{
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"doi": "10.6084/M9.FIGSHARE.17372082.V1",
"url": "https://tandf.figshare.com/articles/journal_contribution/Aromatic_glycosides_from_the_aerial_part_of_i_Bupleurum_chinense_i_/17372082/1",
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"creators": [
{
"name": "Liu, Yan",
"givenName": "Yan",
"familyName": "Liu"
},
{
"name": "Lu, Dong-Xv",
"givenName": "Dong-Xv",
"familyName": "Lu"
},
{
"name": "Huang, Jin",
"givenName": "Jin",
"familyName": "Huang"
},
{
"name": "Pan, Juan",
"givenName": "Juan",
"familyName": "Pan"
},
{
"name": "Guan, Wei",
"givenName": "Wei",
"familyName": "Guan"
},
{
"name": "Yang, Bing-You",
"givenName": "Bing-You",
"familyName": "Yang"
},
{
"name": "Kuang, Hai-Xue",
"givenName": "Hai-Xue",
"familyName": "Kuang"
}
],
"titles": [
{
"title": "Aromatic glycosides from the aerial part of Bupleurum chinense"
}
],
"publisher": {
"name": "Taylor & Francis"
},
"container": {},
"subjects": [
{
"subject": "Biochemistry"
},
{
"subject": "Space Science"
},
{
"subject": "Biotechnology"
},
{
"subject": "Environmental Sciences not elsewhere classified"
},
{
"subject": "Chemical Sciences not elsewhere classified"
},
{
"subject": "Ecology"
},
{
"subject": "FOS: Biological sciences",
"schemeUri": "http://www.oecd.org/science/inno/38235147.pdf",
"subjectScheme": "Fields of Science and Technology (FOS)"
},
{
"subject": "Biological Sciences not elsewhere classified"
},
{
"subject": "Developmental Biology"
},
{
"subject": "Plant Biology"
}
],
"contributors": [],
"dates": [
{
"date": "2021-12-22",
"dateType": "Created"
},
{
"date": "2024-02-07",
"dateType": "Updated"
},
{
"date": "2021",
"dateType": "Issued"
}
],
"publicationYear": 2021,
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"rights": "Creative Commons Attribution 4.0 International",
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"descriptions": [
{
"description": "A new aromatic glycoside (1) and twelve (2–13) known aromatic glycosides were isolated from the n-butyl alcohol of the 70% EtOH extract of the aerial part of Bupleurum chinense. Among them, compounds 4–7, 9, 11–13 were isolated from Umbelliferae plants for the first time. Their structures were elucidated by NMR and MS spectroscopy, and the absolute configuration of compound 1 was elucidated by single-crystal X-ray diffraction. Compounds 6 and 10 showed moderate cytotoxic activities on MGC-803 cell lines with IC50 values of 8.63 ± 0.08 and 13.65 ± 1.73 μM, respectively.",
"descriptionType": "Abstract"
}
],
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