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1.
Phytochem Rev ; 15: 161-195, 2016.
Article in English | MEDLINE | ID: mdl-27065758

ABSTRACT

After the sensational rediscovery of living exemplars of the Cretaceous relict Metasequoia glyptostroboides-a tree previously known exclusively from fossils from various locations in the northern hemisphere, there has been an increasing interest in discovery of novel natural products from this unique plant source. This article includes the first complete compilation of natural products reported from M. glyptostroboides during the entire period in which the tree has been investigated (1954-2014) with main focus on the compounds specific to this plant source. Studies on the biological activity of pure compounds and extracts derived from M. glyptostroboides are reviewed for the first time. The unique potential of M. glyptostroboides as a source of bioactive constituents is founded on the fact that the tree seems to have survived unchanged since the Cretaceous era. Since then, its molecular defense system has resisted the attacks of millions of generations of pathogens. In line with this, some recent landmarks in Metasequoia paleobotany are covered. Initial spectral analysis of recently discovered intact 53 million year old wood and amber of Metasequoia strongly indicate that the tree has remained unchanged for millions of years at the molecular level.

2.
Fitoterapia ; 95: 109-14, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24631762

ABSTRACT

Metasequoia glyptostroboides, a tree native to China, is described as a living fossil and has existed for millions of years. The oldest fossils recorded have been dated to the late Cretaceous era. During the time of its existence, the molecular defence system of the tree has apparently resisted millions of generations of pathogens, which encouraged search for novel natural product from this source. Eight compounds have been characterised from needles of M. glyptostroboides, including the novel natural product 6-carboxydihydroresveratrol 3-O-ß-glucopyranoside. The structure determinations were based on extensive use of 2D NMR spectroscopic techniques and high-resolution mass spectrometry.


Subject(s)
Cupressaceae/chemistry , Free Radical Scavengers/chemistry , Glucosides/chemistry , Lipoxygenase Inhibitors/chemistry , Stilbenes/chemistry , Biological Assay , Biological Products , Biphenyl Compounds/pharmacology , Free Radical Scavengers/isolation & purification , Free Radical Scavengers/pharmacology , Glucosides/isolation & purification , Glucosides/pharmacology , Lipoxygenase Inhibitors/isolation & purification , Lipoxygenase Inhibitors/pharmacology , Magnetic Resonance Spectroscopy , Mass Spectrometry , Molecular Structure , Picrates/pharmacology , Plant Leaves/chemistry , Plants, Medicinal , Stilbenes/isolation & purification , Stilbenes/pharmacology , Trees
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