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A New Group of Plant-Derived Naphthoquinone Pesticides
β Scribed by Khambay, Bhupinder P. S.; Batty, David; Beddie, David G.; Denholm, Ian; Cahill, Matthew R.
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 228 KB
- Volume
- 50
- Category
- Article
- ISSN
- 1526-498X
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β¦ Synopsis
A series of compounds with structures based on insecticidal/acaricidal naphthoquinones isolated from Calceolaria andina has been synthesised. A feature of the series is the lack of resistance shown by strains resistant to established classes of pesticides. The importance for activity of the tetra-substituted carbon atom in the side-chain, as observed in the natural products, has been investigated. In analogues with acyclic side-chains the position of the tetrasubstituted carbon for optimum activity was dependent on the length of the sidechain. With cyclic side-chains, activity was dependent on the size of the ring, the number and position of the substituents therein. Activity of the compounds examined was particularly high against Bemisia tabaci and T etranychus urticae in direct-contact tests, but was much lower than expected in leaf-dip tests. A partial improvement based on formulation has been demonstrated.
π SIMILAR VOLUMES
The growth of the white-rot basidiomycete Pleurotus sajor-caju in malt-agar plates was inhibited by three naturally occurring, plant-derived naphthoquinones: juglone, lawsone, and plumbagin. The latter two compounds exerted the most potent antifungal activity, and lawsone killed the mycelium at conc