Prenylflavans from Tephrosia watsoniana

The aerial parts of tephrosia watsoniana afforded five new flavonoids named tephrowatsin A, B, C, D and E. Their structures and stereochemistries were established by spectroscopic methods and chemical transformations.     

New natural rotenoid and pterocarpanoid analogues from Neorautanenia Amboensis

Four new natural rotenoid and pterocarpanoid analogues, neobanone, rotenonone, 12a-hydroxyisomillettone and neobanol were isolated from the benzene extract of the root of Neorautanenia amboensis. The structures were determined by investigation of IR, UV, MS, ¹H-NMR, CD and oxidative conversions.     

Prenylated flavonoids from Tephrosia purpurea seeds

Two new prenylated flavonoids, purpuritenin purpureamethide, have been characterized from the seeds of Tephrosia purpurea together with the known c     

A prenylated flavan from Tephrosia madrensis

5,7-Dimethoxy-8-prenylflavan has been isolated and identified from aerial parts of Tephrosia madrensis.     

Extracts from Tephrosia vogelii for the protection of stored legume seeds against damage by three bruchid species

Aliquots of powdered dried leaves of Tephrosia vogelii (Leguminosae – Papilionoideae) were extracted with hexane, acetone and ethanol. The extracts were tested for their potential to protect stored legume seeds from damage by the bruchids Acanthoscelides obtectus, Callosobruchus maculatus and Callosobruchus chinensis (Coleoptera – Bruchidae). While the acetone and ethanol extracts were ineffective except for a significant but low effect on A. obtectus, the hexane extract had a relatively high efficacy, providing similar control of all three bruchid species. This effect was manifested in slowly‐reduced adult survival within 7 days and in reduced numbers of eggs laid and of F₁ progeny produced, resulting in seed damage averaging 7.1% compared to 99.8% in the untreated controls after one generation. These findings are discussed in the context of previously identified constituents of T. vogelii, the rotenoids rotenone, tephrosin and deguelin.     

A laboratory assessment of the potential molluscicidal activity of some Nigerian plant species used as anthelmintics

Laboratory studies were conducted to determine the potential molluscicidal activity of five Nigerian plant species used in alternative medicine practice as anthelmintics. Laboratory-bred adult Biomphalaria pfeifferi, the snail host of Schistosoma mansoni in Nigeria, and their viable 0- to 24-hour-old egg masses were separately exposed for 24 hours, in replicated bioassays, to 7.81–4 000 mg l^?1 concentrations of crude ethanolic extracts of the leaves and roots of Annona senegalensis, Anogeissus leiocarpus, Crotalaria retusa, Dalbergia sissoo and Vernonia amygdalina. Fruits and stem bark of D. sissoo were also investigated. The 24-hour LC50 and LC90 values of extracts for target organisms were calculated using probit analysis. Susceptibility of target organisms to extracts varied with the plant species and morphological part. Egg masses and adult snails were most susceptible to D. sissoo fruit extract (LC90 values of 89.29 and 74.33 mg l^?1, respectively) and least susceptible to V. amygdalina leaf extract (LC90 values of 11 864.09 and 6 241.61 mg l^?1, respectively). Concentration-dependent behavioural responses and embryo deaths at the gastrula/exogastrula and/or prehatch snail stages of development were observed in exposed snails and egg masses, respectively. Tested extracts of A. senegalensis, A. leiocarpus, C. retusa and V. amygdalina did not show appreciable toxicities to B. pfeifferi egg masses or adults. For demonstrating significant molluscicidal activity (LC90 < 100 mg l^?1) and toxicities to egg masses, we recommend further studies on the ethanolic extracts of D. sissoo fruits and roots.     

Molluscicidal activity of affinin and other isobutylamides from the asteraceae

Unsaturated aliphatic isobutylamides from Asteraceae, Rutaceae and Piperaceae are potential agents to control schistosomiasis. Affinin (N-isobutyl-2,6,8-decatrienamide) from Heliopsis longipes has strong molluscicidal activity against Physa occidentalis (ld₅₀ca 100 μM) and the cercariae of the fluke. The amide has also been shown to be present in Wedelia parviceps flowers.     

Viridiflorin,an isoflavone from Tephrosia viridiflora

A new isoflavone, viridiflorin, has been isolated from Tephrosia viridiflora. Its structure was established as 4′,5,7-trihydroxy-2′,5′-dimethoxy-6-prenylisoflavone based on spectral evidence and chemical transformation.     

Inducibly-formed isoflavonoids from leaves of soybean

Isoformononetin, glyceollins I, II and 2-isopentenyl-3,6a,9-trihydroxypterocarpan (glyceocarpin) accumulated in soybean (Glycine max) leaves after treatment with aqueous sodium iodoacetate or a cell suspension of the bacterium, Pseudomonas pisi. These compounds were also accompanied by two previously unreported pterocarpans, glyceofuran its 9-O-methyl derivative. Glyceocarpin is described for the first time as a plant product.     

Further studies on the isoflavones of Tephrosia maxima

A new 7,8-methylenedioxyisoflavone, maxima isoflavone H, was isolated from Tephrosia maxima along with the known isoflavone, maxima isoflavone B.     

Molluscicidal saponins from Gundelia tournefortii

From the roots of Gundelia tournefortii seven saponins have been isolated mainly by DCCC. The main saponins (A and B) were characterized, mainly by ¹³C and ¹H NMR spectroscopy, as oleanolic acid 3-O-(2-[α-l-arabinopyranosyl(1 → 3) -β-d-gentiotriosyl(1 → 6) -β-d-glucopyranosyl]gb-d-xylopyranoside) (saponin A) and oleanolic acid 3-O-(2-[α-l-arabinopyranosyl] (1 → 3)-β-d-gentiobiosyl (1 → 6)-β-d-glucopyranosyl β-d-xylopyranoside) (saponin B). The other saponins are also derived from oleanolic acid and contain more sugar units. The saponin mixture and the saponins A and B possess strong molluscicidal activity against the schistosomiasis transmitting snail Biomphalaria glabrata.