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Several Other Compounds (several + other_compound)
Selected AbstractsReview of issues concerning the use of reproductive inhibitors, with particular emphasis on resolving human-wildlife conflicts in North AmericaINTEGRATIVE ZOOLOGY (ELECTRONIC), Issue 1 2010Kathleen A. FAGERSTONE Abstract This manuscript provides an overview of past wildlife contraception efforts and discusses the current state of research. Two fertility control agents, an avian reproductive inhibitor containing the active ingredient nicarbazin and an immunocontraceptive vaccine, have received regulatory approval with the Environmental Protection Agency and are commercially available in the USA. OvoControl G Contraceptive Bait for Canada Geese and Ovo Control for pigeons are delivered as oral baits. An injectable immunocontraceptive vaccine (GonaCon Immunocontraceptive Vaccine) was registered with the Environmental Protection Agency for use in female white-tailed deer in September 2009. An injectable product (GonaCon Immunocontraceptive Vaccine) is registered for use in female white-tailed deer. Both products are labeled for use in urban/suburban areas where these species are overabundant. Several other compounds are currently being tested for use in wildlife in the USA, Europe, Australia and New Zealand that could have promise in the future. The development and use of reproductive inhibitors for resolving human,wildlife conflicts will depend on a number of factors, including meeting the requirements of regulatory agencies for use in the environment and on the biological and economical feasibility of their use. Use will also be dependent on health and safety issues and on public acceptance of the techniques. [source] The New Metabolite (S)-Cinnamoylphosphoramide from Streptomyces sp. and Its Total SynthesisEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 30 2008Melanie Quitschau Abstract The tunicate-associated strain Streptomyces sp. JP90 produces the unprecedented metabolite cinnamoylphosphoramide (1) among several other compounds. Structure elucidation was accomplished by NMR spectroscopic studies and efficient total synthesis. The absolute configuration at phosphorus was determined by synthesis of both enantiomers of 1 performing a resolution of the corresponding diastereomeric phosphoramides of L -phenylalanine ethyl ester. Unusual cinnamic acid derivative 1 represents the first bacterial organophosphoramide. As it matches the Schrader's formula for insecticidal organophosphates, its biological activity was investigated. A weak inhibition of acetylcholinesterase was observed in in vitro tests, and water-soluble analogues of 1 were prepared. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008) [source] Backhousia citriodora F. Muell.,Rediscovery and chemical characterization of the L -citronellal form and aspects of its breeding systemFLAVOUR AND FRAGRANCE JOURNAL, Issue 5 2001J. C. Doran Abstract The rare L -citronellal form of Backhousia citriodora F. Muell. was first reported in 1950 but attempts to relocate it were unsuccessful until 1996. The quest to relocate trees of this type has been driven by interest in L -citronellal for perfumery. The common, citral form of the species is already under cultivation for oil production in Australia. This paper reports on the rediscovery of the L -citronellal form, first in 1996 in a year-old provenance/progeny trial of B. citriodora in south-eastern Queensland, and then in a natural population on Queensland's Sunshine Coast in 1998. The three L -citronellal trees in the trial gave foliar oil concentrations (g/100 g dry weight) of 3.2, 2.2 and 1.8, respectively, when sampled in November 1996. The same trees sampled in March 1999 gave pale yellow oils consisting of 85,89% citronellal, 6,9% isopulegol isomers with small quantities of citronellol (approx. 3%) and several other compounds. Data on the physicochemical properties of these oils are given in the paper. Seed from a single mature L -citronellal tree gave progeny of both the L -citronellal and citral form in a ratio of approximately 1 : 1. Propagation material from many more plants of the L -citronellal form needs to be collected and assembled in breeding populations. This would form the basis of a selection and breeding programme, should this chemotype show economic potential. Copyright © 2001 John Wiley & Sons, Ltd. [source] Barley polyamine oxidase: characterisation and analysis of the cofactor and the N-terminal amino acid sequencePHYTOCHEMICAL ANALYSIS, Issue 3 2001Anna Radová Abstract This paper reports the first purification method developed for the isolation of an homogeneous polyamine oxidase (PAO) from etiolated barley seedlings. The crude enzyme preparation was obtained after initial precipitation of the extract with protamine sulphate and ammonium sulphate. The enzyme was further purified to a final homogeneity (by the criteria of isoelectric focusing and SDS,PAGE) using techniques of low pressure chromatography followed by two FPLC steps. The purified yellow enzyme showed visible absorption maxima of a flavoprotein at 380 and 450,nm: the presence of FAD as the cofactor was further confirmed by measuring the fluorescence spectra. Barley PAO is an acidic protein (pI 5.4) containing 3% of neutral sugars: its molecular mass determined by SDS,PAGE was 56,kDa, whilst gel permeation chromatography revealed the higher value of 76 kDa. The N-terminal amino acid sequence of barley PAO shows a high degree of similarity to that of maize PAO and to several other flavoprotein oxidases. The polyamines spermine and spermidine were the only two substrates of the enzyme with Km values 4,×,10,5 and 3,×,10,5,M and pH optima of 5.0 and 6.0, respectively. Barley polyamine oxidase is markedly inhibited by acridine dyes and hydrazines. Weak inhibition was observed with substrate analogues, aminoaldehydes, metal chelating agents and several other compounds. Copyright © 2001 John Wiley & Sons, Ltd. [source] | ||||||||||