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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
Auteur
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.
Texte du rabat
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
Résumé
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.
Contenu
Pregnane.- Gymnepregoside O.- Telosmoside A11.- Asclepias Fruticosa Saponin 12.- Asclepias Fruticosa Saponin 13.- Asclepias Incarnata Saponin 78.- Asclepias Incarnata Saponin 93.- Telosmoside A12.- Hoyacarnoside K.- Asclepias Incarnata Saponin 79.- Asclepias Fruticosa Saponin 16.- Hoyacarnoside T.- Asclepias Incarnata Saponin 92.- Cynafoside D.- Araujia Sericifera Glycoside 16.- Gymnepregoside L.- Leptadenia Hastata Saponin 25.- Causiaroside II.- Tacca Chantrieri Saponin 8.- Stephanoside P.- Gymnemaroside B.- Hainaneoside B.- Marstomentoside O.- Marstomentoside P.- Periplocoside F.- Auriculoside A.- Cynanchum Caudatum Saponin 61.- Cynanchum Caudatum Saponin 64.- Wilfoside C 1G.- Nigroside A.- Asclepias Fruticosa Saponin 14.- Asclepias Fruticosa Saponin 15.- Teikaside B-IVa.- Asclepias Incarnata Saponin 16.- Asclepias Incarnata Saponin 17.- Asclepias Fruticosa Saponin 17.- Asclepias Fruticosa Saponin 18.- Cynafoside C.- Leptadenia Hastata Saponin 30.- Araujia Sericifera Glycoside 20.- Leptadenia …