Spectroscopic Data of Steroid Glycosides 2

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Volume 2

ISBN: 0387311602
ISBN 13: 9780387311609
Herausgeber: Anwer Basha/Viqar Uddin Ahmad
Verlag: Springer Verlag GmbH
Umfang: x, 706 S., 682 s/w Illustr., 706 p. 682 illus.
Erscheinungsdatum: 05.04.2007
Auflage: 1/2007
Produktform: Gebunden/Hardback
Einband: GEB

Spectroscopic Data of Steroid Glycosides Dr. Viqar Uddin Ahmad, HEJ Research Institute of Chemistry, University of Karachi, Karachi, Pakistan Dr. Anwer Basha, Abbott Laboratories, Abbott Park, Illinois, USA 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 cm1 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 13CNMR (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

Artikelnummer: 1272302 Kategorie:

Beschreibung

InhaltsangabeStigmastane.- 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 Sapon

Autorenporträt

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.

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