Zc(=o)oy, Wherein Z Is An Acyclic Radical Bonded To The C=o By A Carbon And Y Is An Organic Radical Bonded To The Oxygen By A Carbon Patents (Class 514/546)
Abstract: An environmentally safe insecticide and its method of use are disclosed. The inventive insecticide comprises an effective concentration of an alkyl ester of lactic acid. Ethyl lactate is a preferred alkyl ester of lactic acid. Reduction in insect infestation is achieved by applying the insecticide of the invention to an infested substrate. Typical substrates include plants, crops, trees, animals, and humans, and surfaces that come into contact with plants, crops, trees, animals, and humans.
Abstract: Peptide-based compounds including heteroatom-containing, three-membered rings efficiently and selectively inhibit specific activities of N-terminal nucleophile (Ntn) hydrolases. The activities of those Ntn having multiple activities can be differentially inhibited by the compounds described. For example, the chymotrypsin-like and PGPH activities of the 20S proteasome can be selectively inhibited with the inventive compounds. The peptide-based compounds include an electron withdrawing group adjacent to the ring functionality, and the peptide include at least three peptide units. Among other therapeutic utilities, the peptide-based compounds exhibit anti-inflammatory and inhibition of cell proliferation, involving therapeutic applications for these compounds.
Type:
Grant
Filed:
May 11, 2000
Date of Patent:
December 14, 2004
Assignee:
Yale University
Inventors:
Craig M. Crews, Mikael Elofsson, Ute Splittgerber, Ny Sin, Kyung Bo Kim
Abstract: A method for preventing an initial hepatic encephalopathic episode in persons at risk for hepatic encephalopathic episodes by administering to the person a therapeutically effective amount of at least one phenyl butyrate compounds or a salt, derivative or metabolite of phenyl butyrate in a pharmaceutically acceptable vehicle.
Type:
Application
Filed:
December 1, 2003
Publication date:
November 18, 2004
Inventors:
Marshall L. Summar, Sharron Ema Gargosky
Abstract: A compound according to formula one that is useful as a fungicide is provided. Additionally, processes to make and use same are provided.
Type:
Grant
Filed:
June 9, 2003
Date of Patent:
November 9, 2004
Assignee:
Dow AgroSciences LLC
Inventors:
Carla Jean Rasmussen Klittich, Jeannie Rachel Cetusic, Marilene Tenguan Iamauti, Irene Mae Morrison, Michael Thomas Sullenberger, William Chi-Leung Lo, Ann Marie Buysse, Brent Jeffrey Rieder, John Todd Mathieson, Monica Britt Olson, Michael John Ricks
Abstract: A method of screening pheromone compounds for mitogen-activated protein (MAP) kinase modulating activity and for employing such pheromone compounds in compositions suitable for the prevention or treatment of diseases, conditions, and symptoms thereof benefitting from modulation of MAP kinase activity.
Abstract: The present invention relates to methods for regulating the release of TGF-&bgr; from living cells in vitro or in vivo, comprising bringing the cells into contact with an effective amount of a NAALADase inhibitor. Such methods are believed to be useful for affecting neuroregeneration, cell proliferation, cell differentiation, extracellular matrix formation, myelination, inflammation, immune function, liver function, pancreatic function, angiogenesis, or wound healing; and/or for preventing or treating diabetes.
Type:
Grant
Filed:
August 1, 2002
Date of Patent:
October 19, 2004
Assignee:
Guilford Pharmaceuticals Inc.
Inventors:
Barbara S. Slusher, Xi-Chun May Lu, Krystyna Wozniak
Abstract: Provided are a mating disruption agent toward the peach twig borer and a mating disruption method comprising the use of the mating disruption agent. The attraction inhibition of this mating disruption agent, which gets rid of harmful insects without the use of insecticide, is extremely effective and flawless right up to the post harvest of fruits such as peaches. More specifically, provided is a mating disruption agent comprising 5-decenyl acetate having an E/Z ratio of 65/35 to 100/0 and 5-decen-1-ol having an E/Z ratio of 65/35 to 100/0 wherein the 5-decen-1-ol is 10% by weight or less based on total weight of the 5-decenyl acetate and 5 -decen-1-ol. Also provided is a method of peach twig borer mating disruption comprising use of the mating disruption agent.
Abstract: The present invention provides substituted 3,3-diphenyl indanone, indane and indole compounds, as well as analogues thereof, which are specific, potent and safe inhibitors of mammalian cell proliferation. The compounds can be used to inhibit mammalian cell proliferation in situ as a therapeutic approach towards the treatment or prevention of diseases characterized by abnormal cell proliferation, such as cancer.
Type:
Grant
Filed:
January 10, 2002
Date of Patent:
October 5, 2004
Assignees:
Children's Medical Center Corporation, President & Fellows of Harvard College, Nuchem Pharmaceuticals, Inc.
Inventors:
Carlo Brugnara, Jose Halperin, Rudolf Fluckiger, Emile M. Bellott, Jr., Richard John Lombardy, John J. Clifford, Ying-Duo Gao, Reem M. Haidar, Eugene W. Kelleher, Adel M. Moussa, Yesh P. Sachdeva, Minghua Sun, Heather N. Taft
Abstract: Carnitine is injected in-ovo in incubating eggs of poultry in order to improve the well-being of poultry and/or prevent or alleviate ascites. A small amount of carnitine injected in ovo shows an efficacy similar to conventional feeding techniques requiring larger amounts of carnitine.
Type:
Application
Filed:
May 17, 2004
Publication date:
September 30, 2004
Inventors:
Robert G. Teeter, Stanley L. Van Hooser, Kevin Q. Owen
Abstract: The present invention relates to the preparation and biological activity of 3-deoxy-Dmyo-inositol ether lipid analogs as inhibitors of phosphatidylinositol-3-kinase signaling and cancer cell growth. The compounds of the present invention are useful as anti-tumor 5 agents which effectively inhibit the growth of mammalian cells.
Type:
Application
Filed:
December 11, 2003
Publication date:
September 30, 2004
Inventors:
Alan P. Kozikowski, Lixin Qiao, Garth Powis
Abstract: There is disclosed a method of treating an infection in a person in need of such treatment, which comprises the administration to such person of an effective amount of at least one compound represented by formula (I)
Abstract: The invention relates to a blend, and a process for its use, which is made up of specific castor polyesters and anionic surfactants, which when used to clean the hair provide detergency and cleaning attributes, but surprisingly also provide the hair with gloss.
Type:
Grant
Filed:
January 13, 2003
Date of Patent:
September 7, 2004
Assignee:
Zenitech LLC
Inventors:
Kenneth Klein, Irwin Paleksky, Anthony J. O'Lenick, Jr.
Abstract: The present invention relates to the use of an alkanoyl L-carnitine, or a pharmaceutically acceptable salt thereof, for the preparation of a medicament for the treatment of anhedonia.
Abstract: The present invention provides pharmaceutical compositions including: a combination of a compound of the formula (I) wherein R1 is C1-C6 alkyl and R2 is independently —H or —OH, or a pharmaceutically acceptable salt thereof; and a phorbol compound. The present invention also provides for these and other compositions and their use for the treatment of established cancers or tumors.
Abstract: This invention provides O-&agr;-acyloxyalkyl ethers of the venlafaxine metabolite 4-[2-(Dimethylamino-1-(1-hydroxycyclohexyl)ethyl]phenol, represented by Formula (I): 1
Type:
Application
Filed:
October 24, 2003
Publication date:
July 29, 2004
Applicant:
Wyeth
Inventors:
John P. Yardley, Magid A. Abou-Gharbia, John W. Ullrich
Abstract: This invention relates to novel compounds of Formula (I) to (VII), and compositions thereof, useful in the treatment of disease states mediated by the chemokine, Interleukin-8 (IL-8).
Abstract: The invention relates to oil composition comprising 0.1 to 59.8% by weight of a triglyceride, 40 to 99.7% by weight of a diglyceride, 0.1 to 10% by weight of a monoglyceride and at most 5% by weight of a free fatty acid, wherein contents of &ohgr;3 type unsaturated acyl groups having at least 20 carbon atoms and monoenoic acyl groups in acyl groups constituting the diglyceride are 15 to 89.5% by weight and 10 to 84.5% by weight, respectively; and oral medicinal compositions and foods comprising such an oil composition.
The oil composition effectively develops physiological functions derived from &ohgr;3 type unsaturated fatty acids, such as inhibition of platelet aggregation, and is excellent in effect of facilitating combustion of body fat, oxidation stability, flavor and the like, and also excellent in flowability.
Abstract: A powder containing a high amount of conjugated linoleic acid or other oil is provided. The powder contains either triglycerides containing CLA, free fatty acids of CLA, or alkylesters of CLA, or another desired oil. The powder is free flowing and has good organoleptic properties. The powder may be used as a dietary supplement or combined with foodstuffs to form a food product suitable for consumption by animals or humans.
Abstract: The present invention relates to an environmentally acceptable synthesis method of polyol esters that produces no toxic by-products methods during the synthesis and the resultant esters are environmentally friendly insecticides. The present invention also provides for the use of these esters in a mixture as safe effective insecticides.
Type:
Grant
Filed:
April 24, 2002
Date of Patent:
June 29, 2004
Assignee:
Ava Chemical Ventures L.L.C.
Inventors:
William A. Farone, Tracy Palmer, Gary Joseph Puterka
Abstract: The use of one or more quaternary ammonium ester compositions to disinfect contact lenses and preserve ophthalmic lens compositions is described. Ophthalmic lens compositions containing one or more quaternary ammonium ester compositions and methods of making and using the same are also described.
Type:
Application
Filed:
April 11, 2003
Publication date:
June 17, 2004
Inventors:
Joseph C. Salamone, Richard Ozark, Zhenze Hu, Roya Nicole Borazjani
Abstract: This invention is directed to a method of using a therapeutic composition comprising a compound of an alpha-ketoalkanoic acid (pyruvate) and/or its derivatives for the treatment of cytokine-mediated inflammatory conditions. The compound is an alpha-ketoalkanoic acid, a physiologically acceptable salt of an alpha-ketoalkanoic acid, an ester of an alpha-ketoalkanoic acid, or an amide of an alpha-ketoalkanoic acid. A component for inducing and stabilizing the enol resonance form of the ester at physiological pH values is also disclosed. The cytokine-mediated inflammatory conditions are mediated by, for example, an “early” (Tumor Necrosis Factor (TNF), interleukin-1&bgr; (IL-1&bgr;)) or “late” (high mobility group B-1 (HMGB-1)) mediator of inflammation.
Type:
Application
Filed:
September 15, 2003
Publication date:
June 10, 2004
Applicants:
University of Pittsburgh of the Commonwealth System of Higher Education, North Shore-Long Island Jewish Research Institute
Inventors:
Mitchell P. Fink, Luis Ulloa, Kevin J. Tracey
Abstract: The present invention provides methods and compositions for promoting healing of damaged tissue that result in an increased level of nitric oxide in the vicinity of the damaged tissue. Also provided are methods and compositions for inhibiting unwanted wound healing by inhibiting the activity of nitric oxide in the tissue.
Type:
Grant
Filed:
February 28, 2003
Date of Patent:
June 8, 2004
Assignee:
New York Society for the Ruptured and Crippled Maintaining
the Hospital for Special Surgery
Abstract: The present invention includes compositions and methods for treatment of prostate cancer which involve the use of 12-O-tetradecanoylphorbol-13-acetate combined with a retinoid such as all-trans-retinoic acid or paclitaxol, wherein the drugs are administered together, and further wherein the combined use of these agents results in a synergistic effect on prostate tumor cell growth.
Abstract: A method and lactate compound for four unique purposes: (1) the provision of a fuel energy source to skeletal muscles, hearts and other tissues and organs of humans and other mammals during exercise and recovery; (2) cardiac energy supplementation following ischemia; (3) the maintenance of blood glucose and restoration of liver glycogen; and (4) the provision of fluid and electrolytes to humans and other mammals before, during and after exercise. The lactate compound is preferably a glycerol-lactate ester or a glycerol-acetate ester.
Abstract: A combination of volatile components which act synergistically to effectively attract yellowjackets in the Vespula species group is provided. A preferred formulation includes (E)-2-hexenal and linalool in the first component (A) and acetic acid and isobutanol in the second component (B). The two components are combined such that the vapors of the components blend to effectively attract the targeted yellowjackets. A dispenser may be utilized to release the vapors and may also be included within a trap to provide a means for monitoring or controlling the insects.
Type:
Grant
Filed:
July 31, 2002
Date of Patent:
May 25, 2004
Assignee:
The United States of America as Represented by the Secretary
of Agriculture
Abstract: Double fumarates of L-carnitine or isovaleryl L-carnitine and an amino acid having formula (I) are disclosed which are useful as active ingredients of food supplements, dietary supplements or drugs.
wherein: R is hydrogen or isovaleryl; and
[A+] is a positively charged amino acid selected from the group consisting of creatine, ornithine, lysine, arginine and histidine.
Abstract: The present invention is directed to novel acyloins, their derivatives, methods for their production and their use for the production of novel epothilones and their derivatives. In addition, the invention is directed to the building blocks for epothilone synthesis, methods for their production and the use of synthetic building blocks for the production of epothilones and their derivatives.
Type:
Application
Filed:
April 15, 2003
Publication date:
April 29, 2004
Inventors:
Ludger A. Wessjohann, Gunther Scheid, Uwe Bornscheuer, Erik Henke, Wouter Kuit, Romano Orru
Abstract: Disclosed is a method of treating acute renal failure in a subject. The method comprises the step of administering to the subject an effective amount of a composition comprising a 2-ketoalkanoic acid, a pharmaceutically acceptable salt of a 2-ketoalkanoic acid, an ester of a 2-ketoalkanoic acid, or an amide of a 2-ketoalkanoic acid. Preferably, the composition comprises an enolization agent and an alkyl aralkyl, alkoxyalkyl or carboxyalkyl ester of a 2-ketoalkanoic acid dissolved in a pharmaceutically acceptable vehicle.
Abstract: The present invention is directed to novel dipeptide thereof, represented by the general Formula I:
where R1-R3, X and Y are defined herein. The present invention also relates to the discovery that compounds having Formula I are potent inhibitors of caspases and apoptotic cell death. Therefore, the inhibitors of this invention can retard or block cell death in a variety of clinical conditions in which the loss of cells, tissues or entire organs occurs.
Type:
Grant
Filed:
November 14, 2001
Date of Patent:
April 6, 2004
Assignee:
Cytovia, Inc.
Inventors:
Sui Xiong Cai, Eckard Weber, Yan Wang, Gordon B Mills, Douglas R Green
Abstract: This invention relates to devices, kits, and methods for eliminating termite colonies. The kits, devices, and methods employ a termiticidal bait matrix containing
a) a termiticide selected such that the termiticide causes death to about 50 to about 100% of termites within about 24 to about 84 days after the termites begin to ingest the termiticide or the bait matrix comprising the termiticide,
b) a cellulose containing material, and
c) water.
The termiticidal bait matrix can be used in a bait station installed in the ground. The kits are suitable to be used by consumers in their homes.
Type:
Grant
Filed:
March 5, 2001
Date of Patent:
April 6, 2004
Assignee:
University of Florida Research Foundation, Inc.
Inventors:
Philip Frederick Brode, III, Garry Steven Garrett, Leo Timothy Laughlin, Randall Stryker Matthews, Dale Edwin Barker, Daniel James Kinne, Gary Eugene McKibben, Christopher Miles Miller, Timothy Robert Probst
Abstract: The invention relates to 7-[5-hydroxy-2-(hydroxyhydrocarbyl or heteroatom-substituted hydroxy hydrocarbyl)-3-hydroxy-cyclopentyl(enyl)] heptanoic or heptenoic acids and derivatives of said acids, wherein one or more of said hydroxy groups are replaced by an ether group. The compounds of the present invention are potent ocular hypotensives, and are particularly suitable for the management of glaucoma.
Abstract: The present invention provides compositions comprising an anti-angiogenic factor, and a polymeric carrier. Representative examples of anti-angiogenic factors include Anti-Invasive Factor, Retinoic acids and derivatives thereof, and paclitaxel. Also provided are methods for embolizing blood vessels, and eliminating biliary, urethral, esophageal, and tracheal/bronchial obstructions.
Type:
Application
Filed:
March 14, 2003
Publication date:
April 1, 2004
Applicant:
Angiotech Pharmaceuticals, Inc.
Inventors:
William L. Hunter, Lindsay S. Machan, A. Larry Arsenault
Abstract: Pesticidal compositions for the control of pests containing one or more neurally effective substances. In addition, the present invention is directed to a method for controlling pests by applying a pesticidally-effective amount of the pesticidal compositions to a locus where pest control is desired.
Abstract: The invention concerns novel derivatives of 3,3-diphenylpropylamines, methods for their preparation, pharmaceutical compositions containing the novel compounds, and the use of the compounds for preparing drugs. More particularly, the invention relates to novel prodrugs of antimuscarinic agents with superior pharmacokinetic properties compared to existing drugs such as oxybutynin and tolterodine, methods for their preparation, pharmaceutical compositions containing them, a method of using said compounds and compositions for the treatment of urinary incontinence, gastrointestinal hyperactivity (irritable bowel syndrome) and other smooth muscle contractile conditions.
Abstract: A composition is disclosed which is suitable for the prevention and treatment of kidney dysfunctions and diseases and which can therefore take the form of a food supplement or of an actual medicinal drug comprising a combination of acetyl L-carnitine and propionyl L-carnitine or their pharmacologically acceptable salts.
Abstract: The present invention provides a process for the preparation of antimicrobial compound &bgr;-keto aliphatic acid ester, a novel, aliphatic, fatty acid derivative from Bacillus sp.
Type:
Application
Filed:
July 24, 2003
Publication date:
March 18, 2004
Inventors:
Annapurna Jetty, Dattatray M. Akkewar, Kondapuram Vijaya Raghavan
Inventors:
Arne Ptoc k, Ingo Rose, Eberhard Ammermann, Reinhard Stierl, Gisela Lorenz, Siegfried Strathmann, Maria Scherer, Klaus Schelberger, Egon Haden
Abstract: A method has been discovered for attracting Colorado potato beetles to an area of object or area, which method involves treating the object or area with a Colorado potato beetle attracting composition (with or without an insecticide) containing a carrier material and a Colorado potato beetle attracting effective amount of (a) (Z)-3-hexenyl acetate, (±)-linalool, nonanal, and methyl salicylate, (b) (Z)-3-hexenyl acetate, (±)-linalool, and methyl salicylate, (c) (Z)-3-hexen-1-ol, (E)-2-hexen-1-ol, and (±)-linalool, (d) (Z)-3-hexenyl acetate and methyl salicylate, or (e) (Z)-3-hexenyl acetate and (±)-linalool.
Type:
Grant
Filed:
September 13, 2002
Date of Patent:
March 9, 2004
Assignee:
The United States of America as represented by the Secretary
of Agriculture
Abstract: The present invention provides a novel use of L-carnitine, the derivatives thereof and their pharmacologically acceptable salts in combination with antiretroviral drugs for reducing ceramide levels and enhance the activity of the aforesaid antiretroviral drugs for the therapeutic treatment of HIV-infection and AIDS.
Abstract: The present invention features compounds active at both the serotonin reuptake site and the N-methyl-D-aspartate (NMDA) receptor and the use of such compounds for treating different disorders. Compounds having activity at the serotonin reuptake site and the NMDA receptor (“multi-active compounds”) can be used to treat different types of disorders such as depression, obsessive-compulsive disorders (OCD), sleep, disorders, sexual dysfunction, and eating disorders. Preferably, the multi-active compounds are used to treat depression.
Type:
Application
Filed:
November 21, 2001
Publication date:
February 26, 2004
Applicant:
NPS Pharmaceuticals, Inc.
Inventors:
Alan L. Mueller, Scott T. Moe, Manuel F. Balandrin
Abstract: Novel insect repellents having ester bonds such that when deposited on skin, natural skin cleaning agents provide slow release of the active.
Type:
Grant
Filed:
July 10, 2002
Date of Patent:
February 24, 2004
Assignee:
Unilever Home & Personal Care USA Division of Conopco,
Inc.
Inventors:
Frank Meyer, Ferial Khorshahi-Arvanaghi, Bijan Harichian, Victor DeFlorio, Yu-Wen Feng
Abstract: The invention provides B-ring expanded estra-1,3,5(10)-triene compounds of general formula (1) which modulate the polymerization of tubulin and/or the depolymerization of microtubules. The compounds have anti-angiogenic and anti-tumor activity. The invention also provides methods of preparing the compounds, and methods of using the compounds for the treatment of cancer or other mammalian diseases characterized by undesirable angiogenesis. The compounds of the invention are also expected to have utility as research tools.
Type:
Grant
Filed:
August 16, 2002
Date of Patent:
February 24, 2004
Assignee:
The United States of America as represented by the Department
of Health and Human Services
Abstract: The present invention relates to the potentiation of glutamate receptor function using certain sulphonamide derivatives. It also relates to novel sulphonamide derivatives, to processes for their preparation and to pharmaceutical compositions containing them.
Type:
Grant
Filed:
January 23, 2001
Date of Patent:
February 17, 2004
Assignee:
Eli Lilly and Company
Inventors:
Macklin Brian Arnold, David Michael Bender, Buddy Eugene Cantrell, Winton Dennis Jones, Paul Leslie Ornstein, Richard Lee Simon, Edward C. R. Smith, Eric George Tromiczak, Hamideh Zarrinmayeh, Dennis Michael Zimmerman
Abstract: A method for treating a microbial infection or disease in a subject, said method comprising administering to said subject an effective amount of a compound according to the formula (1). Wherein; denotes a single or double bond or an epoxidised bond, and A1 to A13 are independently selected from moieties as depicted in the description. Also claimed are methods for disinfecting surfaces using the above compound, and claims to the above compound.
Type:
Application
Filed:
May 22, 2003
Publication date:
February 12, 2004
Inventors:
Rodney Warren Rickards, Chunjiu Zhao, Stephen Charles Trowell
Abstract: Electrolyte solutions are provided which are useful in electrolyte and fluid therapy, parenteral nutrition and dialysis. The Na:Cl ratio is normalized, plasma and cellular pH are normalized and cellular cofactor ratios are normalized in a manner which decreases toxicity over prior art solutions.