Patents
Patents for C07D 471 - Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups (64,559)
02/2009
02/03/2009US7485649 Inhibitors of checkpoint kinases
02/03/2009US7485648 pyridine or pyrimidine thieno(2,3-e)pyrimidine tricyclic compounds; metabotropic glutamate receptor antagonist; analgesic, anxiolytic agent: pain, migraine, urinary incontinence; neurodegenerative diseases: Alzheimer's disease
02/03/2009US7485643 Bicyclic inhibitors of MEK and methods of use thereof
02/03/2009US7485634 Methods for modulating the activity of receptors are provided. In particular compounds and compositions are provided for modulating the activity of receptors and for the treatment, prevention, or amelioration of one or more symptoms of
02/03/2009US7485630 e.g. 2-{[(3'-Amino-1'-aza-2'-oxobicyclo[6.3.0]-undecyl)-11'-carbonyl]amino}-1,5-pentanedioic acid; tripeptide Gly-Pro-Glu (GPE) mimetic; enzymatic degradation, ischemic injury, hypoxic injury, reperfusion injury, and asphyxia
02/03/2009US7485285 Delivery of antidepressants through an inhalation route
02/03/2009CA2420040C New phenylalanine derivatives
02/03/2009CA2382435C Novel herbicidally active phenyl-substituted heterocycles
02/03/2009CA2274686C Sulfonic acid or sulfonylamino n-(heteroaralkyl)-azaheterocyclylamide compounds
01/2009
01/30/2009CA2712022A1 Enantiomerically pure (-) 2-[1-(7-methyl-2-(morpholin-4-yl)-4-oxo-4h-pyrido[1,2-a]pyrimidin-9-yl)ethylamino]benzoic acid, its use in medical therapy, and a pharmaceutical composition comprising it - 026
01/29/2009WO2009014941A1 3-(4-amidopyrrol-2-ylmethlidene)-2-indolinone derivatives as multi-target protein kinase inhibitors and histone deacetylase inhibitors
01/29/2009WO2009014679A1 Dolasetron trifluoroacetate, polymorphs of dolasetron trifluoroacetate and process for preparation thereof
01/29/2009WO2009014637A2 Heterocyclic amide compounds as protein kinase inhibitors
01/29/2009WO2009014217A1 Bicyclic pyrrole derivative
01/29/2009WO2009013354A1 ARYLMETHYLENE SUBSTITUTED N-ACYL-β-AMINO ALCOHOLS
01/29/2009WO2009013299A2 Novel bradykinin b1 antagonists
01/29/2009WO2009013258A1 Use of rylene derivatives as active components in solar cells and photodetectors
01/29/2009WO2009012721A1 Process for the preparation of risperidone
01/29/2009WO2008142528A3 An improved process for preparing nevirapine
01/29/2009WO2008124849A3 Pyrrolo-pyridine kinase modulators
01/29/2009WO2007114848A3 Chemical compounds
01/29/2009US20090030206 Method for producing quaterrylene-3,4:13, 14-tetracarboxy diimides by direct synthesis
01/29/2009US20090030202 Material for organic electroluminescent element and organic electroluminescent element employing the same
01/29/2009US20090030030 Arylalkenyl and arylalkynyl substituted imidazoquinolines
01/29/2009US20090030029 Novel benzonaphthyridines
01/29/2009US20090030027 Androgen Receptor Modulator Compounds and Methods
01/29/2009US20090030020 7H-Pyrido[3,4-D]Pyrimidin-8-Ones, Their Manufacture and Use as Protein Kinase Inhibitors
01/29/2009US20090030011 1-Aminocarbonyl-, 1-aminosulfoxyl- and 1-aminosulfonyl-substituted triazolopyridines, e.g., 5-chloro-[1,2,3]triazolo[4,5-b]pyridin-1-yl)-(3,4-dihydro-1H-isoquinolin-2-yl)-methanone; these compounds lower triglyceride levels and are used to prevent and treat type II diabetes and arteriosclerosis
01/29/2009US20090030010 3-Amino-pyrazolo[3,4b]pyridines as inhibitors of protein tyrosine kinases, their production and use as pharmaceutical agents
01/29/2009US20090030002 Heterocyclic compounds and their uses
01/29/2009US20090029996 Pyridazin-3(2H)-One Derivatives And Their Use As Pde4 Inhibitors
01/29/2009US20090029988 Hydroxyalkyl Substituted Imidazoquinolines
01/29/2009US20090029987 Pharmaceutical Compositions for the Prevention and Treatment of Complex Diseases and Their Delivery by Insertable Medical Devices
01/29/2009US20090029986 such as 1-{(S)-2-[(5-Bromo-pyrimidin-2-ylamino)-methyl]-piperidin-1-yl}-1-quinolin-2-yl-methanone, used as human orexin receptor antagonist, for the treatment of obesity and insomnia
01/29/2009US20090029980 C-7 Isoxazolinyl Quinolone / Naphthyridine Derivatives Useful as Antibacterial Agents
01/29/2009US20090029939 Pre-organized tricyclic integrase inhibitor compounds
01/29/2009US20090028855 Inhibitors of akt/pkb with anti-tumor activity
01/29/2009DE4497905B4 Verfahren zur Herstellung von Phencynonat-Hydrochlorid mit α-Konfiguration Process for preparing phencynonate hydrochloride with α-configuration
01/29/2009DE102007034620A1 Neue B1-Antagonisten New B1 antagonists
01/29/2009CA2694251A1 Novel b1-antagonists
01/29/2009CA2694224A1 Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof
01/29/2009CA2693967A1 Heterocyclic amide compounds as protein kinase inhibitors
01/28/2009EP2019103A1 Novel compound having affinity for amyloid
01/28/2009EP2019094A1 Heterocyclic type cinnamide derivative
01/28/2009EP2018859A1 Arylmethylene substituted N-acyl-beta-amino alcohols
01/28/2009EP2018167A2 Compositions and methods for fgf receptor kinases inhibitors
01/28/2009EP1814880B1 Imidazo[1,2-a]pyridine compounds, compositions, uses and methods related thereto
01/28/2009EP1495024B1 Dipyridodiazepinones as reverse transcriptase inhibitors
01/28/2009EP1315701B1 Process for the racemisation of 1-benzyl-4-(4-fluorophenyl)-3-hydroxymethyl-1,2,3,6-tetrahydropyridine to be used as intermediate in the synthesis of paroxetine
01/28/2009EP0966443B1 Heteroaryl-hexanoic acid amide derivatives, their preparation and their use as selective inhibitors of mip-1-alpha binding to its ccr1 receptor
01/28/2009CN101356174A Indol-3-yl-carbonyl-spiro-piperidine derivatives
01/28/2009CN101356173A Novel pyridopyrazines and their use as modulators of kinases
01/28/2009CN101356172A 激酶抑制剂 Kinase inhibitors
01/28/2009CN101356171A N4-phenyl-quinaz0line-4-amine derivatives and related compounds as ERBBI type receptor tyrosine kinase inhibitors for the treatment of hyperproliferative diseases
01/28/2009CN101356161A Heterocyclic CETP inhibitors
01/28/2009CN101353349A Perfluoroalkyl chain substituted perylene-3,4:9,10-tetracarboxylic diimide compounds and preparation thereof
01/28/2009CN101353348A 7-[4-(aminomethyl)-4-fluoro-3-(alkoxyimine) pyrrolidine-1-yl] substituted quinoline carboxylic acid derivative and preparation thereof
01/28/2009CN101353347A Preparation of risperidone
01/28/2009CN101353344A Pyrazolyl-substituted heterocycles and their use as phytosanitary products
01/28/2009CN101353320A Matrix metalloprotease inhibitors, medicinal composition containing the same, preparation and use thereof
01/28/2009CN100455582C Hydroxyalkyl substituted pyrido-7-pyrimidin-7-ones
01/28/2009CN100455581C Imidazopyridine derivatives as melanocortin receptor agonists.
01/27/2009US7482462 Immunosuppressants for treating skin disorders, acne, alopecia, estrogen- or androgen-dependent tumors, rheumatoid arthritis, type I and II diabetes, lupus erythematosus, multiple sclerosis, ulcerative colitis, Crohn's disease, psoriasis, contact dermatitis, graft versus host disease, eczema, asthma
01/27/2009US7482456 8-(3-Biaryl)phenylquinoline phosphodiesterase-4 inhibitors
01/27/2009US7482454 Antimicrobial quinolones, their compositions, and uses
01/27/2009US7482453 dissolving clopidogrel in ethyl acetate solvent then adding sulfuric acid; good yield and purity of enantiomer
01/27/2009US7482452 intermediates for p38 MAP kinase inhibitors; industrial scale; 3-cyano-6-oxo-2-thio-1,6-dihydropyridines or pyrimidine, 2,4-diones as starting reactants and 2-cyano-N-phenylthioacetamide; cyclization; diazotization of 3-amino-7H-thieno[2,3-b]pyridin-6-ones, halide displacement
01/27/2009US7482373 useful in the treatment of central or peripheral nervous system disorders; psychological disorders; gastrointestinal disorders
01/27/2009US7482372 Antiinflammatory; cartilage protecting therapeutics; antiarthritic agent; N-{4-[(2-methyl-4-quinolinyl)methoxy]phenyl}-2,4-dioxo-1,3-diazaspiro[4.5]decane-6-carboxamide; 2-(2,5-dioxo-4-imidazolidinyl)-N-{4-[(2-methyl-4-quinolinyl)methoxy]phenyl)acetamide
01/27/2009US7482364 Histamine H3 antagonists; do not contain imidazolyl moiety; such as 1-[4-(4-piperidin-1-ylmethyl-phenyl)-but-3-ynyl]-piperidine
01/27/2009US7482360 Fused tetracyclic mGluR1 antagonists as therapeutic agents
01/27/2009US7482359 Androgen receptor modulators
01/27/2009US7482358 2-(5-cyano-3-pyridyl)-4-(4-fluorophenyl)-4-(6-fluoro-3-pyridyl)-5-methyl-2-imidazoline; obesity, bulimia; antidiabetic agents; neuropeptide Y receptor antagonists
01/27/2009US7482354 Pyrazolo-quinazoline derivatives, process for their preparation and their use as kinase inhibitors
01/27/2009US7482350 4,5-disubstituted-2-aryl pyrimidines
01/27/2009US7482345 P38 kinase inhibiting agents
01/27/2009US7482342 Indazolecarboxamide derivatives, preparation and use thereof as CDK1, CDK2 and CDK4 inhibitors
01/27/2009US7482336 Aminocyclohexanes as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes
01/27/2009CA2335115C Fused azepinone cyclin dependent kinase inhibitors
01/22/2009WO2009012283A1 Compounds and methods for kinase modulation, and indications therefor
01/22/2009WO2009011904A1 Compounds useful as faah modulators and uses thereof
01/22/2009WO2009011871A2 Thiadiazole modulators of pkb
01/22/2009WO2009010988A1 An improved, industrially viable process for the preparation of high purity paliperidone
01/22/2009WO2009010801A1 Spiro condensed barbituric acid derivatives for use as antibacterial
01/22/2009WO2009010791A2 Cyclic ethers
01/22/2009WO2009010530A1 Bicyclic heteroaryl compounds and their use as kinase inhibitors
01/22/2009WO2009010491A1 6-phenyl-1h-imidazo[4,5-c]pyridine-4-carbonitrile derivatives as cathepsin inhibitors
01/22/2009WO2009010488A1 Heterocyclic compounds useful as mk2 inhibitors
01/22/2009WO2009010129A1 Bispidon ligands and the metal complexes thereof
01/22/2009WO2008145842A3 Triazolopyridine carboxamide derivatives, preparation thereof and therapeutic use thereof
01/22/2009WO2008101935A3 New indole derivative compounds and pharmaceutical compositions containing the same
01/22/2009WO2008083367A4 Polycyclic heteroaryl substituted triazoles useful as axl inhibitors
01/22/2009WO2008055013A3 5-oxo-5,8 - dihydro - pyrido - pyrimidines as inhibitors of c-fms kinase
01/22/2009WO2007136465A3 Compositions and methods for fgf receptor kinases inhibitors
01/22/2009US20090023770 1-methoxy-2-methyl-3-[(4-nitrophenyl)sulphonyl]indolizine, used as angiogenesis inhibitors
01/22/2009US20090023769 Organic Compounds
01/22/2009US20090023767 Anticancer agents; initiasting mitosis which causes tumor cell death
01/22/2009US20090023763 Condensed Pyridine Derivatives Useful as A2B Adenosine Receptor Antagonists
01/22/2009US20090023757 Process for preparing bicyclic compounds
01/22/2009US20090023756 Substituted quinazolines as pde10 inhibitors