Abstract: The invention relates to C-glycose compounds of formula (I) where: S? is a monosaccharide radical or a polysaccharide radical derived from a monosaccharide or polysaccharide S; R is a linear or branched alkyl radical; and Z is an ethylenyl CH?CR1(R2) or an acetylenyl C?CR3 radical. The invention also relates to a method for preparing C-glycoside compounds of formula (III), characterized in that the method consists of a step of reacting a sugar (S), in an aqueous solvent or in the absence of a solvent and in the presence of an organic or mineral base (B), with a phosphonate of formula (II) according to the following reaction pattern: Formulas (II), (III).
Type:
Grant
Filed:
November 6, 2009
Date of Patent:
October 29, 2013
Assignees:
Ecole Nationale Supérieure de Chimie de Rennes, Armor Proteines
Abstract: A process for the crosslinking of at least one polymer selected from polysaccharides and derivatives thereof, which is carried out in an aqueous solvent by the action of an effective and non-excessive amount of at least one crosslinking agent, characterized in that it is carried out on a mixture containing at least one low-molecular weight polymer and at least one high-molecular weight polymer. A process for the preparation of an injectable monophase hydrogel of at least one crosslinked polymer selected from polysaccharides and derivatives thereof. Crosslinked polymers and injectable monophase hydrogels respectively obtainable by each of said processes.
Abstract: There are provided composite fibers of alginate and chitosan. Also provided are fiber materials methods of producing composite fibers or films and composite films. In one embodiment there is provided a composite fiber of alginate and chitosan suitable for use in wound management products, wherein chitosan polymer is bonded to alginate polymer along the length of the fiber.
Type:
Grant
Filed:
February 15, 2007
Date of Patent:
October 22, 2013
Assignee:
The University of Bolton Education Corporation
Abstract: The invention is a pharmaceutical composition comprising a carboxyalkylether which lowers triglycerides and elevated HDL, and a statin which inhibits HMG-CoA reductase, thereby reducing LDL, said composition being useful for treating vascular diseases.
Type:
Grant
Filed:
December 20, 2007
Date of Patent:
October 15, 2013
Assignee:
Warner-Lambert Company, LLC
Inventors:
Charles Larry Bisgaier, Roger Schofield Newton
Abstract: Provision of a novel combined therapy with ECyd, which therapy exhibits remarkable antitumor effect and gives less adverse effects. The invention provides an antitumor agent containing, in combination, 1-(3-C-ethynyl-?-D-ribopentofuranosyl) cytosine or a salt thereof and carboplatin.
Abstract: The present invention provides novel methods for the localized delivery of inotropic agents to the heart, including specific regions of the heart, such as the ventricles, for example in a subject undergoing cardiothoracic surgery, with the aim of supporting the myocardial contractile function of the heart.
Abstract: This invention relates to novel saponin compounds of formula II wherein MBz denotes p-methoxybenzoyl, and R is selected from the group comprising C6-10 aryl, C6-10 aryl-C1-4 alkyl-, C1-18 alkanoyl, C3-18 alkenyl, C6-10 aryl-C(O)—, C6-10 aryl-C1-4 alkyl-C(O)—, wherein each of the groups can optionally be substituted. These compounds possess a selective cytostatic activity, useful, e.g., in the treatment of proliferative diseases. The invention further relates to methods of preparation of the novel compounds and to a pharmaceutical composition containing these compounds.
Type:
Grant
Filed:
February 8, 2010
Date of Patent:
October 8, 2013
Assignees:
Uniwersytet W Bialymstoku, Univerzita Palackeho V Olomouci, Bioapex, S.R.O.
Inventors:
Jacek Witold Morzycki, Agnieszka Wojtkielewicz, Jana Oklestkova, Lucie Hoffmannova, Miroslav Strnad
Abstract: The invention relates to novel crystalline phases of 5,6-dichloro-2-(isopropylamino)-1-(?-L-ribofuranosyl)-1H-benzimidazole (Maribavir), pharmaceutical compositions thereof and their use in medical therapy.
Abstract: Cationic hydrophobically modified galactomannan ethers having a cationic degree of substitution (DSC) from 0.01 to 0.5 and hydrophobic degree of substitution (DSH) below 0.001 are readily soluble in aqueous systems and useful to thicken, stabilize and condition cosmetics, detergent compositions and household cleaning products; they further improve the deposition of other ingredients on the treated surface (skin, hair or fabric).
Type:
Grant
Filed:
July 14, 2009
Date of Patent:
October 1, 2013
Assignee:
Lamberti SpA
Inventors:
Valentina Langella, Eva Baldaro, Giuseppe Li Bassi
Abstract: This invention describes processes for the convergent synthesis of calicheamicin derivatives, and similar analogs using bifunctional and trifunctional linker intermediates.
Abstract: The present invention relates to a method for removing impurities from biopolymer material, e.g. polysaccharides, polypeptides or polynucleotides. More particularly, the present invention provides a method of reducing lipopolysaccharide levels in a lipopolysaccharide containing biopolymer material, comprising the successive steps of: a) providing an aqueous solution containing 0.05-50 wt. % of dissolved lipopolysaccharide-containing biopolymer material; 0.001-10 wt.% of a surfactant; 0.05-15 wt. % of solid adsorbent; and at least 50 wt. % of water; b) allowing the adsorbent to adsorb lipopolysaccharides; c) separating the solid adsorbent containing adsorbed lipopolysaccharides from the remaining aqueous solution; and d) recovering the biopolymer material containing a reduced level of lipopolysaccharide from the separated aqueous solution.
Type:
Grant
Filed:
June 19, 2008
Date of Patent:
September 10, 2013
Assignee:
Bender Analytical Holding B.V.
Inventors:
Johannes Caspar Mathias Elizabeth Bender, Pieter Sebastiaan Vermeulen
Abstract: The present disclosure provides bicyclic cyclohexitol nucleoside analogs of formula I and oligomeric compounds comprising these nucleoside analogs. These bicyclic nucleoside analogs are expected to be useful for enhancing properties of oligomeric compounds including for example nuclease resistance.
Type:
Grant
Filed:
February 6, 2009
Date of Patent:
September 10, 2013
Assignee:
Isis Pharmaceuticals, Inc.
Inventors:
Punit P. Seth, Michael T. Migawa, Eric E. Swayze, Quanlai Song, Mingming Han, Bruce S. Ross
Abstract: A method for the chlorination of a sucrose-6-acylate to produce a 4,1?,6?-trichloro-4,1?,6?-trideoxy-galactosucrose-?-acylate wherein said method comprises: (i) reacting the sucrose-6-acylate with a chlorinating agent in a reaction vehicle comprising a tertiary amide in order to chlorinate the 4, V and 6? positions of the sucrose-6-acylate; and (ii) quenching the product stream of (i) to produce a 4,1?,6?-trichloro-4,1?,6?-trideoxy-galactosucrose-6-acylate; wherein before said quenching, a portion of the tertiary amide is removed.
Type:
Grant
Filed:
March 24, 2010
Date of Patent:
September 10, 2013
Assignee:
Tate & Lyle Technology Ltd.
Inventors:
Wayne N. Boutzale, David A. Dentel, Mohamad R. Jaber
Abstract: The present invention relates to a composition comprising an inclusion complex of a cyclodextrin and quinazoline containing zinc-binding moiety based derivatives. The cyclodextrin is preferable a ?-cyclodextrin or a derivative thereof. The quinazolines have enhanced and unexpected properties as inhibitors of epidermal growth factor receptor tyrosine kinase (EGFR-TK) and their use in the treatment of EGFR-TK related diseases and disorders such as cancer. The said derivatives may further act as HDAC inhibitors.
Type:
Grant
Filed:
January 17, 2012
Date of Patent:
August 27, 2013
Assignee:
Curis, Inc.
Inventors:
Xiong Cai, Changgeng Qian, Haixiao Zhai, Rudi Bao
Abstract: The present invention relates to methods of preparing anthocyanins, and methods of preparing precursors of anthocyanins. The methods utilize a coupling reaction between a sugar and a suitable electrophilic precursor to form Eastern half intermediates that are then reacted with Western half intermediates to form the target anthocyanins. Some Eastern half intermediates and electrophilic precursors also form part of the invention.
Abstract: A method of treating Type II diabetes utilizing two off-the-shelf drugs. Intravenous injection of one or both drugs, individually and in combination, can prevent and treat diabetes, restore damaged islet cell functions and reduce or stop the use of oral hypoglycemic agents and insulin.
Abstract: The present invention provides novel compounds with hypocholesteremic activity from crude Embilica officinialis (EO) extracts and methods of use. The invention also provides nutraceuticals.
Type:
Grant
Filed:
June 22, 2009
Date of Patent:
July 23, 2013
Inventors:
Subroto Chatterjee, Mark S. Butler, Brinda Somanadhan