Spectroscopic Data of Steroid Glycosides 4

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.
Cardenolide.- Divostroside.- 17?H-Divostroside.- Hongkelin, Honghelin.- Kwangoside.- Maquiroside A.- Neriaside.- Neridiginoside.- Neriifolin.- Neriifoside.- Odoroside H.- Periplocymarin.- Sarmentocymarin.- Solanoside, 3?-O-Methylevomonoside.- 17?-Solanoside.- Thevofoline.- Uzarigenin 3-O-?-D-Digitalopyranoside.- Vallaroside.- Vanderoside.- Cheirant(H)Oside.- Cheiranthus Allioni Saponin Ch-30.- Chrysolina Polita Saponin 3.- Corchoroside A.- 7,8-Didehydrosyriogenin 3-O-[6-Deoxy-?-D-Allopyranoside].- Gofruside.- Helveticoside.- 17?-Helveticoside.- Malayoside.- Mallotus Philippinensis Saponin 1.- Acovenosigenin A 3-O-?-L-Rhamnopyranoside.- Affinoside S-IX, Sarmentogulomethyloside.- Alliotoxin.- Asclepias Fruticosa Saponin 9.- Asclepias Fruticosa Saponin 30.- Convallaria Majalis Saponin 1.- Convallaria Majalis Saponin 2.- Coroglaucigenin 3-O-?-L-Rhamnopyranoside.- Desglucoerycordin.- Desglucouzarin.- 3-EPI-Digitoxigenin 3-O-?-D-Glucopyranoside.- Evonoloside.- Frugoside.- Glucodigitoxigenin.- Helveticosol.- 17?-Hydroxyuzarigenin 3-O-[6-Deoxy-?-D-Allopyranoside].- Ledienoside.- Malloside.- Oreina Gloriosa Glycoside 4.- Ornithogalum Umbellatum Saponin 3.- Periguloside.- Peripalloside.- Periplorhamnoside.- Rhodexin A.- Syriogenin 3-O-[6-Deoxy-?-D-Allopyranoside].- Corchoside C.- Chrysolina Fastuosa Saponin 3.- Ornithogalum Umbellatum Saponin 4.- Nerizoside.- Decoside.- Nierembergia Aristata Saponin 3.- Acolongifloroside H.- Amboside.- Apocynum Cannabinum Saponin 8.- Candelabrin.- Cerberiopsin I.- Cerberiopsin II.- Christyoside.- Cymarin, Cimarin, k-Strophanthin-?.- Deacetylcerbertin.- De(S)Acetyltanghinin.- 17?H-Deacetyltanghinin.- Desaroside.- Lanadoxin.- Peruvoside.- Pseudocaudoside.- Sarmutoside.- Sinoside.- Sinostroside.- Tanghinigenin ?-L-Acofrioside.- Thevetia Neriifolia Saponin 10.- Affinoside S-III.- Nierembergia Aristata Saponin 1.- Pachomonoside.- Acovenoside A, Venanatin.- Alloemicymarin.- Cerdollaside.- 17?-Cerdollaside.- Cymarol.- Digitalis Lanata Saponin 4.- Digitoxigenin 3-O-[3?-O-Methyl-?-D-Glucopyranoside].- Emicymarin, e-Strophanthin.- Obeside C.- (20R,S)-18,20-Oxido-20,22-Dihydroneriifolin.- Sarnovide.- Streblus Asper Saponin 1.- Strospeside.- Theveneriin, Ruvoside.- Thevetia Neriifolia Saponin 6.- Thevetia Neriifolia Saponin 7.- Adonitoxin.- Asclepias Fruticosa Saponin 8.- Asclepias Fruticosa Saponin 31.- Aspecioside.- Convallotoxin, Convallotoxoside, Corglycone.- Crossopetalum Gaumeri Saponin 1.- Desglucocheirotoxin.- Glucocorotoxigenin.- Kabuloside, Cabuloside.- Nigrescigenin Digitoxoside.- Ornithogalum Nutans Saponin 17.- Perofskoside.- Strophalloside.- Strophanthidin 3-O-?-D-Fucoside.- Strophanthidin 3-O-?-D-Quinovopyranoside.- Adonitoxol.- Alliside, Alloside.- Antiogoside.- Antioside.- ? - Antioside.- Bipindogulomethyloside, Convallaria Majalis Glycoside E1.- Bipindoside.- Chrysolina Polita Saponin 1.- Convallaria Majalis Glycoside E2.- Convallaria Majalis Glycoside G.- Convallatoxol, Perconvol.- Crossopetalum Gaumeri Saponin 2.- De(S)Glucocheirotoxol.- Gitorin.- Glucocannogenol.- Glucocoroglaucigenin.- 12?-Hydroxyfrugoside.- 8?-Hydroxsyriogenin 3-O-[6-Deoxy-?-D-Allopyranoside].- Lokundjoside, Cuspidoside.- Oreina Gloriosa Glycoside 2.- Panoside.- Periplogenin 3-O-?-D-Glucopyranoside.- Strophanolloside.- Strophanthus Gratus Saponin 1.- Affinoside O.- Anodendroside G.- Affinoside S-II.- Anodendroside F.- Cryptanoside A.- Cryptanoside B.- Fugaxin.- Intermedioside.- Sarveroside.- Affinoside S-XI.- Asperoside.- Kamaloside.- Affinoside S-I.- Apocynum Cannabinum Saponin 6.- Apocynum Cannabinum Saponin 7.- Cymarylic Acid.- Musaroside, Sarmutogenin 3-O-?-D-Digitalopyranoside.- Perusitin.- Strophanthindin 3-O-?-D-Digitalopyranoside.- Strophanthojavoside.- Strophothevoside.- Vernadigin.- Affinoside S-IV.- Affinoside S-V.- Affinoside S-VI Affinogenin D-II 3-O-?-D-glucopyranoside.- Bipindaloside.- Digitalis Lanata Saponin 3.- Armethoside.- Streblus Asper Saponin 2.- Alloglaucoside.- Antialloside.- ?-Antiarin.- ?-Antiar
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:: 9780387311623
ISBN: 0387311629
Erscheinungsjahr: 01.05.2007
Verlag: Springer-Verlag GmbH
Gewicht: 1095g
Seiten: 696
Sprache: Englisch
Sonstiges: Buch, 244x165x40 mm, 761 illus.