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Norditerpenoid alkaloids from Consolida orientalis and complete 1H and 13C NMR signal assignments of some lycoctonine-type alkaloids
- Source :
- Journal of natural products. 65(7)
- Publication Year :
- 2002
-
Abstract
- A new norditerpene alkaloid was isolated, 18-demethylpubescenine (1), in addition to four known compounds, 14-demethyltuguaconitine (2), takaosamine (3), gigactonine (4), and delcosine (5), from fresh, whole plants of Consolida orientalis. The structure of 1 was established by spectroscopic methods, including various 2D NMR techniques and HRESIMS. As a result of a detailed NMR study, complete 1H NMR chemical shift assignments for alkaloids 1-5 are presented herein, and some 13C NMR signal assignments for 2-4 have been revised.
- Subjects :
- Stereochemistry
Molecular Conformation
Pharmaceutical Science
Ranunculaceae
Biology
Analytical Chemistry
Gigactonine
chemistry.chemical_compound
Alkaloids
Drug Discovery
Organic chemistry
Nuclear Magnetic Resonance, Biomolecular
Pharmacology
Hungary
Plants, Medicinal
Molecular Structure
Alkaloid
Organic Chemistry
Carbon-13 NMR
biology.organism_classification
Complementary and alternative medicine
chemistry
Proton NMR
Molecular Medicine
Spectrophotometry, Ultraviolet
Lycoctonine
Diterpene
Diterpenes
Two-dimensional nuclear magnetic resonance spectroscopy
Subjects
Details
- ISSN :
- 01633864
- Volume :
- 65
- Issue :
- 7
- Database :
- OpenAIRE
- Journal :
- Journal of natural products
- Accession number :
- edsair.doi.dedup.....2373c7563a002d124232e100f6b008d1