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From Local To Global - Fifty Years Of Research On Salvia Divinorum, Ivan Casselman, Catherine Nock, Hans Wohlmuth, Robert Weatherby, Michael Heinrich

Dr Hans Wohlmuth

Ethnopharmacological relevance: In 1962 ethnopharmacologists, Hofmann and Wasson, undertook an expedition to Oaxaca, Mexico. These two researchers were the first scientists to collect a flowering specimen of Salvia divinorum allowing the identification of this species. While the species' traditional use is confined to a very small region of Mexico, since Hofmann and Wasson's expedition 50 years ago, Salvia divinorum has become globally recognized for its main active constituent, the diterpene salvinorin A, which has a unique effect on human physiology. Salvinorin A is a kappa-opioid agonist and the first reported psychoactive diterpene.

Methods: This review concentrates on the investigation of …

Adulteration Of Ginkgo Biloba Products And A Simple Method To Improve Its Detection, Hans Wohlmuth, Kate Savage, Ashley Dowell, Peter Mouatt

Dr Hans Wohlmuth

Extracts of ginkgo (Ginkgo biloba) leaf are widely available worldwide in herbal medicinal products, dietary supplements, botanicals and complementary medicines, and several pharmacopoeias contain monographs for ginkgo leaf, leaf extract and finished products. Being a high-value botanical commodity, ginkgo extracts may be the subject of economically motivated adulteration. We analysed eight ginkgo leaf retail products purchased in Australia and Denmark and found compelling evidence of adulteration with flavonol aglycones in three of these. The same three products also contained genistein, an isoflavone that does not occur in ginkgo leaf. Although the United States Pharmacopeia – National Formulary (USP-NF) and the …

Antibacterial Anthranilic Derivatives From Geijera Parviflora, Qing-Yao Shou, Linda Banbury, Alan Maccarone, Dane Renshaw, Htwe Mon, Stefani Griesser, Hans Griesser, Stephen Blanksby, Joshua Smith, Hans Wohlmuth

Dr Hans Wohlmuth

Five anthranilic acid derivatives, a mixture I of three new compounds 11′-hexadecenoylanthranilic acid (1), 9′-hexadecenoylanthranilic acid (2), and 7′-hexadecenoylanthranilic acid (3), as well as a new compound 9,12,15-octadecatrienoylanthranilic acid (4) together with a new natural product, hexadecanoylanthranilic acid (5), were isolated from Geijera parviflora Lindl. (Rutaceae). Their structures were elucidated by extensive spectroscopic measurements, and the positions of the double bonds in compounds 1–3 of the mixture I were determined by tandem mass spectrometry employing ozone-induced dissociation. The mixture I and compound 5 showed good antibacterial activity against several Gram-positive strains.