Sugar derivative

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Carbohydrate doai

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C536S123000, C514S061000

Reexamination Certificate

active

07375095

ABSTRACT:
For extending the uses of a compound represented by Chemical formula 1, the object of the present invention is to provide a derivative of cyclic tetrasaccharide whose physicochemical properties are changed from those of cyclic tetrasaccaride, a composition comprising the same, and a process for producing the same. The present invention solves the above object by providing a derivative of cyclic tetrasaccharide, which is produced by the steps of reacting a compound represented by Chemical formula 1 with a reactive reagent and substituting one ore more hydroxyl groups with substituents except hydroxyl group and O-glycosyl group; a composition comprising the same; and a process for producing the derivative of cyclic tetrasaccharide.

REFERENCES:
patent: 5786196 (1998-07-01), Cote et al.
patent: 5889179 (1999-03-01), Cote et al.
patent: 2004/0236097 (2004-11-01), Aga et al.
patent: 1 229 112 (2002-08-01), None
patent: 1 284 286 (2003-02-01), None
patent: 1 360 988 (2003-11-01), None
patent: 1 380 595 (2004-01-01), None
patent: WO 01/90338 (2001-11-01), None
patent: WO 02/10361 (2002-02-01), None
patent: WO 02/057011 (2002-07-01), None
patent: WO 02/072594 (2002-09-01), None
The Merck Index, 13thEdition, p. 794, monograph for “Glucose” © 2001 by Merck & Co., Inc.
Hawley's Condensed Chemical Dictionary, 13thEdition, pp. 540-541, entry for “Glucose” © 1997 by Van Nostrand Reinhold.
M. Yalpani, Polysaccharides: Syntheses, Modifications and Structure/Property Relations, In: Studies in Organic Chemistry, pp. 36:234-299 (1988).
Côté et al., The Hydrolytic and Transferase Action of Alternanase on Oligosaccharides,Carbohydrate Research, 332:373-379 (2001).
Boger, J., et al, “203. Cyclodextrin chemistry. Selective modification of all primary hydroxyl groups of α- and β-cyclodextrins”, Helvetica Chimica Acta. (1978). vol. 61, pp. 2190-2218.
Breslow, Ronald and Anthony Czarnik, “Transaminations by Pyridoxamines selectively attached at C-3 in β-cyclodexrin” J. Am. Chem. Soc. (1983. vol. 103, pp. 1390-1391.
Cote, Gregory and Peter Biely, “Enzymically produced cyclic α-1,3-linked and α-1,6-linked oligosaccharides of D-glucose”, Eur. J. Biochem. (1994). vol. 226, pp. 641-648.
Harada, Aakira, “Design and synthesis of macromolecular systems consisting of cyclodextrins and polymers”, J. Michl (ed.), Molecular Chemistry. (1997).Kluwer Academic Publishers. Netherlands, pp. 361-370.
Hedges, Allan, “Industrial applications of cyclodextrins”, Chem. Rev. (1998). vol. 98, pp. 2035-2044.
Hirst, E. and Elizabeth Percival, “Methyl Ethers of Mono- and Disaccharides”, Whistler et al (eds.) Methods In Carbohydrate Chemistry. (1963). Academic Press Inc., New York. 145-151.
Ichikawa, et al, “Simple preparation of multi-valent cyclodextrin-carbohydrate conjugates”, Tetrahedron: Asymmetry. (2000). vol. 11, pp. 389-392.
Ikeda, et al, “Modifications of the secondary hydroxyl side of α-cyclodextrin and NMR studies of them”, Tetrahedron Letters. (1990). vol. 31, No. 35, pp. 5045-5048.
Khan, et al, “Methods for selective modifications of cyclodextrins”, Chem. Rev. (1998). vol. 98, pp. 1977-1996.
Komiyama, “Kagaku (Science)” (in Japanese), (1989), vol. 59, No. 2, pp. 105-112.
Lee, Cheang Kuan, “Trehalose”, C.K. Lee (ed) Developments In Food Carbohydrate-2. (1980). Applied Science Publishers Ltd. Essex, GB. Chapter 1, pp. 1-89.
Murakami, et al, “Synthesis and chiral recognition property of 3-acetylamino-3-deoxy-8-cyclodextrin”, Chemistry Letters. (1988), No. 3, pp. 553-556.
Suzuki, et al, “Ferrocene-appended cyclodextrins. The effects of temperature, organic solvent, length of spacer, and cavity size in the complexation behavior”, Bull. Chem. Soc. Jpn. (1993). vol. 66, No. 5, pp. 1472-1481.
Szejtli, Jozsef, “Utilization of cyclodextrins in industrial products and processes”, J. Mater. Chem. (1997). vol. 7, No. 4, pp. 575-587.
Szeja, Wieslaw, “Convenient synthesis and application of sucrose sulfates”, Frieder Lichtenthaler (ed.), Carbohydrates as Organic Raw Materials. (1990). VCH, Weineim, Chapter 5, pp. 117-125.
Ueno, A., et al, “Host-guest complexation of ferrocene-appended β-cyclodextrin in organic solvents”, Makromol. Chem., Rapid Commun. (1985). vol. 6, pp. 231-233.
Ueno, Akihiko and Ronald Bewslow, “Selective sulfonation of a secondary hydroxyl group of β-cyclodextrin”, Tetrahedron Letters (1982). vol. 23, No. 34, pp. 3451-3454.
Yoshimoto, K. et al, “Chemical and biochemical studies on carbohydrate esters. XIII. Synthesis of 6-O-, 6,6′- Di-O- and 4,6,4′,6′-Tetra-O-stearoyl-α,α-trehaloses” Chem. Pharm. Bull. (1982). vol. 30, No. 4, pp. 1169-1174.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Sugar derivative does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Sugar derivative, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Sugar derivative will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-3983277

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.