Literature DB >> 23892453

The chemistry and biological activity of the Hyacinthaceae.

Dulcie A Mulholland1, Sianne L Schwikkard, Neil R Crouch.   

Abstract

The 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; ref. 1); the current contribution considers the family at a global level.

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Year:  2013        PMID: 23892453     DOI: 10.1039/c3np70008a

Source DB:  PubMed          Journal:  Nat Prod Rep        ISSN: 0265-0568            Impact factor:   13.423


  15 in total

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2.  Bufadienolides and anti-angiogenic homoisoflavonoids from Rhodocodon cryptopodus, Rhodocodon rotundus and Rhodocodon cyathiformis.

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5.  Acaricidal Activity of Bufadienolides Isolated from Drimia pancration against Tetranychus urticae, and Structural Elucidation of Arenobufagin-3-O-α-L-rhamnopyranoside.

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Journal:  J Org Chem       Date:  2019-08-05       Impact factor: 4.354

7.  Cytotoxic homoisoflavonoids from the bulbs of Bellevalia flexuosa.

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Journal:  Fitoterapia       Date:  2018-02-20       Impact factor: 2.882

8.  Synthesis of Natural Homoisoflavonoids Having Either 5,7-Dihydroxy-6-methoxy or 7-Hydroxy-5,6-dimethoxy Groups.

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Journal:  Molecules       Date:  2016-08-13       Impact factor: 4.411

9.  Identification by Molecular Docking ofHomoisoflavones from Leopoldia comosa as Ligands of Estrogen Receptors.

Authors:  Fedora Grande; Bruno Rizzuti; Maria A Occhiuzzi; Giuseppina Ioele; Teresa Casacchia; Fabrizio Gelmini; Rita Guzzi; Antonio Garofalo; Giancarlo Statti
Journal:  Molecules       Date:  2018-04-12       Impact factor: 4.411

10.  Sulfadiazine Masquerading as a Natural Product from Scilla madeirensis (Scilloideae).

Authors:  Luke P Robertson; Lindon W K Moodie; Darren C Holland; K Charlotte Jandér; Ulf Göransson
Journal:  J Nat Prod       Date:  2020-03-25       Impact factor: 4.050

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