The Hetero Ring Is Three-membered Patents (Class 514/475)
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Publication number: 20140155479Abstract: The present invention relates to tiglien-3-one compounds and their use in methods of treating or preventing protozoal infections, bacterial infections, parasitic infections and cell proliferative disorders. The tiglien-3-one compounds are also used in methods of controlling pests in humans, animals, plants and the environment.Type: ApplicationFiled: November 20, 2013Publication date: June 5, 2014Applicant: QBiotics LimitedInventors: Paul Warren Reddell, Victoria Anne Gordon
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Publication number: 20140155383Abstract: The present invention relates to the use of cathepsin K and/or cathepsin S inhibitors in a method for the treatment and/or prophylaxis of pulmonary hypertension and/or heart failure.Type: ApplicationFiled: May 11, 2012Publication date: June 5, 2014Applicant: BAYER INTELLECTUAL PROPERTY GMBHInventors: Stefan Golz, Martina Delbeck, Heinrich Meier, Andreas Geerts, Thomas Mondritzki, Hubert Trübel
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Patent number: 8741949Abstract: Carnitin-Palmitoyl-Transferase-1 (CPT-1) inhibitor for use in treating and/or preventing disorders caused by delipidation of neural tissue.Type: GrantFiled: June 25, 2009Date of Patent: June 3, 2014Assignee: Meta-IQ ApSInventor: Josephus Dirk Nieland
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Publication number: 20140148398Abstract: Compounds useful for the treatment of giardiasis are described.Type: ApplicationFiled: October 12, 2011Publication date: May 29, 2014Applicants: The United States of America, as represented by the Secretary, Dept. of Health and Human Service, UNIVERSITY OF MARYLAND, COLLEGE PARKInventors: Wei Zheng, Catherine Chen, Juan Jose Marugan, Noel Southall, Christopher P. Austin, Andrey Galkin, Liudmila Kulakova, Osnat Herzberg
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Patent number: 8735447Abstract: The disclosure is in part directed to crystalline forms of 6-O-(4-dimethylaminoethoxy)cinnamoyl fumagillol and variants thereof.Type: GrantFiled: November 16, 2012Date of Patent: May 27, 2014Assignee: Zafgen, Inc.Inventors: Thomas Crawford, Hayley A. Reece
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Patent number: 8735441Abstract: One aspect of the invention relates to inhibitors that preferentially inhibit immunoproteasome activity over constitutive proteasome activity. In certain embodiments, the invention relates to the treatment of immune related diseases, comprising administering a compound of the invention. In certain embodiments, the invention relates to the treatment of cancer, comprising administering a compound of the invention.Type: GrantFiled: October 5, 2012Date of Patent: May 27, 2014Assignee: Onyx Therapeutics, Inc.Inventors: Kevin D. Shenk, Francesco Parlati, Han-jie Zhou, Catherine Sylvain, Mark S. Smyth, Mark K. Bennett, Guy J. Laidig
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Patent number: 8716334Abstract: Novel substituted cyclohexylidene-ethylidene-octahydro-indene compounds and compositions comprising the same are described. The compounds exhibit profound anti-proliferative effects, in comparison to other compounds known for their anti-cancer and anti-hyperproliferative ability. Methods of use of such compounds and compositions are described for treating a variety of cancers, inflammatory and other hyperproliferative diseases and disorders.Type: GrantFiled: June 16, 2009Date of Patent: May 6, 2014Assignee: Ben Gurion University of the Negev Research and Development AuthorityInventors: Shimon Ben Shabat, Amnou Sintov
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Patent number: 8716233Abstract: The present invention is based upon the identification of regions within the NOTCH-1 receptor that, when mutated, lead to increase receptor signaling. The mutations are associated with uncontrolled cellular growth and this growth may be arrested using agents that interfere with NOTCH-1 activity, such as inhibitors of gamma-secretase. Assays for the NOTCH-1 mutations may be used diagnostically or as part of a treatment regimen for cancer patients.Type: GrantFiled: May 22, 2009Date of Patent: May 6, 2014Assignees: The Brigham and Women's Hospital, Inc., Dana-Farber Cancer Institute, Inc.Inventors: Jon C. Aster, Stephen C. Blacklow, A. Thomas Look, Adolfo A. Ferrando, Andrew P. Weng
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Publication number: 20140113000Abstract: The present invention provides methods for producing a non ?-keto peracid that has lower toxicity and lower corrosivity. The present embodiments also provide methods and compositions for reducing microbes on a surface, methods and compositions for preventing and reducing infectious vegetative bacteria on a substrate, and methods and compositions for treating a wound. In particular, compositions of the invention provide for a mixture of an ?-keto peracid and a non ?-keto peracid that works synergistically to reduce microbes on a surface, to prevent vegetative bacteria on a surface and to heal a wound in animals or humans.Type: ApplicationFiled: October 18, 2013Publication date: April 24, 2014Applicant: CHD Bioscience, Inc.Inventors: Edwin D. Neas, John D. Skinner
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Patent number: 8673881Abstract: The invention relates to novel resolvin compounds and pharmaceutical preparations thereof. The invention further relates to methods of treatment using the novel resolvin compounds of the invention.Type: GrantFiled: April 13, 2010Date of Patent: March 18, 2014Assignee: A.T. Resolve SarlInventors: Per Gjorstrup, C. Eric Schwartz
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Patent number: 8673904Abstract: Provided herein are novel epoxide inhibitors of cysteine proteases, compositions comprising the epoxide inhibitors, and packaged pharmaceuticals. Also provided are methods of inhibiting a papain-family cysteine protease and methods of treating or preventing a disease by administering a composition containing an epoxide inhibitor of the invention. The compositions may be administered in combination with another therapeutic agent.Type: GrantFiled: June 13, 2007Date of Patent: March 18, 2014Assignee: The Board of Trustees of the Leland Stanford Junior UniversityInventors: Matthew S. Bogyo, Amir M. Sadaghiani, Steven Verhelst
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Patent number: 8673971Abstract: The present invention discloses 4-nerolidylcatechol and its derivatives isolated from South American/Amazon plants (Pothomorphe species) and their potential use as therapeutical agent for treatment of malarial symptoms, including malarial patients resistant to traditional drugs. The present invention also discloses a method for producing 4-nerolidylcatechol and their derivatives.Type: GrantFiled: December 28, 2007Date of Patent: March 18, 2014Assignee: Instituto Nacional de Pesquisa de Amazonia INPAInventors: Ana Cristina Da Silva Pinto, Márcia Rúbia Silva Melo, Valter Ferreira De Andrade Neto, Francisco Célio Maia Chaves, Pedro Paulo Ribeiro Vieira, Adrian Martin Pohlit
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Publication number: 20140073691Abstract: The invention generally relates to methods of improving thyroid hormone sensitivity or treating a thyroid hormone resistance related disorder in a patient in need thereof, comprising administering a pharmaceutically effective amount of a MetAP-2 inhibitor. Such methods may include administering a MetAP-2 inhibitor at a dose that does not substantially modulate angiogenesis.Type: ApplicationFiled: November 10, 2011Publication date: March 13, 2014Applicant: Zafgen, Inc.Inventor: Thomas E. Hughes
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Publication number: 20140066408Abstract: This invention provides, but is not limited to, novel oleanolic acid derivatives having the formula: wherein the variables are defined herein. Also provided are pharmaceutical compositions, kits and articles of manufacture comprising such compounds, methods and intermediates useful for making the compounds, and methods of using the compounds and compositions.Type: ApplicationFiled: January 14, 2013Publication date: March 6, 2014Applicant: REATA PHARMACEUTICALS, INC.Inventor: REATA PHARMACEUTICALS, INC.
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Publication number: 20140057979Abstract: The present invention provides substances that can be used in a broad range of applications and effectively regulate clock gene expression. Provided is a clock gene expression regulating agent comprising, as an active ingredient, one or more selected from the group consisting of caryophyllene oxide and compounds represented by the following structural formula: wherein X is CH3, NH2 or NHCH3.Type: ApplicationFiled: October 15, 2013Publication date: February 27, 2014Applicant: Shiseido Company, Ltd.Inventors: Yoko Gozu, Shinichiro Haze
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Publication number: 20140056995Abstract: Novel Uses of small molecules, particularly, triterpenoids and ingol diterpenes isolated from Euphorbia neriifolia, are disclosed herein. The triterpenoids are useful as lead compounds for manufacturing a medicament or a pharmaceutical composition for treating cancer; whereas the ingol diterpenes are useful as lead compounds for manufacturing a medicament or a pharmaceutical composition for treating thrombocytopenia.Type: ApplicationFiled: August 27, 2012Publication date: February 27, 2014Applicant: Mackay Memorial HospitalInventors: YU-JEN CHEN, Lie-Chwn Lin, Ching-Pin Lin
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Publication number: 20140051752Abstract: The invention generally relates to methods of treating an overweight or obese subject, and treating overweight- or obesity-related conditions using non-daily administration of e.g, a MetAP-2 inhibitor.Type: ApplicationFiled: November 29, 2011Publication date: February 20, 2014Applicant: ZAFGEN, INC.Inventor: Thomas E. Hughes
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Publication number: 20140045934Abstract: The invention generally relates to methods of treating an overweight or obese subject, and treating overweight- or obesity-related conditions using non-daily administration of e.g., a MetAP-2 inhibitor.Type: ApplicationFiled: October 17, 2013Publication date: February 13, 2014Applicant: ZAFGEN, INC.Inventor: Thomas E. Hughes
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Publication number: 20140045935Abstract: The invention generally relates to methods of treating an overweight or obese subject, and treating overweight- or obesity-related conditions using non-daily administration of e.g, a MetAP-2 inhibitor.Type: ApplicationFiled: October 17, 2013Publication date: February 13, 2014Inventor: Thomas E. Hughes
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Patent number: 8642650Abstract: The invention generally relates to methods of treating an overweight or obese subject, and treating overweight- or obesity-related conditions. In certain embodiments, the invention provides a method of treating an overweight or obese subject including administering a MetAP2 inhibitor in which the amount administered does not substantially modulate angiogenesis.Type: GrantFiled: December 4, 2009Date of Patent: February 4, 2014Assignee: Zafgen, Inc.Inventors: Thomas E. Hughes, James E. Vath
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Publication number: 20140011870Abstract: The invention generally relates to methods of treating an overweight or obese subject, and treating overweight- or obesity-related conditions using effective of amounts of a MetAP-2 inhibitor.Type: ApplicationFiled: November 29, 2011Publication date: January 9, 2014Applicant: Zafgen, Inc.Inventor: Thomas E. Hughes
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Publication number: 20130345302Abstract: Compounds, pharmaceutical compositions including the compounds, and methods of preparation and use thereof are disclosed. The compounds are honokiol analogs. The compounds and compositions can be used to treat and/or prevent a wide variety of cancers, including drug resistant cancers. Representative honokiol analogs include diepoxide honokiol analogues. The compounds are believed to function, at least, by inhibiting angiogenesis and/or inducing apoptosis. Thus, the compounds are novel therapeutic agents for a variety of cancers.Type: ApplicationFiled: July 31, 2013Publication date: December 26, 2013Inventor: Jack L. Arbiser
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Publication number: 20130337024Abstract: Provided are a carotenoid-containing composition containing at least one carotenoid; at least one selected from the group consisting of ascorbic acid, derivatives thereof and salts of the acid and the derivatives; and an emulsifier, the at least one selected from the group consisting of ascorbic acid, derivatives thereof and salts of the acid and the derivatives being contained in an amount, in terms of a number of moles of ascorbic acid, in a range of from 30 times to 190 times a total number of moles of the at least one carotenoid, and the composition having a pH in the range of from 6.5 to 9.0; and a method for preparing the composition.Type: ApplicationFiled: August 20, 2013Publication date: December 19, 2013Applicant: FUJIFILM CorporationInventor: Shinichiro SERIZAWA
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Patent number: 8604078Abstract: The present invention relates to a solid fosfomycin pharmaceutical composition stable in front the coloration, suitable for diabetics and not entailing gastrointestinal problems. The pharmaceutical composition of this invention comprises fosfomycin trometamol, glycine, and optionally other excipients as sucralose, silice dioxide, polyvinylpyrrolidone and flavor; and is substantially free from sugars and sugar alcohols as sucrose, fructose, glucose, xylitol, mannitol, sorbitol or mixtures thereof.Type: GrantFiled: March 19, 2012Date of Patent: December 10, 2013Inventor: Carlos Picornell Darder
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Patent number: 8598215Abstract: Compositions and methods are disclosed which are useful of the treatment and prevention of proliferative disorders.Type: GrantFiled: July 23, 2009Date of Patent: December 3, 2013Assignee: Bristol-Myers Squibb CompanyInventor: Francis Y. F. Lee
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Patent number: 8598229Abstract: The present invention relates to tiglien-3-one compounds and their use in methods of treating or preventing protozoal infections, bacterial infections, parasitic infections and cell proliferative disorders. The tiglien-3-one compounds are also used in methods of controlling pests in humans, animals, plants and the environment.Type: GrantFiled: December 22, 2006Date of Patent: December 3, 2013Assignee: QBiotics LimitedInventors: Paul Warren Reddell, Victoria Anne Gordon
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Publication number: 20130316989Abstract: The invention relates to methods of treating inflammatory disease comprising administering a compound of formula A, a compound of any one of formulae 1-49 or I-III, a lipoxin compound, or an oxylipin compound.Type: ApplicationFiled: August 5, 2013Publication date: November 28, 2013Applicant: RESOLVYX PHARMACEUTICALS, INC.Inventor: Per Gjorstrup
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Publication number: 20130316994Abstract: The invention generally relates in part to methods of reducing hepatobiliary dysfunction and reducing risk of incident hepatobiliary dysfunction, comprising administering a MetAP2 inhibitor to patients in need thereof. The invention also relates in part to methods of effecting weight loss while reducing hepatic injury or risk thereof, comprising administering a MetAP2 inhibitor.Type: ApplicationFiled: November 29, 2011Publication date: November 28, 2013Applicant: Zafgen, Inc.Inventor: Thomas E. Hughes
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Publication number: 20130309324Abstract: The present invention provides O-nitro compounds, pharmaceutical compositions of O-nitro compounds and methods of using O-nitro compounds and/or pharmaceutical compositions thereof to treat or prevent diseases or disorders characterized by abnormal cell proliferation, such as cancer, inflammation, cardiovascular disease and autoimmune disease.Type: ApplicationFiled: July 26, 2013Publication date: November 21, 2013Applicants: RadioRx, Inc., c/o Interwest Venture Partners, Alliant Techsystems Inc.Inventors: Mark D. Bednarski, Susan Knox, Louis F. Cannizzo, Kristin F. Warner, Robert B. Wardle, Stephen P. Velarde, Shoucheng Ning
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Publication number: 20130310451Abstract: The present invention discloses novel compounds useful for the inhibition of IL-6/STAT signaling and/or PI3K/NF-?B signaling in the treatment of associated diseases or conditions, e.g. cancer. A pharmaceutical composition comprising such novel compounds, its use and a method thereof, is also disclosed.Type: ApplicationFiled: July 18, 2011Publication date: November 21, 2013Applicant: GLACTONE PHARMA DEVELOPMENT ABInventors: Ritha Gidlöf, Martin Johansson, Olov Sterner, Eduardo Muñoz
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Patent number: 8586627Abstract: Compounds, pharmaceutical compositions including the compounds, and methods of preparation and use thereof are disclosed. The compounds are honokiol analogs. The compounds and compositions can be used to treat and/or prevent a wide variety of cancers, including drug resistant cancers. Representative honokiol analogs include diepoxide honokiol analogues. The compounds are believed to function, at least, by inhibiting angiogenesis and/or inducing apoptosis. Thus, the compounds are novel therapeutic agents for a variety of cancers.Type: GrantFiled: April 29, 2008Date of Patent: November 19, 2013Inventor: Jack L. Arbiser
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Publication number: 20130289107Abstract: The present invention describes methods and compositions for improving the therapeutic efficacy of therapeutic agents previously limited by suboptimal therapeutic performance by either improving efficacy as monotherapy or reducing side effects. Such methods and compositions are particularly applicable to substituted hexitols such as dianhydrogalactitol and diacetyldianhydrogalactitol.Type: ApplicationFiled: August 17, 2011Publication date: October 31, 2013Applicant: DEL MAR PHARMACEUTICALSInventor: Dennis M. Brown
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Patent number: 8569347Abstract: Compositions and methods are disclosed which are useful of the treatment and prevention of proliferative disorders.Type: GrantFiled: May 20, 2004Date of Patent: October 29, 2013Assignee: Bristol-Myers Squibb CompanyInventor: Francis Y. F. Lee
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Publication number: 20130280286Abstract: The medicament for the prevention or the relief of poisoning by large clostridial cytotoxins (LCTs), in particular Clostridium difficile toxins A and B (TcdA and TcdB), is characterized by containing as active ingredient at least one effector, namely an inhibitor or activator of the autocatalytic protease activity of LCTs (large clostridial cytotoxins).Type: ApplicationFiled: May 30, 2012Publication date: October 24, 2013Applicant: JOHANNES GUTENBERG-UNIVERSITAET MAINZInventors: Christoph VON EICHEL-STREIBER, Jessica REINEKE, Stefan TENZER, Hansjörg SCHILD, Maja RUPNIK
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Publication number: 20130274327Abstract: The purpose is to provide a compound which can overcomes the disadvantages of conventional steroid drugs and NSAID. It is found that specific epoxy monohydroxy forms of eicosapentaenoic acid, docosahexaenoic acid and docosapentaenoic acid which are independently represented by formulae [chemical formula 1], [chemical formula 5] and the like have an inhibitory activity on neutrophils. This compound can inhibit the invasion of neutrophils into tissues and the activation of neutrophils which are observed in acute inflammations.Type: ApplicationFiled: August 4, 2011Publication date: October 17, 2013Inventors: Makoto Arita, Hiroyuki Arai, Yosuke Isobe, Tadafumi Kubota
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Publication number: 20130266578Abstract: The invention generally relates in part to methods of effecting weight loss and/or improving glucose tolerance in a patient in need thereof, comprising administering a MetAP2 inhibitor.Type: ApplicationFiled: April 7, 2011Publication date: October 10, 2013Inventors: Thomas E. Hughes, James E. Vath, Alan D. Cherrington
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Publication number: 20130261099Abstract: Fatty acid inhibitors, pharmaceutical compositions including fatty acid inhibitors, methods for using fatty acid inhibitors to treat a variety of diseases, and methods for preparing fatty acid inhibitors are provided herein.Type: ApplicationFiled: May 24, 2013Publication date: October 3, 2013Applicant: LIFE TECHNOLOGIES CORPORATIONInventor: Bruce BRANCHAUD
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Patent number: 8546382Abstract: Described herein are methods for improving engraftment of hematopoietic cells in an individual following hematopoietic progenitor cell transplantation (e.g., via bone marrow or cord blood transplantation). Methods for increasing hematopoietic progenitor cell proliferation in individuals with bone marrow aplasia are also described. The methods involve administering an agent that inhibits adipogenesis, adipocyte growth, adipocyte differentiation and/or adipocyte proliferation.Type: GrantFiled: April 15, 2010Date of Patent: October 1, 2013Assignee: Children's Medical Center CorporationInventors: Olaia Naveiras, George Daley, Pamela L. Wenzel
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Publication number: 20130237560Abstract: A method of inhibiting excitotoxicity by indirectly activating ?4?2 nicotinic acetylcholine receptors (nAChRs) which indirectly activate synaptic AMPA and NMDA receptors is disclosed. Inhibitors of ?7 nACHRs, such as macrocyclic diterpenoids, more specifically cembranoids or methyllycaconitine (MLA), indirectly activate ?4?2 nAChRs and can be used to treat neurodegenerative diseases, including, but not limited to, Alzheimer's Disease, Parkinson Disease, AIDS related dementia and the delayed effects of stroke. They can also be used to treat diseases associated with neuronal impairment, including, but not limited to glaucoma caused by optical nerve damage, delayed effects of epilepsy; and multiple sclerosis.Type: ApplicationFiled: March 15, 2013Publication date: September 12, 2013Inventors: Peter Andrew Ferchmin, Vesna Ana Eterovic De Ferchmin, Hector Manuel Maldonado
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Publication number: 20130225676Abstract: The present invention concerns an antiviral composition comprising the following components: R-(?)-2-methyl-5-(prop-1-en-2-yl)-cyclohex-2-enone (also called (?) carvone) and S-(+)-2-methyl-5-(prop-1-en-2-yl)-cyclohex-2-enone (also called (+) carvone) and (2E)-3,7-dimethylocta-2,6-dien-1-ol (also called trans-geraniol) in combination with at least one more component chosen among essential oils components for use in treatment and prevention of diseases caused by DNA enveloped viruses, DNA non-enveloped viruses, RNA enveloped viruses and RNA non-enveloped viruses.Type: ApplicationFiled: March 28, 2011Publication date: August 29, 2013Inventor: Christine Coppens
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Patent number: 8513302Abstract: The invention provides uses and methods for reducing nephropathy in persons with diabetes mellitus (particularly Type 2 diabetes), in persons with metabolic syndrome, in persons with triglyceride levels over 215 mg/dL, and in persons with a cholesterol level over 200 mg/dL, by administering an inhibitor of soluble epoxide hydrolase (“sEH”). Optionally, a cis-epoxyeicosantrienoic acid (“EET”) can be administered with the sEH inhibitor. The invention further provides for using EETs in conjunction with one or more sEH inhibitors to reduce hypertension, and for compositions of EETs coated with a material insoluble in an acid of pH 3 but soluble in a solution with a pH of 7.4 or higher.Type: GrantFiled: May 4, 2011Date of Patent: August 20, 2013Assignee: The Regents of the University of CaliforniaInventors: Bruce D. Hammock, Takaho Watanabe, Seung-Jin Ma, Susan E. Bennett, Judith S. Stern, Christophe Morisseau, In-Hae Kim
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Publication number: 20130209488Abstract: The present invention relates to methods, compositions, and diagnostic tests for treating and diagnosing cancer and other related diseases that result in dysregulation of malic enzyme 2. In particular, the methods and compositions include combination therapy, such as with a combination of two or more ME2 inhibitors or a combination of an ME2 inhibitor and an anticancer agent.Type: ApplicationFiled: August 5, 2011Publication date: August 15, 2013Applicant: BETH ISRAEL DEACONESS MEDICAL CENTER, INCInventors: Vikas P. Sukhatme, Jian-Guo Ren
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Publication number: 20130202580Abstract: The present invention relates to the use of a 2,5-dihydroxybenzene derivative represented by Formula (I) or a pharmaceutically acceptable salt, solvate, isomer, or prodrug thereof for the therapeutic and/or prophylactic treatment of, inter alia, actinic keratosis.Type: ApplicationFiled: February 14, 2013Publication date: August 8, 2013Applicant: AmDerma Pharmaceuticals, LLCInventor: AmDerma Pharmaceuticals, LLC
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Publication number: 20130197078Abstract: The disclosure is in part directed to crystalline forms of 6-O-(4-dimethylaminoethoxy)cinnamoyl fumagillol and variants thereof.Type: ApplicationFiled: November 16, 2012Publication date: August 1, 2013Inventors: Thomas Crawford, Hayley A. Reece
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Publication number: 20130189382Abstract: Use of fucoxanthin in the preparation of a product having neuroprotective effect associated with neurodegenerative disorder and improving memory is disclosed in the disclosure. A product having neuroprotective effect associated with neurodegenerative disorder is also disclosed in the disclosure. Fucoxanthin can inhibit oxidative stress of cells and has the effect of preventing or treating Alzheimer's disease and improving memory.Type: ApplicationFiled: September 30, 2010Publication date: July 25, 2013Applicant: Beijing Gingko Group Biological Technology Co., Ltd.Inventors: Yanmei Li, Liang Li
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Patent number: 8481592Abstract: The present invention relates to a pharmaceutical composition for preventing or treating hyperlipidemia, fatty liver, diabetes and obesity comprising a sesquiterpene derivative as an active ingredient. The sesquiterpene derivatives of the present invention leads to decrease in body fat weight, visceral fat weight and total cholesterol levels, triglyceride of plasma and liver tissue, blood glucose and blood insulin levels in a fast state, finally exhibiting efficacies on prevention or treatment of hyperlipidemia, fatty liver, diabetes and obesity.Type: GrantFiled: October 20, 2008Date of Patent: July 9, 2013Assignee: Kwang Dong Pharm Co., Ltd.Inventors: Tae-Sun Park, Ha-Won Kim
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Publication number: 20130172407Abstract: A pharmaceutical composition including oleoylethanolamide (OEA) is administered to inhibit tumor/cancer cell proliferation. The pharmaceutically composition may additionally include vitamin A, carotenoids, ?-3 polyunsaturated fatty acid, ?-6 polyunsaturated fatty acid and/or conjugated linolenic acid. The tumor/cancer may be colorectal cancer, lung adenocarcinoma, breast cancer, hepatoma, oral cancer and/or stomach adenocarcinoma.Type: ApplicationFiled: November 6, 2012Publication date: July 4, 2013Applicant: China Medical UniversityInventor: China Medical University
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Publication number: 20130165495Abstract: A method of inhibiting excitotoxicity by indirectly activating ?4?2 nicotinic acetylcholine receptors (nAChRs) which indirectly activate synaptic AMPA and NMDA receptors is disclosed Inhibitors of ?7 nACHRs, such as macrocyclic diterpenoids, more specifically cembranoids or methyllycaconitine (MLA), indirectly activate ?4?2 nAChRs and can be used to treat neurodegenerative diseases, including, but not limited to, Alzheimer's Disease, Parkinson Disease, AIDS related dementia and the delayed effects of stroke. They can also be used to treat diseases associated with neuronal impairment, including, but not limited to glaucoma caused by optical nerve damage, delayed effects of epilepsy; and multiple sclerosis.Type: ApplicationFiled: November 9, 2012Publication date: June 27, 2013Inventors: Peter Andrew Ferchmin, Vesna Ana Eterovic De Ferchmin, Hector Manuel Maldonado, Khalid El Sayed
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Patent number: 8470879Abstract: Fatty acid inhibitors, pharmaceutical compositions including fatty acid inhibitors, methods for using fatty acid inhibitors to treat a variety of diseases, and methods for preparing fatty acid inhibitors are provided herein.Type: GrantFiled: November 2, 2010Date of Patent: June 25, 2013Assignee: Life Technologies CorporationInventor: Bruce Branchaud
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Publication number: 20130158046Abstract: Fumagillin analog polymer conjugates, methods of making fumagillin analog polymer conjugates, compositions comprising a polymer conjugate of a fumagillin analog, and methods for treating cancer, or treating angiogenic diseases comprising administering to a subject in need thereof an effective amount of a polymer conjugate of a fumagillin analog, are described. Also described are novel fumagillin analogs, methods of making fumagillin analogs, compositions comprising at least one fumagillin analog, and methods for treating cancer, or treating angiogenic diseases comprising administering to a subject in need thereof an effective amount of a fumagillin analog.Type: ApplicationFiled: February 15, 2013Publication date: June 20, 2013Applicant: Mersana Therapeutics, IncInventors: Laura C. Akullian, Russell C. Petter, John J. Kane, Charles E. Hammond, Mao Yin, Aleksandr Yurkovetskiy, Cheri A. Stevenson