Patents
Patents for C07D 401 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom (107,979)
05/2008
05/07/2008CN101175722A Azetidine derivatives as ccr-3 receptor antagonists
05/07/2008CN101172973A A process for the preparation of pyridine-methylsulfinyl compounds
05/07/2008CN100386323C Synthesis of domperidone maleate
05/07/2008CN100386318C Tetrahydroquinoline derivatives and their use as FSH receptor modulators
05/07/2008CN100386314C Pharmaceutical compositions containing azetidine derivatives novel azetidine derivatives and preparation thereof
05/06/2008US7368573 Triamide-substituted heterobicyclic compounds
05/06/2008US7368572 Anticancer agents
05/06/2008US7368566 Process and intermediates for preparing benzazepines
05/06/2008US7368477 Benzofuranyl alkanamine derivatives and uses thereof
05/06/2008US7368467 Calcium channel modulators 2-(alkyl or (hetero)arylalkylthio)-imidazoles and S-oxides thereof; angina, hypertension, congestive heart failure, myocardial ischemia, arrhythmia, diabetes, urinary incontinence, stroke, pain, brain injury, or neuronal disorders
05/06/2008US7368465 Metalloproteinase inhibitors
05/06/2008US7368463 Substituted 4-amino-1-benzylpiperidine compounds
05/06/2008US7368461 Compounds and method for the treatment of overactive bladder
05/06/2008US7368453 Quinazolinone compounds with reduced bioaccumulation
05/06/2008US7368451 N-(3,5-diamino-6-chloropyrazine-2-carbonyl)-N'-(4-{4-[3-(1H-tetrazol-5-yl)propoxy]phenyl}butyl)guanidine hydrochloride; hydrates mucosal surfaces; are absorbed less rapidly, thus have a prolonged pharmacodynamic half-life; skin and respiratory disorders, vision deffects
05/06/2008US7368450 Sodium channel blockers
05/06/2008US7368447 N-(3,5-diamino-6-chloropyrazine-2-carbonyl)-N'-(4-{4-[3-(1H-tetrazol-5-yl)propoxy]phenyl}butyl)guanidine hydrochloride; hydrates mucosal surfaces; are absorbed less rapidly, thus have a prolonged pharmacodynamic half-life; skin and respiratory disorders, vision deffects
05/06/2008US7368445 Fused pyrazole derivatives as TGF-β signal transduction inhibitors for the treatment of fibrosis and neoplasms
05/06/2008US7368444 4-Hydroxy-1-toluenesulfonyl-2,3,4,5-tetrahydro-1H-1-benzazepine, for example; useful as the preventive and/or treatment medicine against diseases caused by stress
05/06/2008CA2430601C Piperazine derivatives
05/06/2008CA2390649C 5-aryl-1h-1,2,4-triazole compounds as inhibitors of cyclooxygenase-2 and pharmaceutical compositions containing them
05/06/2008CA2294352C Polymorphs of 8-chloro-6,11-dihydro-11-(4-piperidylidene)-5h-benzo[5,6] cyclohepta[1,2-b]pyridine
05/02/2008WO2008051873A2 Phenylurea compounds as soluble epoxide hydrolase inhibitors
05/02/2008WO2008051597A1 Process for the preparation of imatinib
05/02/2008WO2008051532A1 2-[1-phenyl-5-hydroxy or methoxy-4alpha-methyl-hexahydroclopenta[f]indazol-5-yl]ethyl phenyl derivatives as glucocorticoid receptor ligands
05/02/2008WO2008051047A1 Aminopyrazole derivatives, process for the preparation thereof, and composition for preventing or treating ischemic diseases containing the same
05/02/2008WO2008050732A1 Iminopyridine derivative and use thereof
05/02/2008WO2008050162A1 Process for the preparation of desloratadine adduct formed with carbon dioxide
05/02/2008WO2008050117A1 Benzoyl amino heterocyclyl compounds as glucokinase (glk) activators
05/02/2008WO2008049994A1 New fluorene derivatives, compositions containing the same and use thereof as inhibitors of the protein chaperone hsp 90
05/02/2008WO2008049950A1 Novel polynitrogenated systems as anti-hiv agents
05/02/2008WO2008049919A2 Rho kinase inhibitors
05/02/2008WO2008049875A1 Novel substituted piperidyl-propane-thiols
05/02/2008WO2008049874A1 Piperidyl-propane-thiol ccr3 modulators
05/02/2008WO2008049806A1 Piperidine or piperazine substituted tetrahydro-naphthalene-1-carboxylic acid mtp inhibiting compounds
05/02/2008WO2008049585A1 Pyridazine derivatives
05/02/2008WO2008049538A1 Substituted dihydropyrazolones and use thereof as hif-prolyl-4 -hydroxylase inhibitors
05/02/2008WO2008019971A3 Arylpiperazine derivatives and uses thereof
05/02/2008WO2008011611A3 Compounds and compositions as itpkb inhibitors
05/02/2008WO2008002676A3 Biaryl compositions and methods for modulating a kinase cascade
05/02/2008WO2007150010A3 Cyclopropyl amine derivatives as histamin h3 receptor modulators
05/02/2008WO2007146341A3 Amorphous and crystalline forms of pantoprazole magnesium salt
05/02/2008CA2667551A1 Novel polynitrogenated systems as anti-hiv agents
05/02/2008CA2667548A1 Substituted piperidyl-propane-thiols
05/02/2008CA2667547A1 Piperidyl-propane-thiol ccr3 modulators
05/02/2008CA2667435A1 Chemical compounds
05/02/2008CA2667316A1 Benzoyl amino heterocyclyl compounds as glucokinase (glk) activators
05/02/2008CA2667235A1 Pyridazine derivatives
05/02/2008CA2667007A1 2-[1-phenyl-5-hydroxy or methoxy-4alpha-methyl-hexahydrocyclopenta[f]indazol-5-yl]ethyl phenyl derivatives as glucocorticoid receptor ligands
05/02/2008CA2666482A1 Soluble epoxide hydrolase inhibitors
05/02/2008CA2664141A1 Piperidine or piperazine substituted tetrahydro-naphthalene-1-carboxylic acid mtp inhibiting compounds
05/02/2008CA2664115A1 New fluorene derivatives, compositions containing the same and use thereof as inhibitors of the protein chaperone hsp 90
05/01/2008US20080103311 Retroviral protease inhibitors
05/01/2008US20080103306 preparation of an imidazole derivative of formula I,** Image-1wherein R1, R2, R3 and R4 are described hereinabove. These compounds can be used in the treatment or prevention of mGluR5 receptor mediated disorders. and treatment of pain, psychosis and memory deficits
05/01/2008US20080103183 New imidazolone and imidazolidinone derivatives as 11b-hsd1 inhibitors
05/01/2008US20080103182 N-[1-(4-Difluoromethoxy-benzyl)-1H-indazol-3-yl]-terephthalamic acid;liver carnitine palmitoyl transferase 1 (L-CPT1) nhibitor; antidiabetic and hypotensive agent; obesity, insulin resistance, hyperglycemia; reduce liver beta -oxidation, consequently inhibit gluconeogenesis
05/01/2008US20080103177 New use of iloperidone
05/01/2008US20080103174 Ether derivatives
05/01/2008US20080103173 Compounds Having Activity At Nk3 Receptor And Uses Thereof In Medicine
05/01/2008US20080103172 as tyrosine, serine/threonine, cyclin-dependent kinases, HER protein; 5-{2-[3-[4-trifluoromethyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazol-2-yl]-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazol-4-yl]-vinyl}-pyridine-3-carbaldehyde; antiproliferative, antiinflammatory agent, neurodegenerative diseases
05/01/2008US20080103163 Nociceptine antagonists; hydrochloride salts of N-amidino-2-{[2-(4-chlorobenzoylamino)-6-methylquinazolin-4-yl]amino}cyclohexylamine, 1-[1-cyclooctylmethyl-3-hydroxymethyl-4-piperidyl]-3-ethyl-1,3-dihydro-2H-benzimidazol-2-one and N-(4-amino-2-methyl-6-quinolyl)-2-[(4-ethylphenoxy)methyl]benzamide
05/01/2008US20080103162 Antipruritics
05/01/2008US20080103161 Bicyclic heterocycles, pharmaceutical compositions containing these compounds, their use and processes for the preparation thereof
05/01/2008US20080103154 3, 4-dihydro-2(IH)-quinolinone and 2(1H)-quinolinone derivatives
05/01/2008US20080103150 and geranylgeranyltransferase inhibitor; 3-chloromethyl-4-cyanobenzyl-5 methyl triazole; antitumor agents; prevent membrane attachment of protein p21ras and block aberrant growth of ras-transformed tumors; capable to inhibit prenylation of Ras proteins, both at enzymatic and cellular level
05/01/2008US20080103148 Preventing ventilator induced pneumonia; utilizing compounds having longer half life on mucosal surfaces
05/01/2008US20080103139 3-Carbamoyl-2-Pyridone Derivative
05/01/2008US20080103136 3-[1-(2-chlorophenyl)ethoxy]-5-imidazo[1,2-a]pyridin-3-ylthiophene-2-carboxyamide; polo like kinase inhibitor; antitumor and anticarcinogenic agent; mitotic phase (M phase) of the cell cycle
05/01/2008US20080103135 Histamine H3 antagonists; do not contain imidazolyl moiety; such as 1-[4-(4-piperidin-1-ylmethyl-phenyl)-but-3-ynyl]-piperidine
05/01/2008US20080102031 4-[(4-N,N-diethylaminocarbonyl)phenyl]-spiro[2H,1-benzopyran-2,4'-piperidine; ligands of delta opioid receptor; analgesic, anxiolitic, antidepressant, analgesic; gastrointestinal disorders, neurodegenerative diseases; side effect reduction
05/01/2008US20080101989 Methods, Compositions and Kits Pertaining to Analyte Determination
05/01/2008US20080100208 Organic light-emitting compound, organic light-emitting device including the compound, and method of manufacturing the organic light-emitting device
04/2008
04/30/2008EP1916245A1 Indole derivative having pgd2 receptor antagonist activity
04/30/2008EP1916240A1 Pyridazine derivatives
04/30/2008EP1916239A1 Pyridone compound
04/30/2008EP1915365A2 Carboxamide compound and use of the same
04/30/2008EP1915364A1 Pyrazole derivatives as therapeutic agents
04/30/2008EP1915363A1 Oxopyridyl quinoline amides as nk3 receptor modulators
04/30/2008EP1915362A1 Amide alkyl pyridiyl quinolines as nk3 receptor modulators
04/30/2008EP1915361A1 Alkylpyridyl quinolines as nk3 receptor modulators
04/30/2008EP1915351A1 Quinazoline derivatives useful in cancer treatment
04/30/2008EP1915350A1 Amide derivatives
04/30/2008EP1915348A1 Azinyl-3-sulfonylindazole derivatives as 5-hydroxytryptamine-6 ligands
04/30/2008EP1915345A1 Fluoro substituted 2-oxo azepan derivatives
04/30/2008EP1716118B1 Tetrahydrobenzo[d]azepin-2- one derivatives and the use thereof for treating cardiovascular diseases
04/30/2008EP1713791B1 5-fluoro- and chloro-pyridin-2-yl-tetrazoles as ligands of the metabotropic glutamate receptor-5
04/30/2008EP1601664B1 Biaryltetrahydroisoquinoline piperidines as selective mch receptor antagonists for the treatment of obesity and related disorders
04/30/2008DE102006050516A1 New pyrazol-3-one compounds are hypoxia-inducible transcription factor-prolyl-4-hydroxylase inhibitors useful e.g. to treat and/or prophylaxis heart-circulation diseases, heart failure, anemia, chronic kidney diseases and renal failure
04/30/2008DE102006050515A1 New substituted dipyridiyl-dihydropyrazolone derivatives are hypoxia-inducible transcription factor-prolyl-4-hydroxylase inhibitors useful to treat/prevent e.g. cardiovascular diseases, heart-circulation diseases, heart failure and anemia
04/30/2008DE102006050513A1 New substituted dihydropyrazolone derivatives are hypoxia-inducible transcription factor-prolyl-4-hydroxylase inhibitors useful to treat/prevent e.g. cardiovascular diseases, heart-circulation diseases, heart failure and anemia
04/30/2008DE102006050512A1 New substituted dihydropyrazole- and dihydrotriazole derivatives are hypoxia-inducible transcription factor-prolyl-4-hydroxylase inhibitors useful to treat/prevent e.g. cardiovascular diseases, heart-circulation diseases and anemia
04/30/2008DE102006050511A1 New substituted dihydrotriazolone compounds are hypoxia-inducible transcription factor-prolyl-4-hydroxylase inhibitors useful to treat or prophylaxis e.g. heart insufficiency, anemia, chronic kidney diseases and renal failure
04/30/2008DE102006050510A1 New substituted dihydropyrazolthione compounds are hypoxia-inducible transcription factor-prolyl-4-hydroxylase inhibitors useful to treat or prevent e.g. heart insufficiency, anemia, chronic kidney diseases and renal failure
04/30/2008CN101171249A Method for producing indole derivative having piperidine ring
04/30/2008CN101171248A 3-mono- and 3,5-disubstituted piperidine derivatives as renin inhibitors
04/30/2008CN101171247A Pyrrole derivatives as DNA gyrase and topoisomerase inhibitors
04/30/2008CN101171245A Indolylamino quinazoline derivatives as antitumor agents
04/30/2008CN101171244A Indazolylamino quinazoline derivatives as antitumor agents
04/30/2008CN101171008A Proton pump inhibitors in the treatment of sleep disturbance due to silent gastro-esophageal reflux
04/30/2008CN101168541A Quinolone carboxylic acid derivatives, preparation method and medical use thereof