Article(id=1201124486272738013, tenantId=1146029695717560320, journalId=1189982191388893191, issueId=1201124478286786612, articleNumber=null, orderNo=null, doi=10.16438/j.0513-4870.2023-0904, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=research-article, receivedDate=1690214400000, receivedDateStr=2023-07-25, revisedDate=1698249600000, revisedDateStr=2023-10-26, acceptedDate=null, acceptedDateStr=null, onlineDate=1764299993341, onlineDateStr=2025-11-28, pubDate=1710172800000, pubDateStr=2024-03-12, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1764299993341, onlineIssueDateStr=2025-11-28, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1764299993341, creator=13701087609, updateTime=1764299993341, updator=13701087609, issue=Issue{id=1201124478286786612, tenantId=1146029695717560320, journalId=1189982191388893191, year='2024', volume='59', issue='3', pageStart='493', pageEnd='788', issueExtLink='null', onlineDate='null', pubDate='null', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1764299991434, creator=13701087609, updateTime=1764300490467, updator=13701087609, preIssue=null, nextIssue=null, ext={EN=IssueExt(id=1201126571420639892, tenantId=1146029695717560320, journalId=1189982191388893191, issueId=1201124478286786612, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1201126571420639893, tenantId=1146029695717560320, journalId=1189982191388893191, issueId=1201124478286786612, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null}, startPage=633, endPage=642, ext={EN=ArticleExt(id=1201124487631692549, articleId=1201124486272738013, tenantId=1146029695717560320, journalId=1189982191388893191, language=EN, title=Anti-COVID-19 mechanism of
Anoectochilus roxburghii liquid based on network pharmacology and molecular docking, columnId=1190335348761793317, journalTitle=Acta Pharmaceutica Sinica, columnName=Original Articles, runingTitle=null, highlight=null, articleAbstract=
Anoectochilus roxburghii liquid (spray, a hospital preparation of Wu Mengchao Hepatobiliary Hospital of Fujian Medical University) has shown a good clinical treatment effect during the COVID-19 pandemic, but its material basis and mechanism of action are still unclear. In this study, network pharmacology and molecular docking methods were used to predict the molecular mechanism of A. roxburghii liquid against COVID-19, and pharmacodynamic experiments in vitro were conducted to study the interaction between the current targets with clear preventive and therapeutic effects and the key components of A. roxburghii liquid. UPLC-MS and database were used to compare and analyze the active ingredients in the liquid, and 17 potential active ingredients with good drug-like properties were screened by in vivo pharmacokinetics process in SwissADME database. SwissTargetPrediction and GeneCards were searched to find 93 common targets. Cytoscape 3.8.2 software was used to construct the "component-target" network map, and the Metascape platform was used for gene function annotation and pathway enrichment analysis. It was found that the extract could regulate the positive response to external stimuli, inflammatory response, cytokine production and other biological processes by binding the active ingredients such as isorhamnetin, kaempferol, luteolin, quercetin and apigenin to the common targets (NOS3, MPO, MMP3, etc.), and play an anti-COVID-19 role. In the angiotensin-converting enzyme 2 (ACE2) activity inhibition assay, it was found that the stock solution of A. roxburghii liquid (for spray), and the supernatant after removing polysaccharides (mainly containing flavonoids) could to some extent inhibit the activity of ACE2. Crucially, in the experiment of 2019-nCOV-S pseudovirus infecting HEK-293T-ACE2 cells, we found that A. roxburghii liquid may exert anti-COVID-19 effects by blocking the binding of SARS-CoV-S protein to ACE2.
, correspAuthors=Dan JIA, Cheng-jian ZHENG, authorNote=null, correspAuthorsNote=null, copyrightStatement=Copyright ©2024 Acta Pharmaceutica Sinica. All rights reserved., copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, authorCompany=null, fund=null, authors=null, authorsList=Jin ZHU, Yan-bin WU, De-fu HUANG, Bing-ke BAI, Xu-hui HE, Dan JIA, Cheng-jian ZHENG), CN=ArticleExt(id=1201124490165052405, articleId=1201124486272738013, tenantId=1146029695717560320, journalId=1189982191388893191, language=CN, title=基于网络药理学与分子对接的金线莲液抗COVID-19作用机制研究, columnId=1190335348896011050, journalTitle=药学学报, columnName=研究论文, runingTitle=null, highlight=null, articleAbstract=
金线莲液(喷雾用) 在COVID-19大流行期间表现出良好的临床治疗效果, 但其物质基础及作用机制尚不明确。本研究拟通过网络药理学及分子对接的方法预测金线莲液防治新冠的分子机制, 结合体外药效学实验对当前具有明确新冠防治效果的靶点与金线莲液重点成分的相互作用进行研究。首先运用UPLC-MS结合数据库比对分析金线莲液中活性成分, 经SwissADME数据库体内药代动力学过程筛选得到类药性较好的潜在活性成分17个, SwissTargetPrediction、GeneCards检索获得化合物疾病共有靶点93个。随后运用Cytoscape 3.8.2软件构建“成分-靶点”网络图, 以Metascape平台进行基因功能注释和富集通路分析, 发现金线莲液主要通过异鼠李素、山柰酚、木犀草素、槲皮素、芹菜素等活性成分与共有靶点(NOS3、MPO、MMP3等) 结合, 调节对外部刺激的积极反应、炎症反应、细胞因子产生等生物过程, 发挥抗COVID-19的作用。血管紧张素转换酶2 (angiotensin-converting enzyme 2, ACE2) 活性测定实验表明金线莲液(喷雾用) 原液及除去多糖后的上清液(主要为黄酮类成分) 对ACE2酶活性有一定的抑制作用。最后, 采用2019-nCOV-S蛋白假病毒感染HEK-293T-ACE2细胞, 发现金线莲液可能主要通过阻断新冠病毒S蛋白与ACE2的结合发挥抗病毒作用。
, correspAuthors=贾丹, 郑承剑, authorNote=null, correspAuthorsNote=
, copyrightStatement=版权所有©《药学学报》编辑部2024, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=PGb3nPKxA9YcOIRtPJaFgw==, magXml=2LvB5s0r2lyBLnwmT81K1Q==, pdfUrl=null, pdf=oFs4WG52TXc4UN/EkXfQLQ==, pdfFileSize=5708342, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=6SKvNDpv1Kj7EIYWyWzZxA==, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=ynZbcWSpbZ73YFs8ZE8ogQ==, mapNumber=null, authorCompany=null, fund=null, authors=
, authorsList=朱瑾, 吴岩斌, 黄德福, 白冰珂, 何旭辉, 贾丹, 郑承剑)}, authors=[Author(id=1201124492178317388, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1201124486272738013, orderNo=0, firstName=null, middleName=null, lastName=null, nameCn=null, orcid=null, stid=null, country=null, authorPic=null, dead=0, email=null, emailSecond=null, emailThird=null, correspondingAuthor=0, authorType=1, ext={EN=AuthorExt(id=1201124492316729434, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1201124486272738013, authorId=1201124492178317388, language=EN, stringName=Jin ZHU, firstName=Jin, middleName=null, lastName=ZHU, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=
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2, address=2. School of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, China, bio=null, bioImg=null, bioContent=null, aboutCorrespAuthor=null), CN=AuthorExt(id=1201124492794880135, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1201124486272738013, authorId=1201124492547416180, language=CN, stringName=吴岩斌, firstName=岩斌, middleName=null, lastName=吴, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=
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Interaction network of ingredients and target genes of Anoectochilus roxburghii liquid , figureFileSmall=TRPbkWg6sp4LUxuI0fQE4A==, figureFileBig=6SKvNDpv1Kj7EIYWyWzZxA==, tableContent=null), ArticleFig(id=1201124497572192644, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1201124486272738013, language=EN, label=null, caption=null, figureFileSmall=FgSEXKVMgC/J8xN+MKI12g==, figureFileBig=OhjYzIE43XrlvN1xKRSR0A==, tableContent=null), ArticleFig(id=1201124497664467334, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1201124486272738013, language=CN, label=Figure 2, caption=
GO enrichment analysis of key targets of Anoectochilus roxburghii liquid for COVID-treatment (A) and KEGG signaling pathways enrichment analysis bubble chart of Anoectochilus roxburghii liquid for COVID-treatment (B) , figureFileSmall=FgSEXKVMgC/J8xN+MKI12g==, figureFileBig=OhjYzIE43XrlvN1xKRSR0A==, tableContent=null), ArticleFig(id=1201124497790296462, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1201124486272738013, language=EN, label=null, caption=null, figureFileSmall=MoCWGdZROSmlsCGzg61Fig==, figureFileBig=QslVvssvYwZQSFTopkG41A==, tableContent=null), ArticleFig(id=1201124497937097112, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1201124486272738013, language=CN, label=Figure 3, caption=
Heat map of the docking binding energy of active ingredients with key targets (A) and the docking binding energy of active ingredients with key targets for COVID-2019 (B) , figureFileSmall=MoCWGdZROSmlsCGzg61Fig==, figureFileBig=QslVvssvYwZQSFTopkG41A==, tableContent=null), ArticleFig(id=1201124498054537631, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1201124486272738013, language=EN, label=null, caption=null, figureFileSmall=VJCI5LyKS1jc20YwrxZkVA==, figureFileBig=XyqnyOOG0b2AJ1s3gb1CUQ==, tableContent=null), ArticleFig(id=1201124498222309796, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1201124486272738013, language=CN, label=Figure 4, caption=
Molecular docking of MMP3-luteolin (A), MMP3-quercetin (B), MPO-isorhamnetin (C), MPO-kaempferol (D), NOS3-apigenin (E), and NOS3-quercetin (F) , figureFileSmall=VJCI5LyKS1jc20YwrxZkVA==, figureFileBig=XyqnyOOG0b2AJ1s3gb1CUQ==, tableContent=null), ArticleFig(id=1201124498343944617, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1201124486272738013, language=EN, label=null, caption=null, figureFileSmall=uV6JlWZuoNV0IZCfYP7QKw==, figureFileBig=APmuii8A2NmFfO1MMYh8Uw==, tableContent=null), ArticleFig(id=1201124498469773746, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1201124486272738013, language=CN, label=Figure 5, caption=
Inhibition of ACE2 activity (A) and molecular docking of luteolin and quercetin to ACE2 (B). ARL: Anoectochilus roxburghii liquid; PEARL: Polysaccharide extraction of Anoectochilus roxburghii liquid; CPEARL: Concentrated polysaccharide extraction of Anoectochilus roxburghii liquid; SARL: Supernatant of Anoectochilus roxburghii liquid; CSARL: Concentrated supernatant of Anoectochilus roxburghii liquid. n = 3, x ± s. **P < 0.01, ***P < 0.001 , figureFileSmall=uV6JlWZuoNV0IZCfYP7QKw==, figureFileBig=APmuii8A2NmFfO1MMYh8Uw==, tableContent=null), ArticleFig(id=1201124498587214264, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1201124486272738013, language=EN, label=null, caption=null, figureFileSmall=DDseCMtApLnfbcoklMWguA==, figureFileBig=1S7DmNSYcfst8EcMk6fQ/g==, tableContent=null), ArticleFig(id=1201124498721431997, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1201124486272738013, language=CN, label=Figure 6, caption=
Infection of COVID-19-spike protein pseudoviru with HEK-293T-ACE2 cell. A: Control; B: Anoectochilus roxburghii liquid; Scale bar: 100 μm , figureFileSmall=DDseCMtApLnfbcoklMWguA==, figureFileBig=1S7DmNSYcfst8EcMk6fQ/g==, tableContent=null), ArticleFig(id=1201124498855649729, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1201124486272738013, language=EN, label=null, caption=null, figureFileSmall=null, figureFileBig=null, tableContent=
| No. | Formula | Compound | Classification | Theoretical mass (m/z) | Retention time/min | Peak area |
| 1 | C6H6N2O | Nicotinamide | Alkaloid | 123.055 8 | 0.75 | 175 834 136.016 |
| 2 | C28H32O16 | Isorhamnetin-3-O-neohesperosid* | Flavonoids | 625.176 8 | 5.55 | 96 062 483.793 |
| 3 | C28H32O16 | Narcissoside | Flavonoids | 625.176 8 | 5.55 | 96 062 483.793 |
| 4 | C21H20O12 | Hyperoside | Flavonoids | 465.103 3 | 5.08 | 47 853 655.447 |
| 5 | C21H20O12 | Isoquercitrin | Flavonoids | 465.103 3 | 5.08 | 47 853 655.447 |
| 6 | C21H20O12 | Quercetin-7-O-beta-D-glucopyranoside | Flavonoids | 465.103 3 | 5.08 | 47 853 655.447 |
| 7 | C6H6O3 | 5-Hydroxymethylfurfural | Aldehyde | 127.039 5 | 1.98 | 40 657 683.314 |
| 8 | C15H10O5 | Apigenin | Flavonoids | 271.060 6 | 7.58 | 37 623 873.521 |
| 9 | C7H6O2 | 4-Hydroxybenzaldehyde | Aldehyde | 123.044 6 | 3.73 | 32 495 217.177 |
| 10 | C15H10O7 | Quercetin | Flavonoids | 303.050 5 | 6.78 | 31 608 529.603 |
| 11 | C16H12O7 | Isorhamnetin | Flavonoids | 317.066 1 | 7.99 | 28 387 619.612 |
| 12 | C22H22O12 | Isorhamnetin 7-O-glucoside | Flavonoids | 479.118 9 | 5.72 | 24 938 679.992 |
| 13 | C22H22O12 | Isorhamnetin-3-O-beta-D-glucoside | Flavonoids | 479.118 9 | 5.72 | 24 938 679.992 |
| 14 | C15H10O6 | Luteolin | Flavonoids | 287.055 5 | 6.81 | 23 014 885.179 |
| 15 | C9H10O3 | Acetovanillone/apocynin | Phenol | 167.070 8 | 4.96 | 12 792 294.561 |
| 16 | C9H8O3 | p-Hydroxy-cinnamic acid | Organic acids | 165.055 1 | 4.37 | 12 552 628.526 |
| 17 | C15H10O6 | Kaempferol | Flavonoids | 287.055 5 | 7.71 | 9 056 013.128 |
| 18 | C10H10O4 | Ferulic acid | Organic acids | 195.065 7 | 4.92 | 7 948 071.827 |
| 19 | C21H20O11 | Luteolin-7-O-glucoside | Flavonoids | 449.108 4 | 5.14 | 6 584 913.682 |
| 20 | C27H30O16 | Rutin | Flavonoids | 611.161 2 | 4.94 | 6 025 519.264 |
| 21 | C21H20O11 | Quercitrin | Flavonoids | 449.108 4 | 5.73 | 4 816 696.133 |
| 22 | C16H18O9 | Chlorogenic acid | Organic acids | 355.102 9 | 3.43 | 2 107 121.727 |
| 23 | C9H8O4 | Caffeic acid | Organic acids | 181.050 1 | 3.69 | 2 074 399.038 |
| 24 | C15H14O6 | Epicatechin | Flavonoids | 291.086 8 | 3.96 | 894 546.032 |
| 25 | C21H20O11 | Isoorientin | Flavonoids | 449.108 4 | 4.53 | 349 859.148 |
| 26 | C9H8O3 | trans-3-Hydroxycinnamic acid | Organic acids | 165.055 1 | 5.3 | 212 170.466 |
| 27 | C9H8O3 | 2-Hydroxycinnamic acid | Organic acids | 165.055 1 | 5.67 | 190 088.487 |
| 28 | C21H20O11 | Orientin | Flavonoids | 449.108 4 | 4.64 | 182 962.447 |
| 29 | C30H48O3 | Oleanolic acid* | Organic acids | 457.368 1 | 16.28 | 171 259.272 |
| 30 | C30H48O3 | Ursolic acid* | Organic acids | 457.368 1 | 16.28 | 171 259.272 |
| 31 | C30H26O13 | cis-Tiliroside | Flavonoids | 595.145 1 | 6.88 | 133 964.129 |
), ArticleFig(id=1201124498994061764, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1201124486272738013, language=CN, label=Table 1, caption=
Compounds of Anoectochilus roxburghii liquid (spray) in the acetonitrile phase. Compounds marked with * are unique to the acetonitrile phase
, figureFileSmall=null, figureFileBig=null, tableContent=
| No. | Formula | Compound | Classification | Theoretical mass (m/z) | Retention time/min | Peak area |
| 1 | C6H6N2O | Nicotinamide | Alkaloid | 123.055 8 | 0.75 | 175 834 136.016 |
| 2 | C28H32O16 | Isorhamnetin-3-O-neohesperosid* | Flavonoids | 625.176 8 | 5.55 | 96 062 483.793 |
| 3 | C28H32O16 | Narcissoside | Flavonoids | 625.176 8 | 5.55 | 96 062 483.793 |
| 4 | C21H20O12 | Hyperoside | Flavonoids | 465.103 3 | 5.08 | 47 853 655.447 |
| 5 | C21H20O12 | Isoquercitrin | Flavonoids | 465.103 3 | 5.08 | 47 853 655.447 |
| 6 | C21H20O12 | Quercetin-7-O-beta-D-glucopyranoside | Flavonoids | 465.103 3 | 5.08 | 47 853 655.447 |
| 7 | C6H6O3 | 5-Hydroxymethylfurfural | Aldehyde | 127.039 5 | 1.98 | 40 657 683.314 |
| 8 | C15H10O5 | Apigenin | Flavonoids | 271.060 6 | 7.58 | 37 623 873.521 |
| 9 | C7H6O2 | 4-Hydroxybenzaldehyde | Aldehyde | 123.044 6 | 3.73 | 32 495 217.177 |
| 10 | C15H10O7 | Quercetin | Flavonoids | 303.050 5 | 6.78 | 31 608 529.603 |
| 11 | C16H12O7 | Isorhamnetin | Flavonoids | 317.066 1 | 7.99 | 28 387 619.612 |
| 12 | C22H22O12 | Isorhamnetin 7-O-glucoside | Flavonoids | 479.118 9 | 5.72 | 24 938 679.992 |
| 13 | C22H22O12 | Isorhamnetin-3-O-beta-D-glucoside | Flavonoids | 479.118 9 | 5.72 | 24 938 679.992 |
| 14 | C15H10O6 | Luteolin | Flavonoids | 287.055 5 | 6.81 | 23 014 885.179 |
| 15 | C9H10O3 | Acetovanillone/apocynin | Phenol | 167.070 8 | 4.96 | 12 792 294.561 |
| 16 | C9H8O3 | p-Hydroxy-cinnamic acid | Organic acids | 165.055 1 | 4.37 | 12 552 628.526 |
| 17 | C15H10O6 | Kaempferol | Flavonoids | 287.055 5 | 7.71 | 9 056 013.128 |
| 18 | C10H10O4 | Ferulic acid | Organic acids | 195.065 7 | 4.92 | 7 948 071.827 |
| 19 | C21H20O11 | Luteolin-7-O-glucoside | Flavonoids | 449.108 4 | 5.14 | 6 584 913.682 |
| 20 | C27H30O16 | Rutin | Flavonoids | 611.161 2 | 4.94 | 6 025 519.264 |
| 21 | C21H20O11 | Quercitrin | Flavonoids | 449.108 4 | 5.73 | 4 816 696.133 |
| 22 | C16H18O9 | Chlorogenic acid | Organic acids | 355.102 9 | 3.43 | 2 107 121.727 |
| 23 | C9H8O4 | Caffeic acid | Organic acids | 181.050 1 | 3.69 | 2 074 399.038 |
| 24 | C15H14O6 | Epicatechin | Flavonoids | 291.086 8 | 3.96 | 894 546.032 |
| 25 | C21H20O11 | Isoorientin | Flavonoids | 449.108 4 | 4.53 | 349 859.148 |
| 26 | C9H8O3 | trans-3-Hydroxycinnamic acid | Organic acids | 165.055 1 | 5.3 | 212 170.466 |
| 27 | C9H8O3 | 2-Hydroxycinnamic acid | Organic acids | 165.055 1 | 5.67 | 190 088.487 |
| 28 | C21H20O11 | Orientin | Flavonoids | 449.108 4 | 4.64 | 182 962.447 |
| 29 | C30H48O3 | Oleanolic acid* | Organic acids | 457.368 1 | 16.28 | 171 259.272 |
| 30 | C30H48O3 | Ursolic acid* | Organic acids | 457.368 1 | 16.28 | 171 259.272 |
| 31 | C30H26O13 | cis-Tiliroside | Flavonoids | 595.145 1 | 6.88 | 133 964.129 |
), ArticleFig(id=1201124499115696587, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1201124486272738013, language=EN, label=null, caption=null, figureFileSmall=null, figureFileBig=null, tableContent=
| No. | Formula | Compound | Classification | Parent ions (m/z) | Retention time/min | Peak area |
| 1 | C28H32O16 | Narcissoside | Flavonoids | 625.176 8 | 5.56 | 360 141 730.433 |
| 2 | C6H6N2O | Nicotinamide | Alkaloid | 123.055 8 | 0.77 | 322 069 111.273 |
| 3 | C22H22O12 | Isorhamnetin-3-O-beta-D-glucoside | Flavonoids | 479.118 9 | 5.56 | 125 694 608.876 |
| 4 | C27H30O17 | Quercetin-3-gentiobioside* | Flavonoids | 627.156 1 | 4.42 | 96 208 194.200 |
| 5 | C27H30O17 | Quercetin-3-O-sophoroside* | Flavonoids | 627.156 1 | 4.42 | 96 208 194.200 |
| 6 | C21H20O12 | Hyperoside | Flavonoids | 465.103 3 | 5.08 | 57 386 506.410 |
| 7 | C21H20O12 | Isoquercitrin | Flavonoids | 465.103 3 | 5.08 | 57 386 506.410 |
| 8 | C21H20O12 | Quercetin-7-O-beta-D-glucopyranoside | Flavonoids | 465.103 3 | 5.08 | 57 386 506.410 |
| 9 | C27H30O16 | Rutin | Flavonoids | 611.161 2 | 4.96 | 31 450 367.717 |
| 10 | C6H6O3 | 5-Hydroxymethylfurfural | Aldehyde | 127.039 5 | 1.99 | 31 228 323.705 |
| 11 | C9H8O3 | trans-4-Hydroxycinnamic acid | Organic acids | 165.055 1 | 4.78 | 21 625 266.704 |
| 12 | C16H18O9 | Chlorogenic acid | Organic acids | 355.102 9 | 3.44 | 18 958 348.143 |
| 13 | C21H20O11 | Luteolin-7-O-glucoside | Flavonoids | 449.108 4 | 5.14 | 14 536 593.189 |
| 14 | C21H20O11 | Isoorientin | Flavonoids | 449.108 4 | 4.5 | 8 538 764.556 |
| 15 | C21H20O11 | Orientin | Flavonoids | 449.108 4 | 4.5 | 8 538 764.556 |
| 16 | C9H8O4 | Caffeic acid | Organic acids | 181.0501 | 3.59 | 6 531 741.290 |
| 17 | C9H8O3 | p-Hydroxy-cinnamic acid | Organic acids | 165.055 1 | 4.38 | 4 756 281.886 |
| 18 | C7H6O2 | 4-Hydroxybenzaldehyde | Aldehyde | 123.044 6 | 3.74 | 4 021 347.971 |
| 19 | C21H20O11 | Quercitrin | Flavonoids | 449.108 4 | 5.72 | 3 308 932.566 |
| 20 | C15H10O6 | Luteolin | Flavonoids | 287.055 5 | 6.96 | 3 275 269.978 |
| 21 | C10H10O4 | Ferulic acid | Organic acids | 195.065 7 | 4.93 | 3 118 575.795 |
| 22 | C7H6O5 | Gallic acid* | Organic acids | 171.029 3 | 1.12 | 2 831 396.652 |
| 23 | C15H10O5 | Apigenin | Flavonoids | 271.060 6 | 7.61 | 2 684 751.734 |
| 24 | C9H10O3 | Acetovanillone/apocynin | Phenol | 167.070 8 | 4.96 | 2 413 349.760 |
| 25 | C15H14O6 | Epicatechin | Flavonoids | 291.086 8 | 3.96 | 1 319 571.235 |
| 26 | C22H22O12 | Isorhamnetin 7-O-glucoside | Flavonoids | 479.118 9 | 5.95 | 1 272 598.550 |
| 27 | C30H26O13 | cis-Tiliroside | Flavonoids | 595.145 1 | 6.85 | 1 195 472.445 |
| 28 | C16H12O7 | Isorhamnetin | Flavonoids | 317.066 1 | 7.99 | 1 137 304.267 |
| 29 | C15H10O7 | Quercetin | Flavonoids | 303.050 5 | 6.78 | 944 245.745 |
| 30 | C15H10O6 | Kaempferol | Flavonoids | 287.055 5 | 7.77 | 860 501.732 |
| 31 | C9H8O3 | 2-Hydroxycinnamic acid | Organic acids | 165.055 1 | 5.75 | 766 017.535 |
| 32 | C9H8O3 | trans-3-Hydroxycinnamic acid | Organic acids | 165.055 1 | 5.29 | 482 355.837 |
), ArticleFig(id=1201124499241525716, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1201124486272738013, language=CN, label=Table 2, caption=
Compounds of Anoectochilus roxburghii liquid (spray) in the water phase. Compounds marked with * are unique to the water phase
, figureFileSmall=null, figureFileBig=null, tableContent=
| No. | Formula | Compound | Classification | Parent ions (m/z) | Retention time/min | Peak area |
| 1 | C28H32O16 | Narcissoside | Flavonoids | 625.176 8 | 5.56 | 360 141 730.433 |
| 2 | C6H6N2O | Nicotinamide | Alkaloid | 123.055 8 | 0.77 | 322 069 111.273 |
| 3 | C22H22O12 | Isorhamnetin-3-O-beta-D-glucoside | Flavonoids | 479.118 9 | 5.56 | 125 694 608.876 |
| 4 | C27H30O17 | Quercetin-3-gentiobioside* | Flavonoids | 627.156 1 | 4.42 | 96 208 194.200 |
| 5 | C27H30O17 | Quercetin-3-O-sophoroside* | Flavonoids | 627.156 1 | 4.42 | 96 208 194.200 |
| 6 | C21H20O12 | Hyperoside | Flavonoids | 465.103 3 | 5.08 | 57 386 506.410 |
| 7 | C21H20O12 | Isoquercitrin | Flavonoids | 465.103 3 | 5.08 | 57 386 506.410 |
| 8 | C21H20O12 | Quercetin-7-O-beta-D-glucopyranoside | Flavonoids | 465.103 3 | 5.08 | 57 386 506.410 |
| 9 | C27H30O16 | Rutin | Flavonoids | 611.161 2 | 4.96 | 31 450 367.717 |
| 10 | C6H6O3 | 5-Hydroxymethylfurfural | Aldehyde | 127.039 5 | 1.99 | 31 228 323.705 |
| 11 | C9H8O3 | trans-4-Hydroxycinnamic acid | Organic acids | 165.055 1 | 4.78 | 21 625 266.704 |
| 12 | C16H18O9 | Chlorogenic acid | Organic acids | 355.102 9 | 3.44 | 18 958 348.143 |
| 13 | C21H20O11 | Luteolin-7-O-glucoside | Flavonoids | 449.108 4 | 5.14 | 14 536 593.189 |
| 14 | C21H20O11 | Isoorientin | Flavonoids | 449.108 4 | 4.5 | 8 538 764.556 |
| 15 | C21H20O11 | Orientin | Flavonoids | 449.108 4 | 4.5 | 8 538 764.556 |
| 16 | C9H8O4 | Caffeic acid | Organic acids | 181.0501 | 3.59 | 6 531 741.290 |
| 17 | C9H8O3 | p-Hydroxy-cinnamic acid | Organic acids | 165.055 1 | 4.38 | 4 756 281.886 |
| 18 | C7H6O2 | 4-Hydroxybenzaldehyde | Aldehyde | 123.044 6 | 3.74 | 4 021 347.971 |
| 19 | C21H20O11 | Quercitrin | Flavonoids | 449.108 4 | 5.72 | 3 308 932.566 |
| 20 | C15H10O6 | Luteolin | Flavonoids | 287.055 5 | 6.96 | 3 275 269.978 |
| 21 | C10H10O4 | Ferulic acid | Organic acids | 195.065 7 | 4.93 | 3 118 575.795 |
| 22 | C7H6O5 | Gallic acid* | Organic acids | 171.029 3 | 1.12 | 2 831 396.652 |
| 23 | C15H10O5 | Apigenin | Flavonoids | 271.060 6 | 7.61 | 2 684 751.734 |
| 24 | C9H10O3 | Acetovanillone/apocynin | Phenol | 167.070 8 | 4.96 | 2 413 349.760 |
| 25 | C15H14O6 | Epicatechin | Flavonoids | 291.086 8 | 3.96 | 1 319 571.235 |
| 26 | C22H22O12 | Isorhamnetin 7-O-glucoside | Flavonoids | 479.118 9 | 5.95 | 1 272 598.550 |
| 27 | C30H26O13 | cis-Tiliroside | Flavonoids | 595.145 1 | 6.85 | 1 195 472.445 |
| 28 | C16H12O7 | Isorhamnetin | Flavonoids | 317.066 1 | 7.99 | 1 137 304.267 |
| 29 | C15H10O7 | Quercetin | Flavonoids | 303.050 5 | 6.78 | 944 245.745 |
| 30 | C15H10O6 | Kaempferol | Flavonoids | 287.055 5 | 7.77 | 860 501.732 |
| 31 | C9H8O3 | 2-Hydroxycinnamic acid | Organic acids | 165.055 1 | 5.75 | 766 017.535 |
| 32 | C9H8O3 | trans-3-Hydroxycinnamic acid | Organic acids | 165.055 1 | 5.29 | 482 355.837 |
), ArticleFig(id=1201124499358966232, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1201124486272738013, language=EN, label=null, caption=null, figureFileSmall=null, figureFileBig=null, tableContent=
| No. | Compound | GI absorption | Bioavailability |
| 1 | Nicotinamide | High | 0.55 |
| 2 | 5-Hydroxymethylfurfural | High | 0.55 |
| 3 | Apigenin | High | 0.55 |
| 4 | 4-Hydroxybenzaldehyde | High | 0.55 |
| 5 | Quercetin | High | 0.55 |
| 6 | Isorhamnetin | High | 0.55 |
| 7 | Luteolin | High | 0.55 |
| 8 | trans-4-Hydroxycinnamic acid | High | 0.85 |
| 9 | Acetovanillone/apocynin | High | 0.55 |
| 10 | p-Hydroxy-cinnamic acid | High | 0.85 |
| 11 | Kaempferol | High | 0.55 |
| 12 | trans-Ferulic acid | High | 0.85 |
| 13 | Ferulic acid | High | 0.85 |
| 14 | Gallic acid | High | 0.56 |
| 15 | Caffeic acid | High | 0.56 |
| 16 | Epicatechin | High | 0.55 |
| 17 | trans-3-Hydroxycinnamic acid | High | 0.85 |
), ArticleFig(id=1201124499459629535, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1201124486272738013, language=CN, label=Table 3, caption=
In vivo pharmacokinetic process of potential active ingredients with good drug-like properties
, figureFileSmall=null, figureFileBig=null, tableContent=
| No. | Compound | GI absorption | Bioavailability |
| 1 | Nicotinamide | High | 0.55 |
| 2 | 5-Hydroxymethylfurfural | High | 0.55 |
| 3 | Apigenin | High | 0.55 |
| 4 | 4-Hydroxybenzaldehyde | High | 0.55 |
| 5 | Quercetin | High | 0.55 |
| 6 | Isorhamnetin | High | 0.55 |
| 7 | Luteolin | High | 0.55 |
| 8 | trans-4-Hydroxycinnamic acid | High | 0.85 |
| 9 | Acetovanillone/apocynin | High | 0.55 |
| 10 | p-Hydroxy-cinnamic acid | High | 0.85 |
| 11 | Kaempferol | High | 0.55 |
| 12 | trans-Ferulic acid | High | 0.85 |
| 13 | Ferulic acid | High | 0.85 |
| 14 | Gallic acid | High | 0.56 |
| 15 | Caffeic acid | High | 0.56 |
| 16 | Epicatechin | High | 0.55 |
| 17 | trans-3-Hydroxycinnamic acid | High | 0.85 |
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