## Abstract The label from (__S__)‐[1‐^13^C]norcoclaurine and (__S__)‐[1‐^13^C]co‐claurine was highly and nonrandomly incorporated into (__S__)‐reticuline in benzyltetrahydroisoquinoline‐producing plant cell cultures of __Berberis stolonifera, Eschscholtzia californica__ and __Peumus boldus__. From
γ-Coniceine of conium maculatum L., a revision of the generally accepted structure
✍ Scribed by H. C. Beyerman; M. van Leeuwen; J. Smidt; A. van Veen
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 692 KB
- Volume
- 80
- Category
- Article
- ISSN
- 0165-0513
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The commonly accepted structure of γ‐coniceine, the major alkaloid of Conium maculatum L., is revised on the basis of results obtained in the present study with “active hydrogen” determinations and with regard to nuclear magnetic resonance spectra. Infra‐red spectra also support this revision.
γ‐Coniceine is 2‐n‐propyl‐3,4,5,6‐tetrahydropyridine.
The revised structure of γ‐coniceine (a Δ^1^ ‐ piperideine) seems of interest with a view to the biogenesis of the piperidine alkaloids and related amino‐acids.
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## Abstract A mollusk‐specific toxin, TxVIIA, having potent paralytic activity was isolated from the venom of sea snail __Conus textile__ (Fainzilber M et al., 1991, __Eur J Biochem 202__:589–595). The structure reported above was based upon amino acid analysis and the Edman degradation. We have re