59 research outputs found
The chemistry and biological activity of the Hyacinthaceae
Covering: 1914 to 2012The Hyacinthaceae (sensu APGII), with approximately 900 species in about 70 genera, can be divided into three main subfamilies, the Hyacinthoideae, the Urgineoideae and the Ornithogaloideae, with a small fourth subfamily the Oziroëoideae, restricted to South America. The plants included in this family have long been used in traditional medicine for a wide range of medicinal applications. This, together with some significant toxicity to livestock has led to the chemical composition of many of the species being investigated. The compounds found are, for the most part, subfamily-restricted, with homoisoflavanones and spirocyclic nortriterpenoids characterising the Hyacinthoideae, bufadienolides characterising the Urgineoideae, and cardenolides and steroidal glycosides characterising the Ornithogaloideae. The phytochemical profiles of 38 genera of the Hyacinthaceae will be discussed as well as any biological activity associated with both crude extracts and compounds isolated. The Hyacinthaceae of southern Africa were last reviewed in 2000 (T. S. Pohl, N. R. Crouch and D. A. Mulholland, Curr. Org. Chem., 2000, 4, 1287-1324; ); the current contribution considers the family at a global level
ChemInform Abstract: SYNTH. VON 1-(P-CHLORBENZYL-7-AZAINDOL-3)-ALPHA-PIPERIDYL-METHANOL ALS POTENTIELLEM ANTIMALARIAMITTEL
Synthesis of 1-p-chlorobenzyl-7-azaindole-3-.alpha.-piperidylmethanol as a potential antimalarial agent
RECENT RESEARCH ON RED SQUILL AS A RODENTICIDE
Red squill has been used in rodent control for several hundred years but in the United States its use has decreased since the 1950s. However, there is now a recognized need for rodenticides with different kinds of toxic activity. Red squill is being investigated as an acute rodenticide and an economic crop for the southwestern states. Clones from a prior USDA collection have been assayed by high-performance liquid chromatography and selections are being propagated in California and Arizona. The major toxicant, scilliroside, is relatively fast acting, causing convulsions and death to rats and mice. This glycoside is also strongly emetic to humans, cats and dogs, affording a safety factor uncommon to high-toxicity rodenticides. Our chemical, processing, agronomic, and toxicological studies are a technical basis for further developing this potentially superior rodenticide
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