Document 1277
 DOCN  M9591277
 TI    Four diterpene esters from Euphorbia myrsinites.
 DT    9509
 AU    Oksuz S; Gurek F; Gil RR; Pengsuparp T; Pezzuto JM; Cordell GA;
       Department of Chemistry, Faculty of Pharmacy, University of; Istanbul,
       Turkey.
 SO    Phytochemistry. 1995 Apr;38(6):1457-62. Unique Identifier : AIDSLINE
       MED/95306027
 AB    The Turkish species Euphorbia myrsinites has yielded four new
       tetracyclic diterpene tetraesters from a cytotoxic acetone extract, in
       addition to the known cycloartane-type triterpenoids and betulin. The
       new compounds and their hydrolysis product have been extensively
       characterized by high field spectroscopic techniques, and were shown to
       be four new tetraesters of the parent alcohol, myrsinol.
 DE    Antiviral Agents/*CHEMISTRY/ISOLATION & PURIF/PHARMACOLOGY  Comparative
       Study  Diterpenes/*CHEMISTRY/ISOLATION & PURIF/PHARMACOLOGY
       Esters/CHEMISTRY/ISOLATION & PURIF  HIV-1/ENZYMOLOGY  Molecular
       Conformation  Molecular Structure  Nuclear Magnetic Resonance  *Plants,
       Medicinal  Reverse Transcriptase/*ANTAGONISTS & INHIB  Support, Non-U.S.
       Gov't  Support, U.S. Gov't, P.H.S.  Turkey  JOURNAL ARTICLE

       SOURCE: National Library of Medicine.  NOTICE: This material may be
       protected by Copyright Law (Title 17, U.S.Code).