Isolation, identification and antiviral activities of metabolites of calycosin-7-O-beta-D-glucopyranoside
文献类型:期刊论文
作者 | Chen, Luying1; Li, Zhixiong1![]() ![]() |
刊名 | JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
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出版日期 | 2011-09-10 |
卷号 | 56期号:2页码:382-389 |
关键词 | Calycosin-7-O-beta-D-glucopyranoside Metabolites Antiviral activity |
ISSN号 | 0731-7085 |
DOI | 10.1016/j.jpba.2011.05.033 |
文献子类 | Article |
英文摘要 | In vivo and in vitro metabolites of calycosin-7-O-beta-D-glucopyranoside in rats were identified using a specific and sensitive high performance liquid chromatography-tandem mass spectrometry (HPLC-MS(n)) method. The parent compound and twelve metabolites were found in rat urine after oral administration of calycosin-7-O-beta-D-glucopyranoside. The parent compound and six metabolites were detected in rat plasma. In heart, liver, spleen, lung and kidney samples, respectively, six, eight, seven, nine and nine metabolites were identified, in addition to the parent compound. Three metabolites, but no trace of parent drug, were found in the rat intestinal flora incubation mixture and feces, which demonstrated cleavage of the glycosidic bond of the parent compound in intestines. The main phase I metabolic pathways of calycosin-7-O-beta-D-glucopyranoside in rats were deglycosylation, dehydroxylation and demethylation reactions; phase II metabolism included sulfation, methylation, glucuronidation and glycosylation (probably). Furthermore, two metabolites commonly found in rat urine, plasma and tissues were isolated from feces and characterized by NMR. The antiviral activities of the metabolite calycosin against coxsackie virus B(3) (CVB(3)) and human immunodeficiency virus (HIV) were remarkably stronger than those of calycosin-7-O-beta-D-glucopyranoside. (C) 2011 Elsevier B.V. All rights reserved. |
WOS关键词 | IN-VITRO ; MASS-SPECTROMETRY ; RAT PLASMA ; VIVO ; FRAGMENTATION ; MONGHOLICUS ; GLYCOSIDES ; URINE ; HPLC |
资助项目 | National Science & Technology Major Project "Key New Drug Creation and Manufacturing Program", China[2009ZX09301-001] ; National Science & Technology Major Project "Key New Drug Creation and Manufacturing Program", China[2009ZX09308-005] ; National Science & Technology Major Project "Key New Drug Creation and Manufacturing Program", China[2009ZX09501-030] ; National Science & Technology Major Project "Key New Drug Creation and Manufacturing Program", China[2009ZX09103-334] ; National Science & Technology Major Project "Key New Drug Creation and Manufacturing Program", China[2009ZX09301-005-007] ; National Science & Technology Major Project "Key New Drug Creation and Manufacturing Program", China[2009ZX09501-029] |
WOS研究方向 | Chemistry ; Pharmacology & Pharmacy |
语种 | 英语 |
WOS记录号 | WOS:000292785900028 |
出版者 | ELSEVIER SCIENCE BV |
源URL | [http://119.78.100.183/handle/2S10ELR8/278403] ![]() |
专题 | 上海中药现代化研究中心 |
通讯作者 | Huang, Chenggang |
作者单位 | 1.Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China; 2.Chinese Acad Sci, Kunming Inst Zool, Key Lab Anim Models & Human Dis Mech, Kunming 650223, Peoples R China; 3.China Acad Chinese Med Sci, Inst Chinese Mat Med, Beijing 100700, Peoples R China |
推荐引用方式 GB/T 7714 | Chen, Luying,Li, Zhixiong,Tang, Yihong,et al. Isolation, identification and antiviral activities of metabolites of calycosin-7-O-beta-D-glucopyranoside[J]. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS,2011,56(2):382-389. |
APA | Chen, Luying.,Li, Zhixiong.,Tang, Yihong.,Cui, Xiaolan.,Luo, Ronghua.,...&Huang, Chenggang.(2011).Isolation, identification and antiviral activities of metabolites of calycosin-7-O-beta-D-glucopyranoside.JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS,56(2),382-389. |
MLA | Chen, Luying,et al."Isolation, identification and antiviral activities of metabolites of calycosin-7-O-beta-D-glucopyranoside".JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS 56.2(2011):382-389. |
入库方式: OAI收割
来源:上海药物研究所
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