About: Kuo-Hsiung Lee

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	researcher (en) 연구원 (ko) 研究者 (ja) wetenschapper (nl) дослідник (uk) изилдөөчү (ky) 研究者 (zh)
rdfs:label	李國雄 (zh) Kuo-Hsiung Lee (en) Kuo-Hsiung Lee (nl)
skos:prefLabel	李國雄 (zh) Kuo-Hsiung Lee (en) Kuo-Hsiung Lee (nl)
name	李國雄 (zh) Kuo-Hsiung Lee (en) Kuo-Hsiung Lee (nl)
ResearchGate contributions ID	wds:Q87895492-612a8d64-4c6b-737b-8ba5-0f4d9c8c2611
ResearchGate contributions ID	2066241240
instance of	wds:Q87895492-2DF9B4E9-316D-4769-BB66-9FC2100EBA58
instance of	Homo sapiens
Academic Tree ID	wds:Q87895492-1b528533-4c0c-2a75-c761-45faba5adafd
Academic Tree ID	498149
ResearchGate profile ID	wds:Q87895492-12716642-4e50-2827-a358-fb239544c0fd
ResearchGate profile ID	Kuo-Hsiung-Lee
NORAF ID	wds:Q87895492-90be25a9-4131-e853-6ec5-da6359b5347f
occupation	wds:Q87895492-6ABC0585-8DF1-42DE-92D6-BFE27D54123D
NUKAT ID	wds:Q87895492-523c72dc-4201-6839-3e4c-248fc7b4996b
sex or gender	wds:Q87895492-5972ED53-E23A-43CD-AC11-F6AEAFF7CF75
ISNI	wds:Q87895492-3a8353c6-405b-2fc7-a48b-8750d13ef04f
VIAF ID	wds:Q87895492-386a0537-4e3b-137b-82ba-f3a15e38988a
Library of Congress authority ID	wds:Q87895492-d9c8faeb-4873-8951-5488-e3239d8abcf1
Bibliothèque nationale de France ID	wds:Q87895492-27f8e8c4-4786-765d-ae0d-7d89c45dc1c5
IdRef ID	wds:Q87895492-0c3851b6-4f38-dbaf-e56a-433faf2160c2
SHARE Catalogue author ID	wds:Q87895492-D2EA0A31-903C-455B-A893-6DD12850D89C
date of death	wds:Q87895492-77346fe3-4f70-455c-aaa6-038bb97b2b72
NORAF ID	https://livedata.bibsys.no/authority/3042592
VIAF ID	http://viaf.org/viaf/47009091
Library of Congress authority ID	http://id.loc.gov/authorities/names/n2002159613
Bibliothèque nationale de France ID	http://data.bnf.fr/ark:/12148/cb14588660p#about
IdRef ID	http://www.idref.fr/073331228/id
NORAF ID	3042592
occupation	researcher
NUKAT ID	n2005115737
sex or gender	male
ISNI	0000000116351110
VIAF ID	47009091
Library of Congress authority ID	n2002159613
Bibliothèque nationale de France ID	14588660p
IdRef ID	073331228
SHARE Catalogue author ID	92089
date of death	2021-10-24 00:00:00Z (xsd:dateTime)
ORCID iD	wds:Q87895492-6A8EACAF-5C38-46D4-B33A-AA32FA59FBF8
ORCID iD	https://orcid.org/0000-0002-6562-0070
ORCID iD	0000-0002-6562-0070
ResearcherID	wds:Q87895492-9781A09A-BCE5-4757-8075-49DE279B6DB0
Publons author ID	wds:Q87895492-bf20e305-4d6d-a509-ff7f-1356f1777854
ResearcherID	H-5153-2013
Publons author ID	2628056
Arnet Miner author ID	wds:Q87895492-738d36a1-43d4-5b7d-aa09-7cfa26550c9e
Arnet Miner author ID	5405a3dcdabfae450f3c03d6
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q87895492
is author of	Prenylated benzophenones and xanthones from Hypericum scabrum. New sesquiterpenes from Capsicum annuum Two new protopines argemexicaines A and B and the anti-HIV alkaloid 6-acetonyldihydrochelerythrine from formosan Argemone mexicana Bioactive constituents from the roots of Panax japonicus var. major and development of a LC-MS/MS method for distinguishing between natural and artifactual compounds Two new sesquiterpenoids and anti-HIV principles from the root bark of Zanthoxylum ailanthoides Cytotoxic and anti-HIV Principles from the Rhizomes of Begonia nantoensis. Constituents from the Stems of Hibiscus taiwanensis. Constituents from the stems of Hibiscus taiwanensis. New lignans and cytotoxic constituents from Wikstroemia lanceolata Cytotoxic and anti-HIV principles from the rhizomes of Begonia nantoensis A new anti-HIV alkaloid, drymaritin, and a new C-glycoside flavonoid, diandraflavone, from Drymaria diandra Cardiac glycosides from Antiaris toxicaria with potent cardiotonic activity Cytotoxic cardiac glycosides and coumarins from Antiaris toxicaria Interiotherins C and D, two new lignans from Kadsura interior and antitumor-promoting effects of related neolignans on Epstein-Barr virus activation 2-(3-Methoxyphenyl)-5-methyl-1,8-naphthyridin-4(1H)-one (HKL-1) induces G2/M arrest and mitotic catastrophe in human leukemia HL-60 cells The cytotoxic principles of Hyptis capitata and the structures of the new triterpenes hyptatic acid-A and -B Physanolide A, a novel skeleton steroid, and other cytotoxic principles from Physalis angulata Isolation, structures, and structure - cytotoxic activity relationships of withanolides and physalins from Physalis angulata Rapid Recognition and Targeted Isolation of Anti-HIV Daphnane Diterpenes from Daphne genkwa Guided by UPLC-MSn CHM-1, a new vascular targeting agent, induces apoptosis of human umbilical vein endothelial cells via p53-mediated death receptor 5 up-regulation. Antitumor agents 270. Novel substituted 6-phenyl-4H-furo[3,2-c]pyran-4-one derivatives as potent and highly selective anti-breast cancer agents Antitumor agents. 266. Design, synthesis, and biological evaluation of novel 2-(furan-2-yl)naphthalen-1-ol derivatives as potent and selective antibreast cancer agents. Antitumor agents. 254. Synthesis and biological evaluation of novel neo-tanshinlactone analogues as potent anti-breast cancer agents Antitumor Agents. 239. Isolation, structure elucidation, total synthesis, and anti-breast cancer activity of neo-tanshinlactone from Salvia miltiorrhiza Betulinic acid derivatives as human immunodeficiency virus type 2 (HIV-2) inhibitors Anticancer principles from medicinal piper ( hú jiāo) plants. New cembranolide analogues from the formosan soft coral Sinularia flexibilis and their cytotoxicity. Optimization of 2,4-diarylanilines as non-nucleoside HIV-1 reverse transcriptase inhibitors Cancer preventive agents. Part 8: Chemopreventive effects of stevioside and related compounds Dantaxusins C and D, two novel taxoids from Taxus yunnanensis. Antifeedant and Insecticidal Activity of Quassinoids against the Diamondback Moth(Plutella xylostella)and Structure—Activity Relationships Antitumor agents. 228. five new agarofurans, Reissantins A-E, and cytotoxic principles from Reissantia buchananii. New developments in the chemistry and biology of the bioactive constituents of Tanshen Recent progress on C-4-modified podophyllotoxin analogs as potent antitumor agents Synthesis and biological relationships of 3',6-substituted 2-phenyl-4-quinolone-3-carboxylic acid derivatives as antimitotic agents Cytotoxic aporphinoid alkaloids from thalictrum sessile Cytotoxic Principles fromSaussurea LappaandCorydalis Turtshaninovii f. Yanhusuo Cancer preventive agents, Part 2: Synthesis and evaluation of 2-phenyl-4-quinolone and 9-oxo-9,10-dihydroacridine derivatives as novel antitumor promoters

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