{
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"creators": [
{
"name": "Liang, Jingjing",
"givenName": "Jingjing",
"familyName": "Liang"
},
{
"name": "Peng, Xiaogang",
"givenName": "Xiaogang",
"familyName": "Peng"
},
{
"name": "Zhou, Jia",
"givenName": "Jia",
"familyName": "Zhou"
},
{
"name": "Zhou, Ming",
"givenName": "Ming",
"familyName": "Zhou"
},
{
"name": "Ruan, Hanli",
"givenName": "Hanli",
"familyName": "Ruan"
}
],
"titles": [
{
"title": "Diarylheptanoids from the fresh pericarps of Juglans sigillata"
}
],
"publisher": {
"name": "Taylor & Francis"
},
"container": {},
"subjects": [
{
"subject": "Biochemistry"
},
{
"subject": "Cell Biology"
},
{
"subject": "Pharmacology"
},
{
"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": "Immunology"
},
{
"subject": "FOS: Clinical medicine",
"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": "Cancer"
},
{
"subject": "Inorganic Chemistry"
},
{
"subject": "FOS: Chemical sciences",
"schemeUri": "http://www.oecd.org/science/inno/38235147.pdf",
"subjectScheme": "Fields of Science and Technology (FOS)"
}
],
"contributors": [],
"dates": [
{
"date": "2017-12-29",
"dateType": "Created"
},
{
"date": "2024-03-01",
"dateType": "Updated"
},
{
"date": "2017",
"dateType": "Issued"
}
],
"publicationYear": 2017,
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"rights": "Creative Commons Attribution 4.0 International",
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"descriptions": [
{
"description": "One new diarylheptanoid (3S)-3′, 4″-epoxy-1-(4′-hydroxylphenyl)-7-(3″-hydroxylphenyl) heptane-3-hydroxy (1), together with eleven known ones (2–12), was isolated from the fresh pericarps of Juglans sigillata. Their structures were elucidated on the basis of extensive spectroscopic methods, including HR-ESI-MS, 1D and 2D-NMR. All isolates were evaluated for their cytotoxic activities in vitro against the growth of human cancer cells lines HT-29 and MCF-7 by MTT assay.",
"descriptionType": "Abstract"
}
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