Helvetica Chimica Acta · 1989 · 41 citations · 13 references
PharmacyMedicinal ChemistryPharmacologyCancer PharmacologyDrug DiscoveryStructure-activity RelationshipsMedicinal Plant KnowledgeMedicinal PlantsNatural Product DerivatizationNatural Product Drug DiscoveryStructure-activity Relationship AnalysisActive Compound IsolationAnticancer ActivityAnticancer Natural ProductsBioactive Plant CompoundsCrude Extract PreparationFractionationPharmacological ScreeningPlant-derived Natural Products
Abstract The crude petroleum‐ether extract of the root bark of Hypericum revolutum V AHL (Guttiferae) exhibited in vitro growth‐inhibitory activity against the Co‐115 human colon carcinoma cell line. Activity‐guided fractionation of this extract resulted in the isolation of two new hyperforin derivatives 1 and 2 . The structure of 1 (hyperevolutin A) was established by X‐ray analysis as the 4‐hydroxy‐8‐ exo ‐methyl‐5,7‐ exo ‐bis(3‐methylbut‐2‐enyl)‐1‐(2‐methyl‐1‐oxopropyl)‐8‐ endo ‐(4‐methylpent‐3‐enyl)bicyclo[3.3.1]non‐3‐ene‐2,9‐dione. The structure of the homologue 2 was deduced by comparison of its UV and 1 H‐ and 13 C‐NMR spectra with those of 1 .
13
<i>International Tables for X-ray Crystallography</i>
Acta Crystallographica Section B · 1976 · 14.2K citations · Full text
A New Spray Reagent for Paper Chromatography of Polyols and Cetoses
Paul J. Godin · Nature · 1954 · 189 citations · Full text
N. S. Bystrov, B. K. CHERNOV, V. N. Dobrynin et al. · Tetrahedron Letters · 1975 · 146 citations
[Antibiotic hyperforin from Hypericum perforatum L].
Gurevich Ai, Dobrynin Vn, Kolosov Mn et al. · PubMed · 1971 · 98 citations
Life Sciences, Pharmacotherapy, Antimicrobial Pharmacology +1