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Chemical constituents of the seeds of Citrus reticulata and their bioactivity. 柑橘种子化学成分及其生物活性研究。
IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Pub Date : 2026-02-09 DOI: 10.1080/10286020.2026.2625940
Meng-Jue Rui, Hong-Tao Xu, Jun-Jie Yang, Gui-Xin Chou

Four new limonoids (1-4), reticulactone A (1), 21,23-dihydro-23-ethoxy-21-oxolimonin (2), tetrahydro-20,22-dihydroxy-21,23-diethoxy-nomilin (3), and dasycarinone B (4), as well as 11 known limonoids and one known carbolic acid, were isolated from the EtOH extract of the seeds of Citrus reticulata Blanco. The inhibitory effects of 15 limonoids (1-15) on the proliferation of HepG2 liver cancer cells were evaluated using the CCK-8 assay. Based on their structural characteristics, the results revealed that the typical limonoid compounds 2, 5, 10, and 12 exhibited stronger cytotoxicity compared to other limonoid compounds. Notably, the novel compound 2 demonstrated the strongest cytotoxic activity (IC50 = 18.24 ± 2.78 μM).

从柑橘种子的乙醇提取物中分离得到了4个新的柠檬素(1-4),分别为网状内酯A(1)、21,23-二氢-23-乙氧基-21-oxolimonin(2)、四氢-20,22-二羟基-21,23-二氧基-nomilin(3)、dasycarinone B(4),以及11个已知的柠檬素和1个已知的碳酸。CCK-8法观察15种柠檬素(1-15)对HepG2肝癌细胞增殖的抑制作用。结果表明,典型的类柠檬化合物2、5、10和12比其他类柠檬化合物具有更强的细胞毒性。其中,化合物2具有最强的细胞毒活性(IC50 = 18.24±2.78 μM)。
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引用次数: 0
New α-glucosidase inhibitory isoflavone derivatives from the leaves of Placolobium vietnamense. 新α-葡萄糖苷酶抑制异黄酮衍生物的研究。
IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Pub Date : 2026-02-05 DOI: 10.1080/10286020.2026.2625179
Tuyet T N Huynh, Huong T M Nguyen, Quyen H N Tran, Tuyet T A Nguyen, Thuy T L Nguyen, Trung V Phung, Jirapast Sichaem, Lien T M Do

A new isoflavone-quinone, placovinone E (1), and a new natural isoflavone, placovinone F (2), together with four known isoflavones (3-6), were isolated from the leaves of P. vietnamense. The chemical structures of all isolated compounds were elucidated using spectroscopic techniques (NMR and HRESIMS) and confirmed by comparison with literature data. All isolated compounds were evaluated for their α-glucosidase and xanthine oxidase inhibitory activities. Among them, compound 1 exhibited the strongest α-glucosidase inhibition (IC50 21.6 ± 1.04 µM), which was markedly more potent than the positive control, acarbose (IC50 156.2 ± 5.43 µM). In addition, compound 1 showed the highest xanthine oxidase inhibitory activity (IC50 32.8 ± 0.08 µM), although it remained considerably less potent than the positive control, allopurinol (IC50 2.45 ± 0.01 µM).

从越南参叶中分离到了一种新的异黄酮-醌类化合物placovinone E(1)和一种新的天然异黄酮placovinone F(2),以及四种已知的异黄酮(3-6)。所有分离化合物的化学结构都通过波谱技术(NMR和hresms)进行了鉴定,并与文献资料进行了比较。所有分离得到的化合物均具有α-葡萄糖苷酶和黄嘌呤氧化酶抑制活性。其中,化合物1对α-葡萄糖苷酶的抑制作用最强(IC50为21.6±1.04µM),明显高于阳性对照阿卡波糖(IC50为156.2±5.43µM)。此外,化合物1显示出最高的黄嘌呤氧化酶抑制活性(IC50为32.8±0.08µM),但其抑制活性仍明显低于阳性对照别嘌呤醇(IC50为2.45±0.01µM)。
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引用次数: 0
Transcriptomic profile and gene expression of human breast cancer cell lines treated with herbal extract of clinacanthus nutans leaves. 棘棘叶提取物处理人乳腺癌细胞系的转录组学特征和基因表达。
IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Pub Date : 2026-02-05 DOI: 10.1080/10286020.2026.2625174
Zaleha Md Toha, Norhasyimah Haron, Kristine Sandra Pey Adum, Nik Nur Syazni Nik Mohamed Kamal, Melati Khairuddean, Hasni Arsad

Clinacanthus nutans (CN) is traditionally used in medicine, but its apoptotic effects on breast cancer cells remain unclear. This study investigated the apoptotic potential of CN dichloromethane leaf extract (CNDCM) in MCF-7 cells using RNA-Seq analysis. Differential gene expression analysis identified 843 genes, with 395 upregulated and 448 downregulated. Gene ontology and KEGG pathway analyses revealed apoptosis-related pathways. Key apoptosis-associated genes, including ALDH3A1, CYP1A1, NOS3, MT1X, and CES1, were further validated by RT-qPCR. These findings suggest CNDCM as a potential candidate for breast cancer therapy.

cnan (Clinacanthus nutans)传统上用于医学,但其对乳腺癌细胞的凋亡作用尚不清楚。本研究采用RNA-Seq方法研究CN二氯甲烷叶提取物(CNDCM)对MCF-7细胞的凋亡潜力。差异基因表达分析鉴定出843个基因,其中上调395个,下调448个。基因本体和KEGG通路分析揭示了凋亡相关通路。RT-qPCR进一步验证凋亡相关关键基因ALDH3A1、CYP1A1、NOS3、MT1X、CES1。这些发现表明CNDCM是乳腺癌治疗的潜在候选药物。
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引用次数: 0
Survey of natural products reported by Asian research groups in 2024. 2024年亚洲研究小组报告的天然产物调查。
IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Pub Date : 2026-02-05 DOI: 10.1080/10286020.2026.2617381
Qian-Ru Wang, Shu-Yang Wang, Shuang-Gang Ma, Shi-Shan Yu
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引用次数: 0
Antifungal secondary metabolites from a mangrove-derived fungus Daldinia eschscholtzii TGM23. 红树源真菌Daldinia eschscholtzii TGM23抗真菌次生代谢物研究。
IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Pub Date : 2026-02-04 DOI: 10.1080/10286020.2026.2620992
Xiu Gong, Wei-Kang Chen, Miao Yu, Shi-Ji Chen, Jue-Ying Shi, Yi-Kang Qiu, Guo-Lei Huang, Cai-Juan Zheng

One new compound daldiniaone A (1), along with six known compounds 1-(2,6-dihydroxyphenyl)ethan-1-one (2), 1-(2,6-dihydroxyphenyl)butan-1-one (3), penicilliode B (4), (4-hydroxy-3-methoxyphenyl)acetic acid (5), 2-(4-methoxyphenyl)acetic acid (6), and 2-(2-hydroxyethyl)phenol (7), were obtained from the EtOAc extract of the mangrove-derived fungus Daldinia eschscholtzii TGM23. Their structures were characterized by comprehensive spectral analysis, including nuclear magnetic resonance (NMR), high resolution electrospray ionization mass spectroscopy (HR-ESI-MS), and electronic circular dichroism (ECD) spectra. All the isolated compounds were tested for their inhibitory activity against three plant pathogenic fungi. Compound 6 showed inhibitory activity against Phytophthora capsici, with the EC50 value of 106.5 μg/ml. Compound 7 exhibited inhibitory activity against Botrytis cinerea with the EC50 value of 86.8 μg/ml.

从红树真菌Daldinia eschscholtzii TGM23的EtOAc提取物中分离得到1个新化合物daldiniaone A(1)和6个已知化合物1-(2,6-二羟基苯基)e- 1- One(2)、1-(2,6-二羟基苯基)丁醇-1- One(3)、penicilliode B(4)、(4-羟基-3-甲氧基苯基)乙酸(5)、2-(4-甲氧基苯基)乙酸(6)和2-(2-羟乙基)苯酚(7)。通过核磁共振(NMR)、高分辨率电喷雾质谱(HR-ESI-MS)和电子圆二色性(ECD)等综合光谱分析对其结构进行了表征。对分离得到的化合物进行了对3种植物病原真菌的抑菌活性测定。化合物6对辣椒疫霉具有抑制活性,EC50值为106.5 μg/ml。化合物7对灰霉病菌具有抑制活性,EC50值为86.8 μg/ml。
{"title":"Antifungal secondary metabolites from a mangrove-derived fungus <i>Daldinia eschscholtzii</i> TGM23.","authors":"Xiu Gong, Wei-Kang Chen, Miao Yu, Shi-Ji Chen, Jue-Ying Shi, Yi-Kang Qiu, Guo-Lei Huang, Cai-Juan Zheng","doi":"10.1080/10286020.2026.2620992","DOIUrl":"https://doi.org/10.1080/10286020.2026.2620992","url":null,"abstract":"<p><p>One new compound daldiniaone A (<b>1</b>), along with six known compounds 1-(2,6-dihydroxyphenyl)ethan-1-one (<b>2</b>), 1-(2,6-dihydroxyphenyl)butan-1-one (<b>3</b>), penicilliode B (<b>4</b>), (4-hydroxy-3-methoxyphenyl)acetic acid (<b>5</b>), 2-(4-methoxyphenyl)acetic acid (<b>6</b>), and 2-(2-hydroxyethyl)phenol (<b>7</b>), were obtained from the EtOAc extract of the mangrove-derived fungus <i>Daldinia eschscholtzi</i>i TGM23. Their structures were characterized by comprehensive spectral analysis, including nuclear magnetic resonance (NMR), high resolution electrospray ionization mass spectroscopy (HR-ESI-MS), and electronic circular dichroism (ECD) spectra. All the isolated compounds were tested for their inhibitory activity against three plant pathogenic fungi. Compound <b>6</b> showed inhibitory activity against <i>Phytophthora capsici</i>, with the EC<sub>50</sub> value of 106.5 μg/ml. Compound <b>7</b> exhibited inhibitory activity against <i>Botrytis cinerea</i> with the EC<sub>50</sub> value of 86.8 μg/ml.</p>","PeriodicalId":15180,"journal":{"name":"Journal of Asian Natural Products Research","volume":" ","pages":"1-8"},"PeriodicalIF":1.3,"publicationDate":"2026-02-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146113155","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
An integrative strategy for comprehensive determination of nineteen constituents from Eupatorii Herba and application in pharmacokinetic study by combing UHPLC-QTRAP-MS/MS with gC-MS. UHPLC-QTRAP-MS/MS与gC-MS相结合综合测定冬补药材中19种成分及其在药动学研究中的应用
IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Pub Date : 2026-01-31 DOI: 10.1080/10286020.2026.2617377
Kai-Li Zhang, Zi-Jing Zhang, Zhou-Jing Feng, Ye Shang, Yan Feng, Na Zheng, Lin-Chang Fan, Ya-Meng Zhu, Hui-Zi Ouyang, Jun He

This study developed an integrated ultra-high performance liquid chromatography triple quadrupole linear ion trap tandem mass spectrometry/tandem mass spectrometry (UHPLC-QTRAP-MS/MS) with gas chromatography-mass spectrometry (GC-MS) strategy to quantify 19 constituents of Eupatorii Herba (EH) in rat plasma. The validated method demonstrated acceptable precision (RSD < 13.86%), accuracy (-12.05 to 11.81%), extraction recovery (83.25-116.50%), matrix effect (85.14-115.36%; RSD < 14.10%), and stability (RSD < 13.26%). Key pharmacokinetic findings revealed rapid absorption for all detected analytes, with melilotoside, o-acetyl-p-cresol, and thymol exhibiting the highest systemic exposure. This work provided a validated analytical foundation for further pharmacological research on EH.

本研究建立了一种集成的超高效液相色谱-三重四极杆线性离子阱串联质谱/串联质谱(UHPLC-QTRAP-MS/MS)和气相色谱-质谱(GC-MS)方法,对大鼠血浆中冬芪(EH)的19种成分进行定量分析。验证方法精密度(RSD < 13.86%)、准确度(-12.05 ~ 11.81%)、提取回收率(83.25 ~ 116.50%)、基质效应(85.14 ~ 115.36%,RSD < 14.10%)、稳定性(RSD < 13.26%)均可接受。关键的药代动力学结果显示,所有检测到的分析物都能快速吸收,麝香草苷、邻乙酰-对甲酚和百里酚显示出最高的全身暴露。本研究为EH的进一步药理研究提供了有效的分析基础。
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引用次数: 0
Steroidal glycosides from Tylophora ovata with anti-inflammatory and radical scavenging activities. 具有抗炎和清除自由基活性的卵形霉甾体苷。
IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Pub Date : 2026-01-24 DOI: 10.1080/10286020.2025.2608815
Bing Shao, Hui Wang, Yu Miao, Qing-Jie Zhao, Jie Ren

A chemical investigation on 80% ethanol extract from the whole plants of Tylophora ovata afforded two new C21 steroidal glycosides, ovatacosides A and B (1 and 2). Structural elucidation of both compounds were performed by spectral methods such as 1D and 2D (1H-1H COSY, HMQC, and HMBC) NMR spectroscopy and high resolution mass spectrometry. The isolated components were evaluated in vitro for anti-inflammatory activities against COX-1 and COX-2 and radical scavenging potential using DPPH test. Consequently, 1 exhibited modest selective inhibition on COX-1 (61.9%) at the concentration of 100 μM and significant DPPH scavenging activity (IC50 = 42.9 μM) comparable with positive control Trolox (IC50 = 44.2 μM).

对卵形霉全株80%乙醇提取物进行化学研究,得到两种新的C21甾体苷:卵形霉苷A和卵形霉苷B(1和2)。通过1D和2D (1H-1H COSY, HMQC和HMBC) NMR波谱和高分辨率质谱等光谱方法对两种化合物进行了结构解析。采用DPPH试验对分离得到的各组分体外抗COX-1和COX-2活性及自由基清除能力进行评价。结果表明,在100 μM浓度下,1对COX-1表现出适度的选择性抑制(61.9%),并具有显著的DPPH清除活性(IC50 = 42.9 μM),与阳性对照Trolox (IC50 = 44.2 μM)相当。
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引用次数: 0
Signal pathway and active compounds of Penicillium griseofulvum against triple-negative breast cancer. 灰黄青霉菌抗三阴性乳腺癌的信号通路及活性物质研究。
IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Pub Date : 2026-01-23 DOI: 10.1080/10286020.2026.2615671
Di Li, Jun-Guo Huang, Cheng-Yun Huang, Bai-Hui Lu, Jing Li, Wen-Jing Wang, Xiao-Long Yang

Triple-negative breast cancer (TNBC) is a type of breast cancer that has a high rate of growth and metastasis. In this study, the liquid fermentation product (EX-9) of Penicillium griseofulvum, an endophytic fungus derived from the medicinal plant Delphinium grandiflorum L., has exhibited significant anti-cancer activity against TNBC. We investigated the therapeutic effects and potential mechanisms of EX-9 on TNBC both in vivo and in vitro. Our findings demonstrated that EX-9 exhibited remarkable efficacy against TNBC both in vivo and in vitro, while showing negligible toxicity. The potential mechanism for its anti-TNBC effect involved the inhibition of the PI3K/Akt signaling pathway. Additionally, we employed liquid chromatography-mass spectrometry (LC-MS) technology and network pharmacology methods to uncover the potential pharmacological substance basis of EX-9 in combating TNBC.

三阴性乳腺癌(TNBC)是一种具有高生长和转移率的乳腺癌。在本研究中,来源于药用植物三角飞蓟马的内生真菌青霉菌(Penicillium grisiseofulvum)的液体发酵产物(EX-9)显示出显著的抗癌活性。我们在体内和体外研究了EX-9对TNBC的治疗作用和可能的机制。我们的研究结果表明,EX-9在体内和体外对TNBC都有显著的疗效,而毒性可以忽略不计。其抗tnbc作用的潜在机制涉及抑制PI3K/Akt信号通路。此外,我们还利用液相色谱-质谱(LC-MS)技术和网络药理学方法揭示了EX-9抗TNBC的潜在药理物质基础。
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引用次数: 0
Antimelanogenesis and antioxidant activity of Broussonetia papyrifera leaf extract fermentation broth. 纸莎草叶提取物发酵液的抗黑色素生成及抗氧化活性。
IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Pub Date : 2026-01-19 DOI: 10.1080/10286020.2026.2613432
Bo Dou, Rui-Qi Wu, Xiao-Lai Ma, Xiao-Qun Duan

Broussonetia papyrifera leaves are a medicinal plant rich in bioactive substances. This study utilized microbial fermentation of B. papyrifera leaf extract (BLE) to screen out Lactobacillus rhamnosus and Bifidobacterium papyrifera as the most suitable fermentation strains. The total phenols, total flavonoids, total tannins and total triterpenoids content increased after fermentation. The fermentation broth of L. rhamnosus and BLE (BLFs) could inhibit the tyrosinase, melanin production and related protein expression of mouse melanoma cell B16-F10. The fermentation broth of B. bifidum and BLE (BBFs) exhibited significant antioxidant effects. It indicates that the fermented BLE has great application potential in the fields of medicine, cosmetics and related areas.

纸莎草叶是一种富含生物活性物质的药用植物。本研究利用纸莎草叶片提取物(BLE)进行微生物发酵,筛选出鼠李糖乳杆菌和纸莎草双歧杆菌为最适宜的发酵菌株。发酵后总酚、总黄酮、总单宁和总三萜含量增加。鼠李糖发酵液和BLE (BLFs)对小鼠黑色素瘤细胞B16-F10酪氨酸酶、黑色素生成及相关蛋白表达均有抑制作用。两歧双歧杆菌发酵液和BLE (BBFs)具有显著的抗氧化作用。表明发酵后的BLE在医药、化妆品等相关领域具有很大的应用潜力。
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引用次数: 0
A new nor-28-oleanane glycoside isolated from Syzygium formosum inhibits nitric oxide production in LPS-stimulated RAW264.7 cells. 一种新的正-28-齐墩烷苷可抑制lps刺激RAW264.7细胞中一氧化氮的产生。
IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Pub Date : 2026-01-19 DOI: 10.1080/10286020.2026.2615673
Pham Thi Tham, Pham Thi Thu Giang, Dam Xuan Thang, Vu Thi Thu Hoa, Ngo Thuy Van, Do Thu Chieu, Dao Duy Manh, Pham The Chinh, Bui Huu Tai, Phan Van Kiem

One new nor-28-oleanane glycoside (1) and fifteen known compounds (2 - 16) were separated from a methanol extract of Syzygium formosum leaves. Their structures were elucidated via HRESIMS and NMR spectroscopic analyses. The absolute configuration of 1 was determined based on ECD spectra calculated using TD-DFT methods. Among the isolates, syringin (11) exhibited significant inhibitory activity against NO production in LPS-stimulated RAW264.7 cells, with an IC50 value of 18.4 μM. Compounds 1 - 3 displayed moderate inhibitory effects, with IC50 values of 58.4-79.2 μM.

从合子叶甲醇提取物中分离到1个新的不含-28-齐墩烷糖苷(1)和15个已知化合物(2 ~ 16)。它们的结构通过hresms和NMR分析得到。利用TD-DFT方法计算ECD谱,确定了1的绝对构型。其中紫丁香苷(11)对lps刺激的RAW264.7细胞产生NO具有显著的抑制活性,IC50值为18.4 μM。化合物1 ~ 3具有中等抑制作用,IC50值为58.4 ~ 79.2 μM。
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引用次数: 0
期刊
Journal of Asian Natural Products Research
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