title><addtitle>Bioorg Chem</addtitle><description>[Display omitted] •Nine new guaiane-type sesquiterpenoids were isolated from the roots of Lindera glauca.•Glaucatotone A (1) is a dihomosesquiterpenoid with an unprecedented 5/5/7/6 ring system.•(±)-Glaucatotone B (2a/2b) represent the first norsesquiterpenoids with a (cyclopentylmethyl)cyclohexane skeleton.•1, 2a, 2b and 7 exhibited potent inhibitory effects. Glaucatotones A − I, nine new guaiane-type sesquiterpenoids, along with two reported compounds, namely (1β,5β)-1-hydroxyguaia-4(15),11(13)-dieno-12,5-lactone (10) and pseudoguaianelactone C (11), were isolated from the roots of Lindera glauca. The structures and absolute configurations of these compounds were elucidated by extensive spectroscopic analyses, single-crystal X-ray diffraction, and comparison of experimental and calculated electronic circular dichroism (ECD) data. Structurally, glaucatotone A (1) is characterized as a dihomosesquiterpenoid with an unprecedented 5/5/7/6 ring system. A pair of enantiomers, (±)-glaucatotone B (2a/2b), represent the first rearranged norsesquiterpenoid with a (cyclopentylmethyl)cyclohexane skeleton. 3 is defined as a dinorsesquiterpenoid possessing a 5/7/5 ring system. 4–6 are three guaiane-type norsesquiterpenoids. In vitro bioactivity, 2a selectively inhibited Bcap-37 with IC50 value of 5.60 μM, and 9 selectively inhibited Du-145 with IC50 value of 5.52 μM. The anti-inflammatory activity of 1–9 were tested, and of these compounds, 1, 2a, 2b and 7 exhibited potent inhibitory effects.</description><subject>Anti-inflammatory</subject><subject>Cytotoxicity</subject><subject>Lindera glauca</subject><subject>Norsesquiterpenoids</subject><subject>Sesquiterpenoids</subject><issn>0045-2068</issn><issn>1090-2120</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kM1O3DAUha2Kqgy0b1BVXrLJ1Nd2HIcFEkIwRRqpm3ZtOc4NeJTEg-1QzRt0zSPyJISGdtnVla7Oj85HyGdga2Cgvu7WjQ8h3q0543J-VSDKd2QFrGYFB86OyIoxWRacKX1MTlLaMQYgK_WBHAvNNQgtViRtejs5m0MOIyZ6-fz76facbibr7YhFPuyRJkwPk88Y9zgG3ybaxTDQfI80hpATDR3d-rHFaOndnzD6y-d7asfsCz92vR2GOT8eqHXZP_p8-Ejed7ZP-OntnpKfN9c_rr4V2--b26vLbeGE4rkA0XKolBBca-hkWXWythwbVWunW3SMg3NMSax1I5hWHVZNKxuuVTkTUVKckrMldx_Dw4Qpm8Enh30_TwtTMryGupIApZilcpG6GFKK2Jl99IONBwPMvOI2O7PgNq-4zYJ7tn15a5iaAdt_pr98Z8HFIsB556PHaJLzODpsfUSXTRv8_xteANIClHw</recordid><startdate>20240301</startdate><enddate>20240301</enddate><creator>Pan, Xinyuan</creator><creator>Cai, Jiayi</creator><creator>Liu, Kaohua</creator><creator>Guo, Jiaqi</creator><creator>Li, Siqi</creator><creator>Wang, Ling</creator><creator>Han, Lizhu</creator><creator>Zhou, Kexin</creator><creator>Meng, Xiongyu</creator><creator>Qin, Luping</creator><creator>Li, Huaqiang</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20240301</creationdate><title>Glaucatotones A−I: Guaiane-type sesquiterpenoids from the roots of Lindera glauca with anti-inflammatory activity</title><author>Pan, Xinyuan ; Cai, Jiayi ; Liu, Kaohua ; Guo, Jiaqi ; Li, Siqi ; Wang, Ling ; Han, Lizhu ; Zhou, Kexin ; Meng, Xiongyu ; Qin, Luping ; Li, Huaqiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-13d2176332881f457f49a2eb698c8dec021cc064e98b3086fe7bd4b2865024643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Anti-inflammatory</topic><topic>Cytotoxicity</topic><topic>Lindera glauca</topic><topic>Norsesquiterpenoids</topic><topic>Sesquiterpenoids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pan, Xinyuan</creatorcontrib><creatorcontrib>Cai, Jiayi</creatorcontrib><creatorcontrib>Liu, Kaohua</creatorcontrib><creatorcontrib>Guo, Jiaqi</creatorcontrib><creatorcontrib>Li, Siqi</creatorcontrib><creatorcontrib>Wang, Ling</creatorcontrib><creatorcontrib>Han, Lizhu</creatorcontrib><creatorcontrib>Zhou, Kexin</creatorcontrib><creatorcontrib>Meng, Xiongyu</creatorcontrib><creatorcontrib>Qin, Luping</creatorcontrib><creatorcontrib>Li, Huaqiang</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Bioorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pan, Xinyuan</au><au>Cai, Jiayi</au><au>Liu, Kaohua</au><au>Guo, Jiaqi</au><au>Li, Siqi</au><au>Wang, Ling</au><au>Han, Lizhu</au><au>Zhou, Kexin</au><au>Meng, Xiongyu</au><au>Qin, Luping</au><au>Li, Huaqiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Glaucatotones A−I: Guaiane-type sesquiterpenoids from the roots of Lindera glauca with anti-inflammatory activity</atitle><jtitle>Bioorganic chemistry</jtitle><addtitle>Bioorg Chem</addtitle><date>2024-03-01</date><risdate>2024</risdate><volume>144</volume><spage>107135</spage><epage>107135</epage><pages>107135-107135</pages><artnum>107135</artnum><issn>0045-2068</issn><eissn>1090-2120</eissn><abstract>[Display omitted] •Nine new guaiane-type sesquiterpenoids were isolated from the roots of Lindera glauca.•Glaucatotone A (1) is a dihomosesquiterpenoid with an unprecedented 5/5/7/6 ring system.•(±)-Glaucatotone B (2a/2b) represent the first norsesquiterpenoids with a (cyclopentylmethyl)cyclohexane skeleton.•1, 2a, 2b and 7 exhibited potent inhibitory effects. Glaucatotones A − I, nine new guaiane-type sesquiterpenoids, along with two reported compounds, namely (1β,5β)-1-hydroxyguaia-4(15),11(13)-dieno-12,5-lactone (10) and pseudoguaianelactone C (11), were isolated from the roots of Lindera glauca. The structures and absolute configurations of these compounds were elucidated by extensive spectroscopic analyses, single-crystal X-ray diffraction, and comparison of experimental and calculated electronic circular dichroism (ECD) data. Structurally, glaucatotone A (1) is characterized as a dihomosesquiterpenoid with an unprecedented 5/5/7/6 ring system. A pair of enantiomers, (±)-glaucatotone B (2a/2b), represent the first rearranged norsesquiterpenoid with a (cyclopentylmethyl)cyclohexane skeleton. 3 is defined as a dinorsesquiterpenoid possessing a 5/7/5 ring system. 4–6 are three guaiane-type norsesquiterpenoids. In vitro bioactivity, 2a selectively inhibited Bcap-37 with IC50 value of 5.60 μM, and 9 selectively inhibited Du-145 with IC50 value of 5.52 μM. The anti-inflammatory activity of 1–9 were tested, and of these compounds, 1, 2a, 2b and 7 exhibited potent inhibitory effects.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>38281383</pmid><doi>10.1016/j.bioorg.2024.107135</doi><tpages>1</tpages></addata></record>
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subjects Anti-inflammatory
Cytotoxicity
Lindera glauca
Norsesquiterpenoids
Sesquiterpenoids
title Glaucatotones A−I: Guaiane-type sesquiterpenoids from the roots of Lindera glauca with anti-inflammatory activity
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