Spectroscopic Data of Steroid Glycosides: Volume 4 2007 edition

Marc Notes: '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. Biographical Note: 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. Description for Sales People: 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. Jacket Description/Back: 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 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 13C-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 Table of Contents: 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.- ?-Antiarin.- Asclepias Subulata Saponin 1.- Canescein.- Convallaria Majalis Glycoside E5.- Glucostrophanthidin.- Ornithogalum Nutans Saponin 15.- Ornithogalum Umbellatum Saponin 5.- SArmentoside A, Sarmentoside C.- Sarmentoside E.- Scorpioside.- Thollosid.- Canesceol, Convallaria Majalis Glycoside L.- Convallaria Majalis Glycoside L1.- Convallaria Majalis Glycoside P2.- Glucoevonogenin.- Opposide.- Ornithogalum Nutans Saponin 16.- Ornithogalum Nutans Saponin 18.- Sarhamnoloside.- Sarmentoloside.- Scorpiosidol.- Anodendroside A.- 7,8-Dehydrocerberin.- Affinoside N.- Anodendroside E2.- Acetylobebioside.- Beauwalloside.- Cerberin, Vaneferin.- Cryptograndoside A.- Hongheloside A.- Nerigoside.- Oleandrin, Folinerin, Neriolin, Corrigen, Folianorin.- Anodendroside E1.- 19-O-Acetylfrugoside.- Mansonin.- Rhodexin B.- Strebloside.- Verodoxin, 16-Formylstrospeside.- Panstroside.- Cannodimethoside.- Gitodimethoside.- Antiarojavoside.- Toxicarioside A.- 11?,19-Dihydroxydigitoxigenin 3-O-[3?-O-Methyl-?-D-glucopyranoside].- Sarmentoside A Acid.- Thollosidic Acid.- Acocantherin, Ouabain, g-Strophanthin, g-Strophanthoside.- Acolongifloroside K.- Cerbertin.- Peruvoside 2?-Acetate.- Tanghinin.- 16-Acetylstrospeside.- Acoschimperoside P.- Acovenoside B.- Cryptostegia Madagascariensis Saponin 3.- Neritaloside.- Obeside B.- 18,20-Oxido-20,22-Dihydroneriifolin 2?-Acetate.- Vallarosolanoside.- Acetyladonitoxin.- Arguayoside.- Taucidoside.- 19-Acetylglucocoroglaucigenin.- Chrysolina Polita Saponin 2.- Oleandrigenin 3-O-?-D-Glucopyranoside.- Lophopetalum Toxicum Glycoside B.- Affinoside S-VII.- Chrysolina Americana Saponin 1.- Adigoside.- Digitoxigenin ?-D-Glucoside Melonyl Ester.- Digitoxigenin Bisdigitoxoside.- Acetylobeside B.- Monoacetylacoschimperoside P.- Digitalis Lanata Saponin 6.- Terminalia Arjuna Saponin 1.- Digitalis Lanata Saponin 5.- Digoxigenin Bisdigitoxoside.- Gitoxigenin Bisdigitoxoside.- Rhodexoside.- Convallaria Majalis Saponin 3.- Tamarindus Indica Saponin 1.- Chrysolina Fastuosa Saponin 5.- ?16-Adynerigenin ?-Odorobioside.- Bulloside.- Periplogenin Digitoxocymaroside.- Sarmentogenin Digitoxocymaroside.- Coroloside.- Digitalis Lanata Saponin 1.- Glucoevatromonoside.- Oxystelmoside.- Uzarigenin Canarobioside.- Erychroside.- Erychrosol.- Oreina Gloriosa Glycoside 3.- Ornithogalum Nutans Saponin 20.- Neriumoside B-2.- Chrysolina Herbacea Saponin 1.- Sarmentogenin Dicymaroside.- Beaumontia Brevituba Saponin 3.- 16-Desacetyl-16-Anhydrocryptograndoside B.- Gitaloxigenin Bisdigitoxoside.- Beaumontia Brevituba Saponin 6.- Beaumontia Brevituba Saponin 7.- Echubioside.- Odorobioside K.- Odoroside D.- Cheiranthoside III.- Securidaside, Hyrcanoside.- 6?-O-(4?-Hydroxy-E-Cinnamoyl) Desglucouzarin.- Calotropis Procera Saponin 1.- Cheiroside A, Cheiroside H.- Convallaria Majalis Glycoside Y.- Convallaria Majalis Glycoside Z.- Corchorus Olitorius Saponin 1.- Corchorus Olitorius Saponin 2.- Digitoxigenin Glucosidoglucomethyloside.- Evobioside.- Glucodigifucoside.- Glucodigigulomethyloside.- Glucogitoroside.- Neoglucodigifucoside.- Ornithogalum Nutans Saponin 21.- Convallaria Majalis Glycoside U.- Gypsobioside.- 17?-Gypsobioside.- Chrysolina Fuliginosa Glycoside 1.- Oreina Gloriosa Glycoside 1.- Ornithogalum Nutans Saponin 5.- Vijaloside.- Neriumoside A-2.- Anhydrodigitalin.- Apobioside.- Cerbera Odollam Saponin 1.- Obebioside D.- Apocynum Cannabinum Saponin 5.- Glucosyldivaricoside.- Glucosyldivostroside.- Neoodorobioside G.- Obebioside A.- Odorobioside G.- Oxystelmine.- Periplocin, Periplocoside.- Thevetia Ahouai Saponin 3.- Thevetia Neriifolia Saponin 1.- Thevetia Neriifolia Saponin 3.- Uzarigenin 3-O-?-D-Glucopyranosyl-(1?4)-?-Ddigitalopyranoside.- Cheiranthoside II.- Cheiranthoside X.- Cheiranthus Allioni Saponin Ch-31.- Convallaria Majalis Glycoside F.- Erysimoside.- Glucocheirant(H) Oside.- Gluocosylgofruside.- Mallotus Japonicus Saponin MJ-V.- Olitoriside, Olitorin.- Xysmalorin.- Rhodexin C.- Cheiranthoside VI.- Cheiranthoside VII.- Convallaria Majalis Glycoside P1.- Convallaria Majalis Glycoside S.- Crossopetalum Gaumeri Saponin 3.- Digitoxigenin Gentiobioside.- Digitoxigenin ?-D-Sophoroside.- 3-Epi-Digitoxigenin ?-D-Gentiobioside.- Erycordin.- Erysimosol.- Euonymoside A.- Euonymuside A.- Glucoevonoloside.- Glucogitofucoside.- Glucosylfrugoside.- Gulosarmentoglucoside.- Mallotus Japonicus Saponin MJ-VI.- Mallotus Japonicus Saponin MJ-VII.- Ornithogalum Umbellatum Saponin 2.- Urezin.- Uzarigenin ?-Cellobioside.- Uzarigenin 3-O-Sophoroside.- UZarin.- Ornithogalum Nutans Saponin 19.- Digitalis Cariensis Saponin 1.- Basikuloside.- Cerbera Odollam Saponin 2.- Apocynum Cannabinum Saponin 1.- Chrysolina Fuliginosa Glycoside 2.- Cerbera Manghas Glycoside 1.- CErbera Manghas Glycoside 2.- 8?-Hydroxy-?16-Digitoxigenin ?-Odorobioside.- Glucolanadoxin.- Strophanthin, k-Strophanthin-?.- Strophanthus Divaricatus Saponin 1.- Strophanthus Divaricatus Saponin 2.- Asclepias Fruticosa Saponin 34.- Acobioside A.- Allodigitalin, Allodigitalinum Verum.- Digitalin, Digitalinum Verum.- Emicin.- Neodigitalinum Verum, Neodigitalin.- Obebioside C.- Sargenoside.- Streptocaulon Glycoside 4.- k-Strophanthol-?, Glucocymarol.- Thevetia Neriifolia Saponin 8.- Adonis Vernalis Saponin 1.- Cheiranthoside I.- Cheiranthoside VIII, Cheirotoxin.- Cheiranthoside IX.- Convallaria Majalis Glycoside H1.- Convalloside, Bogoroside.- Coronillobioside.- Crossopetalum Gaumeri Saponin 4.- Crotalaria Retusa Glycoside.- Erycanoside.- Eryscenoside.- Glucostrophalloside.- Neoconvalloside.- Nigrescigenin Digilanidobioside.- Cheirotoxol.- Convallatoxoloside.- Coronillobiosidol.- Glucoalliside.- Glucobipindogulomethyloside.- Glucolokundjoside.- Glucopanoside.- 4?-O-?-D-Glucopyranosyl-12?-Hydroxyfrugoside.- Neoconvallatoxoloside.- Cheiranthoside IV.- Subalpinosid.- Cryptanoside C.- Glucokamaloside.- Chrysolina Grossa Saponin 1.- Strophanthidin ?-D-Glucopyranosyl-(1?4)-?-D-Digitalopyranoside.- Glucocanescein.- Acetylobebioside A.- ?16-Adynerigenin ?-Neribioside.- Cryptograndioside B, Glucosylcryptograndoside.- Funingenoside L.- Funingenoside O.- Glucosylnerigoside.- Hongheloside C.- Thevetia Ahouai Saponin 4.- Urechitoxin, Oleandrin Monoglucoside.- 19-Acetylglucofrugoside.- Cryptostigmin II.- Glucostrebloside.- Glucoverodoxin.- Neo-Glucoverodoxin.- Wattoside E.- Asclepias Fruticosa Saponin 33.- Glucogitodimethoside.- Panstrosin.- Chrysolina Polita Saponin 4.- Oreina Gloriosa Saponin 1.- 16-O-Acetyldigitalinum Verum.- Acospectoside A, 1-O-Acetylacobioside.- Cryptostigmin III.- Glucoacovenoside B.- Obebioside B.- Streptocaulon Glycoside 1.- Adonis Vernalis Saponin 2.- Adonis Vernalis Saponin 3.- Rhodexin D.- Digitoxin.- Digoxin.- Gitoxin, Bigitalin, Gitoxoside.- Ornithogalum Nutans Saponin 22.- Digitalis Lanata Saponin 7.- Ornithogalum Nutans Saponin 12.- 16-O-Acetylglucogitodimethoside.- Sarmentogenin Bisdigitoxooleandroside.- Chrysolina Fuliginosa Glycoside 3.- Chrysolina Fuliginosa Glycoside 4.- Diginatin.- Digitalis Lanata Saponin 2.- Digitoxigenin Glucosidobisdigitoxoside.- Acetylobebioside B.- Ornithogalum Nutans Saponin 24.- Ornithogalum Nutans Saponin 9.- ?-Acetyldigitoxin, Acedoxin.- ?-Acetyldigitoxin.- Sarmentogenin Digitoxodicymaroside.- Gitaloxin.- Ornithogalum Nutans Saponin 23.- Ornithogalum Nutans Saponin 14.- Ornithogalum Nutans Saponin 2.- Neriumoside C-1.- Sarmentogenin Tricymaroside.- ?-Acetyldigoxin, Digoride B.- ?-Acetyldigoxin, Digoride A.- Digithapsin A.- Ornithogalum Nutans Saponin 4.- Mandevilla Pentlandiana Saponin 3.- Ornithogalum Nutans Saponin 7.- Cerapioside.- Corchorus Olitorius Saponin 3.- Digitalis Cariensis Glycoside G4.- Ornithogalum Nutans Saponin 3.- Ornithogalum Nutans Saponin 1.- Neriumoside B-1.- Ornithogalum Nutans Saponin 6.- ?16-Adynerigenin ?-Gentiobiosyl ?-D-Sarmentoside.- ?16-Adynerigenin ?-Neritrioside.- Adonis Aestivalis Saponin 1.- Adynerigenin ?-Neritrioside.- Beaumontia Murtonii Saponin 1.- Beaumontia Murtonii Saponin 2.- ?16-Digitoxigenin ?-Neritrioside.- Ornithogalum Nutans Saponin 25.- Beaumontia Brevituba Saponin 1.- Beaumontia Brevituba Saponin 4.- Beaumontia Brevituba Saponin 5.- Digitoxigenin ?-Oleatrioside (Gentiobiosyl Beaumontoside).- Echujin.- Gentiobiosylodoroside A.- Odoroside K.- Odorotrioside G.- Ornithogalum Nutans Saponin 8.- Ornithogalum Nutans Saponin 10.- Cellobiosyl Digigulomethyloside.- Digifucocellobioside.- Evonoside.- Gitorocellobioside.- Neoevonoside.- Gypsotrioside.- Acetylgitaloxin.- Neriumoside A-1.- ?16-Adynerigenin ?-Odorotrioside.- Ornithogalum Nutans Saponin 11.- Adynerigenin ?-Odorotrioside.- Apocynum Cannabinum Saponin 2.- Apocynum Cannabinum Saponin 3.- Apocynum Cannabinum Saponin 4.- ?16-Digitoxigenin ?-Odorotrioside.- ?16-8?-Hydroxydigitoxigenin ?-Neritrioside.- Biondianoside A.- Cerbera Manghas Saponin 2.- Cerbera Manghas Saponin 3.- Gitoxigenin ?-Oleatrioside.- 8?-Hydroxydigitoxigenin ?-Neritrioside.- Neriagenin ?-Neritrioside.- Nerium Odorum Saponin 2.- Obetrioside A.- Odoroside G.- Thevetia Neriifolia Saponin 2.- Thevetia Neriifolia Saponin 4.- Thevetia Neriifolia Saponin 5.- Thevetin B, Cerberoside.- 4?-O-?-Cellobiosylgofruside.- Glucoolitoriside.- Glucoerysimoside.- Neoglucoerysimoside.- Olitoriusin.- 4?-O-?-Cellobiosylfrugoside.- Euonymusoside A.- Glucoerycordin.- Glucoerysimol.- Uzaroside.- Digithapsin B.- Cryptostigmin I.- Apobasinoside.- Streptocaulon Glycoside 2.- Ornithogalum Nutans Saponin 13.- Cellostrophanthoside.- De(s)acetyltanghinoside.- k-Strophanthoside, k-Strophanthin-?.- 17?H-Strophanthoside.- Thevetia Neriifolia Saponin 9.- Thevetin A.- Acovenoside C, Gentiobiosidoacovenoside A.- Alloneogitostin.- Gitostin.- Neogitostin.- k-Strophanthol-?.- 4?-O-?-Cellobiosyl-12?-Hydroxyfrugoside.- Glucoconvallatoxoloside.- Mandevilla Pentlandiana Saponin 2.- Cheiranthoside V.- Ornithogalum Umbellatum Saponin 1.- Strophanthoside-19-Carboxylic Acid.- Thevetia Neriifolia Saponin 11.- Beaumontia Brevituba Saponin 2.- Funingenoside K.- Funingenoside N.- Gentiobiosylnerigoside.- Gentiobiosyloleandrin.- Honghelotrioside A.- Sinapoylerysimoside.- Digoxoside.- Chrysolina Polita Saponin 5.- Tanghinoside.- 14-O-Acetylacovenoside C.- Obetrioside B.- Purpureaglycoside A, Descetyllanatoside A, Deslanatoside, Deslanoside A.- 3 -Di-Dehydro-Deacetyllanatoside C.- Purpureaglycoside B, Desacetyldigilanide B, Desacetyllanatoside B, Deslanoside B.- Deslanoside C, Deslanide, Deslanoside, Deacetyllanatoside C.- Oxyline.- Digitalis Cariensis Glucoside G1.- Lanatoside A, Digilanide A.- Adonis Aestivalis Saponin 2.- Alepposide B.- Glucogitaloxin.- Lanatoside B, Purpureaglycoside B Acetate, Digilanide B.- Lanatoside C, Celanide, Digilanide C, Cedilanid, Ceglunate, Digilanogen C.- Mandevilla Pentlandiana Saponin 4.- Sugoroside.- Lanatoside D.- Extensumside A.- Streptocaulon Glycoside 3.- Lanatoside E, Digilanide E.- Cerbera Manghas Saponin 1.- Nerium Odorum Saponin 1.- Lanatoside F.- Cryptostigmin IV.- Funingenoside M.- Funingenoside P.- Sinapoylglucoerysimoside.- Glucodigoxoside.- Gitoxin Cellobioside.- Alepposide A.- Glucoacetyldigoxide.- Mandevilla Pentlandiana Saponin 5.- Elaeodendroside H.- Elaeodendroside D.- Elaeodendroside K.- Elaeodendroside L.- 3?-Didehydrogomphoside.- Elaeodendroside B?.- Elaeodendroside C.- 3?-EPI-Gomphoside.- Gomphoside.- Gomphotin.- 3?-EPI-19-Norafroside.- 5,6-Dehydrouscharidin.- Elaeodendroside O.- 14?,17?-Epoxy-5,6-Dehydrocalotropin.- 5,6-Dehydrocalactin.- Elaeodendroside I.- Elaeodendroside R.- Humistratin, 7,8-Dehydrocalotropin.- Uscharidin.- Asclepias Fruticosa Saponin 29.- Calactin.- Calotropin, Pekilocerin A.- 3?-Didehydroafroside.- Elaeodendroside S.- Afroside.- Asclepias Fruticosa Saponin 27.- 3?-EPI-Afroside.- Gomphotoxin.- 17?-Hydroxygomphoside.- 4 -Hydroxygomphoside.- Elaeodendroside B.- Elaeodendroside M.- Affinoside D.- Elaeodendroside A.- Elaeodendroside J.- Elaeodendroside N.- Affinoside C.- 3?-EPI-19-Norgomphoside 3?-Acetate.- Affinoside Q.- Affinoside T.- 5,6-Dehydrocalotoxin.- Elaeodendroside P.- Elaeodendroside Q.- Gomphocarpus Sinaicus Saponin 1.- 16?-Hydroxy-5,6-Dehydrocalotropin.- 15?-Hydroxy-5,6-Dehydrocalotropin.- 15?-Hydroxy-7,8-Dehydrocalotropin.- Affinoside Le.- Asclepias Fruticosa Saponin 7.- Calotoxin.- 16?-Hydroxycalactin.- 17?-Hydroxycalactin.- 16?-Hydroxycalotropin.- 15?-Hydroxycalotropin.- Asclepias Fruticosa Saponin 28.- 4 -Hydroxyafroside.- 17?-Hydroxyafroside.- 3-EPI-17?-Hydroxyafroside.- Affinoside J.- Gomphacil.- Affinoside B.- Affinoside F.- Affinoside P.- Affinoside R.- Affinoside S.- Affinoside K, 3?-Demethylaffinoside A.- Labriformidin.- Affinoside E.- Affinoside La.- Desglucosyrioside, Eriocarpin.- Syriobioside.- Ghalakinoside.- 5,6-Dehydroasclepin.- Affinoside H.- Affinoside I, ?16-Affinoside M.- 19-Deoxyuscharin.- 2?-O-Acetylcerleaside A.- Asclepin.- Elaeodendroside F.- Elaeodendroside G.- Affinoside A.- Affinoside M, 3?-EPI-Affinoside A.- 3?-EPI-Afroside 3-O-Acetate.- Affinoside Lb.- Affinoside G.- Affinoside Lc.- Affinoside Ld.- Affinoside Lf.- Affinoside Lg.- Uscharin.- 16?-Acetoxy-5,6-Dehydrocalotropin.- 16?-Hydroxy-5,6-Dehydroasclepin.- Asclepias Fruticosa Saponin 5.- Voruscharin.- 16?-Acetoxycalactin.- 16?-Acetoxycalotropin.- 16?-Hydroxyasclepin.- 16?-Hydroxyaffinoside A.- Asclepias Tuberosa Saponin 1.- Buchaninoside.- Asclepias Fruticosa Saponin 6.- 16?-Hydroxyuscharin.- 16?-Acetoxy-3?-EPI-19-Norgomphoside 3?-Acetate.- Asclepias Tuberosa Saponin 2.- Labriformin.- 16?-Acetoxyasclepin.- Asclepias Tuberosa Saponin 3.- 3?-O-?-D-Glucopyranosylcalotropin.- 3?-O-?-D-Glucopyranosyl-16?-Hydroxycalotropin.- 3-O-?-Gentiobiosyl-16?-Hydroxycalotropin.- Thevetioside I.- Cerleaside A.- Thevetioside A.- Thevetioside B.- Elaeodendroside E.- 16?-Acetoxy-5,6-Dehydroasclepin.- Thevetia Ahouai Saponin 1.- Cerleaside B.- Thevetioside C.- Thevetioside D.- Syrioside.- Funingenoside I.- Funingenoside J.- Parefuningoside.- Thevetioside E.- Funingenoside C.- Funingenoside G.- Thevetia Ahouai Saponin 2.- ?16-Neriagenin ?-Neritrioside.- Thevetioside F.- Thevetioside H.- Thevetioside J.- Thevetia Neriifolia Saponin 12.- Funingenoside A.- Funingenoside H.- Thevetioside G.- Funingenoside B.- Funingenoside E.- Thevetioside I?.- Funingenoside D.- Funingenoside F.- Pregnane.- Scleronephthya Pallida Saponin 2.- Scleronephthya Pallida Saponin 1.- Cladiella Krempfi Glycoside 1.- Eunicea Pinta Saponin 1.- Brucea Javanica Saponin 1.- Pregnedioside A.- Pregnedioside B.- Muricea Glycoside 1.- Pseudoplexaura Wagenaari Saponin 1.- Calocin.- Calocinin.- Hemidine.- Indicine.- Periploca Sepium Glycoside E, Periplocoside N.- Periplocogenin.- Holantosine B.- Holantosine D.- Holantosine F.- N-Demethylholacurtine.- 17-EPI-N-Demethylholacurtine.- Marsin.- Basikoside A.- Locin.- Agave Americana Glycoside 1.- Eunicea Saponin 1.- Diginin.- 17-EPI-Holacurtine. Publisher Marketing: 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, - 13C-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.