Abstract: Steroid compounds are disclosed that have a formula represented by the following: and wherein m, n, t, u1, u2, v1, v2, R1a, R1b, R2a, R2b, R3a, R3b, R3c, R3d, and Y are as described herein. The compounds may be prepared as pharmaceutical compositions, and may be used for the treatment or prevention of a variety of conditions in mammals including humans, including by way of non-limiting example, inflammatory conditions, autoimmune disorders, cancer, and graft-versus-host disease.
Type:
Grant
Filed:
November 28, 2011
Date of Patent:
November 29, 2016
Assignees:
New York University, Memorial Sloan-Kettering Cancer Center
Inventors:
Dan R. Littman, Jun R. Huh, Nicolas Gabriel Albert Manel, Daniel A. Ryan, David Y. Gin, Mary S. Gin, Michael R. Krout
Abstract: The invention provides compounds, methods, pharmaceutical compositions, and kits for the treatment of proliferative disorders such as cancer. In one aspect, the methods comprise compounds that inhibit the activity of protein kinases, such as cell division cycle (Cdc) kinase. In another aspect, the methods comprise compounds that inhibit Cdc7 and/or Dbf4 activity. In another aspect, the methods comprise compounds that exhibit anti-proliferative properties useful in treating diseases such as cancer. Compounds useful for any of the methods include compounds of the Formula (A) or (B): or pharmaceutically acceptable salts thereof. Exemplary compounds of Formula (A) or (B) include granaticin A, granaticin B, dihydrogranaticin A, dihydrogranaticin B, medermycin, and actinorhodin.
Type:
Grant
Filed:
November 9, 2015
Date of Patent:
November 15, 2016
Assignee:
Sloan-Kettering Institute for Cancer Research
Inventors:
Mark G. Frattini, Hakim Djaballah, Thomas J. Kelly
Abstract: Provided are an attractant for bone marrow stem cells containing at least one of cinnamtannin B1 and pentagalloylglucose, and a method for attracting bone marrow stem cells in which bone marrow stem cells are attracted by the attractant.
Abstract: The present invention relates to a chemically modified heparin, with an antifactor II activity of less than 10 IU/mg, an antifactor Xa activity of less than 10 IU/mg and an average molecular weight (Mw) between about 6.5 and 9.5 kDa. Also disclosed is a method of preparing the heparin and its medical use, including treatment of malaria.
Type:
Grant
Filed:
December 19, 2012
Date of Patent:
November 1, 2016
Assignee:
DILAFORETTE AB
Inventors:
Hans-Peter Ekre, Ulf Lindahl, Erik Holmer, Per-Olov Eriksson, Anna Leitgeb, Mats Wahlgren, Stefania Tiddia, Lino Liverani
Abstract: A solid substrate for the extraction, stabilization, and storage of proteins is provided. The substrate includes: a polysaccharide, such as melezitose under a substantially dry state. The substrate is configured to extract proteins from a sample and stabilize the extracted proteins in a dry format under ambient conditions for a prolonged period of time. Methods for collecting and recovering the proteins stored in the dry solid substrate are also described.
Type:
Grant
Filed:
April 25, 2014
Date of Patent:
November 1, 2016
Assignee:
General Electric Company
Inventors:
Ernest William Kovacs, Erik Leeming Kvam, Bing Li, Frank John Mondello
Abstract: The present invention relates to pharmaceutical compositions comprising dapagliflozin and cyclodextrin, preferably (2-hydroxy)propyl-b-cyclodextrin or ?-cyclodextrin, preferably as inclusion complex. The invention further relates to a process for producing said pharmaceutical compositions. Finally, the invention relates to the use of cyclodextrin for producing dapagliflozin-containing dosage forms and to methods of purification of dapagliflozin.
Abstract: The present invention relates to chemically modified heparin for use in the treatment of sickle cell disease, with an antifactor II activity of less than 10 IU/mg, an antifactor Xa activity of less than 10 IU/mg and an average molecular weight (Mw) between about 6.5 and 9.5 kDa.
Type:
Grant
Filed:
December 19, 2012
Date of Patent:
November 1, 2016
Assignee:
DILAFORETTE AB
Inventors:
Hans-Peter Ekre, Anna Leitgeb, Mats Wahlgren, Dagmar Pikas
Abstract: The present invention relates to a chemically modified glycosaminoglycan with an antifactor II activity of less than 10 IU/mg, an antifactor Xa activity of less than 10 IU/mg and an average molecular weight (Mw, weight average) from about 4.6 to 6.9 kDa. Also disclosed is a method of preparing the modified glycosaminoglycan and its medical uses.
Type:
Grant
Filed:
December 19, 2012
Date of Patent:
October 25, 2016
Assignee:
Dilafor AB
Inventors:
Hans-Peter Ekre, Ulf Lindahl, Erik Holmer, Per-Olov Eriksson
Abstract: A kit for bonding to biological hard tissues, containing a phosphorylated polysaccharide, a polyvalent metal salt other than phosphates, and a solvent. The adhesive composition for biological hard tissues provided by the kit for bonding to biological hard tissues is suitably used in for medical uses, such as cement for bones or dental cement.
Type:
Grant
Filed:
October 9, 2015
Date of Patent:
October 25, 2016
Assignees:
National University Corporation Okayama University, Junsei Educational Institution
Abstract: The antimicrobial composition of the present invention comprises a cationic active ingredient, a quaternized sugar-derived surfactant, and an optional foam boosting surfactant. These formulations have a high cidal activity in a short amount of time and provide stable copious foam. The formulations of the present invention also exhibit enhanced tissue (e.g. skin) compatibility as defined by an in vitro whole toxicology assessment method.
Type:
Grant
Filed:
December 5, 2014
Date of Patent:
October 25, 2016
Assignee:
Ecolab USA Inc.
Inventors:
Daniel E. Pedersen, Angela R. Eder, Charles Allen Hodge
Abstract: The present invention relates to cellulose mixed esters, processes for preparing these and uses of the cellulose mixed esters, for example in coating compositions. The cellulose mixed esters have glass transition temperatures that fall within an appropriate range to allow for film formation to occur at ambient temperatures and have a total degree of substitution per anhydroglucose unit of about 2.5 to about 3.5; a residual hydroxyl functionality per anhydroglucose unit of 0 to about 0.5; a degree of substitution per anhydroglucose unit by C2-C6 ester groups of about 0.5 to about 2.8; and a degree of substitution per anhydroglucose unit by Ievulinyl ester groups of about 0.2 to about 2.6.
Type:
Grant
Filed:
December 5, 2012
Date of Patent:
October 4, 2016
Assignee:
Resene Paints Limited
Inventors:
Mark Glenny, Colin Gooch, Simon Hinkley, Jennifer Mason, Cameron Tristram, Dennis Williams
Abstract: Pharmaceutical/cosmetic compositions containing a dermatologically effective amount of hyaluronic acid, at least one retinoid and/or salt and/or derivative thereof, at least one oligosaccharide and at least one inhibitor of hyaluronic acid degradation, formulated into a physiologically acceptable medium therefor, are useful for the treatment of wrinkles, fine lines, fibroblast depletions and scars.
Abstract: The present invention relates to a process for dewatering a slurry comprising microfibrillated cellulose wherein the process comprises the following steps of, providing a slurry comprising microfibrillated cellulose and liquid, subjecting the slurry to an electric field inducing the liquid of the slurry to flow and separating the liquid from the microfibrillated cellulose. The invention also relates to microfibrillated cellulose dewatered according to the process.
Type:
Grant
Filed:
May 11, 2012
Date of Patent:
September 20, 2016
Assignee:
Stora Enso OYJ
Inventors:
Isto Heiskanen, Kaj Backfolk, Ari Kotilainen, Valentas Gaidelis, Jonas Sidaravicius
Abstract: The invention provides semisynthetic derivatives of Nystatin A1, water soluble salts and complexes, pharmaceutical compositions and plant protection products comprising the derivatives and their use, as antifungal antibiotics (Formula 1a).
Type:
Grant
Filed:
March 7, 2013
Date of Patent:
September 20, 2016
Assignee:
BLIRT S.A.
Inventors:
Edward Borowski, Natalia Salewska, Joanna Boros-Majewska, Maria Milewska, Malgorzata Wysocka, Slawomir Milewski, Andrzej Skladanowski, Adam Treder, Ewa Sadowska, Izabela Chabowska
Abstract: The present invention relates to a process for purifying a slurry comprising cellulose, such as microfibrillated cellulose, wherein the process comprises the following steps: —providing a slurry comprising cellulose and liquid, —subjecting the slurry to an electric field inducing the liquid of the slurry to flow, —separating the liquid from the cellulose thus obtaining a liquid depleted slurry, —adding a washing liquid, such as an organic solvent, to the liquid depleted slurry—subjecting the liquid depleted slurry to an electric field inducing the washing liquid of the slurry to flow and—separating the washing liquid from the cellulose, thus obtaining a purified cellulose. The invention also relates to cellulose such as microfibrillated cellulose obtainable from said process.
Type:
Grant
Filed:
May 11, 2012
Date of Patent:
September 20, 2016
Assignee:
Stora Enso OYJ
Inventors:
Isto Heiskanen, Kaj Backfolk, Ari Kotilainen, Valentas Gaidelis, Jonas Sidaravicius
Abstract: The present invention relates to methods for disinfecting or decontaminating a material or for preventing an infection or contamination of a material. The invention further relates to compositions which are suitable for disinfecting a material or for preventing an infection or contamination of a material and to uses of such compositions. The invention further relates to a medical use of chitosan and to a pharmaceutical composition comprising the chitosan. The invention further relates to a method of treating a microbial infection and to an aqueous solution comprising chitosan. The invention moreover relates to a chitosan or a pharmaceutical composition comprising a chitosan for an epithelial cell growth stimulating treatment of a patient's tissue and to a method of stimulating the growth of epithelial cells. The invention also relates to a tissue dressing material.
Type:
Grant
Filed:
September 1, 2010
Date of Patent:
September 13, 2016
Assignee:
Medoderm GmbH
Inventors:
Karsten Henco, Thomas Freier, Rivelino Montenegro
Abstract: Provided are a cosmetic solution and a method for producing the cosmetic solution, the cosmetic solution being easy to store and also easy to handle during use, and moreover having a high moisturizing function, without the use of a preservative. Hyaluronic acid/or a hyaluronic acid compound is dispersed in a polyvalent alcohol, also, an organic acid and/or organic acid salt different from the hyaluronic acid and/or hyaluronic acid compound is dispersed in a polyvalent alcohol such that it contains no water. The solution contains 0.01 to 2.0 wt % hyaluronic acid and/or hyaluronic acid compound 97 wt % or more polyvalent alcohol, is weakly acidic; i.e. 5?pH<7 due to the organic acid and/or organic acid salt.
Abstract: The present invention relates to a pharmaceutical composition for preventing or treating a menopausal symptom, comprising cinnamic acid, shanzhiside methylester or a mixture thereof as an active ingredient. The composition of the present invention exhibits an excellent estrogenic activity, and is effectively utilized for treating or preventing diverse menopausal symptoms generated by estrogen deficiency during perimenopause, menopause and postmenopause.
Type:
Grant
Filed:
December 26, 2008
Date of Patent:
September 6, 2016
Assignee:
Natural Endotech Co., Ltd.
Inventors:
Jae-Soo Kim, Bo-Yeon Kwak, Kwontaek Yi, Jaekyoung Lee
Abstract: Edible compositions useful for weight management in male animals are disclosed. The compositions comprise one or more isoflavones or isoflavone metabolites and are particularly useful for reducing or preventing the accumulation of body fat. Also disclosed are methods useful for weight management in an animal utilizing compositions comprising one or more isoflavones. The compositions and methods are particularly useful for the reduction or prevention of body fat accumulation during periods of excess caloric intake, and preferably have a sparing effect on lean body mass.