Isolation and identification of two new compounds from the twigs and leaves of Cephalotaxus fortunei. View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2019-04-11

AUTHORS

Qingmei Feng, Bingxin Li, Yuan Feng, Xingyu Li, Xiaorui Ma, Haifeng Wang, Gang Chen

ABSTRACT

Two new compounds, namely 5-hydroxy-7-methoxy-6-methylchromone (1), and sesquiterpene X (6), together with 21 known compounds were isolated from the twigs and leaves of Cephalotaxus fortunei Hook. f. The structures of 1-23 were elucidated on the basis of spectroscopic analysis (1D/2D NMR, HR-ESI-MS and IR) and comparison with literature. The absolute configuration of compound 6 was determined by means of electronic circular dichroism calculation. The in vitro anti-inflammatory activities of all compounds were assayed in RAW 264.7 cells by assessing lipopolysaccharide-induced nitric oxide production. Compounds 1 and 6 exhibited weak effects with percentage inhibitions of 24% and 35.60%, respectively. In addition, compounds 4, 9, and 14 have the potential to be developed as therapeutic agents for inflammatory diseases because of their significant anti-inflammatory activities and high content in C. fortunei. More... »

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11418-019-01308-5

DOI

http://dx.doi.org/10.1007/s11418-019-01308-5

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1113378545

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/30976949


Indexing Status Check whether this publication has been indexed by Scopus and Web Of Science using the SN Indexing Status Tool
Incoming Citations Browse incoming citations for this publication using opencitations.net

JSON-LD is the canonical representation for SciGraph data.

TIP: You can open this SciGraph record using an external JSON-LD service: JSON-LD Playground Google SDTT

[
  {
    "@context": "https://springernature.github.io/scigraph/jsonld/sgcontext.json", 
    "about": [
      {
        "id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/1115", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Pharmacology and Pharmaceutical Sciences", 
        "type": "DefinedTerm"
      }, 
      {
        "id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/11", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Medical and Health Sciences", 
        "type": "DefinedTerm"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "Shenyang Pharmaceutical University", 
          "id": "https://www.grid.ac/institutes/grid.412561.5", 
          "name": [
            "School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China.", 
            "Key Laboratory of Computational Chemistry-Based Natural Antitumor Drug Research and Development, Wenhua Road 103, Shenyang, Liaoning Province, 110016, China."
          ], 
          "type": "Organization"
        }, 
        "familyName": "Feng", 
        "givenName": "Qingmei", 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Shenyang Pharmaceutical University", 
          "id": "https://www.grid.ac/institutes/grid.412561.5", 
          "name": [
            "School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China.", 
            "Key Laboratory of Computational Chemistry-Based Natural Antitumor Drug Research and Development, Wenhua Road 103, Shenyang, Liaoning Province, 110016, China."
          ], 
          "type": "Organization"
        }, 
        "familyName": "Li", 
        "givenName": "Bingxin", 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Shenyang Pharmaceutical University", 
          "id": "https://www.grid.ac/institutes/grid.412561.5", 
          "name": [
            "School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China.", 
            "Key Laboratory of Computational Chemistry-Based Natural Antitumor Drug Research and Development, Wenhua Road 103, Shenyang, Liaoning Province, 110016, China."
          ], 
          "type": "Organization"
        }, 
        "familyName": "Feng", 
        "givenName": "Yuan", 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Shenyang Pharmaceutical University", 
          "id": "https://www.grid.ac/institutes/grid.412561.5", 
          "name": [
            "School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China.", 
            "Key Laboratory of Computational Chemistry-Based Natural Antitumor Drug Research and Development, Wenhua Road 103, Shenyang, Liaoning Province, 110016, China."
          ], 
          "type": "Organization"
        }, 
        "familyName": "Li", 
        "givenName": "Xingyu", 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Shenyang Pharmaceutical University", 
          "id": "https://www.grid.ac/institutes/grid.412561.5", 
          "name": [
            "School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China.", 
            "Key Laboratory of Computational Chemistry-Based Natural Antitumor Drug Research and Development, Wenhua Road 103, Shenyang, Liaoning Province, 110016, China."
          ], 
          "type": "Organization"
        }, 
        "familyName": "Ma", 
        "givenName": "Xiaorui", 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Shenyang Pharmaceutical University", 
          "id": "https://www.grid.ac/institutes/grid.412561.5", 
          "name": [
            "School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China.", 
            "Key Laboratory of Computational Chemistry-Based Natural Antitumor Drug Research and Development, Wenhua Road 103, Shenyang, Liaoning Province, 110016, China."
          ], 
          "type": "Organization"
        }, 
        "familyName": "Wang", 
        "givenName": "Haifeng", 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Shenyang Pharmaceutical University", 
          "id": "https://www.grid.ac/institutes/grid.412561.5", 
          "name": [
            "School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China. chengang1152001@163.com.", 
            "Key Laboratory of Computational Chemistry-Based Natural Antitumor Drug Research and Development, Wenhua Road 103, Shenyang, Liaoning Province, 110016, China. chengang1152001@163.com."
          ], 
          "type": "Organization"
        }, 
        "familyName": "Chen", 
        "givenName": "Gang", 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "https://doi.org/10.1081/scc-120003635", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1006833680"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1080/14786410802267510", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1008719797"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/0031-9422(89)80203-1", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1018071409"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.bmcl.2013.08.045", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1018764368"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1248/cpb.37.2819", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1025801573"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.tet.2004.06.070", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1026785742"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s0031-9422(03)00021-9", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1030638245"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.ejphar.2007.07.005", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1032505247"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/hlca.200390174", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1033069702"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1248/cpb.51.378", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1033135052"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.bmcl.2015.01.056", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1037755060"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.bmcl.2015.01.056", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1037755060"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.jep.2009.02.024", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1037839541"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1146/annurev.pharmtox.010909.105812", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1043364888"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1673/031.010.1301", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1048093970"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/0031-9422(90)85187-k", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1048941507"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s0040-4039(01)97839-6", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1052159551"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jacs.6b08424", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055876160"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jo01044a010", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055998227"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/np049836w", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1056229737"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/np049836w", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1056229737"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/np0498657", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1056229757"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/np0498657", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1056229757"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/np970445+", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1056239027"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/np970445+", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1056239027"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1055/s-2006-958109", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1057471133"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1055/s-2006-960961", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1057472871"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.biopha.2017.02.066", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1084061765"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.19540/j.cnki.cjcmm.20170308.003", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1091248956"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/cbdv.201800137", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1103994143"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2019-04-11", 
    "datePublishedReg": "2019-04-11", 
    "description": "Two new compounds, namely 5-hydroxy-7-methoxy-6-methylchromone (1), and sesquiterpene X (6), together with 21 known compounds were isolated from the twigs and leaves of Cephalotaxus fortunei Hook. f. The structures of 1-23 were elucidated on the basis of spectroscopic analysis (1D/2D NMR, HR-ESI-MS and IR) and comparison with literature. The absolute configuration of compound 6 was determined by means of electronic circular dichroism calculation. The in vitro anti-inflammatory activities of all compounds were assayed in RAW 264.7 cells by assessing lipopolysaccharide-induced nitric oxide production. Compounds 1 and 6 exhibited weak effects with percentage inhibitions of 24% and 35.60%, respectively. In addition, compounds 4, 9, and 14 have the potential to be developed as therapeutic agents for inflammatory diseases because of their significant anti-inflammatory activities and high content in C. fortunei.", 
    "genre": "research_article", 
    "id": "sg:pub.10.1007/s11418-019-01308-5", 
    "inLanguage": [
      "en"
    ], 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1042407", 
        "issn": [
          "1340-3443", 
          "1861-0293"
        ], 
        "name": "Journal of Natural Medicines", 
        "type": "Periodical"
      }
    ], 
    "name": "Isolation and identification of two new compounds from the twigs and leaves of Cephalotaxus fortunei.", 
    "productId": [
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s11418-019-01308-5"
        ]
      }, 
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1113378545"
        ]
      }, 
      {
        "name": "nlm_unique_id", 
        "type": "PropertyValue", 
        "value": [
          "101518405"
        ]
      }, 
      {
        "name": "pubmed_id", 
        "type": "PropertyValue", 
        "value": [
          "30976949"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s11418-019-01308-5", 
      "https://app.dimensions.ai/details/publication/pub.1113378545"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2019-04-16T06:22", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-uberresearch-data-dimensions-target-20181106-alternative/cleanup/v134/2549eaecd7973599484d7c17b260dba0a4ecb94b/merge/v9/a6c9fde33151104705d4d7ff012ea9563521a3ce/jats-lookup/v90/0000000377_0000000377/records_106810_00000003.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "http://link.springer.com/10.1007/s11418-019-01308-5"
  }
]
 

Download the RDF metadata as:  json-ld nt turtle xml License info

HOW TO GET THIS DATA PROGRAMMATICALLY:

JSON-LD is a popular format for linked data which is fully compatible with JSON.

curl -H 'Accept: application/ld+json' 'https://scigraph.springernature.com/pub.10.1007/s11418-019-01308-5'

N-Triples is a line-based linked data format ideal for batch operations.

curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/pub.10.1007/s11418-019-01308-5'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s11418-019-01308-5'

RDF/XML is a standard XML format for linked data.

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s11418-019-01308-5'


 

This table displays all metadata directly associated to this object as RDF triples.

174 TRIPLES      20 PREDICATES      50 URIs      16 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s11418-019-01308-5 schema:about anzsrc-for:11
2 anzsrc-for:1115
3 schema:author Nd8ef3cf9b4f042448df85e4ae3bbb4d0
4 schema:citation https://doi.org/10.1002/cbdv.201800137
5 https://doi.org/10.1002/hlca.200390174
6 https://doi.org/10.1016/0031-9422(89)80203-1
7 https://doi.org/10.1016/0031-9422(90)85187-k
8 https://doi.org/10.1016/j.biopha.2017.02.066
9 https://doi.org/10.1016/j.bmcl.2013.08.045
10 https://doi.org/10.1016/j.bmcl.2015.01.056
11 https://doi.org/10.1016/j.ejphar.2007.07.005
12 https://doi.org/10.1016/j.jep.2009.02.024
13 https://doi.org/10.1016/j.tet.2004.06.070
14 https://doi.org/10.1016/s0031-9422(03)00021-9
15 https://doi.org/10.1016/s0040-4039(01)97839-6
16 https://doi.org/10.1021/jacs.6b08424
17 https://doi.org/10.1021/jo01044a010
18 https://doi.org/10.1021/np049836w
19 https://doi.org/10.1021/np0498657
20 https://doi.org/10.1021/np970445+
21 https://doi.org/10.1055/s-2006-958109
22 https://doi.org/10.1055/s-2006-960961
23 https://doi.org/10.1080/14786410802267510
24 https://doi.org/10.1081/scc-120003635
25 https://doi.org/10.1146/annurev.pharmtox.010909.105812
26 https://doi.org/10.1248/cpb.37.2819
27 https://doi.org/10.1248/cpb.51.378
28 https://doi.org/10.1673/031.010.1301
29 https://doi.org/10.19540/j.cnki.cjcmm.20170308.003
30 schema:datePublished 2019-04-11
31 schema:datePublishedReg 2019-04-11
32 schema:description Two new compounds, namely 5-hydroxy-7-methoxy-6-methylchromone (1), and sesquiterpene X (6), together with 21 known compounds were isolated from the twigs and leaves of Cephalotaxus fortunei Hook. f. The structures of 1-23 were elucidated on the basis of spectroscopic analysis (1D/2D NMR, HR-ESI-MS and IR) and comparison with literature. The absolute configuration of compound 6 was determined by means of electronic circular dichroism calculation. The in vitro anti-inflammatory activities of all compounds were assayed in RAW 264.7 cells by assessing lipopolysaccharide-induced nitric oxide production. Compounds 1 and 6 exhibited weak effects with percentage inhibitions of 24% and 35.60%, respectively. In addition, compounds 4, 9, and 14 have the potential to be developed as therapeutic agents for inflammatory diseases because of their significant anti-inflammatory activities and high content in C. fortunei.
33 schema:genre research_article
34 schema:inLanguage en
35 schema:isAccessibleForFree false
36 schema:isPartOf sg:journal.1042407
37 schema:name Isolation and identification of two new compounds from the twigs and leaves of Cephalotaxus fortunei.
38 schema:productId N39c1c52b4ae4485486e403ade813556a
39 N7dd012c6ea6d4464a10d8cf942692fe7
40 Nb673c8b3f20d49dd859cc7a0391dc1a7
41 Nd238ce01d35d46d4b5ce1e5e0fa8d24b
42 schema:sameAs https://app.dimensions.ai/details/publication/pub.1113378545
43 https://doi.org/10.1007/s11418-019-01308-5
44 schema:sdDatePublished 2019-04-16T06:22
45 schema:sdLicense https://scigraph.springernature.com/explorer/license/
46 schema:sdPublisher N43a83e4a438e48f2976bbf901777e32f
47 schema:url http://link.springer.com/10.1007/s11418-019-01308-5
48 sgo:license sg:explorer/license/
49 sgo:sdDataset articles
50 rdf:type schema:ScholarlyArticle
51 N39c1c52b4ae4485486e403ade813556a schema:name doi
52 schema:value 10.1007/s11418-019-01308-5
53 rdf:type schema:PropertyValue
54 N43a83e4a438e48f2976bbf901777e32f schema:name Springer Nature - SN SciGraph project
55 rdf:type schema:Organization
56 N44aef6f740b94e9c83f76d4a6fbf4f2a rdf:first N4acd7f41ebfb4870b79b192cca0f19b0
57 rdf:rest Nc05e793e73e048c9939fe6b30ae10df5
58 N4acd7f41ebfb4870b79b192cca0f19b0 schema:affiliation https://www.grid.ac/institutes/grid.412561.5
59 schema:familyName Feng
60 schema:givenName Yuan
61 rdf:type schema:Person
62 N5d4fc123c67b40fc9f75b1263474c2e5 schema:affiliation https://www.grid.ac/institutes/grid.412561.5
63 schema:familyName Feng
64 schema:givenName Qingmei
65 rdf:type schema:Person
66 N7dd012c6ea6d4464a10d8cf942692fe7 schema:name dimensions_id
67 schema:value pub.1113378545
68 rdf:type schema:PropertyValue
69 N869450cced6d4fccaf4749d596bd7151 schema:affiliation https://www.grid.ac/institutes/grid.412561.5
70 schema:familyName Ma
71 schema:givenName Xiaorui
72 rdf:type schema:Person
73 N89d2b7832c2849f099b8467bad041032 rdf:first Nba2d3c0b8bda4b68a5b77855928e33da
74 rdf:rest N44aef6f740b94e9c83f76d4a6fbf4f2a
75 N937947e01d6547d39b46a864d947aff8 schema:affiliation https://www.grid.ac/institutes/grid.412561.5
76 schema:familyName Wang
77 schema:givenName Haifeng
78 rdf:type schema:Person
79 N9fb752cfe696433fb6ad37e09f5ad098 rdf:first Ndf8cbc39f02241a2a7c258ed709f2c87
80 rdf:rest rdf:nil
81 Nb673c8b3f20d49dd859cc7a0391dc1a7 schema:name pubmed_id
82 schema:value 30976949
83 rdf:type schema:PropertyValue
84 Nba2d3c0b8bda4b68a5b77855928e33da schema:affiliation https://www.grid.ac/institutes/grid.412561.5
85 schema:familyName Li
86 schema:givenName Bingxin
87 rdf:type schema:Person
88 Nc05e793e73e048c9939fe6b30ae10df5 rdf:first Ncbd6600ea32a4d51ba011022ac6dac50
89 rdf:rest Nf66bed0c8be34b9da621e70363d960f6
90 Ncbd6600ea32a4d51ba011022ac6dac50 schema:affiliation https://www.grid.ac/institutes/grid.412561.5
91 schema:familyName Li
92 schema:givenName Xingyu
93 rdf:type schema:Person
94 Nd238ce01d35d46d4b5ce1e5e0fa8d24b schema:name nlm_unique_id
95 schema:value 101518405
96 rdf:type schema:PropertyValue
97 Nd8ef3cf9b4f042448df85e4ae3bbb4d0 rdf:first N5d4fc123c67b40fc9f75b1263474c2e5
98 rdf:rest N89d2b7832c2849f099b8467bad041032
99 Ndf8cbc39f02241a2a7c258ed709f2c87 schema:affiliation https://www.grid.ac/institutes/grid.412561.5
100 schema:familyName Chen
101 schema:givenName Gang
102 rdf:type schema:Person
103 Nf66bed0c8be34b9da621e70363d960f6 rdf:first N869450cced6d4fccaf4749d596bd7151
104 rdf:rest Nfca49732617e4569bd0b71f9fd3c6634
105 Nfca49732617e4569bd0b71f9fd3c6634 rdf:first N937947e01d6547d39b46a864d947aff8
106 rdf:rest N9fb752cfe696433fb6ad37e09f5ad098
107 anzsrc-for:11 schema:inDefinedTermSet anzsrc-for:
108 schema:name Medical and Health Sciences
109 rdf:type schema:DefinedTerm
110 anzsrc-for:1115 schema:inDefinedTermSet anzsrc-for:
111 schema:name Pharmacology and Pharmaceutical Sciences
112 rdf:type schema:DefinedTerm
113 sg:journal.1042407 schema:issn 1340-3443
114 1861-0293
115 schema:name Journal of Natural Medicines
116 rdf:type schema:Periodical
117 https://doi.org/10.1002/cbdv.201800137 schema:sameAs https://app.dimensions.ai/details/publication/pub.1103994143
118 rdf:type schema:CreativeWork
119 https://doi.org/10.1002/hlca.200390174 schema:sameAs https://app.dimensions.ai/details/publication/pub.1033069702
120 rdf:type schema:CreativeWork
121 https://doi.org/10.1016/0031-9422(89)80203-1 schema:sameAs https://app.dimensions.ai/details/publication/pub.1018071409
122 rdf:type schema:CreativeWork
123 https://doi.org/10.1016/0031-9422(90)85187-k schema:sameAs https://app.dimensions.ai/details/publication/pub.1048941507
124 rdf:type schema:CreativeWork
125 https://doi.org/10.1016/j.biopha.2017.02.066 schema:sameAs https://app.dimensions.ai/details/publication/pub.1084061765
126 rdf:type schema:CreativeWork
127 https://doi.org/10.1016/j.bmcl.2013.08.045 schema:sameAs https://app.dimensions.ai/details/publication/pub.1018764368
128 rdf:type schema:CreativeWork
129 https://doi.org/10.1016/j.bmcl.2015.01.056 schema:sameAs https://app.dimensions.ai/details/publication/pub.1037755060
130 rdf:type schema:CreativeWork
131 https://doi.org/10.1016/j.ejphar.2007.07.005 schema:sameAs https://app.dimensions.ai/details/publication/pub.1032505247
132 rdf:type schema:CreativeWork
133 https://doi.org/10.1016/j.jep.2009.02.024 schema:sameAs https://app.dimensions.ai/details/publication/pub.1037839541
134 rdf:type schema:CreativeWork
135 https://doi.org/10.1016/j.tet.2004.06.070 schema:sameAs https://app.dimensions.ai/details/publication/pub.1026785742
136 rdf:type schema:CreativeWork
137 https://doi.org/10.1016/s0031-9422(03)00021-9 schema:sameAs https://app.dimensions.ai/details/publication/pub.1030638245
138 rdf:type schema:CreativeWork
139 https://doi.org/10.1016/s0040-4039(01)97839-6 schema:sameAs https://app.dimensions.ai/details/publication/pub.1052159551
140 rdf:type schema:CreativeWork
141 https://doi.org/10.1021/jacs.6b08424 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055876160
142 rdf:type schema:CreativeWork
143 https://doi.org/10.1021/jo01044a010 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055998227
144 rdf:type schema:CreativeWork
145 https://doi.org/10.1021/np049836w schema:sameAs https://app.dimensions.ai/details/publication/pub.1056229737
146 rdf:type schema:CreativeWork
147 https://doi.org/10.1021/np0498657 schema:sameAs https://app.dimensions.ai/details/publication/pub.1056229757
148 rdf:type schema:CreativeWork
149 https://doi.org/10.1021/np970445+ schema:sameAs https://app.dimensions.ai/details/publication/pub.1056239027
150 rdf:type schema:CreativeWork
151 https://doi.org/10.1055/s-2006-958109 schema:sameAs https://app.dimensions.ai/details/publication/pub.1057471133
152 rdf:type schema:CreativeWork
153 https://doi.org/10.1055/s-2006-960961 schema:sameAs https://app.dimensions.ai/details/publication/pub.1057472871
154 rdf:type schema:CreativeWork
155 https://doi.org/10.1080/14786410802267510 schema:sameAs https://app.dimensions.ai/details/publication/pub.1008719797
156 rdf:type schema:CreativeWork
157 https://doi.org/10.1081/scc-120003635 schema:sameAs https://app.dimensions.ai/details/publication/pub.1006833680
158 rdf:type schema:CreativeWork
159 https://doi.org/10.1146/annurev.pharmtox.010909.105812 schema:sameAs https://app.dimensions.ai/details/publication/pub.1043364888
160 rdf:type schema:CreativeWork
161 https://doi.org/10.1248/cpb.37.2819 schema:sameAs https://app.dimensions.ai/details/publication/pub.1025801573
162 rdf:type schema:CreativeWork
163 https://doi.org/10.1248/cpb.51.378 schema:sameAs https://app.dimensions.ai/details/publication/pub.1033135052
164 rdf:type schema:CreativeWork
165 https://doi.org/10.1673/031.010.1301 schema:sameAs https://app.dimensions.ai/details/publication/pub.1048093970
166 rdf:type schema:CreativeWork
167 https://doi.org/10.19540/j.cnki.cjcmm.20170308.003 schema:sameAs https://app.dimensions.ai/details/publication/pub.1091248956
168 rdf:type schema:CreativeWork
169 https://www.grid.ac/institutes/grid.412561.5 schema:alternateName Shenyang Pharmaceutical University
170 schema:name Key Laboratory of Computational Chemistry-Based Natural Antitumor Drug Research and Development, Wenhua Road 103, Shenyang, Liaoning Province, 110016, China.
171 Key Laboratory of Computational Chemistry-Based Natural Antitumor Drug Research and Development, Wenhua Road 103, Shenyang, Liaoning Province, 110016, China. chengang1152001@163.com.
172 School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China.
173 School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China. chengang1152001@163.com.
174 rdf:type schema:Organization
 




Preview window. Press ESC to close (or click here)


...