File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Pseudolaric acids: Isolation, bioactivity and synthetic studies

TitlePseudolaric acids: Isolation, bioactivity and synthetic studies
Authors
Chiu, PLeung, LTKo, BCB
Issue Date2010
PublisherRoyal Society of Chemistry. The Journal's web site is located at http://www.rsc.org/npr
Citation
Natural Product Reports, 2010, v. 27 n. 7, p. 1066-1083 How to Cite?
DOI: http://dx.doi.org/10.1039/b906520m
AbstractThe pseudolaric acids are diterpenoids isolated from the root bark of Pseudolarix amabilis, or the golden larch. Pseudolaric acids A and B are the major antifungal and anti-angiogenic congeners of this family of compounds. This review presents the results of the isolation, biological and synthetic studies of these natural products. © 2010 The Royal Society of Chemistry.
Persistent Identifierhttp://hdl.handle.net/10722/125253
ISSN
0265-0568
2021 Impact Factor: 15.111
2020 SCImago Journal Rankings: 2.703
ISI Accession Number ID
WOS:000279111100005
Funding AgencyGrant Number
University of Hong Kong
University Grants Committee of the Hong Kong Special Administrative RegionAoE/P-10/01
Funding Information:

We thank the University of Hong Kong for a postdoctoral fellowship for LTL and support from the University Grants Committee of the Hong Kong Special Administrative Region, Areas of Excellence Scheme Grant AoE/P-10/01.

References
References in Scopus
Grants
Institute of molecular technology for drug discovery and synthesis

 

DC FieldValueLanguage
dc.contributor.authorChiu, Pen_HK
dc.contributor.authorLeung, LTen_HK
dc.contributor.authorKo, BCBen_HK
dc.date.accessioned2010-10-31T11:20:11Z-
dc.date.available2010-10-31T11:20:11Z-
dc.date.issued2010en_HK
dc.identifier.citationNatural Product Reports, 2010, v. 27 n. 7, p. 1066-1083en_HK
dc.identifier.issn0265-0568en_HK
dc.identifier.urihttp://hdl.handle.net/10722/125253-
dc.description.abstractThe pseudolaric acids are diterpenoids isolated from the root bark of Pseudolarix amabilis, or the golden larch. Pseudolaric acids A and B are the major antifungal and anti-angiogenic congeners of this family of compounds. This review presents the results of the isolation, biological and synthetic studies of these natural products. © 2010 The Royal Society of Chemistry.en_HK
dc.languageengen_HK
dc.publisherRoyal Society of Chemistry. The Journal's web site is located at http://www.rsc.org/npren_HK
dc.relation.ispartofNatural Product Reportsen_HK
dc.subject.meshAngiogenesis Inhibitors-
dc.subject.meshAnti-Infective Agents-
dc.subject.meshBiological Products - chemical synthesis - chemistry - isolation and purification - pharmacology-
dc.subject.meshDiterpenes - chemical synthesis - chemistry - isolation and purification - pharmacology-
dc.subject.meshDrugs, Chinese Herbal - chemical synthesis - chemistry - isolation and purification - pharmacology-
dc.titlePseudolaric acids: Isolation, bioactivity and synthetic studiesen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0265-0568&volume=27&issue=7&spage=1066&epage=1083&date=2010&atitle=Pseudolaric+acids:+isolation,+bioactivity+and+synthetic+studiesen_HK
dc.identifier.emailChiu, P: pchiu@hku.hken_HK
dc.identifier.emailLeung, LT: h0104628@graduate.hku.hken_HK
dc.identifier.authorityChiu, P=rp00680en_HK
dc.identifier.authorityLeung, LT=rp00734en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/b906520men_HK
dc.identifier.pmid20405078-
dc.identifier.scopuseid_2-s2.0-77954676306en_HK
dc.identifier.hkuros174391en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-77954676306&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume27en_HK
dc.identifier.issue7en_HK
dc.identifier.spage1066en_HK
dc.identifier.epage1083en_HK
dc.identifier.eissn1460-4752-
dc.identifier.isiWOS:000279111100005-
dc.publisher.placeUnited Kingdomen_HK
dc.relation.projectInstitute of molecular technology for drug discovery and synthesis-
dc.identifier.scopusauthoridChiu, P=11140148700en_HK
dc.identifier.scopusauthoridLeung, LT=36196831900en_HK
dc.identifier.scopusauthoridKo, BCB=7102833927en_HK
dc.identifier.issnl0265-0568-

Export via OAI-PMH Interface in XML Formats

OR

Export to Other Non-XML Formats