At 3-position Patents (Class 514/355)
-
Patent number: 8263527Abstract: Insecticidal compositions suitable for use in preparation of insecticidal liquid fertilizers comprising a pyrethroid, a hydrated aluminum-magnesium silicate, and at least one dispersant selected from the group consisting of a sucrose ester, a lignosulfonate, an alkylpolyglycoside, a naphthalenesulfonic acid formaldehyde condensate and a phosphate ester are disclosed.Type: GrantFiled: September 9, 2011Date of Patent: September 11, 2012Assignee: FMC CorporationInventor: Timothy Martin
-
Publication number: 20120220463Abstract: The present invention relates to crystalline complexes of 4-hydroxy benzoic acid and selected pesticides. It also relates to agriculturally useful compositions of the complexes.Type: ApplicationFiled: October 28, 2010Publication date: August 30, 2012Applicant: BASF SEInventors: Heidi Emilia Saxell, Rafel Israels, Ansgar Schaefer, Matthias Bratz, Hans Wolfgang Hoeffken, Ingo Brode, Elisa Nauha, Maija Nissinen
-
Patent number: 8252818Abstract: Compounds of formula (I): are inhibitors of p38 kinase and are useful in the treatment of conditions or disease states mediated by p38 kinase activity or mediated by cytokines produced by the activity of p38.Type: GrantFiled: February 26, 2010Date of Patent: August 28, 2012Assignee: GlaxoSmithKline LLCInventors: Nicola Mary Aston, Paul Bamborough, Ann Louise Walker
-
Publication number: 20120214851Abstract: The invention relates to a composition comprising at least one aminobenzamide compound or a salt thereof for controlling animal parasites, veterinary pharmaceutical compositions comprising at least one aminobenzamide of formula (I) for preventing infection with diseases transmitted through parasites, its use for the preparation of a veterinary pharmaceutical for controlling animal parasites, and a method for preventing infection with diseases transmitted through parasites.Type: ApplicationFiled: April 26, 2012Publication date: August 23, 2012Applicant: BAYER CROPSCIENCE AGInventors: Ulrich GÖRGENS, Akihiki YANAGI, Kazue YANAGI, Keisuke YANAGI, Kasumi YANAGI, Katsuaki WADA, Tetsuya MURATA, Yukiyoshi WATANABE, Jun MIHARA, Koichi ARAKI
-
Publication number: 20120207810Abstract: The present invention relates to drug delivery systems comprising ocular implant, which include organic molecules, capable of modulating tyrosine kinase signal transduction in order to regulate, modulate and/or inhibit abnormal cell proliferation, in combination with a polymer, which polymer serves to control, modify, modulate and/or slow the release of the therapeutic component into the environment of the eye in which said composite is placed.Type: ApplicationFiled: February 15, 2012Publication date: August 16, 2012Inventors: Lon T. SPADA, Jane Guo SHIAH, Patrick HUGHES, Thomas C. MALONE, Gerald W. DEVRIES, Jeffrey L. EDELMAN, Julie A. WURSTER
-
Publication number: 20120207773Abstract: The present invention provides materials and methods for making a subject non-responsive to an antigen. Methods of the invention may comprise contacting the subject with the antigen and a compound that induces anergy. In some embodiments, the antigen may be an autoimmune antigen, examples of which include, but are not limited to acetylcholine receptor for myasthenia gravis, glutamic acid decarboxylase for type I diabetes mellitus and rheumatoid factor in rheumatoid arthritis, hi some embodiments, the present invention provides a method of transplanting an organ, tissue, or cells into a subject (e.g., a mammal such as a human).Type: ApplicationFiled: August 17, 2010Publication date: August 16, 2012Inventor: Jun Hayashi
-
Patent number: 8236346Abstract: The present invention provides methods for reducing A? deposition, A? neurotoxicity and microgliosis in an animal or human afflicted with a cerebral amyloidogenic disease, such as Alzheimer's disease (AD), by administering therapeutically effective amounts of the (R)-enantiomer of the dihydropyridine compound nilvadipine, also known as (?)-nilvadipine, to the animal or human. Further provided are methods for reducing the risk of A? deposition, A? neurotoxicity and microgliosis in animals or humans suffering from traumatic brain injury by administering (?)-nilvadipine after the traumatic brain injury and continuing treatment for a prescribed period of time thereafter.Type: GrantFiled: October 3, 2008Date of Patent: August 7, 2012Assignee: Alzheimer's Institute of America, IncInventors: Michael J. Mullan, Daniel Paris, Robert A. Ivey, III
-
Pharmaceutical compositions for reducing amyloid deposition, amyloid neurotoxicity, and microgliosis
Patent number: 8236347Abstract: The present invention provides methods for reducing A? deposition, A? neurotoxicity and microgliosis in an animal or human afflicted with a cerebral amyloidogenic disease, such as Alzheimer's disease (AD), by administering therapeutically effective amounts of the (R)-enantiomer of the dihydropyridine compound nilvadipine, also known as (?)-nilvadipine, to the animal or human. Further provided are methods for reducing the risk of A? deposition, A? neurotoxicity and microgliosis in animals or humans suffering from traumatic brain injury by administering (?)-nilvadipine after the traumatic brain injury and continuing treatment for a prescribed period of time thereafter.Type: GrantFiled: February 1, 2010Date of Patent: August 7, 2012Assignee: Alzheimer's Institute of America, Inc.Inventors: Michael J. Mullan, Daniel Paris, Robert A. Ivey, III -
Publication number: 20120190542Abstract: The present invention relates to pesticidal mixtures, compositions and uses thereof comprising a component (A) and a component (B), wherein components (A) and (B) are: (A) a carboxylic acid amide fungicide; and (B) a benzamide fungicide; with the proviso that the mixture does not comprise: 1). fluopicolide and mandipropamid and clothianidin; or 2). fluopicolide and mandipropamid and imidacloprid; or 3). fluopicolide and mandipropamid and thiamethoxam. The invention also relates to mixtures, compositions and uses thereof wherein component (A) is metalaxyl-M and component (B) is a benzamide fungicide.Type: ApplicationFiled: March 29, 2010Publication date: July 26, 2012Applicant: SYNGENTA CROP PROTECTION, LLCInventors: Patrick John Doyle, Gilberto Olaya-Huertas, Paul John Kuhn, Allison Tally
-
Patent number: 8227493Abstract: Soluble granule pesticidal compositions comprise Flonicamid, a dispersant, and a wetting agent are disclosed.Type: GrantFiled: April 13, 2005Date of Patent: July 24, 2012Assignee: FMC CorporationInventors: Hong Liu, Robin Dexter, Timothy Martin, Craig Martin
-
Publication number: 20120184520Abstract: [Problem] The present invention provides a compound which is useful as an active ingredient of a pharmaceutical composition, in particular, a pharmaceutical composition for preventing and/or treating VAP-1-related diseases. [Means for Solution] The present inventors have conducted intensive studies on a compound having a VAP-1 inhibitory activity, and as a result, they have found that a compound of the present invention or a salt thereof exhibits an excellent VAP-1 inhibitory activity and is useful for preventing and/or treating VAP-1-related diseases, in particular, diabetic nephropathy or diabetic macular edema, thereby completing the present invention. The present invention further relates to a pharmaceutical composition, in particular, a pharmaceutical composition for preventing and/or treating VAP-1-related diseases, which comprises the compound of the present invention or a salt thereof, and an excipient.Type: ApplicationFiled: September 15, 2010Publication date: July 19, 2012Applicant: Astellas Pharma Inc.Inventors: Kousei Yoshihara, Daisuke Suzuki, Susumu Yamaki, Yuji Koga, Norio Seki, Jiro Fujiyasu, Masahiro Neya
-
Publication number: 20120184585Abstract: The invention relates to fatty acid niacin conjugates; compositions comprising an effective amount of a fatty acid niacin conjugate; and methods for treating or preventing an metabolic disease comprising the administration of an effective amount of a fatty acid niacin conjugate.Type: ApplicationFiled: March 22, 2012Publication date: July 19, 2012Applicant: CATABASIS PHARMACEUTICALS, INC.Inventors: Jill C. Milne, Michael R. Jirousek, Jean E. Bemis, Chi B. Vu
-
Publication number: 20120178783Abstract: This invention provides the compound having the structure wherein n is 1-10; X is C—R11 or N; wherein R11 is H, OH, SH, F, Cl, SO2R7, NO2, trifluoromethyl, methoxy, or CO—R7, wherein R7 is alkyl, alkenyl, alkynyl, C3-C8 cycloalkyl, or aryl; Z is R2 is H or NR3R4, wherein R3 and R4 are each independently H, C1-C6 alkyl, or C3-C8 cycloalkyl; R5 is OH or SH; and R6, R12, R13, and R14 are each independently H, OH, SH, F, Cl, SO2R15, NO2, trifluoromethyl, methoxy, or CO—R15, wherein R15 is alkyl, alkenyl, alkynyl, C3-C8 cycloalkyl, or aryl, or a salt of the compound, which is useful in the treatment of tumors.Type: ApplicationFiled: March 21, 2012Publication date: July 12, 2012Inventors: John S. Kovach, Francis Johnson
-
Patent number: 8211922Abstract: The present invention is directed to nicotinamide derivatives, and their use in treating lipoprotein abnormalities, alone or in combination with a statin.Type: GrantFiled: January 20, 2010Date of Patent: July 3, 2012Assignee: Cortria CorporationInventors: Robert Bender, Stefan Chlopicki, Jerzy Gebicki
-
Patent number: 8211947Abstract: The present invention relates to a pharmaceutical composition and method for treating and preventing musculoskeletal and connective tissue diseases of unknown etiology, such as different forms of arthritis and other rheumatic conditions, comprising a combination of therapeutic agents that improve the processes of blood circulation and angiogenesis in the affected tissues, as well as other supporting therapies. Among the components of herein proposed pharmaceutical composition, are: vitamin K, polyunsaturated fatty acids (blood thinner), and niacin (vasodilator and hypolipidemic agent).Type: GrantFiled: January 28, 2008Date of Patent: July 3, 2012Inventor: Guillermo Selman-Housein Sosa
-
Patent number: 8207109Abstract: A food supplement with a “slimming” effect is disclosed which strengthens the skeletal muscle, protecting the cardio-vascular apparatus of the user, and has as its characterising components propionyl L-carnitine, coenzyme Q10 nicotinamide, riboflavin and pantothenic acid.Type: GrantFiled: June 13, 2001Date of Patent: June 26, 2012Assignee: Sigma-Tau Industrie Farmaceutiche Riunite SpAInventor: Franco Gaetani
-
Publication number: 20120156146Abstract: A method of improving the appearance of facial texture may comprise the step of applying a composition comprising an effective amount of a material that regulates hyaluronic acid synthesis to an area of textured facial skin, wherein the composition is applied for a period of time sufficient for the material to improve the appearance of the facial texture. In some embodiments, the material that regulates hyaluronic acid synthesis is hexyldecanol. The method may also include the step of identifying facial texture on a facial skin surface. In particular embodiments, the facial skin texture is selected from the group consisting of macro-texture, micro-texture, and combinations thereof.Type: ApplicationFiled: November 17, 2011Publication date: June 21, 2012Inventors: Tomohiro HAKOZAKI, Leo Timothy Laughlin, II
-
Publication number: 20120157315Abstract: The present invention consists in microcapsules, uses and method of microencapsulation with improved properties regarding agglomeration, bleeding and control of the reaction. The invention is especially suitable for chemical compounds with at least one carboxamide group, preferably for microencapsulation of those compounds wherein the carbonyl group is attached to a nitrogen atom or nitrogenated heterocycle and wherein the microencapsulation reaction may be too vigorous.Type: ApplicationFiled: April 30, 2009Publication date: June 21, 2012Inventors: Victor Casana Giner, Miguel Gimeno Sierra, Barbara Gimeno Sierra
-
Patent number: 8202999Abstract: The invention relates to compounds of structural formulas (I), (VII) and (XI): or a pharmaceutically acceptable salt, solvate, clathrate, or prodrug thereof, wherein X1, X2, X3, Y, Z, L, R1, R2, R3, R18 and n are defined herein. These compounds are useful as immunosuppressive agents and for treating and preventing inflammatory conditions, allergic disorders, and immune disorders.Type: GrantFiled: January 6, 2006Date of Patent: June 19, 2012Assignee: Synta Pharmaceuticals Corp.Inventors: Lijun Sun, Shoujun Chen, Zhi-Qiang Xia, Jun Jiang, Yu Xie, Junyi Zhang
-
Publication number: 20120149716Abstract: Methods of treating, preventing, and managing tuberculosis and other related disorders are disclosed. The methods comprise the administration of a PDE4 modulator, or a pharmaceutically acceptable salt, solvate, hydrate, clathrate, stereoisomer, or prodrug thereof, optionally in combination with a second active agent and/or other conventional therapies. Pharmaceutical compositions, single unit dosage forms, and kits suitable for use in such methods are also disclosed.Type: ApplicationFiled: February 9, 2010Publication date: June 14, 2012Inventor: Jerome B. Zeldis
-
Publication number: 20120148560Abstract: A pharmaceutical composition for treating or preventing one or both of neural anoxia and reperfusion injury, which includes a pharmacological activator of the PKG pathway, and methods of treating or preventing medical conditions using a pharmacological activator of the PKG pathway.Type: ApplicationFiled: December 15, 2011Publication date: June 14, 2012Applicant: Florida Atlantic UniversityInventors: Kenneth DAWSON-SCULLY, Sara Louise Milton
-
Publication number: 20120148515Abstract: A cosmetic composition formulated for topical application to skin is provided. The composition includes a safe and effective amount of cyclohexane-1,2,3,4,5,6-hexyl; a safe and effective amount of an N-acyl amino acid compound; and a dematologically acceptable vehicle.Type: ApplicationFiled: November 17, 2011Publication date: June 14, 2012Inventors: Tomohiro HAKOZAKI, Leo Timothy Laughlin, II
-
Publication number: 20120148510Abstract: A method of improving the appearance of facial pores is provided. The method includes the step of applying a composition having an effective amount of a material that regulates IL-1 and/or hyaluronic acid synthesis to an area of facial pores, wherein the composition is applied for a period of time sufficient for the material to improve the appearance of the facial pores. In some embodiments, the material that regulates IL-1 and/or hyaluronic acid synthesis is hexyldecanol. The method may also include the step of identifying facial pores on a facial skin surface.Type: ApplicationFiled: November 17, 2011Publication date: June 14, 2012Inventors: Tomohiro HAKOZAKI, Leo Timothy Laughlin, II
-
Publication number: 20120149719Abstract: A powder-particle dosage form obtained by granulating an excipient and/or a disintegrating agent with a liquid in which a bitter taste masking base is dissolved and/or suspended, and a drug having solubility in water (20° C.) of not higher than 1 g/mL is dissolved or suspended, or a tablet obtained by compressing the powder-particle dosage form could mask bitter taste of a drug.Type: ApplicationFiled: February 23, 2012Publication date: June 14, 2012Inventors: Yoichi TANIGUCHI, Yoshitaka Tomoda, Kazuaki Yoshioka, Toshitada Toyoda, Chieko Imamoto
-
Publication number: 20120142744Abstract: The present invention relates to novel combinations of fatty acid derivatives and pyridine carboxy derivatives, including fatty acid esters with glycerol and 3-carboxy pyridine derivates such as niacinamide. Such combinations have surprisingly shown antiviral and anti-microbial activity and the use for the treatment of inflammatory conditions and infections is disclosed herein.Type: ApplicationFiled: November 23, 2011Publication date: June 7, 2012Inventor: Morten Sloth WEIDNER
-
Publication number: 20120135078Abstract: A xanthine oxidase inhibitor for use in the treatment of angina is described. The angina may be stable angina pectoris and the treatment may be to eliminate, reduce or alleviate one or more symptoms of angina pectoris (such as chest pain), or may be prophylactic. The xanthine oxidase inhibitor may be used in combination with one or more additional therapeutic agents, such as anti-anginal agents. Pharmaceutical compositions, medicaments and kits for the treatment of angina are also described.Type: ApplicationFiled: June 1, 2010Publication date: May 31, 2012Applicant: University of DindeeInventor: Allan Struthers
-
Publication number: 20120122682Abstract: The present invention relates to formulation comprising at least (i) two pesticidal compounds A and B dissolved in a lactic acid ester and wherein a) both A and B have melting points below 900C b) both A and B are selected from the following list: pyraclos-trobin, metalaxyl, mefenoxam, trifloxystrobin, imazalil, pro-chloraz and ipconazole with the proviso that A is different from B (ii) at least one pesticidal compound C present in solid particles, and having a melting point of 900C and above, and to their use as seed treatment formulation as well as their use for plant protection, including seed and crop protection.Type: ApplicationFiled: July 20, 2010Publication date: May 17, 2012Applicant: BASF SEInventors: Rafel Israels, Katharine Klamczynski, Marco Kuhns, Ulf Schlotterbeck
-
Publication number: 20120122935Abstract: The present invention relates to a method for treating or preventing necrotizing enterocolitis (NEC) in a human neonate in need thereof, comprising administering to the neonate a pharmaceutically effective amount of a composition comprising a poly(ADP-ribose) synthetase/polymerase (PARP) inhibitor. Also contemplated herein is an infant food or treatment composition comprising a PARP inhibitor in an amount that is 5 to 500 times greater than a daily recommended intake dosage for the PARP inhibitor.Type: ApplicationFiled: August 16, 2011Publication date: May 17, 2012Applicant: NATIONWIDE CHILDREN'S HOSPITAL, INC.Inventors: Peter J. Giannone, John A. Bauer
-
Publication number: 20120114628Abstract: The present invention relates to the use, especially the cosmetic and/or therapeutic use, of the protein DJ-1, of polypeptides derived from this protein or of analogues thereof, of a nucleic acid sequence coding for such a polypeptide or of a modulator of the activity, stability or expression of such a polypeptide, especially for preventing and/or treating the signs of skin dryness. The invention also relates to the use of the protein DJ-1, of polypeptides derived from this protein or of analogues thereof or of a nucleic acid sequence coding for such a polypeptide, as a marker for evaluating the state of dryness of an epithelium.Type: ApplicationFiled: November 19, 2009Publication date: May 10, 2012Applicant: L'OREALInventors: Dominique Bernard, Lucie Simonetti, Isabelle Castiel
-
Publication number: 20120115851Abstract: An objective of the present invention is to provide compounds that can effectively suppress the concentration of phosphorus in serum to effectively prevent or treat diseases induced by an increase in concentration of phosphate in serum. The compounds according to the present invention are compounds represented by formula (I) and pharmaceutically acceptable salts and solvates thereof: wherein A represents an optionally substituted five- to nine-membered unsaturated carbocyclic moiety or a five- to nine-membered unsaturated heterocyclic moiety, and represents a single bond or a double bond, R5 represents optionally substituted aryl or the like, Z represents —N?CHR6R7 or the like, R6 and R7 represent H, optionally substituted alkyl, optionally substituted aryl or the like, R101 and R102 together form ?O, and R103 and R104 represent H, or R101 and R104 together from a bond, and R102 and R103 together form a bond.Type: ApplicationFiled: January 18, 2012Publication date: May 10, 2012Applicant: KYOWA HAKKO KIRIN CO., LTD.Inventors: Nobuaki Eto, Rika Nagao, Tetsuko Kazama
-
Publication number: 20120108602Abstract: DGAT-1 inhibitor compounds of formula (1), pharmaceutically-acceptable salts and pro-drugs thereof are described, together with pharmaceutical compositions, processes for making them and their use in treating, for example, obesity wherein, for example, Ring A is optionally substituted 2,6-pyrazindiyl; X is ?0; Ring B is optionally substituted 1,4-phenylene; Y1 is a direct bond or —O—; Y2 is —(CH2)r— wherein r is 2 or 3; n is 0 or n is 1 when Y1 is a direct bond between Ring B and Ring C and when Ring B is 1,4-phenylene and Ring C is (4-6C)cycloalkane; Ring C is optionally substituted (4-6C)cycloalkane, (7-10C)bicycloalkane, (8-12C)tricycloalkane, phenylene or pryidindiyl; L is a direct bond or —O—; p is 0, 1 or 2 and when p is 1 or 2 RA1 and RA2 are each independently hydrogen or (1-4C)alkyl; Z is carboxy or a mimic or bioisostere thereof.Type: ApplicationFiled: May 5, 2011Publication date: May 3, 2012Applicant: AstraZeneca ABInventors: Udo Andreas BAUER, Jonas Gunnar BARLIND, Petra JOHANNESSON, Jan Magnus JOHANSSON, Alexander Tobias NOESKE, Annika Ulrika PETERSSON, Alan Martin BIRCH, Roger John BUTLIN, Clive GREEN, Andrew LEACH, Ragnar HOVLAND
-
Publication number: 20120108553Abstract: The present invention is directed to nicotinamide, nicotinamide derivatives and prostaglandin mimetics, alone or in combination with an NSAID, and their use in treating pain, inflammation, and/or gastrointestinal toxicty,Type: ApplicationFiled: May 3, 2011Publication date: May 3, 2012Applicant: Cortria CorporationInventor: Alexander KRANTZ
-
Publication number: 20120108580Abstract: The present invention relates to the use of specific fungicidal active substances, alone or in combination, for controlling mycoses in plants of the palm family and to a method for using said specific fungicidal active substances for controlling said mycoses in the field of plant protection and the protection of materials.Type: ApplicationFiled: April 14, 2011Publication date: May 3, 2012Applicant: BAYER CROPSCIENCE AGInventors: Dirk Ebbinghaus, Kerstin Hesse, Marie-Claire Grosjean-Cournoyer, David Chamberlin
-
Publication number: 20120108651Abstract: The present invention provides compositions and methods based on genetic polymorphisms that are associated with response to statin treatment (particularly for reducing the risk of venous thrombosis). For example, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by these nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and variant proteins, and methods of using the nucleic acid molecules and proteins as well as methods of using reagents for their detection.Type: ApplicationFiled: November 1, 2011Publication date: May 3, 2012Applicants: Leiden University Medical Center (LUMC) Acting On Behalf of Academic Hospital Leiden (AZL), CELERA CORPORATIONInventors: Lance BARE, James J. DEVLIN, Frits R. ROSENDAAL, Pieter H. REITSMA, Irene D. BEZEMER
-
Publication number: 20120100122Abstract: A pharmaceutical composition containing a mitochondrial electron transport chain enhancer (or an antioxidant) and a compound of formula (I) shown in the specification. This pharmaceutical composition can be used to treat neurodegenerative disorders.Type: ApplicationFiled: October 18, 2011Publication date: April 26, 2012Applicant: ChemiGenInventor: Yansheng Du
-
Publication number: 20120095042Abstract: Provided are compounds of formula (I) wherein m is 0, 1 or 2; RI is a mono- or bicyclic heterocyclic ring system including one, two or three heteroatoms selected from nitrogen, sulphur and oxygen; R2 is selected from hydrogen, methyl and ethyl; I) R3 is hydrogen, methyl, or ethyl; and R4 and R5 are independently selected from ethyl and isopropyl; and R3, R4 and R5 together have at least 6 carbon atoms: or II) any two or all of R3, R4 and R5 form together with the carbon atom to which they are attached 3-para-menthyl, bornyl, or adamantyl; having cooling properties, their use as cooling agent and compositions including them.Type: ApplicationFiled: May 4, 2010Publication date: April 19, 2012Inventor: Stefan Michael Furrer
-
Publication number: 20120095063Abstract: The present invention relates to compositions and methods for prophylactic and/or therapeutic treatment of conditions related to mitochondrial function. In various aspects, the present invention comprises administering one or more compounds selected from the group consisting of epicatechin, an epicatechin derivative, catechin, a catechin derivative, nicorandil, and a nicorandil derivative in an amount effective to stimulate mitochondrial function in cells. The methods and compositions described herein provide for reducing infarct size in the heart following permanent ischemia or ischemia/reperfusion (IR) event or method for delaying, attenuating or preventing adverse cardiac remodeling, and can assist in prevention of impaired mitochondria biogenesis and thus prevention of the consequences of impaired mitochondrial biogenesis in various diseases and conditions, as well as provide for the active therapy of mitochondrial depletion that may have already occurred.Type: ApplicationFiled: April 17, 2010Publication date: April 19, 2012Inventors: Francisco Villareal, Pam R. Taub, Alan S. Maisel, George F. Schreiner, Anne Murphy, Katrina Yamazaki, Guillermo Ceballos
-
Patent number: 8158146Abstract: The present invention provides a pharmaceutical composition comprising benazepril and amlodipine wherein the benazepril and the amlodipine are in physical contact with one another, and methods for making the same.Type: GrantFiled: September 28, 2005Date of Patent: April 17, 2012Assignee: Teva Pharmaceutical Industries Ltd.Inventors: Mali Kadosh, Fanny Leska
-
Patent number: 8158825Abstract: The present invention relates to a novel class of modified malonate derivatives. The modified malonate compounds can be used to treat cancer. The modified malonate compounds can also inhibit histone deacetylase and are suitable for use in selectively inducing terminal differentiation, and arresting cell growth and/or apoptosis of neoplastic cells, thereby inhibiting proliferation of such cells. Thus, the compounds of the present invention are useful in treating a patient having a tumor characterized by proliferation of neoplastic cells. The compounds of the invention may also be useful in the prevention and treatment of TRX-mediated diseases, such as autoimmune, allergic and inflammatory diseases, and in the prevention and/or treatment of diseases of the central nervous system (CNS), such as neurodegenerative diseases.Type: GrantFiled: June 21, 2006Date of Patent: April 17, 2012Assignee: Merck Sharp & Dohme Corp.Inventors: Jonathan Grimm, Paul Harrington, Richard Heidebrecht, Jr., Thomas Miller, Karin Otte, Phieng Siliphaivanh, David Sloman, Matthew Stanton, Kevin Wilson, David Witter, Solomon Kattar, Paul Tempest
-
Publication number: 20120088723Abstract: This invention provides a medicament for the treatment of cancer, which cause a reduction of cancer. This invention relates to use of a compound which has inhibitory activities against prostaglandin E2 receptor (EP4 receptor) and is represented by the following general formula (I), (II), (III), or (IV), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition comprising the compound or the salt for the manufacture of a medicament for the treatment of cancer. The invention relates to a method for treatment of cancer comprising administering the compound or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition comprising the compound or the salt to humans or animals. The compound or a pharmaceutically acceptable salt thereof, or the pharmaceutical composition may be used in combination with one or more second active agents.Type: ApplicationFiled: April 22, 2010Publication date: April 12, 2012Applicant: RAQUALIA PHARMA INC.Inventors: Yukinori Take, Shinichi Koizumi, Takako Okumura, Kazuhiko Nonomura
-
Publication number: 20120088661Abstract: The present invention relates to fungicidal mixtures comprising, as active components, 1) azolylmethyloxiranes of the general formula I wherein the variables have the meanings described in the application, 2) a fungicidal compound II, and 3) optionally a further fungicidal compound II, where the compounds II of components 2 and 3 independently of one another are selected from the group consisting of the compounds described in the application, with the proviso that components 2 and 3 are not identical, and to the use of the fungicidal mixtures for controlling phytopathogenic fungi and to the compositions comprising them.Type: ApplicationFiled: June 15, 2010Publication date: April 12, 2012Applicant: BASF SEInventors: Jochen Dietz, Egon Haden, Jens Renner, Sarah Ulmschneider, Alice Glättli, Marianna Vrettou-Schultes, Silke Stolz
-
Publication number: 20120088662Abstract: The present invention relates to fungicidal mixtures comprising, as active components, 1) azolylmethyloxiranes of the general formula I in which the variables have the meanings described in the application, and 2) a fungicidal compound II, where the compounds II of component 2 are selected from among the compounds described in the application, and to the use of the fungicidal mixtures for controlling phytopathogenic fungi and to the compositions comprising them.Type: ApplicationFiled: June 11, 2010Publication date: April 12, 2012Applicant: BASF SEInventors: Jochen Dietz, Egon Haden, Jens Renner, Sarah Ulmschneider, Alice Glättli, Marianna Vrettou-Schultes, Silke Stolz
-
Publication number: 20120090055Abstract: The present invention relates to a method of applying an aqueous, pesticide-comprising dispersion of a polyurethane which is a reaction product of at least one polyol (A) and at least one polyisocyanate (B) to plants or plant parts. The invention furthermore relates to an aqueous pesticide-comprising dispersion of a polyurethane which is a reaction product of at least one polyol (A) and at least one polyisocyanate (B). Furthermore, it relates to the use of the dispersion for controlling phytopathogenic fungi and/or undesired plant growth and/or undesired insect or mite attack and/or for regulating the growth of plants, by allowing the dispersion to act on the respective pests, their environment and/or the plants or plant parts to be protected from the respective pests, the soil and/or on undesired plants and/or the use plants and/or their environment.Type: ApplicationFiled: June 7, 2010Publication date: April 12, 2012Applicant: BASF SEInventors: Karl-Heinrich Schneider, Sven Harmsen, Michael Merk, Erich Birner, Marc Nolte, Cedric Dieleman, Alexander Kopf, Birgit Blanz, Steffen Henkes
-
Publication number: 20120088665Abstract: The present invention relates to fungicidal mixtures comprising, as active components, 1) sulfur-containing triazole compounds I as described in the application, and 2) a fungicidal compound II, where the compounds II of component 2 are selected from among the compounds described in the application, and to the use of the fungicidal mixtures for controlling phytopathogenic fungi and to compositions comprising them.Type: ApplicationFiled: June 11, 2010Publication date: April 12, 2012Applicant: BASF SEInventors: Jochen Dietz, Thomas Grote, Egon Haden, Bernd Müller, Jan Klaas Lohmann, Jens Renner, Sarah Ulmschneider, Alice Glättli, Marianna Vrettou-Schultes, Wassilios Grammenos
-
Publication number: 20120083463Abstract: The present invention relates to active compound combinations consisting, firstly, of a known halogen-substituted derivative (component A) and, secondly, of further known pesticidally active compounds (component B), which active compound combinations are suitable for controlling animal and microbial pests.Type: ApplicationFiled: July 8, 2011Publication date: April 5, 2012Applicant: Bayer CropScience AGInventors: Michael MAUE, Friedrich August MÜHLTHAU, Isabelle ADELT, Markus HEIL, Peter JESCHKE, Tobias KAPFERER, Alexander SUDAU, Heike HUNGENBERG
-
Patent number: 8143267Abstract: Disclosed is a pharmaceutical composition, comprising two analgesic compounds and/or pharmaceutically acceptable salts thereof consisting of nimesulide and/or at least one pharmaceutically acceptable salt thereof and oxycodone and/or at least one pharmaceutically acceptable salt thereof, said two analgesic compounds in an amount sufficient to provide an analgesic effect in a human patient. Also disclosed is a method of effectively treating pain in humans or other mammals, comprising orally administering to the patient an oral dosage form comprising two analgesic compounds consisting of nimesulide and/or at least one pharmaceutically acceptable salt thereof and oxycodone and/or at least one pharmaceutically acceptable salt thereof, said two analgesic compounds in an amount sufficient to provide an analgesic effect in a human patient.Type: GrantFiled: January 25, 2002Date of Patent: March 27, 2012Assignee: Purdue Pharma L.P.Inventors: Ronald M. Burch, Richard S Sackler, Paul D Goldenheim
-
Publication number: 20120070497Abstract: Disclosed are methods and compositions related to the use of boswellic acids (such as acetyl-11-keto-?-boswellic acid, 11-keto-?-boswellic acid, ?-boswellic acid, acetyl-?-boswellic acid, 9,11-dehydro-?-boswellic acid, acetyl-9,11-dehydro-?-boswellic acid, ?-boswellic acid, acetyl-?-boswellic acid, 11-dehydro-?-boswellic acid, acetyl-9,11-dehydro-?-boswellic acid, lupeolic acid, acetyl lupeolic acid, 12-ursene-2-diketone, incensole, incensole acetate, a derivative, in particular an ester thereof, a pharmaceutically acceptable salt thereof, a combination thereof, or a preparation containing one or more of these compounds) for the human medical or veterinary prophylaxis and/or treatment of: a) damage to and/or inflammation of the islets of Langerhans and/or b) damage to the B-cells of the islets of Langerhans.Type: ApplicationFiled: September 22, 2011Publication date: March 22, 2012Applicant: Fraunhofer-Gesellschaft zur Forderung der angewandten Forschung e.V.Inventor: Hermann P.T. Ammon
-
Publication number: 20120070472Abstract: Chronotherapeutic formulations of cardiovascular drugs are disclosed. The formulations comprise at least one cardiovascular drug that exhibits an in vivo elimination half-life of less than about 8 hours; wherein the formulation exhibits the following in vivo profile following administration to a subject: a) a delay in release of therapeutic levels of the at least one drug for about 2 to about 8 hours; b) a Tmax at about 8 to about 12 hours; c) a drug plasma level within 50% of the peak for greater than or equal to 12 hours; and d) a peak-to-trough ratio of drug plasma levels greater than or equal to about 4.Type: ApplicationFiled: October 11, 2011Publication date: March 22, 2012Applicant: Circ Pharma Research & Development LimitedInventors: John Devane, Jackie Butler
-
Publication number: 20120052095Abstract: Nanoemulsified topical formulation comprising curcumin, tetrahydroxycurcumin (BDMC) and curcuminoid either alone or in combinations in an amount of 0.001% to 50% together with one or more pharmaceutically, nutraceutically or dietically acceptable excipient(s) or inactive ingredients, useful for the treatment of inflammation, various skin and oral disorders, mucosal disorders and other diseases associated or related thereof.Type: ApplicationFiled: June 1, 2011Publication date: March 1, 2012Applicant: LAILA PHARMACEUTICALS PVT. LTD.Inventors: Ramchand Nanappan Chaniyilparampu, Madhavi Mungala, Anuj Kapoor, Ganga Raju Gokaraju, Rama Raju Gokaraju, Bhupathiraju Kiran, Trimurtulu Golakoti, Anitha Krishnan Nair, Malliga Raman Murali, Kavitha Parthasarathy
-
Publication number: 20120053137Abstract: This invention relates to a method of treating addiction using a composition containing quercetin. Preferably, it also contains vitamin B3, and vitamin C.Type: ApplicationFiled: August 23, 2011Publication date: March 1, 2012Applicant: Quercegen Pharmaceuticals LLCInventor: Thomas Christian Lines