Phytochemistry LettersPub Date : 2026-02-01Epub Date: 2026-01-08DOI: 10.1016/j.phytol.2025.104108
Qiongyan Fang , Yafang Ding , Xue Wu , Xinyi Yu , Xuting Lan , Jie Wang
{"title":"A pair of polyketide lactone enantiomers from the South China Sea sponge Hippospongia lachne","authors":"Qiongyan Fang , Yafang Ding , Xue Wu , Xinyi Yu , Xuting Lan , Jie Wang","doi":"10.1016/j.phytol.2025.104108","DOIUrl":"10.1016/j.phytol.2025.104108","url":null,"abstract":"<div><div>(±)-Hippetitone, a pair of polyketide lactone enantiomers, was isolated from the South China Sea sponge <em>Hippospongia lachne</em>. The planar structures and relative configurations of these enantiomers were elucidated through HRESIMS and NMR data analysis. The enantiomers were successfully resolved using a normal-phase chiral column. Their absolute configurations were determined by comparing the calculated electronic circular dichroism (ECD) spectra with the experimentally obtained ones. In an in vitro anti-inflammatory assay, the enantiomers markedly reduced LPS-induced IL-6 production in RAW 264.7 cells at 10 <em>μ</em>M, with inhibition rates of 71.9 % and 64.4 %, respectively.</div></div>","PeriodicalId":20408,"journal":{"name":"Phytochemistry Letters","volume":"71 ","pages":"Article 104108"},"PeriodicalIF":1.4,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145925095","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Phytochemistry LettersPub Date : 2026-02-01Epub Date: 2026-01-05DOI: 10.1016/j.phytol.2026.104111
Ling Li , Lin Feng , Lihua Peng , Weilin Qiao , Wei Li , De-an Guo
{"title":"Two new naphthopyrones and a new prenylisoflavone from Berchemia lineata","authors":"Ling Li , Lin Feng , Lihua Peng , Weilin Qiao , Wei Li , De-an Guo","doi":"10.1016/j.phytol.2026.104111","DOIUrl":"10.1016/j.phytol.2026.104111","url":null,"abstract":"<div><div>Two new naphthopyrones, berchelineatones A and B (<strong>1</strong> and <strong>2</strong>), together with a new prenylisoflavone (<strong>3</strong>), were isolated from <em>Berchemia lineata</em>. Their structures were primarily determined by high-resolution mass spectrometry, NMR spectroscopy, and X-ray crystallographic data analysis. Notably, compounds <strong>1</strong> and <strong>2</strong> exhibited potent inhibition on nitric oxide (NO) production induced by lipopolysaccharide (LPS) in RAW264.7 macrophages, with IC<sub>50</sub> values of 2.52 and 2.06 <em>μ</em>M, respectively.</div></div>","PeriodicalId":20408,"journal":{"name":"Phytochemistry Letters","volume":"71 ","pages":"Article 104111"},"PeriodicalIF":1.4,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145925096","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Bioinformatics-based discovery of a new norsesquiterpenoid from agarwood targeting CHRM2 and regulating the PI3K-Akt pathway in liver cancer","authors":"Zi-Xiao Jiang, Jian Feng, Wen-Cheng Hou, Mei-Ran Wang, Shu-Nan Zhang, Hao-Jie Liang, Yang-Yang Liu","doi":"10.1016/j.phytol.2025.104101","DOIUrl":"10.1016/j.phytol.2025.104101","url":null,"abstract":"<div><div>A novel norsesquiterpenoid isolated from agarwood, features a rare oxaspiro[4.5]decane structure. It selectively inhibits human liver cancer cell proliferation (SMMC-7721) with an IC<sub>50</sub> of 18.82 μM, while showing weaker effects on gastric and ovarian cancer cells. Network pharmacology and molecular docking identified muscarinic acetylcholine receptor M2 (CHRM2) as a target, suggesting compound 1 disrupts the PI3K-Akt pathway. ADMET predictions indicate favorable pharmacokinetics. These findings position compound 1 as a promising CHRM2 antagonist for liver cancer therapy, highlighting the potential of natural product-based drug discovery.</div></div>","PeriodicalId":20408,"journal":{"name":"Phytochemistry Letters","volume":"71 ","pages":"Article 104101"},"PeriodicalIF":1.4,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145786882","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Phytochemistry LettersPub Date : 2026-02-01Epub Date: 2026-01-02DOI: 10.1016/j.phytol.2025.104099
Payar Hossain , Md. Hossain Rasel , Md. Jahirul Islam Mamun , Md. Abdul Alim , S.M. Naim Uddin
{"title":"Exploring the therapeutic potentials of Bischofia javanica: Evidence of analgesic, antidiarrheal, and hypoglycemic activities","authors":"Payar Hossain , Md. Hossain Rasel , Md. Jahirul Islam Mamun , Md. Abdul Alim , S.M. Naim Uddin","doi":"10.1016/j.phytol.2025.104099","DOIUrl":"10.1016/j.phytol.2025.104099","url":null,"abstract":"<div><div><em>Bischofia javanica</em> (Euphorbiaceae) has been used for a long time to manage ulcers, bone fractures, dislocations, inflammation, and tuberculosis. This study evaluated the analgesic, antidiarrheal, and hypoglycemic effects of the methanolic fruit extract (MFBJ) and n-hexane fraction (NHF) of the plant. At 400 mg/kg, both reduced pain in the writhing test (56.74 % and 51.63 %; p < 0.001) and prolonged hot plate response times. MFBJ also showed stronger antidiarrheal (68.65 %) and hypoglycemic (5.92 ± 0.03 mmol/L; p < 0.001) effects. Findings suggest therapeutic potential, warranting further characterisation of bioactive compounds.</div></div>","PeriodicalId":20408,"journal":{"name":"Phytochemistry Letters","volume":"71 ","pages":"Article 104099"},"PeriodicalIF":1.4,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145883576","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Phytochemistry LettersPub Date : 2026-02-01Epub Date: 2026-01-14DOI: 10.1016/j.phytol.2025.104105
Pragati Gupta , Kamal Dev , Chirag N. Patel , Gurjot Kaur
{"title":"Harnessing phytoconstituents to treat COVID-19 triggered acute respiratory distress syndrome: Insights from network pharmacology, and molecular modeling","authors":"Pragati Gupta , Kamal Dev , Chirag N. Patel , Gurjot Kaur","doi":"10.1016/j.phytol.2025.104105","DOIUrl":"10.1016/j.phytol.2025.104105","url":null,"abstract":"<div><div>Developing effective therapies for COVID-19-triggered acute respiratory distress syndrome (ARDS) remains a major challenge. Inflammatory signaling molecules have emerged as promising druggable targets. This study employed an integrated network pharmacology and molecular modeling strategy to investigate the anti-inflammatory phytoconstituents (PCs) against COVID-19-triggered ARDS. Putative targets of PCs and disease genes were retrieved from multiple databases, followed by PPI and enrichment analyses, along with network visualization. Network pharmacology identified key phytoconstituents: 1-dehydro-6-gingerol, apigenin-7-glucoside, and quercetin, and crucial targets including EGFR, JAK2, RELA, HSP90AA1, and PIK3CA from the F-B-PCs-T-P network. Enriched inflammatory pathways included Toll-like receptor, PI3K-Akt, NOD-like receptor, and HIF-1 signaling. Molecular docking and dynamics simulations further confirmed stable, high-affinity interactions between these targets and selected PCs. Specifically, apigenin-7-glucoside showed strong binding with JAK2 and RELA, while quercetin favoured JAK2 and EGFR. Overall, the findings underscore the therapeutic potential of these PCs and validate integrated <em>in silico</em> approaches (in) drug discovery.</div></div>","PeriodicalId":20408,"journal":{"name":"Phytochemistry Letters","volume":"71 ","pages":"Article 104105"},"PeriodicalIF":1.4,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145976718","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Phytochemistry LettersPub Date : 2026-02-01Epub Date: 2025-12-06DOI: 10.1016/j.phytol.2025.104093
Bin Wang , Gang Ke , Yue-Ping Lan , En Yuan , Pu-Zhao Zhang
{"title":"Five new cassane diterpenoids from Pterolobium macropterum","authors":"Bin Wang , Gang Ke , Yue-Ping Lan , En Yuan , Pu-Zhao Zhang","doi":"10.1016/j.phytol.2025.104093","DOIUrl":"10.1016/j.phytol.2025.104093","url":null,"abstract":"<div><div>Five previously undescribed tetracyclic cassane-type diterpenoids with an <em>α</em>, <em>β</em>-unsaturated butenolide moiety were isolated from the seeds of <em>Pterolobium macropterum</em> and structurally characterized by a combination of IR, UV, HRESIMS, 1D and 2D NMR spectroscopic data. The cytotoxicity of all isolated compounds was evaluated against human glioma U251 cells and U-87 MG cells. Compound <strong>1</strong> exhibited moderate activity with IC<sub>50</sub> values of 22.78 <em>μ</em>M in human glioma U251 cells and 73.68 <em>μ</em>M in U-87 MG cells, respectively.</div></div>","PeriodicalId":20408,"journal":{"name":"Phytochemistry Letters","volume":"71 ","pages":"Article 104093"},"PeriodicalIF":1.4,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145682294","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Phytochemistry LettersPub Date : 2026-02-01Epub Date: 2026-01-30DOI: 10.1016/S1874-3900(26)00019-4
{"title":"Announcements of the Phytochemical Society of Europe","authors":"","doi":"10.1016/S1874-3900(26)00019-4","DOIUrl":"10.1016/S1874-3900(26)00019-4","url":null,"abstract":"","PeriodicalId":20408,"journal":{"name":"Phytochemistry Letters","volume":"71 ","pages":"Article 104129"},"PeriodicalIF":1.4,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146077317","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Phytochemistry LettersPub Date : 2026-02-01Epub Date: 2025-12-13DOI: 10.1016/j.phytol.2025.104095
Bel Youssouf G. Mountessou , Gesquiere Laure M. Tiani , Joseph Tchamgoue , Rukesh Maharjan , Aron Trucksess , Rainer Kalscheuer , Muhammad I. Choudhary , Simeon F. Kouam
{"title":"Cytotoxic secondary metabolites from submerged cultures of Chaetomium sp. isolated from decaying wood","authors":"Bel Youssouf G. Mountessou , Gesquiere Laure M. Tiani , Joseph Tchamgoue , Rukesh Maharjan , Aron Trucksess , Rainer Kalscheuer , Muhammad I. Choudhary , Simeon F. Kouam","doi":"10.1016/j.phytol.2025.104095","DOIUrl":"10.1016/j.phytol.2025.104095","url":null,"abstract":"<div><div>This study aimed to investigate the chemical constituents of a <em>Chaetomium</em> strain (CECA 170) isolated from decaying wood and to assess their antimicrobial and cytotoxic activities. One previously unreported macrolide (<strong>1</strong>), one ketone-derived isoxazolidine (<strong>2</strong>), and one naturally occurring chromone (<strong>3</strong>), along with four known metabolites (<strong>4 −7</strong>), were isolated from the submerged culture of <em>Chaetomium</em> sp. The structures of the new compounds were established by extensive spectroscopic and spectrometric analyses (NMR, MS). The known compounds were identified by comparing their experimental data with previously published literature. Compound <strong>1</strong> exhibited cytotoxic activities against human breast cancer cells (MCF-7) and HeLa cervical cancer cells, with IC<sub>50</sub> values of 7.84 µM and 18.7 µM, respectively. In contrast, compound <strong>2</strong> displayed stronger cytotoxicity against HeLa cells (IC<sub>50</sub> = 14.3 µM) than MCF-7 cells (IC<sub>50</sub> = 18.5 µM). However, none of the tested compounds showed antimicrobial activity on the evaluated microorganisms. These results underscore the potential of fungi from underexplored niches, like decaying wood, for the discovery of new chemotherapeutic leads.</div></div>","PeriodicalId":20408,"journal":{"name":"Phytochemistry Letters","volume":"71 ","pages":"Article 104095"},"PeriodicalIF":1.4,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145737441","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Phytochemistry LettersPub Date : 2026-02-01Epub Date: 2025-11-26DOI: 10.1016/j.phytol.2025.104087
Ahmed H. Eissa, Helnan A. Aboseada, Seif-Eldin N. Ayyad
{"title":"Sesquiterpenoids with antibacterial and cytotoxic activities from the soft coral Litophyton arboreum","authors":"Ahmed H. Eissa, Helnan A. Aboseada, Seif-Eldin N. Ayyad","doi":"10.1016/j.phytol.2025.104087","DOIUrl":"10.1016/j.phytol.2025.104087","url":null,"abstract":"<div><div>A chemical investigation of the CH<sub>2</sub>Cl<sub>2</sub>/MeOH extract of the Red Sea soft coral <em>Litophyton arboreum</em> led to the isolation of a new eudesmane-type sesquiterpenoid, 11-acetoxy-5<em>β</em>,8<em>β</em>-epidioxy-6-eudesmene (<strong>1</strong>), together with three known analogues (<strong>2</strong>–<strong>4</strong>)<strong>.</strong> The structures of the isolated metabolites were elucidated using comprehensive spectroscopic techniques, including NMR and HRESIMS, supported by detailed comparison with reported data of related analogues. The antiproliferative properties of metabolites <strong>1</strong>–<strong>4</strong> were evaluated against Hep G2 and NCI-H1299 human cancer cell lines. Among them, compounds <strong>1</strong> and <strong>4</strong> exhibited weak cytotoxic activity against NCI-H1299, with IC<sub>50</sub> values of 39.8 ± 0.93 and 43.1 ± 0.61 μM, respectively, compared to doxorubicin as a reference. The antibacterial screening revealed that the isolated sesquiterpenoids displayed weak to moderate activity, with inhibition observed at relatively high concentrations (50–150 µg/mL). Compounds <strong>1</strong>, <strong>3</strong>, and <strong>4</strong> showed selective inhibition of <em>Bacillus cereus</em> and <em>Staphylococcus aureus</em>, whereas Gram-negative bacteria were less affected. Although MIC values could not be determined owing to limited sample availability, the results suggest a weak but measurable antibacterial potential consistent with other eudesmane-type sesquiterpenoids. The combined cytotoxic and antibacterial data indicate that these metabolites may serve as useful scaffolds for future structure–activity and mechanistic studies.</div></div>","PeriodicalId":20408,"journal":{"name":"Phytochemistry Letters","volume":"71 ","pages":"Article 104087"},"PeriodicalIF":1.4,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145616957","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Phytochemistry LettersPub Date : 2026-02-01Epub Date: 2025-11-21DOI: 10.1016/j.phytol.2025.104084
Xu-Ping Zhang, Xue-Kai Zhao, Wei-Guang Wang, Qian-Qian Yin, Lu Gao
{"title":"New γ-lactams from Paraphoma sp. AC-G1 isolated from Artemisia argyi","authors":"Xu-Ping Zhang, Xue-Kai Zhao, Wei-Guang Wang, Qian-Qian Yin, Lu Gao","doi":"10.1016/j.phytol.2025.104084","DOIUrl":"10.1016/j.phytol.2025.104084","url":null,"abstract":"<div><div>Phomalactones A (<strong>1</strong>) and B (<strong>2</strong>), two new <em>γ</em>-lactam derivatives, and one known compound, namely, phaeosphaeride A (<strong>3</strong>), were isolated from <em>Paraphoma</em> sp. AC-G1, an endophytic fungus isolated from <em>Artemisia argyi</em>. Their structures were determined using 1D and 2D NMR spectra, HRESIMS, and optical rotation measurements. Compounds <strong>1–3</strong> were assessed for their antimicrobial activities on <em>Ralstonia solanacearum</em>, <em>Fusarium oxysporum</em>, and <em>Alternaria alternata</em>. The results showed that compounds <strong>1</strong> and <strong>3</strong> exhibited significant inhibition on <em>F. oxysporum</em>.</div></div>","PeriodicalId":20408,"journal":{"name":"Phytochemistry Letters","volume":"71 ","pages":"Article 104084"},"PeriodicalIF":1.4,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145570901","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}