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Furostanol saponin

Grunweller, S., E. Schroder, and J. Kesselmeier. Biological activities of furostanol saponins from Nicotiana tabacum. Phytochemistry 1990 29(8) 2485-2490. [Pg.370]

Allium chinense Max. A. odorum L. A. sativum L. A. tuberosum Roxb. A. uliginosum G. Don Da Suan (Garlic) (bulb) Allicin, allistatin, glucominol, neo-allicin, steroidal saponins, polysaccharides, furostanol saponins, proto-isoerubosides, diallyl sulfide.33 49 438 490-510 Antibacterial, antimutagenic, anticarcinogenesis, carminative, antiarrhythmic, lower plasma cholesterol and low-density lipoproteins, prevent thrombosis, hypotensive and vessel protective effect. [Pg.24]

Furanocoumarin Furanodiene Furanodienone Furostanol saponins Furylisobutyl ketone Furylmethyl ketone Furylpropyl ketone Fustin Galactan... [Pg.428]

Gupta, R.K., Thain, D.C., and Thakur, R.S. 1986. Two furostanol saponins from Trigonella foenum-... [Pg.329]

Yoshikawa, Mv Murakami, T., Komatsu, H., Murakami, N., Yamahara, J. and Matsuda, H. (1 997) Medicinal foodstuffs. IV. Fenugreek seed. (1) Structures of trigoneosides la, lb, lla, Ilia, 11 lb, new furostanol saponins from the seeds of Indian Trigonella foenum-graecum. Chemical and Pharmaceutical Bulletin 45(1), 81-87. [Pg.259]

Zhang JB, Yu B, Hui YZ (2000) Recent Progress in Research of Furostanol Saponins. Youji Huaxue 20 663... [Pg.128]

Zhang J, Ma B, Kang L, Yu H, Yang Y, Yan X, Dong F (2006) Furostanol Saponins from the Fresh Rhizomes of Polygonatum kingianum. Chem Pharm Bull 54 931... [Pg.128]

Dong M, Feng X-Z, Wang B-X, Wu L-J, Ikejima T (2001) Two Novel Furostanol Saponins from the Rhizomes of Dioscorea panthaica Prain et Burkill and Their Cytotoxic Activity. Tetrahedron 57 501... [Pg.140]

Braca A, Prieto JM, De Tommasi N, Tome F, Morelli I (2004) Furostanol Saponins and Quercetin Glycosides from the Leaves of Helleborus viridis L. Phytochemistry 65 2921... [Pg.140]

Perrone A, Plaza A, Bloise E, Nigro P, Hamed AI, Belisario MA, Pizza C, Piacente S (2005) Cytotoxic Furostanol Saponins and a Megastigmane Glucoside from Tribulus parvispinus. J Nat Prod 68 1549... [Pg.141]

Combarieu ED, Fuzzati N, Lovati M, Mercalli E (2003) Furostanol Saponins from Tribulus terrestris. Fitoterapia 74 583... [Pg.141]

Kostova I, Dinchev D, Rentsch GH, Dimitrov V, Ivanova A (2002) Two New Sulfated Furostanol Saponins from Tribulus terrestris. Z Naturforsch 57c 33... [Pg.141]

Research of furostanol saponins (steroid saponins with tetrahydrofurane ring E) 00MI25. [Pg.30]

Steroidal glycosides from Hosta plantaginea var. japonica were less active on HL-60 cells [14]. The spirostanol saponins (19-21) showed dose-dependent cytostatic activities (IC50 from 1 to 3 ig/ml), while the furostanol saponin and C22-steroid were inactive (ICso> 10 ig/ml). [Pg.637]

De Combarieu E, Fuzzati N, Lovati M, Mercalli E (2003) Furostanol saponins from Tribulus terrestris. Fitoterapia 74(6) 583-591 de Meyts P, Cession-Fossion A (1966) Ephedrine as a sympathicomi-metic amine with indirect action in the rat. Comptes Rendus des Seances de la Societe de Biologie et de Ses FUiales 160(11) 2224-2227 (in French)... [Pg.304]

Liu YZ, Liang F, Cui LJ, Xia M, Zhao LY, Yang YC, Shi JG, Abliz Z. Multi-stage mass spectrometry of furostanol saponins combined with electroapray ionization in positive and negative ion modes. Rapid Commun Mass Spectrom 2004 18 235-238. [Pg.611]

Keywords Extracts of Ruscus aculeatus, Venoconstrictor effect, Ruscogenin, Spirostanol saponins, Furostanol saponins... [Pg.179]

In 1972, a group of Research Laboratory of Invemi Della Beffa, Milan, Italy confirmed two furostanol saponins l-0-[a-L-rhamnopyranosyl-(l—>2)-a-L-arabinopyranosyl(l)]-ip,3p,22a,26-tetrahydroxy-furosta-5(6),25(27)-dien-26-P-D-glucopyranoside (13) and l-0-[P-D-glucopyranosyl-(l—>3)-a-... [Pg.191]

In 1998, six novel spirostanol saponins and five novel furostanol saponins were confirmed from the fresh imderground parts of Ruscus aculeatus L. by spectroscopic analysis, nuclear magnetic resonance spectrometry (NMR) and acid hydrolysis. [Pg.191]

Second, five novel furostanol saponins are follows 26-O-P-D-glucopyranosyl-22-0-methyl-(25R)-furost-5-ene-ip,3p,22i , 26-tetrol -0- O-a-L-rhamnopyranosyl-(l- 2)-P-D-galactopyranoside (21), 26-0-P-D-... [Pg.194]

Among their antitumor activity for leukemia HL-60 cells by a MTT assay on each 11 sample concentration of 10 pig/mL of six novel spirostanol saponins (15-20) and five novel furostanol saponins (21-25), percentage of cell growth inhibition (%) of ruscogenin 1-0- 0-a-L-rhamnopyranosyl-(l—>2)-3,4,6-tri-0-acetyl- 3-D-galactopyranoside 1 (18) was the highest 98.2%, followed by 82.5% for 26-0- 3-D-glucopyranosyl-22-0-methyl-(25R)-furost-5-ene-113,3 3,22(, 26-tetrol 1 -0-i 0-a-L-rhamnopyranosyl-( 1 —>2)-3,4,6-tri-O-... [Pg.198]

Fig. 105.1 Basic structures of spirostanol and furostanol saponins (left and middle, respectively) (R = sugar) and the structure of cholesterol (right)... Fig. 105.1 Basic structures of spirostanol and furostanol saponins (left and middle, respectively) (R = sugar) and the structure of cholesterol (right)...
As illustrated by consideration of 1-16, a number of modifiers are commonly used in the trivial nomenclature of furostanol saponins. Where an analogous spirostanol glycsoide has been reported previously with a trivial name, the prefix proto can be added to give the name of the furostanol, for example protodioscin (3) derived from dioscin (1). The methyl prefix is used to indicate that the glycoside is a C-22 methyl acetal (22-methoxy) furostanol (as in methylprotodioscin, (4)), while pseudo indicates -unsaturation... [Pg.3230]


See other pages where Furostanol saponin is mentioned: [Pg.291]    [Pg.247]    [Pg.247]    [Pg.344]    [Pg.49]    [Pg.56]    [Pg.63]    [Pg.643]    [Pg.309]    [Pg.824]    [Pg.222]    [Pg.3225]    [Pg.3225]    [Pg.3227]    [Pg.3228]    [Pg.3228]    [Pg.3229]    [Pg.3229]    [Pg.3230]    [Pg.3232]    [Pg.3233]    [Pg.3239]   
See also in sourсe #XX -- [ Pg.415 ]

See also in sourсe #XX -- [ Pg.49 , Pg.56 , Pg.63 ]

See also in sourсe #XX -- [ Pg.633 , Pg.646 ]




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