1 Introduction.- 2 Biodiversity of Bryophytes.- 3 Chemical Diversity of Bryophytes.- Typical Components of Bryophytes.- Chirality of Terpenoids from the Marchantiophyta.- Essential Oils of some Marchantiophyta Species.- Chemical Constituents of in vitro Cultured Cells and Field Gametophytes of some Marchantiophyta Species.- 4 Chemical Constituents of the Marchantiophyta.- Monoterpenoids.- Sesquiterpenoids.- Diterpenoids.- Steroids and Triterpenoids.- Aromatic compounds.- Flavonoids.- Acetogenins and Lipids.- Miscellaneous.- 5 Chemical Constituents of Bryophyta.- Terpenoids.- Steroids and Triterpenoids.- Aromatic Compounds.- Flavonoids.- Acetogenins and Lipids.- 6 Chemical Constituents of Anthocerotophyta.- Terpenoids.- Sterols.- Aromatic Compounds.- Lipids.- Miscellaneous.- 7 Biologically Active Compounds of the Marchantiophyta and Bryophyta.- Fragrance.- Pungency and Bitterness.- Allergenic Contact Dermatitis.- Antibacterial, Antifungal, and Antiviral Activities.- Insect Antifeedant Activity.- Antioxidant Activity.- Antithrombin Activity.- Brine Shrimp Lethality Activity.- Calcium Inhibitory Activity.- Cathepsin B and L Inhibitory Activity.- Cytotoxic and Apoptotic Activity.- Farnesoid X-receptor (FXR) Receptor Activation.- a-Glucosidase Inhibitory Activity.- Insecticidal Activity.- Liver X Receptor Alpha (LXRa) Agonist Activity.- Muscle Relaxant Activity.- Nematode Larval Motility Inhibition Activity.- Neuroprotective Activity.- Nitric Oxide Production Inhibition.- Plant Growth Inhibitory Activity.- Piscicidal Activity.- Tublin Polymerization Inhibition.- Vasorelaxation.- 8 Chemosystematics of the Marchantiophyta.- Chemosystematics of Haplomitriopsida.- Chemosystematics of Marchantiopsida.- Chemosystematics of Jungermanniopsida.- Conclusion.- 9 Chemical Relationships Between Algae, Bryophytes, and Pteridophytes.- Similarities Between Liverworts, Mosses, and Hornworts.- Similarities Between Algae and Bryophytes.- Similarities Between Bryophytes and Pteridophytes.-
Yoshinori Asakawa
Yoshinori Asakawa obtained his first degree in biology at Tokushima University, and then went to graduate school at Hiroshima University in 1964 to study organic chemistry. He has been actively involved in bryophyte research since the early 1970s, from the time when he was a postdoctoral with Professor Guy Ourisson at the Institut de Chimie, Université Louis-Pasteur, Strasbourg, France. He has studied not only bryophyte constituents and their biosynthesis but also bioactive secondary metabolites of pteridophytes, inedible mushrooms, and aromatic and medicinal plants, as well as the biotransformation of secondary metabolites by fungi and mammals, and oxidation reactions of organic peracids. He has authored and co-authored more than 550 original papers, 24 reviews, and 27 books and monographs. For his outstanding research, Prof. Asakawa was awarded the first Hedwig Medal from the International Association of Bryologists, the Phytochemistry Prize and Certification from Elsevier, the International Symposium on Essential Oils Award, the Jack Cannon International Gold Medal, the Japanese Society of Pharmacognosy Award, and the Tokushima Newspaper Award. He has been Editor of Phytomedicine and Spectroscopy, and a member of the Editorial Advisory Boards of numerous scientific journals, including Phytochemistry, PhytochemistryLetters, PlantaMedica, Flavor and Fragrance Journal, Fitoterapia, Natural ProductCommunications, Natural Product Research, Malaysian Journal of Sciences, Current Chemical Biology, Scientia Pharmaceutica, and Journal of Traditional and Complementary Medicine, among others. He has served twice as Dean of the Faculty of Pharmaceutical Sciences at Tokushima Bunri University, and is currently Director of the Institute of Pharmacognosy (1986–present). Prof. Asakawa has been President of the Phytochemical Society of Asia since 2007.
Agnieszka Ludwiczuk
Agnieszka Ludwiczuk studied chemistry at the Faculty of Chemistry, Maria Curie-Skłodowska University, Lublin, Poland, and received her Master’s degree in 1998. In this same year she started to work at the Department of Pharmacognosy with the Medicinal Plants Unit, Medical University of Lublin, initially as a Scientific and Technical Worker, then as a Research Assistant, and since 2007 as Assistant Professor. In 2005, she obtained her Ph.D. degree in pharmaceutical sciences. From April 2007 until March 2010 she worked as a postdoctoral at Tokushima Bunri University, Tokushima, Japan, under the direction of Prof. Yoshinori Asakawa. Her scientific output to date comprises some 50 scientific papers published in international and domestic journals concerning natural products chemistry, separation methods, extraction techniques, and biological activity. She is currently working on bioactivity-guided isolation and the structural characterization of compounds from medicinal, aromatic, and spore-forming plants. She is also focused on the chemical relationships of algae, bryophytes, and ferns. Her scientific interests cover in addition the chemosystematics of non-vascular plants from the division Marchantiophyta, and selected vascular plants from the families Apiaceae and Lamiaceae, based on their terpenoid, aromatic and phenolic constituents, and the biotransformation of pure secondary metabolites from plant materials for the production of useful substances.
Fumihoro Nagashima
Fumihiro Nagashima studies natural product chemistry at the graduate school of Tokushima Bunri University (TBU), Tokushima, Japan. He was appointed as a Research Assistant in the Faculty of Pharmaceutical Sciences at TBU in 1990, and obtained his Ph.D. degree in 1991 under the direction of Prof. Yoshinori Asakawa. He was promoted to Associate Professor at TBU in 2007. He is currently studying bioactive constituents of southern hemisphere liverworts and Madagascan medicinal plants and has published 80 original papers and four reviews. Recently, he has isolated many new sesquiterpenoids, diterpenoids, bibenzyls, and bis-bibenzyls having new skeletons from the Jungermanniales and Marchantiales. Some of these compounds have exhibited potent cytotoxicity against several cancer cell lines and antimicrobial activity.