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Journal of Asian Natural Products Research最新文献

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Exploring the therapeutic potential of Annona reticulata extract: molecular docking, dynamics, and ADMET properties for cancer treatment and anti-inflammatory activity. 探索网纹花提取物的治疗潜力：用于癌症治疗和抗炎活性的分子对接、动力学和 ADMET 特性。
IF 1.3 3区 医学
Journal of Asian Natural Products Research Pub Date : 2024-12-13 DOI: 10.1080/10286020.2024.2435983
Pratheep Thangaraj, Ekambaram Gayathiri, Palanisamy Prakash, Dhivya Viswanathan, Mostafizur Rahaman, Saravanan Pandiaraj, Nagarajan S, Rekha Anantharaman, Rajakumar Govindasamy
{"title":"Exploring the therapeutic potential of <i>Annona reticulata</i> extract: molecular docking, dynamics, and ADMET properties for cancer treatment and anti-inflammatory activity.","authors":"Pratheep Thangaraj, Ekambaram Gayathiri, Palanisamy Prakash, Dhivya Viswanathan, Mostafizur Rahaman, Saravanan Pandiaraj, Nagarajan S, Rekha Anantharaman, Rajakumar Govindasamy","doi":"10.1080/10286020.2024.2435983","DOIUrl":"10.1080/10286020.2024.2435983","url":null,"abstract":"<p><p>Colorectal cancer remains a global health challenge, prompting the exploration of natural compounds for treatment. <i>Annona reticulata</i> shows promise as a source of activity biomolecules. This study analyzed the dynamics, molecular docking and ADMET properties of the extract, highlighting interaction with inflammatory protein. Key findings include compounds with binding energies of -9.61 and -9.01 kcal/mol for 5fia and 7cx2 receptors. Simulations over 100 ns assessed RMSD, RMSF, SASA, and H-bonding, confirming stability and favorable ADME/toxicity profiles. These results highlight <i>A. reticulata</i> as a promising candidate for developing anti-inflammatory and anticancer drugs.[Figure: see text].</p>","PeriodicalId":15180,"journal":{"name":"Journal of Asian Natural Products Research","volume":" ","pages":"1-23"},"PeriodicalIF":1.3,"publicationDate":"2024-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142822191","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
Urolithin B inhibits LPS-induced macrophage M1 polarization via miR155-5p mediated MAPK/NF-кB pathway. 尿素B通过miR155-5p介导的MAPK/NF-кB途径抑制lps诱导的巨噬细胞M1极化。
IF 1.3 3区 医学
Journal of Asian Natural Products Research Pub Date : 2024-12-13 DOI: 10.1080/10286020.2024.2435984
Wulipan Tuohudaali, Teng-Fei Ji, Wan-Ting Ding, Chen-Yang Li, Jian-Shen Bianba, Ren Ci, Jun Zhao
{"title":"Urolithin B inhibits LPS-induced macrophage M1 polarization via miR155-5p mediated MAPK/NF-кB pathway.","authors":"Wulipan Tuohudaali, Teng-Fei Ji, Wan-Ting Ding, Chen-Yang Li, Jian-Shen Bianba, Ren Ci, Jun Zhao","doi":"10.1080/10286020.2024.2435984","DOIUrl":"https://doi.org/10.1080/10286020.2024.2435984","url":null,"abstract":"<p><p>This study investigated inhibiting mechanisms of Urolithin B (Uro B) on macrophage M1 polarization. Uro B (50 μM) could inhibit the PGE2, COX-2, NO, iNOS, TNF-α, IL-1β and IL-6 levels compared with model group (<i>P</i> < 0.05) as well as the CD86 and F4/80 expression. The miR155-5p overexpression could increase the p38 MAPK, JNK, ERK mRNA activities (<i>P</i> < 0.05), Uro B (50 μM) could reverse changes in these indicators (<i>P</i> < 0.05). Moreover, Uro B (50 μM) could inhibit the TLR4, Src, IκBα, NF-κBp65 and their phosphorylated protein expression (<i>P</i> < 0.05). Therefore, Uro B may inhibit macrophage M1 polarization via miR155-5p mediated MAPK/NF-кB pathway.</p>","PeriodicalId":15180,"journal":{"name":"Journal of Asian Natural Products Research","volume":" ","pages":"1-10"},"PeriodicalIF":1.3,"publicationDate":"2024-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142822206","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
Tripterygium wilfordii polyglycoside tablets attenuated the progression of hepatocellular carcinoma by targeting IL-6 and downstream signaling pathways in a multi-target manner. 雷公藤多苷片通过多靶点靶向IL-6及下游信号通路，减缓了肝癌的进展。
IF 1.3 3区 医学
Journal of Asian Natural Products Research Pub Date : 2024-12-13 DOI: 10.1080/10286020.2024.2435992
Pei-You Ren, Jian-Ying Zhang, Lei Zhao, Xiang-Jun Sun
{"title":"<i>Tripterygium wilfordii</i> polyglycoside tablets attenuated the progression of hepatocellular carcinoma by targeting IL-6 and downstream signaling pathways in a multi-target manner.","authors":"Pei-You Ren, Jian-Ying Zhang, Lei Zhao, Xiang-Jun Sun","doi":"10.1080/10286020.2024.2435992","DOIUrl":"https://doi.org/10.1080/10286020.2024.2435992","url":null,"abstract":"<p><p><i>Tripterygium wilfordii</i> polyglycoside tablets (TWPT) have traditionally been used to treat certain inflammatory diseases. This study validated TWPT as a novel application in hepatocellular carcinoma treatment through multiple targets, thereby expanding its clinical medication scope. TWPT exhibited a low toxicity and a significantly antihepatoma effects <i>in vitro</i> and <i>in vivo</i>. Through network pharmacology analysis, we found TWPT attenuated the progression of hepatocellular carcinoma by multi-targeting, including IL-6, MMP9, TNF-α and VEGFA. Additionally, TWPT targeted IL-6 to regulate downstream pathways, including the PI3K/Akt, JAK2/STAT3, and MAPK signaling pathways. Thus, TWPT could be developed as a potential therapeutic drug for hepatocellular carcinoma.</p>","PeriodicalId":15180,"journal":{"name":"Journal of Asian Natural Products Research","volume":" ","pages":"1-21"},"PeriodicalIF":1.3,"publicationDate":"2024-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142822186","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
Characterization of metabolic profile of Dazhu Hongjingtian and evaluation of its anti-hypoxic constituents. 大竹红景天代谢谱特征及抗缺氧成分评价。
IF 1.3 3区 医学
Journal of Asian Natural Products Research Pub Date : 2024-12-12 DOI: 10.1080/10286020.2024.2434550
Chun-Yan Ou, Xia Gao, Jia-Jia Wang, Xia-Lin Chen, Liang Cao, Zhen-Zhong Wang, Chen-Feng Zhang, Wei Xiao
{"title":"Characterization of metabolic profile of Dazhu Hongjingtian and evaluation of its anti-hypoxic constituents.","authors":"Chun-Yan Ou, Xia Gao, Jia-Jia Wang, Xia-Lin Chen, Liang Cao, Zhen-Zhong Wang, Chen-Feng Zhang, Wei Xiao","doi":"10.1080/10286020.2024.2434550","DOIUrl":"https://doi.org/10.1080/10286020.2024.2434550","url":null,"abstract":"<p><p>Dazhu Hongjingtian (DZ) is renowned for its diverse pharmacological activities, yet its metabolic pathways remain to be fully elucidated. In this study, the metabolic profile after oral administration of DZ extract (DZE) in rats was systematically identified by the UPLC/Q-TOF-MS/MS method for the first time. A total of 94 components, including 32 prototypes and 62 metabolites, were tentatively characterized in rat plasma and various tissues samples. Furthermore, 6 constituents (salidroside, quercetin, 4-hydroxycinnamic acid, 5-hydroxymethylfurfural, <i>p</i>-tyrosol, and gallic acid) derived from plasma prototypes were identified as bioactive by assessing cell viabilities of OGD-injured RSC96 cells.</p>","PeriodicalId":15180,"journal":{"name":"Journal of Asian Natural Products Research","volume":" ","pages":"1-19"},"PeriodicalIF":1.3,"publicationDate":"2024-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142813304","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
Culcinoside E, a new sulfated steroidal biglycoside from the starfish Culcita novaeguineae. Culcinoside E：一种从新海星Culcita novaeguineae中提取的磺化甾体大糖苷。
IF 1.3 3区 医学
Journal of Asian Natural Products Research Pub Date : 2024-12-03 DOI: 10.1080/10286020.2024.2434564
Le Thi Vien, Tran Thi Hong Hanh, Tran Hong Quang, Nguyen Dang Ngai, Dao Viet Ha, Nguyen Xuan Cuong
{"title":"Culcinoside E, a new sulfated steroidal biglycoside from the starfish <i>Culcita novaeguineae</i>.","authors":"Le Thi Vien, Tran Thi Hong Hanh, Tran Hong Quang, Nguyen Dang Ngai, Dao Viet Ha, Nguyen Xuan Cuong","doi":"10.1080/10286020.2024.2434564","DOIUrl":"https://doi.org/10.1080/10286020.2024.2434564","url":null,"abstract":"<p><p>Using various chromatographic separations, six steroid glycoside derivatives, including one new compound named culcinoside E (<b>1</b>), were isolated from the methanol extract of the starfish <i>Culcita novaeguineae</i>. Their structures were confirmed by detailed analysis of the 1D, 2D NMR, and HR ESI QTOF mass spectra. Among isolated compounds, culcinoside E (<b>1</b>), diplasterioside A (<b>5</b>), and thornasteroside A (<b>6</b>) inhibited growth of <i>Enterococcus faecalis</i>, whereas culcitoside C<sub>1</sub> (<b>3</b>) was active on <i>Candida albicans</i>.</p>","PeriodicalId":15180,"journal":{"name":"Journal of Asian Natural Products Research","volume":" ","pages":"1-7"},"PeriodicalIF":1.3,"publicationDate":"2024-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142768182","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
Preclinical determination of wound-healing activity of halibut oil cream in rat model of burn wound 临床前测定大比目鱼油膏在大鼠烧伤模型中的伤口愈合活性。
IF 1.3 3区 医学
Journal of Asian Natural Products Research Pub Date : 2024-12-01 DOI: 10.1080/10286020.2024.2368835
ST Shukla , Anu Kaushik , Samiullah Allahbaksh Auti , Dinesh Kumar , Supriya Kumar Das
{"title":"Preclinical determination of wound-healing activity of halibut oil cream in rat model of burn wound","authors":"ST Shukla ,&nbsp;Anu Kaushik ,&nbsp;Samiullah Allahbaksh Auti ,&nbsp;Dinesh Kumar ,&nbsp;Supriya Kumar Das","doi":"10.1080/10286020.2024.2368835","DOIUrl":"10.1080/10286020.2024.2368835","url":null,"abstract":"<div><div>This study investigated the effects of halibut oil cream, containing omega-3 fatty acids, vitamins A and D, and hydroxyproline, on burn wound healing in rats. Acute dermal toxicity tests confirmed its nontoxicity. Wistar rats were divided into five groups: a control, a positive control treated with silver sulfadiazine 1% (SSD), and three groups treated with 3%, 9%, and 27% halibut oil cream Formulation (HBOF). The SSD and HBOF groups showed significant healing improvements compared to the control. Histopathological analysis indicated increased collagen production in the HBOF groups, suggesting halibut oil cream’s potential as a topical treatment for burn wounds.</div></div>","PeriodicalId":15180,"journal":{"name":"Journal of Asian Natural Products Research","volume":"26 12","pages":"Pages 1455-1474"},"PeriodicalIF":1.3,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141468156","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
Sesquilignans PD from Zanthoxylum nitidum var. tomentosum exerts antitumor effects via the ROS/MAPK pathway in liver cancer cells 从 Zanthoxylum nitidum var. tomentosum 中提取的 Sesquilignans PD 可通过 ROS/MAPK 途径对肝癌细胞产生抗肿瘤作用。
IF 1.3 3区 医学
Journal of Asian Natural Products Research Pub Date : 2024-12-01 DOI: 10.1080/10286020.2024.2371032
Cai-Wen Fan , Li Luo , Mei-Shan Li , Yun-Qiong Gu , Yi-Lin Fang , Feng Qin , Heng-Shan Wang
{"title":"Sesquilignans PD from Zanthoxylum nitidum var. tomentosum exerts antitumor effects via the ROS/MAPK pathway in liver cancer cells","authors":"Cai-Wen Fan ,&nbsp;Li Luo ,&nbsp;Mei-Shan Li ,&nbsp;Yun-Qiong Gu ,&nbsp;Yi-Lin Fang ,&nbsp;Feng Qin ,&nbsp;Heng-Shan Wang","doi":"10.1080/10286020.2024.2371032","DOIUrl":"10.1080/10286020.2024.2371032","url":null,"abstract":"<div><div>Sesquilignans <strong>PD</strong> is a natural phenylpropanoid compound that was isolated from <em>Zanthoxylum nitidum</em> var. <em>tomentosum</em>. In this study, we assessed the antitumor effect of <strong>PD</strong> on SK-Hep-1 and HepG2 cells and the underlying molecular mechanisms. The results revealed that <strong>PD</strong> markedly inhibited the proliferation and migration of both liver cancer cells. Moreover, <strong>PD</strong> induced apoptosis, autophagy, and reactive oxygen species (ROS) production in liver cancer cells. Notably, <strong>PD</strong> increased the protein levels of p-p38 MAPK and p-ERK1/2 in liver cancer cells. This is the first report on the anticancer effect of <strong>PD</strong>, which is mediated <em>via</em> increased ROS production and MAPK signaling activation.</div></div>","PeriodicalId":15180,"journal":{"name":"Journal of Asian Natural Products Research","volume":"26 12","pages":"Pages 1530-1542"},"PeriodicalIF":1.3,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141492125","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
The changes of intestinal microbiota and metabolomics during the inhibition of bladder cancer by liquiritigenin 利尿苷抑制膀胱癌过程中肠道微生物群和代谢组学的变化
IF 1.3 3区 医学
Journal of Asian Natural Products Research Pub Date : 2024-12-01 DOI: 10.1080/10286020.2024.2366010
Zhao Zhai , Jie Fu , Meng-Liang Ye , Jing-Yue Wang , Hao-Jian Zhang , Hang Yu , Xin-Yu Yang , Hui Xu , Jia-Chun Hu , Jin-Yue Lu , Heng-Tong Zuo , Yi Zhao , Jian-Ye Song , Yong Zhang , Yan Wang , Nian-Zeng Xing
{"title":"The changes of intestinal microbiota and metabolomics during the inhibition of bladder cancer by liquiritigenin","authors":"Zhao Zhai ,&nbsp;Jie Fu ,&nbsp;Meng-Liang Ye ,&nbsp;Jing-Yue Wang ,&nbsp;Hao-Jian Zhang ,&nbsp;Hang Yu ,&nbsp;Xin-Yu Yang ,&nbsp;Hui Xu ,&nbsp;Jia-Chun Hu ,&nbsp;Jin-Yue Lu ,&nbsp;Heng-Tong Zuo ,&nbsp;Yi Zhao ,&nbsp;Jian-Ye Song ,&nbsp;Yong Zhang ,&nbsp;Yan Wang ,&nbsp;Nian-Zeng Xing","doi":"10.1080/10286020.2024.2366010","DOIUrl":"10.1080/10286020.2024.2366010","url":null,"abstract":"<div><div>Liquiritigenin is a natural medicine. However, its inhibitory effect and its potential mechanism on bladder cancer (BCa) remain to be explored. It was found that it could be visualized that the transplanted tumours in the low-dose liquiritigenin -treated group and the high-dose liquiritigenin -treated group were smaller than those in the model group. Liquiritigenin treatment led to alterations in Lachnoclostridium, <em>Escherichia-Shigella, Alistipes</em> and <em>Akkermansia</em>. Non-targeted metabolomics analysis showed that a total of multiple differential metabolites were identified between the model group and the high-dose liquiritigenin-treated group. This provides a new direction and rationale for the antitumour effects of liquiritigenin.</div></div>","PeriodicalId":15180,"journal":{"name":"Journal of Asian Natural Products Research","volume":"26 12","pages":"Pages 1445-1454"},"PeriodicalIF":1.3,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141310757","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
Phosphatidylcholine and ceramide derivatives from white rot fungus Microporus xanthropus PP17-20 白腐霉菌 PP17-20 的磷脂酰胆碱和神经酰胺衍生物。
IF 1.3 3区 医学
Journal of Asian Natural Products Research Pub Date : 2024-12-01 DOI: 10.1080/10286020.2024.2368834
Phongphan Jantaharn , Audomsak Churat , Sirirat Juanan , Ek Sangvichien , Wiyada Mongkolthanaruk , Nuttika Suwannasai , Thanaset Senawong , Sirirath McCloskey
{"title":"Phosphatidylcholine and ceramide derivatives from white rot fungus Microporus xanthropus PP17-20","authors":"Phongphan Jantaharn ,&nbsp;Audomsak Churat ,&nbsp;Sirirat Juanan ,&nbsp;Ek Sangvichien ,&nbsp;Wiyada Mongkolthanaruk ,&nbsp;Nuttika Suwannasai ,&nbsp;Thanaset Senawong ,&nbsp;Sirirath McCloskey","doi":"10.1080/10286020.2024.2368834","DOIUrl":"10.1080/10286020.2024.2368834","url":null,"abstract":"<div><div>The undescribed phosphatidylcholine (<strong>1</strong>), along with twelve known compounds, was isolated from the cultures of white rot fungus <em>Microporus xanthropus</em> PP17-20. In this work the fungus was cultivated in Yeast-Malt extract medium to explore active compound production. The chemical structures were elucidated on the basis of spectroscopic and HRESIMS data. Several isolated compounds were evaluated for anti-proliferative activity against A549 and MCF-7 cancer cell lines.</div></div>","PeriodicalId":15180,"journal":{"name":"Journal of Asian Natural Products Research","volume":"26 12","pages":"Pages 1551-1556"},"PeriodicalIF":1.3,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141468155","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
Discovery of sesquiterpene lactones with anti-inflammatory effect from Youngia japonica 从莬丝子中发现具有抗炎作用的倍半萜内酯
IF 1.3 3区 医学
Journal of Asian Natural Products Research Pub Date : 2024-12-01 DOI: 10.1080/10286020.2024.2370401
Xian-Sheng Ye , Kuan Lin , Chang-Long Leng , Yu-Ran Gui , Shu-Xiu Zhu , Hui-Ying Liu , Yi-Yuan Xia , Bin-Lian Sun , Wei Liu , Xi-Ji Shu
{"title":"Discovery of sesquiterpene lactones with anti-inflammatory effect from Youngia japonica","authors":"Xian-Sheng Ye ,&nbsp;Kuan Lin ,&nbsp;Chang-Long Leng ,&nbsp;Yu-Ran Gui ,&nbsp;Shu-Xiu Zhu ,&nbsp;Hui-Ying Liu ,&nbsp;Yi-Yuan Xia ,&nbsp;Bin-Lian Sun ,&nbsp;Wei Liu ,&nbsp;Xi-Ji Shu","doi":"10.1080/10286020.2024.2370401","DOIUrl":"10.1080/10286020.2024.2370401","url":null,"abstract":"<div><div>The preliminary study revealed that the ethyl acetate eluate of <em>Youngia japonica</em> (YJ-E) could inhibit the expression of key proteins of p-p65, p-IκBα, p-IKKα/β, and p-AKT in LPS stimulated BV2 cell. Further phytochemical study led to the isolation of eight compounds from YJ-E, including one new sesquiterpene lactone. Their structures were elucidated by several spectroscopic data, and comparing the NMR data of known compound. In addition, all of the isolates were evaluated for the anti-inflammatory effect. As a result, compounds <strong>3</strong> and <strong>4</strong> distinctly attenuated the expressions of p-IκBα, p-p65, and p-AKT in LPS stimulated BV2 cell, respectively.</div></div>","PeriodicalId":15180,"journal":{"name":"Journal of Asian Natural Products Research","volume":"26 12","pages":"Pages 1557-1564"},"PeriodicalIF":1.3,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141498137","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
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