Spectroscopic Data of Steroid Glycosides 1

Academic/professional/technical: Research and professional
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This book is the first work of its kind in the field of steroid glycosides. It serves as an essential reference guide containing spectroscopic, physical and biological activity data of over 3500 steroid glycosides, offering the structures and the data of the naturally occurring glycosides of steroids. An extra effort has been made to include the data from Chinese publications which are generally not available in the libraries of Western countries. All compounds are arranged according to the structure of the aglycone, and, in its own class, according to the increasing molecular weight, making this book extremely useful for the structure elucidation of new natural products, particularly glycosides. The book offers a practical desk reference for all scientists and students interested in steroid glycosides and their biological and medicinal importance.
Cholestane.- Asterias Vulgaris Saponin 1.- Asterias Vulgaris Saponin 2.- Moniloside A.- Certonardoside N.- Rathbunioside R1.- Moniloside B.- Ornithogalum Saundersiae Saponin 12.- Ornithogalum Saundersiae Saponin 8.- Amurensoside D.- Attenuatoside A-II.- Pycnopodioside A.- Rathbunioside R2.- Solasteroside S1.- Tumacoside B.- Lilium Henryi Saponin I.- Alloside A.- Limnantheoside B.- Borealoside C.- Moniloside C.- Oreasteroside A.- Antarcticoside H.- Attenuatoside B-II.- Attenuatoside C.- Coscinasteroside F.- Blechnoside B.- 2,22-Dideoxyecdysterone 3-O-?-D-Glucopyranoside.- Silen(E)Oside E, Blechnoside A.- 5?-Silen(E)Oside E.- Antarcticoside D.- Antarcticoside E.- Echinasteroside C.- Tenuifolioside A.- Tenuifolioside B.- Limnantheoside A.- Borealoside D.- Moniloside D.- Poraster Superbus Saponin 1.- Coscinasteroside E.- Pavoninin-2.- Ornithogalum Saundersiae Saponin 3.- Ornithogalum Saundersiae Saponin 1.- Ornithogalum Saundersiae Saponin 2.- Pfaffia Iresinoides Saponin 3.- Laeviuscoloside H.- 2-Deoxy-20-Hydroxyecdysone 22-O-?-D-Glucopyranoside.- Silen(e)oside F.- Forbeside I, Laeviuscoloside I, Henricioside H1.- Antarcticoside I.- Poraster Superbus Saponin 2.- Tumacoside A.- Pfaffia Iresinoides Saponin 1.- Pfaffia Iresinoides Saponin 2.- Silen(e)oside A.- Silen(e)oside D.- Echinasteroside G.- Riisein A.- Riisein B.- Pectinioside F.- Silen(e)oside C.- Pavoninin-1.- Ornithogalum Saundersiae Saponin 13.- Pavoninin-3.- Pavoninin-5.- Pavoninin-6.- Ornithogalum Saundersiae Saponin 9.- Pavoninin-4.- Amurensoside C.- Amurensoside A.- Longicaudoside A.- Melandrioside A.- Certonardoside H4.- Luridoside B.- Pisasteroside D.- Pisasteroside E.- Scoparioside D.- Sileneoside H.- Amurensoside B.- Aphelasteroside A.- Coscinasteroside B.- Glacialoside A.- Glacialoside B.- Helianthoside.- Heliaster Helianthus Saponin 1.- Luridoside A.- Myxoderma Platyacanthum Saponin 1.- Oreasteroside I.- Oreaster Reticulatus Saponin 1.- Pisasteroside B.- Pycnopodioside B.- Scoparioside A.- Scoparioside B.- Downeyoside C.- Aphelasteroside B.- Asterosaponin P1.- Indicoside B.- Longicaudoside B.- Oreasteroside H.- Scoparioside C.- Validoside B.- Distolasteroside D5.- Downeyoside F.- Downeyoside J.- Downeyoside K.- Granulatoside B.- Asterosaponin D2, Distolasteroside D2.- Laeviuscoloside B.- Downeyoside L.- Asterosaponin D1, Distolasteroside D1.- Mediasteroside M2.- Indicoside C.- Pycnopodioside C.- Ornithogalum Thyrsoides Saponin 20.- Schubertoside A.- Tribulus Cistoides Saponin 8.- Ornithogalum Thyrsoides Saponin 18.- Ornithogalum Thyrsoides Saponin 19.- Schubertoside B.- Dimorphoside A.- Galtonia Candicans Saponin 4.- Heliaster Helianthus Saponin 2.- Certonardoside L.- Lnepisorus Ussuriensis Saponi 1.- Polianthes Tuberosa Saponin 2.- Attenuatoside A-1.- Certonardoside H3.- Crossasteroside C.- Culcitoside C4.- 5-Deoxyisonodososide.- Mediasteroside M1.- Oreasteroside B.- Oreasteroside C.- Oreasteroside E.- Antarcticoside G.- Asteriidoside F.- Eryloside K.- Eryloside A.- Ornithogalum Saundersiae Saponin 4.- Polypodasaponin.- Polypodoside B.- Galtonia Candicans Saponin 5.- Tribulus Cistoides Saponin 9.- Tribulus Cistoides Saponin 12.- Allium Porrum Saponin 5.- Certonardoside M.- Nolina Recurvata Saponin 1.- Poranoside A, 22-Dehydrohalityloside E.- Reineckea Carnea Saponin 3.- Tribulus Cistoides Saponin 13.- Tribulus Cistoides Saponin 14.- Crossasteroside B.- Halityloside E.- Halityloside F.- Laeviuscoloside F.- Mediasteroside M3.- Mediasteroside M4.- Oreasteroside D.- Asterosaponin D3.- Attenuatoside B-I.- Crossasteroside D.- Culcitoside C5.- Granulatoside A, Echinasteroside B2.- Isonodososide.- Nodososide.- 6-EPI-Nodososide.- Dimorphoside B.- Eryloside L.- Polypodoside C.- Tribulus Cistoides Saponin 10.- Ornithogalum Saundersiae Saponin 11.- Camassioside.- Chrysolinina Varians Saponin 2.- Cocinnasteoside A.- Fritillaria Thunbergii Saponin 1.- Galtonia Candicans Saponin 9.- Tribulus Cistoides Saponin 11.- Allium Ostrowskianum Saponin 1.- Alloside B.- Antarcticosid
This book is an essential reference guide to spectroscopic, physical and biological activity data of over 3500 steroid glycosides, offering the structures and the data of the naturally occurring glycosides of steroids. All compounds are arranged according to the structure of the aglycone, and, in its own class, by the increasing molecular weight, making Spectroscopic Data of Steroid Glycosides extremely useful for the structure elucidation of new natural products, particularly glycosides.
Editiert von: Anwer Basha, Viqar Uddin Ahmad
Professor Viqar Uddin Ahmad has been associated with the HEJ Research Institute of Chemistry since its establishment in 1967. Prof. Viqar's currents interests are on isolation and structure elucidation of new natural products. Some of them have interesting biological activities. For example: VArious eudesmane sesquiterpenes which showed antibacterial activity against Escherichia coli, Klebsiella ozaenoe, K. pneumonieae, Proteus vulgaris, Shigella boddi, Staphylococcus aureus, S. pyogenes andB. anthracis; some triterpenoidal and steroidal saponins exhibited toxicity in Brine Shrimp Lethality bioassay and antibacterial activity against Pseudomonas pseudomaliae, Co-rynebactterium xerosis etc. One of the saponins isolated from a Trukish plant manifested hypotensive activity in anaesthetized rat.
Prof. Viqar Uddin Ahmad availed a Fulbright Fellowship of nine months in 1993. during his stay at Cornell University, Itacha, USA. Prof. Viqar Uddin Ahmad worked on the twelve step total synthesis of and alkaloid isolated from an insect. Prof. Viqar also dilivered lecturers in the chemistry departments of Central Michighan University, Michighan, Georgia Tech, Atlanta, georgia, State University, Atlanta, Georgia and Cornell University, Ithaca.
Autor: Anwer Basha
ISBN-13:: 9780387311593
ISBN: 0387311599
Erscheinungsjahr: 01.05.2007
Verlag: Springer-Verlag GmbH
Gewicht: 1207g
Seiten: 696
Sprache: Englisch
Sonstiges: Buch, 241x159x45 mm, 661 illus.