Patents
Patents for C07D 209 - Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom (45,780)
02/2003
02/27/2003WO2003016302A1 Diamine derivatives
02/27/2003WO2003016277A1 Cyclohept`b!indole derivatives as spla2 inhibitors
02/27/2003WO2003016276A2 3-substituted oxindole beta-3 agonists
02/27/2003WO2003016259A2 Compounds containing lactic acid elements, method for the production and use thereof as pharmaceutically active substances
02/27/2003WO2003016246A1 Fluorous nucleophilic substitution of alcohols and reagents for use therein
02/27/2003WO2003015917A1 Amine elimination process for making single-site catalysts
02/27/2003WO2003015769A1 Aminoalkyl-substituted aromatic bicyclic compounds, method for the production thereof and their use as medicaments
02/27/2003WO2003015517A1 Agonists and antagonists of 5h3-like receptors of invertebrate s as pesticides
02/27/2003WO2003000181A3 Dipeptidyl peptidase inhibitors for the treatment of diabetes
02/27/2003WO2002085301A3 Indole, azaindole and related heterocyclic amidopiperazine derivatives
02/27/2003WO2002051813A3 PROCESS FOR THE PREPARATION OF α-AMINOSUBSTITUTED CARBOXYLIC ACID AMIDES
02/27/2003WO2001098267A8 3-azabicyclo (3.1.0) hexane derivatives having opioid receptor affinity
02/27/2003US20030040639 Reacting polymer bound chemical intermediate compound with complex to produce complex compound; reacting with nucleophile(s); benzene derivative is decomplexed, optionally derivatised, cleaved from the support
02/27/2003US20030040538 Novel substituted tricyclic compounds
02/27/2003US20030040518 For therapy of neurodegenerative diseases and for the regeneration or prevention of degeneration of lesioned and damaged neurons degeneration of lesioned and damaged neurons
02/27/2003US20030040434 Color developers; recording images
02/27/2003CA2457727A1 Amine elimination process for making single-site catalysts
02/27/2003CA2457037A1 Aminoalkyl-substituted aromatic bicyclic compounds, method for the production thereof and their use as medicaments
02/27/2003CA2456841A1 Cyclohexyl and piperidine diamine derivatives useful as activated blood coagulation factor x inhibitors
02/27/2003CA2456290A1 Agonists and antagonists of 5h3-like receptors of invertebrate s as pesticides
02/26/2003EP1285651A1 Melanin concentrating hormone antagonists
02/26/2003EP1284966A2 Process for the synthesis of amine ethers from secondary amino oxides
02/26/2003EP1284965A1 Method for producing indols
02/26/2003EP1284964A1 Process for the preparation of indole derivatives and intermediates of the process
02/26/2003EP1284963A1 Novel calcium receptor active molecules and method for preparing same
02/26/2003EP1284947A1 Method for formulating organic compounds
02/26/2003EP1284730A1 Aralkyl ester soft drugs
02/26/2003EP1284728A1 Pharmaceuticals for treating obesity
02/26/2003EP1150976B1 3-(thio-substituted amido)-lactams useful as inhibitors of matrix metalloproteinase
02/26/2003EP1141409A4 A system and methods for nucleic acid sequencing of single molecules by polymerase synthesis
02/26/2003EP1003903B1 Process for preparing enantiomerically enriched n-derivatised lactams
02/26/2003EP0674621B1 Enantiomers of carbazole derivatives as 5-ht1-like agonists
02/26/2003CN1399635A Piperazing derivatives as 5-HT1B antagonists
02/25/2003US6525215 HIV protease inhibitors
02/25/2003US6525087 Use of known agonists of the central cannabinoid receptor CB1
02/25/2003US6525083 Antidiabetic agents, antilipemic agents, anticholesterol agents
02/25/2003US6525079 Antiparasitic compounds such as 4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)-1,2,3 -triazole
02/25/2003US6525072 Prevention and treatment of cellular disorders such as cancer
02/25/2003US6525070 Bipiperidine derivatives as modulators of CCR3 activity and as H1 antagonists
02/25/2003US6525068 Hydronaphtalene compounds, prepared by a rhodium catalyzed ring opening reaction in the presence of phosphine ligand
02/25/2003US6525036 Compounds and compositions as protease inhibitors
02/25/2003US6525020 For drug delivery
02/25/2003US6524382 Pigmented vitreous material
02/20/2003WO2003014732A1 Apparatuses and methods for creating and testing pre-formulations and systems for same
02/20/2003WO2003014255A1 Fluorescent diketopyrrolopyrrole analogues
02/20/2003WO2003014083A1 Spiro compounds
02/20/2003WO2003014082A1 Cyclopenta ` b ! indole derivatives as spla2 inhibitors
02/20/2003WO2003014081A1 Process for producing optically active azetidine-2-carboxylic acid
02/20/2003WO2003014069A1 Fluoro linkers and their use as linkers for enzyme-activated drug conjugates
02/20/2003WO2003014064A1 Naphthylurea and naphthylacetamide derivatives as vanilloid receptor 1 (vr1) antagonists
02/20/2003WO2003013512A2 Crystalline forms of fluvastatin sodium
02/20/2003WO2003013510A1 3-arylsulfonyl-7-piperazinyl- indoles, -benzofurans and -benzothiophenes with 5-ht6 receptor affinity for treating cns disorders
02/20/2003WO2003013484A2 N-monoacylated derivatives of o-phenylenediamines, their six membered heterocyclic analogues and their use as pharmaceutical agents
02/20/2003WO2002074742A3 Cdk-inhibitory indirubin derivatives having an increased solubility
02/20/2003WO2002068399B1 Aryl carbamate derivatives, preparation and use thereof
02/20/2003WO2002048097B1 Compounds, compositions and methods for treatment of parasitic infections
02/20/2003WO2002024635A3 Aminoalcohol derivatives
02/20/2003US20030036559 Thermodynamically stable modification of 1-(4-carbazolyl-oxy-3-[2- (2-methoxyphenoxy) -ethylamino] -2-propanole process for its preparation and pharmaceutical compositions containing it
02/20/2003US20030036538 Are designed to produce both Type 1 and Type 2 phototherapeutic effect at once using dual wavelength light source that will produce singlet oxygen and free radicals at the lesion of interest.
02/20/2003US20030035836 Oral controlled release pharmaceutical composition for once-a-day therapy for the treatment and prophylaxis of cardiac and circulatory diseases
02/20/2003CA2456599A1 Spiro compounds
02/20/2003CA2455754A1 Amine derivatives
02/20/2003CA2454072A1 Crystalline forms of fluvastatin sodium
02/20/2003CA2453245A1 Fluoro linkers and their use as linkers for enzyme-activated drug conjugates
02/19/2003EP1284260A1 Tyrosine phosphatase inhibitors
02/19/2003EP1283836A2 Neuroprotective and anti-proliferative compounds
02/19/2003EP1283825A1 N-substituted peptidyl nitriles as cysteine cathepsin inhibitors
02/19/2003EP1192191B1 Method for producing condensation compounds
02/19/2003EP1020179A4 Peptide derivatives or pharmaceutically acceptable salts thereof, method for producing the same, use of said derivatives and pharmaceutical composition
02/19/2003CN1398264A 吲哚-3-基衍生物 Indol-3-yl derivative
02/19/2003CN1398252A Dehydroamino acids compounds
02/19/2003CN1397550A Novel benzene amine compound, its prepn. process and medicinal compsns. contg. them
02/19/2003CN1397549A Novel derivative of 2-azadicyclo-(2,2,1) heptane, its prepn. and use
02/19/2003CN1101815C 3-aminochromanylsulfonyl (thio) ureas, processes for their prepn. their use, and pharmaceutical prepn. comprising them
02/18/2003US6521788 Process for the preparation of 1-aminomethyl-1-cyclohexaneacetic acid
02/18/2003US6521667 Calcilytic compounds
02/18/2003US6521658 Cell proliferation inhibitors
02/18/2003US6521657 Indole derivatives which are agonists of the progesterone receptor and useful for treatment of carcinoma and adenocarcinomas of uterine leiomyomata, endometriosis or polycystic ovary syndorme in a mammal
02/18/2003US6521638 2,3-dihydro-1H-isoindole derivatives useful as modulators of dopamine D3 receptors (antipsychotic agents)
02/18/2003US6521603 Fungicides for the control of take-all disease of plants
02/18/2003CA2420042A1 Carboxylic acid derivatives, processes for the preparation thereof and pharmaceutical agents comprising the same as active ingredient
02/13/2003WO2003011872A1 Platelet adp receptor inhibitors
02/13/2003WO2003011858A1 Substituted isoindoles and e use thereof
02/13/2003WO2003011834A1 Novel vinyl n-(2-benzoylphenyl)-l-tyrosine derivatives and their use as antidiabetics etc
02/13/2003WO2003011833A1 Indazole or indole derivatives, their use in human medicine and more particularly in cancerology
02/13/2003WO2003011827A1 Process for the preparation of 3-spiro'cyclohexam-1,3'-'3h!indolin-2'-one! derivatives
02/13/2003WO2003011815A1 Bicyclic heteroaromatic alanines
02/13/2003WO2003011812A1 NOVEL AMINE DERIVATIVE HAVING HUMAN β-TRYPTASE INHIBITORY ACTIVITY AND DRUGS CONTAINING THE SAME
02/13/2003WO2003011808A1 Retinoid derivatives with antiangiogenic, antitumoral and proapoptotic activities
02/13/2003WO2003011396A1 Tetrahydroindolone and purine derivatives linked to arylpiperazines
02/13/2003WO2003011290A1 Methods for inhibiting or reversing tau filament formation polymerization
02/13/2003WO2003011284A1 5-arylsulfonyl indoles having 5-ht6 receptor affinity
02/13/2003WO2002076988A3 Tert. alkylphenoxy substituted polycyclic compounds
02/13/2003WO2002059082A8 Aryl and aminoaryl substituted serotonin receptor agonist and antagonist ligands
02/13/2003WO2002055492A3 An improved process for preparing pure ondansetron hydrochloride dihydrate
02/13/2003WO2002033110A3 PRODUCTION OF α-HYDROXY-CARBOXYLIC ACIDS USING A COUPLED ENZYME SYSTEM
02/13/2003US20030032666 Crystalline forms
02/13/2003US20030032644 Substituted polycyclic aryl and heteroaryl tertiary-heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity
02/13/2003US20030032626 Substituted naphthyl indole derivatives as inhibitors of plasminogen activator inhibitor type-1 (PAI-1)
02/13/2003US20030032581 Pharmaceuticals for treating obesity