{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,13]],"date-time":"2026-04-13T17:25:53Z","timestamp":1776101153318,"version":"3.50.1"},"reference-count":55,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2026,7,1]],"date-time":"2026-07-01T00:00:00Z","timestamp":1782864000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2026,7,1]],"date-time":"2026-07-01T00:00:00Z","timestamp":1782864000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2026,7,1]],"date-time":"2026-07-01T00:00:00Z","timestamp":1782864000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2026,7,1]],"date-time":"2026-07-01T00:00:00Z","timestamp":1782864000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2026,7,1]],"date-time":"2026-07-01T00:00:00Z","timestamp":1782864000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2026,7,1]],"date-time":"2026-07-01T00:00:00Z","timestamp":1782864000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2026,7,1]],"date-time":"2026-07-01T00:00:00Z","timestamp":1782864000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"funder":[{"DOI":"10.13039\/501100012166","name":"National Key Research and Development Program of China","doi-asserted-by":"publisher","award":["2024YFC3506600"],"award-info":[{"award-number":["2024YFC3506600"]}],"id":[{"id":"10.13039\/501100012166","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Phytochemistry"],"published-print":{"date-parts":[[2026,7]]},"DOI":"10.1016\/j.phytochem.2026.114843","type":"journal-article","created":{"date-parts":[[2026,3,3]],"date-time":"2026-03-03T00:26:58Z","timestamp":1772497618000},"page":"114843","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":0,"special_numbering":"C","title":["Guaiane-type sesquiterpenoids with acetylcholinesterase inhibitory activities from the roots of Stellera chamaejasme"],"prefix":"10.1016","volume":"247","author":[{"given":"Cheng-Yu","family":"Chu","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xuan","family":"Liu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Si-Hui","family":"Mi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ming","family":"Bai","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xiao-Xiao","family":"Huang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shao-Jiang","family":"Song","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.phytochem.2026.114843_bib53","doi-asserted-by":"crossref","first-page":"246","DOI":"10.1016\/j.jgr.2020.07.001","article-title":"Quantitative aspects of the hydrolysis of ginseng saponins: Application in HPLC-MS analysis of herbal products","volume":"45","author":"Abashev","year":"2021","journal-title":"J. Ginseng Res."},{"key":"10.1016\/j.phytochem.2026.114843_bib1","doi-asserted-by":"crossref","first-page":"196","DOI":"10.1016\/j.fitote.2015.11.018","article-title":"Chemical modification of arglabin and biological activity of its new derivatives","volume":"110","author":"Adekenov","year":"2016","journal-title":"Fitoterapia"},{"key":"10.1016\/j.phytochem.2026.114843_bib2","doi-asserted-by":"crossref","DOI":"10.1016\/j.fitote.2022.105250","article-title":"Acylated sucroses and butenolide analog from the leaves of Tripterygium wilfordii Hook. F. And their potential anti-tyrosinase effects","volume":"161","author":"Ai","year":"2022","journal-title":"Fitoterapia"},{"key":"10.1016\/j.phytochem.2026.114843_bib3","doi-asserted-by":"crossref","first-page":"628","DOI":"10.1016\/j.ejmech.2018.03.076","article-title":"An overview of quinazolines: pharmacological significance and recent developments","volume":"151","author":"Alagarsamy","year":"2018","journal-title":"Eur. J. Med. Chem."},{"key":"10.1016\/j.phytochem.2026.114843_bib4","doi-asserted-by":"crossref","first-page":"3214","DOI":"10.1021\/acs.jafc.9b08303","article-title":"Characterization of guaiene synthases from Stellera chamaejasme L. flowers and their application in De novo production of (-)-Rotundone in yeast","volume":"68","author":"An","year":"2020","journal-title":"J. Agric. Food Chem."},{"key":"10.1016\/j.phytochem.2026.114843_bib5","doi-asserted-by":"crossref","first-page":"2904","DOI":"10.1021\/ol200889s","article-title":"Stelleralides A\u2013C, novel potent anti-HIV daphnane-type diterpenoids from Stellera chamaejasme L","volume":"13","author":"Asada","year":"2011","journal-title":"Org. Lett."},{"key":"10.1016\/j.phytochem.2026.114843_bib6","doi-asserted-by":"crossref","DOI":"10.1016\/j.phytochem.2023.113784","article-title":"Yuexiandajisu diterpenoids from Euphorbia ebracteolata Hayata (Langdu roots): an overview","volume":"213","author":"Bailly","year":"2023","journal-title":"Phytochemistry"},{"key":"10.1016\/j.phytochem.2026.114843_bib7","doi-asserted-by":"crossref","first-page":"5648","DOI":"10.1063\/1.464913","article-title":"Density\u2010functional thermochemistry. III. The role of exact exchange","volume":"98","author":"Becke","year":"1993","journal-title":"J. Chem. Phys."},{"key":"10.1016\/j.phytochem.2026.114843_bib8","doi-asserted-by":"crossref","DOI":"10.1016\/j.pscia.2024.100051","article-title":"Chemical composition and neuroprotective activity of hemp seed aqueous extract and their chemotaxonomic significance","volume":"2","author":"Bu","year":"2024","journal-title":"Pharm. Sci. Adv."},{"key":"10.1016\/j.phytochem.2026.114843_bib9","doi-asserted-by":"crossref","DOI":"10.1016\/j.phytochem.2019.112233","article-title":"Bioactive chemical constituents from the seed testa of Vernicia fordii as potential neuroinflammatory inhibitors","volume":"171","author":"Chen","year":"2020","journal-title":"Phytochemistry"},{"key":"10.1016\/j.phytochem.2026.114843_bib10","doi-asserted-by":"crossref","DOI":"10.1016\/j.phytochem.2020.112628","article-title":"Guaiane-type sesquiterpenoids from the roots of Stellera chamaejasme L. and their neuroprotective activities","volume":"183","author":"Cheng","year":"2021","journal-title":"Phytochemistry"},{"key":"10.1016\/j.phytochem.2026.114843_bib11","doi-asserted-by":"crossref","DOI":"10.1016\/j.phytochem.2023.113725","article-title":"Daphnane-type diterpenoids from Stellera chamaejasme L. and their inhibitory activity against hepatocellular carcinoma cells","volume":"212","author":"Cheng","year":"2023","journal-title":"Phytochemistry"},{"key":"10.1016\/j.phytochem.2026.114843_bib12","doi-asserted-by":"crossref","DOI":"10.1016\/j.phytochem.2022.113275","article-title":"Stellerasespenes A\u2012E: sesquiterpenoids from Stellera chamaejasme and their anti-neuroinflammatory effects","volume":"201","author":"Cheng","year":"2022","journal-title":"Phytochemistry"},{"key":"10.1016\/j.phytochem.2026.114843_bib13","doi-asserted-by":"crossref","DOI":"10.1016\/j.trac.2024.117711","article-title":"Advanced technologies targeting isolation and characterization of natural products","volume":"175","author":"Dong","year":"2024","journal-title":"TrAC Trends Anal. Chem."},{"key":"10.1016\/j.phytochem.2026.114843_bib14","doi-asserted-by":"crossref","DOI":"10.1016\/j.fitote.2020.104714","article-title":"Chamaejasmins, cytotoxic guaiane sesquiterpenes from the root of Stellera chamaejasme L","volume":"146","author":"El Desoky","year":"2020","journal-title":"Fitoterapia"},{"key":"10.1016\/j.phytochem.2026.114843_bib15","doi-asserted-by":"crossref","first-page":"2764","DOI":"10.2174\/092986710791859324","article-title":"New therapeutic strategy for parkinson's and alzheimer's disease","volume":"17","author":"Esposito","year":"2010","journal-title":"Curr. Med. Chem."},{"key":"10.1016\/j.phytochem.2026.114843_bib16","series-title":"Gaussian 09, Revision D.01","author":"Frisch","year":"2013"},{"key":"10.1016\/j.phytochem.2026.114843_bib17","first-page":"529","article-title":"Research progress on chemical diversity of saponins in Panax ginseng","volume":"16","author":"Geng","year":"2024","journal-title":"Chin. Herb. Med."},{"key":"10.1016\/j.phytochem.2026.114843_bib18","doi-asserted-by":"crossref","first-page":"767","DOI":"10.1021\/jp807366r","article-title":"Calculation of electronic circular dichroism spectra with time-dependent double-hybrid density functional theory","volume":"113","author":"Goerigk","year":"2009","journal-title":"J. Phys. Chem. A"},{"key":"10.1016\/j.phytochem.2026.114843_bib19","doi-asserted-by":"crossref","first-page":"490","DOI":"10.1002\/(SICI)1096-987X(199604)17:5\/6<490::AID-JCC1>3.0.CO;2-P","article-title":"Merck molecular force field. I. Basis, form, scope, parameterization, and performance of MMFF94","volume":"17","author":"Halgren","year":"1996","journal-title":"J. Comput. Chem."},{"key":"10.1016\/j.phytochem.2026.114843_bib20","doi-asserted-by":"crossref","first-page":"225","DOI":"10.1177\/1747519820961047","article-title":"A new 11,10-guaiane-type sesquiterpenoid from the roots of Stellera chamaejasme Linn","volume":"45","author":"Hu","year":"2021","journal-title":"J. Chem. Res."},{"key":"10.1016\/j.phytochem.2026.114843_bib21","doi-asserted-by":"crossref","first-page":"261","DOI":"10.1016\/j.jep.2003.08.008","article-title":"Screening for acetylcholinesterase inhibitory activity in plants used in Thai traditional rejuvenating and neurotonic remedies","volume":"89","author":"Ingkaninan","year":"2003","journal-title":"J. Ethnopharmacol."},{"key":"10.1016\/j.phytochem.2026.114843_bib22","doi-asserted-by":"crossref","first-page":"443","DOI":"10.1016\/j.fitote.2019.03.024","article-title":"Stelleraguaianone B and C, two new sesquiterpenoids from Stellera chamaejasme L","volume":"134","author":"Jing","year":"2019","journal-title":"Fitoterapia"},{"key":"10.1016\/j.phytochem.2026.114843_bib23","doi-asserted-by":"crossref","first-page":"113","DOI":"10.1016\/j.intimp.2018.04.008","article-title":"A new flavonoid from Stellera chamaejasme L., stechamone, alleviated 2,4-dinitrochlorobenzene-induced atopic dermatitis-like skin lesions in a murine model","volume":"59","author":"Jo","year":"2018","journal-title":"Int. Immunopharmacol."},{"key":"10.1016\/j.phytochem.2026.114843_bib24","doi-asserted-by":"crossref","first-page":"2125","DOI":"10.1039\/C8RA09743G","article-title":"Isolation of maltol derivatives from Stellera chamaejasme and the anti-atopic properties of maltol on skin lesions in DNCB-stimulated mice","volume":"9","author":"Jo","year":"2019","journal-title":"RSC Adv."},{"key":"10.1016\/j.phytochem.2026.114843_bib25","doi-asserted-by":"crossref","DOI":"10.1016\/j.pscia.2023.100021","article-title":"Emerging role of antioxidants in Alzheimer's disease: insight into physiological, pathological mechanisms and management","volume":"2","author":"Kamaljeet","year":"2024","journal-title":"Pharm. Sci. Adv."},{"key":"10.1016\/j.phytochem.2026.114843_bib26","first-page":"1","article-title":"Water extract of Humulus japonicus improves age-related cognitive decline by inhibiting acetylcholinesterase activity and the acetylcholine signaling pathway","volume":"31","author":"Kim","year":"2025","journal-title":"Mol. Med. Rep."},{"key":"10.1016\/j.phytochem.2026.114843_bib27","doi-asserted-by":"crossref","first-page":"801","DOI":"10.1039\/C3OB42010H","article-title":"Design, synthesis and evaluation of novel tacrine\u2013rhein hybrids as multifunctional agents for the treatment of Alzheimer's disease","volume":"12","author":"Li","year":"2014","journal-title":"Org. Biomol. Chem."},{"key":"10.1016\/j.phytochem.2026.114843_bib28","doi-asserted-by":"crossref","first-page":"234","DOI":"10.1055\/s-2004-815540","article-title":"New lignans and cytotoxic constituents from Wikstroemia lanceolata","volume":"70","author":"Lin","year":"2004","journal-title":"Planta Med."},{"key":"10.1016\/j.phytochem.2026.114843_bib29","doi-asserted-by":"crossref","first-page":"4198","DOI":"10.1016\/j.bmc.2014.05.042","article-title":"Topoisomerase II inhibitors from the roots of Stellera chamaejasme L","volume":"22","author":"Liu","year":"2014","journal-title":"Bioorg. Med. Chem."},{"key":"10.1016\/j.phytochem.2026.114843_bib30","doi-asserted-by":"crossref","first-page":"184","DOI":"10.1097\/HM9.0000000000000118","article-title":"Chemical nature of metabolic activation of natural products in traditional Chinese medicines possibly associated with toxicities","volume":"4","author":"Liu","year":"2024","journal-title":"Acupunct. Herb. Med."},{"key":"10.1016\/j.phytochem.2026.114843_bib31","doi-asserted-by":"crossref","first-page":"2521","DOI":"10.1016\/S0024-3205(02)02034-9","article-title":"Acetylcholinesterase inhibitory activity of some Amaryllidaceae alkaloids and narcissus extracts","volume":"71","author":"L\u00f3pez","year":"2002","journal-title":"Life Sci."},{"key":"10.1016\/j.phytochem.2026.114843_bib32","doi-asserted-by":"crossref","first-page":"289","DOI":"10.1016\/j.phymed.2007.02.002","article-title":"Acetylcholinesterase inhibitors from plants","volume":"14","author":"Mukherjee","year":"2007","journal-title":"Phytomedicine"},{"key":"10.1016\/j.phytochem.2026.114843_bib33","doi-asserted-by":"crossref","first-page":"128","DOI":"10.1016\/j.phytochem.2013.04.012","article-title":"Acylated sucroses and acylated quinic acids analogs from the flower buds of Prunus mume and their inhibitory effect on melanogenesis","volume":"92","author":"Nakamura","year":"2013","journal-title":"Phytochemistry"},{"key":"10.1016\/j.phytochem.2026.114843_bib54","series-title":"Recent Advances in Natural Products Analysis","first-page":"621","article-title":"Analysis of carbohydrates (monosaccharides, polysaccharides)","author":"Niaz","year":"2020"},{"key":"10.1016\/j.phytochem.2026.114843_bib34","doi-asserted-by":"crossref","first-page":"129","DOI":"10.1016\/j.fitote.2019.02.017","article-title":"Antimicrobial guaianolide sesquiterpenoids from leaves of the Saudi Arabian plant Anvillea garcinii","volume":"134","author":"Perveen","year":"2019","journal-title":"Fitoterapia"},{"key":"10.1016\/j.phytochem.2026.114843_bib35","doi-asserted-by":"crossref","first-page":"10105","DOI":"10.1021\/acs.jpcb.7b06693","article-title":"Combining explicit quantum solvent with a polarizable continuum model","volume":"121","author":"Provorse Long","year":"2017","journal-title":"J. Phys. Chem. B"},{"key":"10.1016\/j.phytochem.2026.114843_bib36","doi-asserted-by":"crossref","first-page":"711","DOI":"10.1055\/s-0031-1298380","article-title":"Neolignans and sesquiterpenes from cell cultures of Stellera chamaejasme","volume":"78","author":"Qiao","year":"2012","journal-title":"Planta Med."},{"key":"10.1016\/j.phytochem.2026.114843_bib37","doi-asserted-by":"crossref","DOI":"10.1016\/S0076-6879(83)91010-8","article-title":"Reassessment of Ellman's reagent","author":"Riddles","year":"1983","journal-title":"Methods Enzymol."},{"key":"10.1016\/j.phytochem.2026.114843_bib38","first-page":"213","article-title":"Thymelaeaceae","volume":"13","author":"Wang","year":"2007","journal-title":"Flora China"},{"key":"10.1016\/j.phytochem.2026.114843_bib39","doi-asserted-by":"crossref","first-page":"7726","DOI":"10.3390\/molecules28237726","article-title":"Terpenoids from the roots of Stellera chamaejasme (L.) and their bioactivities","volume":"28","author":"Wu","year":"2023","journal-title":"Molecules"},{"key":"10.1016\/j.phytochem.2026.114843_bib40","doi-asserted-by":"crossref","DOI":"10.1016\/j.fitote.2022.105171","article-title":"Chamaejasnoids A-E, a 2,3-seco-guaiane sesquiterpenoid with a 5\/6\/7 bridged ring system and related metabolites from Stellera chamaejasme L","volume":"158","author":"Wu","year":"2022","journal-title":"Fitoterapia"},{"key":"10.1016\/j.phytochem.2026.114843_bib41","doi-asserted-by":"crossref","DOI":"10.1080\/21505594.2025.2479103","article-title":"Multifaceted quorum-sensing inhibiting activity of 3-(Benzo[d][1,3]dioxol-4-yl)oxazolidin-2-one mitigates Pseudomonas aeruginosa virulence","volume":"16","author":"Wu","year":"2025","journal-title":"Virulence"},{"key":"10.1016\/j.phytochem.2026.114843_bib42","series-title":"In-silico Discovery of the Hapten-based Interaction Between Idiosyncratic Hepatotoxic Ingredients of Polygonum multiflorum and HLA-B\u221735:01","author":"Xiao","year":"2025"},{"key":"10.1016\/j.phytochem.2026.114843_bib43","doi-asserted-by":"crossref","first-page":"2195","DOI":"10.1021\/acs.jnatprod.8b00386","article-title":"Structurally diverse sesquiterpenoids from the endangered ornamental plant Michelia shiluensis","volume":"81","author":"Xiong","year":"2018","journal-title":"J. Nat. Prod."},{"key":"10.1016\/j.phytochem.2026.114843_bib44","first-page":"192","article-title":"Animal models of Alzheimer's disease: preclinical insights and challenges","volume":"2","author":"Xu","year":"2023","journal-title":"Acta Mater. Medica"},{"key":"10.1016\/j.phytochem.2026.114843_bib45","doi-asserted-by":"crossref","first-page":"2712","DOI":"10.1021\/acs.jnatprod.5b00660","article-title":"Stelleralides D\u2013J and anti-HIV daphnane diterpenes from Stellera chamaejasme","volume":"78","author":"Yan","year":"2015","journal-title":"J. Nat. Prod."},{"key":"10.1016\/j.phytochem.2026.114843_bib46","doi-asserted-by":"crossref","first-page":"61","DOI":"10.1016\/j.phytochem.2014.07.013","article-title":"Phytotoxic flavonoids from roots of Stellera chamaejasme L. (Thymelaeaceae)","volume":"106","author":"Yan","year":"2014","journal-title":"Phytochemistry"},{"key":"10.1016\/j.phytochem.2026.114843_bib47","doi-asserted-by":"crossref","first-page":"1162","DOI":"10.1016\/j.bmcl.2019.03.031","article-title":"Further sesquiterpenoids from the rhizomes of Homalomena occulta and their anti-inflammatory activity","volume":"29","author":"Yang","year":"2019","journal-title":"Bioorg. Med. Chem. Lett."},{"key":"10.1016\/j.phytochem.2026.114843_bib48","article-title":"The food and medicine homologous Chinese medicine from Leguminosae species: a comprehensive review on bioactive constituents with neuroprotective effects on nervous system","volume":"2","author":"Ye","year":"2025","journal-title":"Food Med. Homol."},{"key":"10.1016\/j.phytochem.2026.114843_bib49","doi-asserted-by":"crossref","DOI":"10.1016\/j.phytochem.2023.113588","article-title":"Diversity of sesquiterpenoids from Stellera chamaejasme with neuroprotective effects","volume":"208","author":"Yuan","year":"2023","journal-title":"Phytochemistry"},{"key":"10.1016\/j.phytochem.2026.114843_bib55","doi-asserted-by":"crossref","first-page":"1225","DOI":"10.1055\/s-2007-981590","article-title":"Investigation of the hydrolysis of ginsenosides by high performance liquid chromatography-electrospray lonization mass spectrometry","volume":"73","author":"Zhang","year":"2007","journal-title":"Planta. Med."},{"key":"10.1016\/j.phytochem.2026.114843_bib50","first-page":"1","article-title":"Simultaneous determination of nine compounds from the roots of Euphorbia fischeriana, Euphorbia ebracteolata and Stellera chamaejasme and their anti-tumor activities","author":"Zhang","year":"2024","journal-title":"J. Asian Nat. Prod. Res."},{"key":"10.1016\/j.phytochem.2026.114843_bib51","doi-asserted-by":"crossref","DOI":"10.1016\/j.ecoenv.2020.111424","article-title":"Inflammatory lncRNA AK039862 regulates paraquat-inhibited proliferation and migration of microglial and neuronal cells through the Pafah1b1\/Foxa1 pathway in co-culture environments","volume":"208","author":"Zhang","year":"2021","journal-title":"Ecotoxicol. Environ. Saf."},{"key":"10.1016\/j.phytochem.2026.114843_bib52","first-page":"548","article-title":"Mechanism of action of protopanaxadiol ginsenosides on hepatocellular carcinoma and network pharmacological analysis","volume":"16","author":"Zhou","year":"2024","journal-title":"Chin. Herb. Med."}],"container-title":["Phytochemistry"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0031942226000762?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0031942226000762?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2026,4,13]],"date-time":"2026-04-13T16:32:28Z","timestamp":1776097948000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0031942226000762"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,7]]},"references-count":55,"alternative-id":["S0031942226000762"],"URL":"https:\/\/doi.org\/10.1016\/j.phytochem.2026.114843","relation":{},"ISSN":["0031-9422"],"issn-type":[{"value":"0031-9422","type":"print"}],"subject":[],"published":{"date-parts":[[2026,7]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Guaiane-type sesquiterpenoids with acetylcholinesterase inhibitory activities from the roots of Stellera chamaejasme","name":"articletitle","label":"Article Title"},{"value":"Phytochemistry","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.phytochem.2026.114843","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2026 Published by Elsevier Ltd.","name":"copyright","label":"Copyright"}],"article-number":"114843"}}