+

WO2007028145A3 - Agents and methods for reducing protein tyrosine phosphatase 1b activity in the central nervous system - Google Patents

Agents and methods for reducing protein tyrosine phosphatase 1b activity in the central nervous system Download PDF

Info

Publication number
WO2007028145A3
WO2007028145A3 PCT/US2006/034467 US2006034467W WO2007028145A3 WO 2007028145 A3 WO2007028145 A3 WO 2007028145A3 US 2006034467 W US2006034467 W US 2006034467W WO 2007028145 A3 WO2007028145 A3 WO 2007028145A3
Authority
WO
WIPO (PCT)
Prior art keywords
reduce
activity
nervous system
central nervous
methods
Prior art date
Application number
PCT/US2006/034467
Other languages
French (fr)
Other versions
WO2007028145A2 (en
Inventor
Louis Herlands
Original Assignee
Dara Biosciences Inc
Louis Herlands
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Dara Biosciences Inc, Louis Herlands filed Critical Dara Biosciences Inc
Publication of WO2007028145A2 publication Critical patent/WO2007028145A2/en
Publication of WO2007028145A3 publication Critical patent/WO2007028145A3/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/38Heterocyclic compounds having sulfur as a ring hetero atom
    • A61K31/381Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0043Nose
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/007Pulmonary tract; Aromatherapy
    • A61K9/0073Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy

Landscapes

  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Otolaryngology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pulmonology (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

The present invention provides pharmaceutical compositions and methods for administration to the central nervous system to reduce protein tyrosine phosphatase 1B (PTP1B) activity, reduce peripheral glucose concentrations, reduce glucose production, reduce lipid, triglyceride and/or cholesterol levels (e.g., in blood, plasma or serum), and/or food intake, and/or to treat a metabolic disorder such as diabetes mellitus (e.g., type I or type II), metabolic syndrome, hyperglycemia, insulin resistance, glucose intolerance and/or obesity, and/or to treat disorders such as leptin resistance, gonadotropin deficiency, heart failure, ischemia, atherosclerosis, coronary artery disease, hyperlipidemia, hypertriglyceridemia, hypercholesterolemia, familial lipoprotein lipase deficiency, hypertension, amenorrhea, cancer (including tumor forming cancers), neurodegenerative disease, and/or polycystic ovary syndrome. Also provided is a delivery device comprising a pharmaceutical composition of the invention.
PCT/US2006/034467 2005-09-02 2006-09-01 Agents and methods for reducing protein tyrosine phosphatase 1b activity in the central nervous system WO2007028145A2 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US71406205P 2005-09-02 2005-09-02
US60/714,062 2005-09-02
US78596506P 2006-03-24 2006-03-24
US60/785,965 2006-03-24

Publications (2)

Publication Number Publication Date
WO2007028145A2 WO2007028145A2 (en) 2007-03-08
WO2007028145A3 true WO2007028145A3 (en) 2007-10-11

Family

ID=37809651

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2006/034467 WO2007028145A2 (en) 2005-09-02 2006-09-01 Agents and methods for reducing protein tyrosine phosphatase 1b activity in the central nervous system

Country Status (1)

Country Link
WO (1) WO2007028145A2 (en)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2009001043A (en) 2006-08-08 2009-02-06 Sanofi Aventis Arylaminoaryl-alkyl-substituted imidazolidine-2,4-diones, processes for preparing them, medicaments comprising these compounds, and their use.
EP2025674A1 (en) 2007-08-15 2009-02-18 sanofi-aventis Substituted tetra hydro naphthalines, method for their manufacture and their use as drugs
US8242092B2 (en) 2008-02-05 2012-08-14 Brent Townshend Protein tyrosine phosphatase inhibitors
US8470841B2 (en) 2008-07-09 2013-06-25 Sanofi Heterocyclic compounds, processes for their preparation, medicaments comprising these compounds, and the use thereof
WO2010068601A1 (en) 2008-12-08 2010-06-17 Sanofi-Aventis A crystalline heteroaromatic fluoroglycoside hydrate, processes for making, methods of use and pharmaceutical compositions thereof
KR20120060207A (en) 2009-08-26 2012-06-11 사노피 Novel crystalline heteroaromatic fluoroglycoside hydrates, pharmaceuticals comprising these compounds and their use
US8586624B2 (en) 2009-12-16 2013-11-19 N30 Pharmaceuticals, Inc. Thiophene inhibitors of S-nitrosoglutathione reductase
WO2011107494A1 (en) 2010-03-03 2011-09-09 Sanofi Novel aromatic glycoside derivatives, medicaments containing said compounds, and the use thereof
US8933024B2 (en) 2010-06-18 2015-01-13 Sanofi Azolopyridin-3-one derivatives as inhibitors of lipases and phospholipases
US8530413B2 (en) 2010-06-21 2013-09-10 Sanofi Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments
TW201215387A (en) 2010-07-05 2012-04-16 Sanofi Aventis Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament
TW201221505A (en) 2010-07-05 2012-06-01 Sanofi Sa Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament
TW201215388A (en) 2010-07-05 2012-04-16 Sanofi Sa (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments
US8871758B2 (en) 2011-03-08 2014-10-28 Sanofi Tetrasubstituted oxathiazine derivatives, method for producing them, their use as medicine and drug containing said derivatives and the use thereof
WO2012120054A1 (en) 2011-03-08 2012-09-13 Sanofi Di- and tri-substituted oxathiazine derivates, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof
US8901114B2 (en) 2011-03-08 2014-12-02 Sanofi Oxathiazine derivatives substituted with carbocycles or heterocycles, method for producing same, drugs containing said compounds, and use thereof
EP2683704B1 (en) 2011-03-08 2014-12-17 Sanofi Branched oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof
US8710050B2 (en) 2011-03-08 2014-04-29 Sanofi Di and tri- substituted oxathiazine derivatives, method for the production, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof
WO2013037390A1 (en) 2011-09-12 2013-03-21 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
WO2013045413A1 (en) 2011-09-27 2013-04-04 Sanofi 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
US11168093B2 (en) 2018-12-21 2021-11-09 Celgene Corporation Thienopyridine inhibitors of RIPK2

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003041729A1 (en) * 2001-09-26 2003-05-22 Albert Einstein College Of Medicine Of Yeshiva University Ptp1b inhibitors and ligands
US6602867B1 (en) * 1999-01-12 2003-08-05 Abbott Laboratories Triazole compounds with dopamine-D3-receptor affinity
US20040186124A1 (en) * 2003-01-06 2004-09-23 Wynne Graham Michael (2-carboxamido)(3-amino)thiophene compounds
US20050124656A1 (en) * 2002-01-29 2005-06-09 Applied Research Systems Ars Substituted methylene amide derivatives as modulators of protein tyrosine phosphatases(ptps)

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6602867B1 (en) * 1999-01-12 2003-08-05 Abbott Laboratories Triazole compounds with dopamine-D3-receptor affinity
WO2003041729A1 (en) * 2001-09-26 2003-05-22 Albert Einstein College Of Medicine Of Yeshiva University Ptp1b inhibitors and ligands
US20050124656A1 (en) * 2002-01-29 2005-06-09 Applied Research Systems Ars Substituted methylene amide derivatives as modulators of protein tyrosine phosphatases(ptps)
US20040186124A1 (en) * 2003-01-06 2004-09-23 Wynne Graham Michael (2-carboxamido)(3-amino)thiophene compounds

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
GIROUX ET AL.: "Nassal Drug deposition, controlled particle dispersion: Applying vertical flow to optimize hasal drug deposition", DRUG DELIVERY TECHNOLOGY, vol. 5, no. 3, March 2005 (2005-03-01), pages 44 - 49 *
IVERSEN ET AL.: "Structure-based Design of a Low Molecular Weight, Nonphosphorus, Nonpeptide, and Highly Selective Inhibitor of Protein-tyrosine Phosphatase 1B", J. BIOL. CHEM., vol. 275, no. 14, April 2000 (2000-04-01), pages 10300 - 10307, XP002902040, DOI: doi:10.1074/jbc.275.14.10300 *
PETTI ET AL.: "Temporal quantitation of mutant kit tyrosine signaling attenuated by a novel thiophene kinase inhibitor OSI-930", MOL. CANCER, vol. 4, June 2005 (2005-06-01), pages 1188 - 1197 *

Also Published As

Publication number Publication date
WO2007028145A2 (en) 2007-03-08

Similar Documents

Publication Publication Date Title
WO2007028145A3 (en) Agents and methods for reducing protein tyrosine phosphatase 1b activity in the central nervous system
BR0318046A (en) Hydroxyl Compounds and Cholesterol Control Compositions and Related Jobs
Volpe et al. Cellular death, reactive oxygen species (ROS) and diabetic complications
Davidson et al. Comparative effects of lipid-lowering therapies
Kuivenhoven et al. Effectiveness of inhibition of cholesteryl ester transfer protein by JTT-705 in combination with pravastatin in type II dyslipidemia
Bustanji et al. Pancreatic lipase inhibition activity of trilactone terpenes of Ginkgo biloba
Chen et al. Erinacine S, a rare sesterterpene from the mycelia of Hericium erinaceus
WO2015200078A8 (en) Fatty acids and their use in conjugation to biomolecules
Yan et al. Effects of the long-acting human glucagon-like peptide-1 analog liraglutide on plasma omentin-1 levels in patients with type 2 diabetes mellitus
Petyaev State of the art paper improvement of hepatic bioavailability as a new step for the future of statin
WO2007002365A3 (en) Modulation of amino acid metabolism in the hypothalamus
Wu et al. In vivo pharmacodynamic and pharmacokinetic effects of metformin mediated by the gut microbiota in rats
WO2008078176A9 (en) Methods, compounds, and compositions for treating metabolic disorders and diabetes
Wu et al. Neohesperidin exerts lipid-regulating effects in vitro and in vivo via fibroblast growth factor 21 and AMP-activated protein kinase/sirtuin type 1/peroxisome proliferator-activated receptor gamma coactivator 1α signaling axis
WO2006031293A3 (en) Methods and compositions for the treatment of obesity, insulin related diseases and hypercholesterolemia
Siddiqui et al. Saroglitazar, a dual PPAR α/γ agonist, improves atherogenic dyslipidemia in patients with non-cirrhotic nonalcoholic fatty liver disease: a pooled analysis
Cheng et al. Ursolic acid alleviates lipid accumulation by activating the AMPK signaling pathway in vivo and in vitro
EP1968561B8 (en) Treatment of diabetic nephropathy
Cotugno et al. Clinical efficacy of bariatric surgery versus liraglutide in patients with type 2 diabetes and severe obesity: a 12-month retrospective evaluation
Lavasani et al. Study of the pharmacokinetic changes of Tramadol in diabetic rats
Pari et al. Antihyperlipidemic effect of coumarin in experimental type 2 diabetic rats
Sheik et al. Anti-hyperglycemic, anti-hyperlipidemic, and anti-inflammatory effect of the drug Guggulutiktaka ghrita on high-fat diet-induced obese rats
BRPI0406772A (en) Compound, processes for preparing an amino acid phenolic ether and compound, pharmaceutical composition, methods for reducing glucose, free fatty acids, cholesterol, and plasma triglyceride levels, for treating obesity, autoimmune diseases, inflammation, immune disease, and a disorder associated with insulin resistance, and intermediate
Abdel-Magid GPR40 receptor agonists for the treatment of type 2 diabetes and related diseases
Rozema et al. Characterization of glucocerebrosides and the active metabolite 4, 8-sphingadienine from Arisaema amurense and Pinellia ternata by NMR and CD spectroscopy and ESI-MS/CID-MS

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application
NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 06802934

Country of ref document: EP

Kind code of ref document: A2

点击 这是indexloc提供的php浏览器服务,不要输入任何密码和下载