Spectroscopic Data of Steroid Glycoside 4

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Volume 4

ISBN: 0387311629
ISBN 13: 9780387311623
Herausgeber: Viqar Uddin Ahmad/Anwer Basha
Verlag: Springer Verlag GmbH
Umfang: x, 696 S., 761 s/w Illustr., 696 p. 761 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: 1272318 Kategorie:

Beschreibung

InhaltsangabeCardenolide.- 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.-

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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