Patents
Patents for C07D 487 - Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups (57,272)
02/2006
02/23/2006US20060040958 Antiproliferative agents; anticancer agents; antiinflammatroy agents; Alzheimer's disease; viricides; fungicides
02/23/2006US20060040957 Bicyclic pyrimidine matrix metalloproteinase inhibitors
02/23/2006US20060040944 5-Aza-7-deazapurine derivatives for treating Flaviviridae
02/23/2006US20060040943 3-Furanyl analogs of toxoflavine as kinase inhibitors
02/23/2006US20060040942 Antiinflammatory agents; autoimmune disease
02/23/2006US20060040941 7-Aminoimidazotriazones
02/23/2006US20060040940 Imidazopyridines pyrimidines and triazines for enhancing cognition as gaba-a-alphas 5 receoptor subtype ligands
02/23/2006US20060040936 Substituted N-arylsulfonylheterocyclic amines as gamma-secretase inhibitors
02/23/2006US20060040935 Method of treating impotence due to spinal cord injury
02/23/2006US20060040934 Use of STAT-6 inhibitors as therapeutic agents
02/23/2006US20060040930 Novel substituted [1,4] benzodioxino[2,3-e] isoindole derivatives, method for preparing and pharmaceutical compositions containing same
02/23/2006US20060040916 Carbapenem compound crystals and injection preparations
02/23/2006US20060040914 Meso-substituted porphyrins
02/23/2006US20060040913 2-Aza-21-carba-5,10,15,20-tetra(3-methoxyphenyl)prophyrin (NC-m-TMPP; for photodynamic therapy, of cancerous and other diseased tissues, Barrett's Oesophagus, ARMD, keratinosis, diabetic neuropathy, peripheral vascular disease, coronary artery disease, disorders arising from bacterial or viral infection
02/23/2006US20060040912 Compounds for pdt
02/23/2006US20060040906 Piperazine urea derivatives as melanocortin-4 receptor agonists
02/23/2006CA2577274A1 Anti-inflammatory agents
02/23/2006CA2577261A1 Aryl-substituted polycyclic amines, method for the production thereof, and use thereof as a medicament
02/23/2006CA2577255A1 Aryl-substituted polycyclic amines, method for the production thereof, and use thereof as a medicament
02/23/2006CA2577060A1 Substituted benzofused heterocycles
02/23/2006CA2576421A1 Inhibitors of hcv replication
02/23/2006CA2575979A1 Novel serotonin receptor ligands and their uses thereof
02/23/2006CA2573772A1 Heterocyclyls as selective melanin concentrating hormone receptor antagonists for the treatment of obesity and related disorders
02/23/2006CA2573688A1 (1s,5s)-3-(5,6-dichloro-3-pyridinyl)-3,6-diazabicyclo[3.2.0]heptane
02/23/2006CA2567782A1 Heterocyclic condensed compounds useful as antidiuretic agents
02/22/2006EP1627876A1 Heterocyclic condensed compounds useful as antidiuretic agents
02/22/2006EP1626975A2 PROCESS FOR SYNTHESIZING ß-LACTAMASE INHIBITOR IN INTERMEDIATES
02/22/2006EP1626973A1 (1s,5s)-3-(5,6-dichloro-3-pyridinyl)-3,6-diazabicyclo 3.2.0]heptane is an effective analgesic agent
02/22/2006EP1626972A1 PROCESS FOR SYNTHESIZING ß-LACTAMASE INHIBITOR INTERMEDIATES
02/22/2006EP1626971A1 6-cyclylmethyl- and 6-alkylmethyl-substituted pyrazolopyrimidines
02/22/2006EP1626967A1 Substituted pyrazoles
02/22/2006EP1456210B1 Pyrazolyl-substituted triazoloquinoxalines
02/22/2006EP1385839B1 3-substituted quinoline-4-carboxamide derivatives as nk-3 and nk-2 receptor antagonists
02/22/2006EP1224187B1 Certain alkylene diamine-substituted heterocycles
02/22/2006CN1738823A Porphyrin derivatives
02/22/2006CN1738822A Fungicidal triazolopyrimidines, method for the production thereof, use thereof for controlling harmful fungi, and agents containing said fungicidal triazolopyrimidines
02/22/2006CN1738821A Novel pyrazolopyrimidines as cyclin dependent kinase inhibitors
02/22/2006CN1738814A Indolyl pyrazinone derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis
02/22/2006CN1738797A Substituted aryl thioureas and related compounds; inhibitors of viral replication
02/22/2006CN1738625A Benzo (1,2,5) thiadiazole ALS CRF-antagonisten
02/22/2006CN1738615A Diaminotriazoles useful as inhibitors of protein kinases
02/21/2006US7002021 Diketopyrrolopyrrole pigments
02/21/2006US7002009 2-(1-isopropoxycarbonyloxy-2-methylpropyl)-7,8-dimethoxy-4(5H),10-dioxo-2H-1,2,3-triazolo[4,5-c][1]benzazepine; diffraction peaks at diffraction angles in a powder X-ray diffraction pattern; pure, stable crystal
02/21/2006US7001914 Compounds
02/21/2006US7001911 Fused cyclic modulators of nuclear hormone receptor function
02/21/2006US7001910 substituted pyrimidinyl-amino-ethoxy benzyl-thiazolidine-diones; hypoglycemic agents
02/21/2006US7001902 Cyclization in presence of Lawesson's reagent
02/21/2006US7001900 Central nervous system disorders
02/21/2006US7001677 Electroluminescent devices comprising diketopyrrolopyrroles
02/21/2006US7001588 Expanded porphyrin compositions for tumor inhibition
02/21/2006CA2309340C Pyrimidine derivatives for labeled binding partners
02/16/2006WO2006017822A2 Quinazoline derivatives and their use in the treatment of thrombocythemia
02/16/2006WO2006017443A2 Aryl-amino substituted pyrrolopyrimidine multi-kinase inhibiting compounds
02/16/2006WO2006017409A2 1,3-disubstituted heteroaryl nmda/nr2b antagonists
02/16/2006WO2006017054A2 Tricyclic-heteroaryl compounds useful as kinase inhibitors
02/16/2006WO2006016093A1 Immunomodulating oxopyrrazolocinnolines as cd80 inhibitors
02/16/2006WO2005121146A3 1, 2, 4-triazolo[1,5a]pyrimidines and use thereof for controlling plant-pathogenic fungi
02/16/2006WO2005118544A3 Cycloalkyl substituted pyrimidinediamine compounds and their uses
02/16/2006WO2005110414A3 Hiv integrase inhibitors
02/16/2006WO2005097799A8 Pyrazolo`4,3-d! pyrimidines
02/16/2006WO2005097107A8 Diphenyl - indol-2-on compounds and their use in the treatment of cancer
02/16/2006WO2005080352A3 Quinazoline derivatives and therapeutic use thereof
02/16/2006WO2005042475A3 Carbamoyl esters that inhibit cholinesterase and release pharmacologically active agents
02/16/2006US20060036093 Pyrimidinone compounds
02/16/2006US20060035937 (1S,5S)-3-(5,6-dichloropyridin-3-YL)-3,6-diazabicyclo[3.2.0]heptane benzenesulfonate
02/16/2006US20060035936 Pain and disorders associated with the nicotinic acetylcholine receptor
02/16/2006US20060035912 Pyrrolopyrimidine derivatives useful in cancer treatment
02/16/2006US20060035910 Substituted 8-perfluoroalkyl-6,7,8,9-tetrahydropyrimido[1,2-a] pyrimidin-4-one derivatives
02/16/2006US20060035909 2,6,9-trisubstituted 8-azapurines such as 2-(4-aminocyclohexylamino)-6-benzylamino-9-isopropyl-8-azapurine, used as cyclin-dependent kinase inhibitors, in the treatment of skin disorders, viral infections, cancer, arthritis, lupus, diabetes, multiple sclerosis, restenosis, polycystic kidney disease, gout
02/16/2006US20060035899 Use of cysteine derivatives for the preparation of a medicament intended to treat pathologies which result from the formation of the heterotrimeric G protein
02/16/2006US20060035898 morpholin-4-yl-{3-[3-(1H-pyrazol-4-yl)-1H-pyrazolo[3,4-b]pyridin-5-yl-phenyl}-methanone; FMS-like tyrosine kinase 3 (FLT3), is implicated in cancers, including leukemia, such as acute myeloid leukemia (AML), acute lymphoblastic leukemia (ALL), and myelodysplasia
02/16/2006US20060035891 (1S, 2R)-N4-(2-Aminocarbonylcyclopent-1-yl)-5-fluoro-N2-[4-(4-methylpiperazin-1-yl)-3-methylphenyl]-2,4-pyrimidinediamine, having antiproliferative activity, used to inhibit cellular proliferation and to treat proliferate diseases such as cancers
02/16/2006US20060035886 Process for preparing pyrrolotriazine aniline compounds useful as kinase inhibitors
02/16/2006US20060035885 8-Substituted-6,7,8,9-tetrahydropyrimido [1,2-a] pyrimidin-4-one derivatives
02/16/2006US20060035883 Novel serotonin receptor ligands and their uses thereof
02/16/2006US20060035876 Combination therapy of an SODm and a corticosteroid for prevention and/or treatment of inflammatory bone or joint disease
02/16/2006DE102004033405A1 New 7-phenylamino-quinolone or 1,8-naphthyridone derivatives, useful e.g. for treating type II diabetes or arteriosclerosis, are inhibitors of glycogen phosphorylase
02/16/2006CA2576949A1 Pyrazolo[1,5-a]pyrimidine derivatives
02/16/2006CA2575808A1 Aryl-amino substituted pyrrolopyrimidine multi-kinase inhibiting compounds
02/16/2006CA2575430A1 1,3-disubstituted heteroaryl nmda/nr2b antagonists
02/16/2006CA2573848A1 Constrained cyano compounds
02/15/2006EP1625847A1 Pharmaceutical composition comprising a tetrahydrotriazolo[4,3-a]pyrazine
02/15/2006EP1625131A1 Process and apparatus for preparing metal or nonmetal phthalocyanine
02/15/2006EP1625130A2 Hiv integrase inhibitors
02/15/2006EP1625129A1 Heterocyclyl-substituted dihydroquinazolines and use thereof as an antiviral agent
02/15/2006EP1625116A1 Process for the preparation of carbostyril derivatives,such as aripiprazole and its intermediates
02/15/2006EP1624935A2 Anti-adhesion composites and methods os use thereof
02/15/2006EP1624874A2 3-amino-4-phenylbutanoic acid derivatives as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes
02/15/2006EP1453835B1 Adenosine a 2a receptor antagonists
02/15/2006CN1735616A Pyrrolobenzodiazepines
02/15/2006CN1735615A Methods for the preparation of pyrrolotriazine compounds useful as kinase inhibitors
02/15/2006CN1735614A Pyrazolopyrimidines as cyclin-dependent kinase inhibitors
02/15/2006CN1733725A Process for preparing 2-iminopyrrolidine derivatives
02/15/2006CN1242511C Electrolytic solution for secondary battery and secondary battery including the same
02/15/2006CN1241925C New [3,4-a: 3.4-c] carbazole compound, its preparation method and drug composition containing them
02/15/2006CN1241924C Method for preparing enkephalinase and angiotensin-converting enzyme inhibitor intermediate and its intermediate
02/14/2006US6998487 Structure including at least three planar moieties, which are linearly configured such that one planar moiety is located between two neighboring planar moieties and shares an atom with each of the moieties
02/14/2006US6998485 3a,8a-Bis-azidomethyl-3a,4,8a,9-tetrahydro-3H,8H-bis[1,2,3]triazolo[1,5-a;1'',5''-d]pyrazine; provides low molecular weight energetic compounds with multiple energetic groups
02/14/2006US6998483 improves yields by avoiding the use of chlorosulphonic acid so no imidazotriazinonesulphonyl chlorides are formed as intermediates ; 4-ethoxy-3-(5-methyl-4-oxo-7-propyl-3,4-dihydroimidazol[5,1-fl-[1,2,4]triazin-2-yl)benzenesulphonic acid
02/14/2006US6998402 7-(1-Acetylpentyl)-5-methyl-2-(4-methylbenzyl)imidazo[5,1-f][1,2,4]triazin-4(3H)-one; learning enhancement, concentration power, learning power, memory power; enzyme inhibitors of phosphodiesterase isoenzyme