Abstract
One of the main goals of the chemistry of naturally occurring compounds is screening for promising biologically active substances of plant origin. In this connection, steroidal glycosides studied in several directions present significant interest. On the one hand, these products are utilized as initial compounds from which to synthesize hormonal preparations and medicines1; on the other hand, steroidal glycosides are of increased interest as biologically active material.
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M.D. Maskovskiy. Medicines,Meditsina, Moscow (1995) (In Russian).
P.K. Kintia, G.V. Lazuryevskiy, N.N. Balashova, I.T. Balashova, A.I. Suruzhiu, and V.A. Lyakh, Structure and Biological Activity of Steroidal Glycosides of the Spirostane and Furostan Series,Shtiintsa, Kishinev (1987) (In Russian).
D.V. Ioffe, Natural compounds possessing antisclerotic properties, Khim. Prirodn. Soedin. 2:275 (1984) (In Russian).
P.K. Kintia, M.N Mats, S.A. Shvets, and L.P. Degtyaryova, Contraceptive activity of some steroidal glycosides, Rastit. Resur. 24:263 (1988) (In Russian).
C. Sannié and H. Lapin, Recherches sur les sapogenines a noyau sterolique. Identification de les genines sur de petites quantites de plantes. Bull. Soc. Chim. Fr. 19: 1080 (1952).
S. Kiyosawa and M. Huton, Detection of prototype compounds of diosgenin and other spirostanol glycosides. Chem. Pharm. Bull. 16: 1162 (1968).
M.E. Wall, C.R. Eddy, M.L. McClennan, and M.E. Klumpp, Detection and estimation of steroidal sapogenins in plant tissues. Anal. Chem. 24: 1337 (1952).
R. Tschesche, B.T. Tjoa, G. Wulff, and R.V. Noronha, Steroid Saponine mit mehr als einer Zuckerkette III. Convallamarosid, ein weiteres 22-Hydroxyfurostanol Saponin, Tetrahedron Lett. 49: 5141 (1968).
P.K. Agrawal, D.C. Jain, and R.K. Gupta, Carbon 13-NMR spectroscopy of steroidal sapogenins and steroidal saponins Phytochemistry 24: 2479 (1985).
E.V. Gutsu, P.K. Kintia, S.A. Shvets, and G.V. Lazuryevskiy, Steroidal glycosides from Capsicum annuum roots. Structure of capsicosides A1, B1, C1. Rhim. Prirodn. Soedin. 6:708 (1986) (In Russian).
V.V. Krokhmalyuk, P.K. Kintia, and V.Ya. Chirva, Gas-liquid chromatography of monosaccharides of triterpene glycosides. Izv. AN MSSR 1: 103 (1975) (In Russian).
S. Hakomori, A rapid permethylation of glycolipids and polysaccharides catalyzed by methylsulfonyl carbanion in dimethyl sulfoxide, J. Biochem. (Tokyo) 55: 205 (1964).
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Shvets, S.A., Kintia, P.K., Naibi, M.A. (1996). Steroidal Glycosides from Petunia hybrida L. Seeds and Their Biological Activity. In: Waller, G.R., Yamasaki, K. (eds) Saponins Used in Traditional and Modern Medicine. Advances in Experimental Medicine and Biology, vol 404. Springer, Boston, MA. https://doi.org/10.1007/978-1-4899-1367-8_23
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DOI: https://doi.org/10.1007/978-1-4899-1367-8_23
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