Molecular structures and antiviral activities of naturally occurring and modified cassane furanoditerpenoids and friedelane triterpenoids from Caesalpinia minax
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AbstractFurther investigation of the active components of the chloroform fraction of the seeds of Caesalpinia minax led to the isolation of a new cassane furanoditerpenoid, caesalmin H (1). together with two known furanoditerpenoid lactones, caesalmin B (2) and bonducellpin D (3). Reduction of the naturally abundant caesalmin D (9). E (10) and F (11) resulted in three new furanoditerpenoid derivatives 4-6. Phytochemical study of the stem of the same plant and subsequent reduction afforded mo friedelane triterpenoids (7-8), which were identified by spectroscopic methods, Compounds 1-2 and 4-8 were corroborated by single crystal X-ray analysis. The factors governing the reduction of cassane furanoditerpenoids and friedelane triterpenoids were investigated by correlating the crystallographic results with density functional theory. The inhibitor activities of 2-8 on the Para3 virus were evaluated by cytopathogenic effects (CPE) reduction assay. (C) 2002 Elsevier Science Ltd. All rights reserved.
All Author(s) ListJiang RW, Ma SC, He ZD, Huang XS, But PPH, Wang H, Chan SP, Ooi VEC, Xu HX, Mak TCW
Journal nameBioorganic and Medicinal Chemistry
Year2002
Month7
Day1
Volume Number10
Issue Number7
PublisherPERGAMON-ELSEVIER SCIENCE LTD
Pages2161 - 2170
ISSN0968-0896
LanguagesEnglish-United Kingdom
Web of Science Subject CategoriesBiochemistry & Molecular Biology; BIOCHEMISTRY & MOLECULAR BIOLOGY; Chemistry; Chemistry, Medicinal; CHEMISTRY, MEDICINAL; Chemistry, Organic; CHEMISTRY, ORGANIC; Pharmacology & Pharmacy

Last updated on 2020-13-10 at 02:35