Spectroscopic Data of Steroid Glycosides 2

Academic/professional/technical: Research and professional
 Buch
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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.
Stigmastane.- Colebrin E.- Vernonia Colorata Glycoside 4.- Acodontasteroside C.- Acodontasteroside B.- Chrysolina Geminata Saponin 1.- Chrysolina Hyperici Saponin 7.- Sophoroside 1.- Sophoroside 2.- Echinasteroside F.- Nardoa Tuberculata Saponin 1.- Halityloside A 6-O-Sulfate.- Asparagus Adscendens Saponin 1.- Amaranthus Spinosus Saponin 1.- Halityloside H 6-O-Sulfate.- 4?-O-Methylhalityloside A 6-O-Sulfate.- Moniloside I.- Pistia Stratiotes Saponin 1.- Moniloside H.- Moniloside G.- Chrysolina Brunsvicensis Saponin 1.- Chrysolina Geminata Saponin 2.- Ajugasalicioside D.- Sitoindoside III.- Sitoindoside IV.- Mycaloside I.- Ajugasalicioside H.- Pectinioside C.- Furostane.- Terrestrinin A.- Kryptogenin 26-O-?-D-Glucopyranoside.- Trillium Kamtschaticum Saponin Tk.- Tumaquenone.- Funkioside B.- Asparagoside B.- Torvoside G.- Polygonatum Odoratum Glycoside 1.- Allium Ampeloprasum Saponin 2.- Agamenoside J.- Nolinofuroside A.- Protoyonogenin.- Protoneoyonogenin.- Hosta Plantaginea Saponin 2.- Aspidistra Sichuanensis Saponin 1.- Tupstroside G.- Wattoside B.- Tupiloside H.- Wattoside D.- Ruscus Aculeatus Saponin 1.- Nolinofuroside G.- Allium Vineale Saponin 2.- Cordyline Stricta Saponin 7.- Nolinofuroside C.- Anemarrhenasaponin-I.- Anemarrhenasaponin-II.- Filicinoside B.- Petunioside I.- Prototokoronin.- Protoneotokorin.- Reineckia Carnea Saponin RS-2.- Downeyoside A.- Downeyoside B.- Costus Spicatus Saponin 1.- Dracaena Surculosa Saponin 5.- Nolinofuroside B.- Torvoside E.- Agave Americana Saponin 1.- Metanarthecium Saponin 2.- Anemarrhenasaponin Ia.- Cordyline Stricta Saponin 5.- Filicinoside A.- Allium Nutans Saponin 3.- Nolinofuroside D.- Tuberoside R.- Metanarthecium Saponin 1.- Dracaena Surculosa Saponin 1.- Dracaena Surculosa Saponin 4.- Cordyline Stricta Saponin 6.- Allium Macrostemon Saponin 1.- Pardarinoside B.- Allium Karataviense Saponin 7.- Pardarinoside A.- Reineckea Carnea Saponin 5.- Nolinofuroside H.- Allium Giganteum Saponin 8.- Nolina Recurvata Saponin 8.- Metanarthecium Glycoside FG-3.- Asparoside B?.- Asparagus Cochinchinensis Saponin 1.- Smilax Nigrescens Saponin 1.- Triteleia Lactea Saponin 3.- Afromontoside.- Aspacochioside C.- Tribol.- Chinenoside III.- Desglucoruscoside, Ruscoponticoside E.- Metanarthecium Glycoside FG-2.- Alliofuroside A.- Trigoneoside VIII.- Trigoneoside IIa.- Trigoneoside IIb.- Trillium Kamtschaticum Saponin Tf.- Ascalonicoside B.- Lilium Brownii Saponin 1.- Ruscus Aculeatus Saponin 3.- Anemarrhenasaponin IV, Timosaponin B III Pseudoprototimosaponin A-III.- Anemarsaponin B.- Anemarsaponin C.- Asparasaponin II.- Dracaena Concinna Saponin 2.- Dioscorea Gracillima Saponin A, Protobioside.- Macrostemonoside F.- Nolinofuroside E.- Nolinofuroside F.- Torvoside F.- Trigofoenoside A.- Trigoneoside XIIa.- Trigoneoside XIIb.- Tuberoside A (Allium).- Tuberoside F? (Solanum).- Asparagus Cochinchinensis Saponin ASP-IV.- Aspacochioside A.- 22-Methoxy - ASP-IV.- Nicotianoside E.- Torvoside A.- Torvoside B.- Trigoneoside IIIa.- Trigoneoside IIIb.- Smilax Sieboldii Saponin 4.- Trigoneoside 1a.- Trigoneoside 1b.- Trigoneoside XIb.- Costus Spicatus Saponin 2.- Costus Spicatus Saponin 3.- Dracaena Concinna Saponin 1.- Icogenin.- Trillium Kamtschaticum Saponin Td, Rhapis Humilis Saponin HSt4.- Chinenoside V.- Kingianoside D.- Tribulus Terrestris Saponin 5.- Triquetroside C1.- Triquetroside C2.- Asparagus Cochinchinensis Saponin ASP-V.- Aspacochioside B.- Ascalonicoside A1.- Ascalonicoside A2.- Macranthoside I.- Macrostemonoside L.- Melongoside O.- Ophiopojaponin B.- Polygonatum Saponin 25-EPI-PO-8.- Timosaponin D.- Trillium Kamtschaticum Saponin Te.- Asparagoside E.- Disporoside C.- Melongoside N.- Officinalisinin - I.- Petunioside L.- Timosaponin B-II.- Trigofoenoside B.- Trigoneoside Xa.- Trigoneoside Xb.- Allium Giganteum Saponin 7.- Metanarthecium Glycoside FG-4.- Metanarthecium Glycoside FG-5.- Metanarthecium Glycoside FG-1.- Solanum Lyratum Saponin 2.- Dracaena Concinna Saponin 3.- Dracaena Concinna S
Spectroscopic Data of Steroid Glycosides 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. All compounds are arranged according to the structure of the aglycone, and, in its own class, according to the increasing molecular weight, making Spectroscopic Data of Steroid Glycosides extremely useful for the structure elucidation of new natural products, particularly glycosides.Spectroscopic Data of Steroid Glycosides offers a practical desk reference for all scientists and students interested in steroid glycosides and their biological and medicinal importance.
The following data of the steroid glycosides, as available in published literature, are included: - Name of the compound, Chemical name of compound and its structure, - Source, name of the genus, species, authors, family of the biological source from which the glycoside has been isolated, - Melting point, - Specific rotation, - Molecule weight, - Molecular formula, - UV spectral data : maxima, e or log e , solvent, - IR peaks in cm -1 with medium in which the spectrum was taken e.g. KBr, nujol, etc, - Proton magnetic resonance (PMR) chemical shifts, multiplicity of the peaks, coupling constants with assignments, - 13 C-NMR (CMR) chemical shifts with assignments, - Mass spectral data with the technique used (e.g. Electron Impact (E.I.), Fast Atom Bombardment (FAB), positive ion or negative ion mode or any other technique, - CD or ORD data, - Biological Activity, - Full reference from which data have been taken.
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.
Autor: Anwer Basha
ISBN-13:: 9780387311609
ISBN: 0387311602
Erscheinungsjahr: 01.05.2007
Verlag: Springer-Verlag GmbH
Gewicht: 1095g
Seiten: 706
Sprache: Englisch
Sonstiges: Buch, 244x165x40 mm, 682 illus.