Patents
Patents for C07D 233 - Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings (34,408)
10/2007
10/16/2007CA2209229C Novel sulfamate compound containing n-substituted carbamoyl group and method for preparing the same
10/11/2007WO2007115269A2 Orally bioavailable caffeic acid related anticancer drugs
10/11/2007WO2007114338A1 Acid secretion inhibitor
10/11/2007WO2007113634A1 Novel dipeptidyl peptidase iv inhibitors and processes for their preparation and pharmaceutical compositions containing them
10/11/2007WO2007113235A1 Process for preparing 6,7-dihydro-5h-imidazo[1,5-a]pyridin-8-one
10/11/2007US20070238754 1-Cyclohexylmethyl-5-(2,5-dimethoxy-phenyl)-2-methyl-1H-pyrrole-3-carboxylic acid cyclohexylamide and 2-(5-Chloro-2-methoxy-phenyl)-1-(2-cyclohexyl-ethyl)-5-methyl-1H-imidazole-4-carboxylic acid cyclohexylamide; treating obesity, eating disorders; antidiabetic agents; antiinflammatory agents; drug abuse
10/11/2007US20070238740 Nitrosated And Nitrosylated Cardiovascular Compounds, Compositions And Methods Of Use
10/11/2007CA2682846A1 Novel dipeptidyl peptidase iv inhibitors and processes for their preparation and pharmaceutical compositions containing them
10/11/2007CA2648003A1 Orally bioavailable caffeic acid related anticancer drugs
10/11/2007CA2647862A1 Acid secretion inhibitor
10/11/2007CA2647616A1 Process for preparing 6,7-dihydro-5h-imidazo[1,5-a]pyridin-8-one
10/10/2007EP1841750A1 Heterocyclic modulators of the glucocorticoid receptor, ap-1, and/or nf-kb activity and use thereof
10/10/2007EP1841504A2 Substituted biaryl compounds as factor xia inhibitors
10/10/2007EP1399163B1 Compounds, methods and compositions useful for the treatment of bovine viral diarrhea virus (bvdv) infection and hepatitis c virus (hcv) infection
10/10/2007EP1232150B1 Urea derivatives as anti-inflammatory agents
10/10/2007EP1142879B1 Imidazole compounds and medicinal use thereof
10/10/2007CN101052638A 4-(condensed cyclicmethyl)-imidazole-2-thiones acting as alpha2 adrenergic agonists
10/10/2007CN100341858C Process for synthesis of sodium glycididazole
10/09/2007US7279582 For example (2S, 3S, 5S)-2-(2,6-dimethylphenoxyacetyl)amino-3-hydroxy-5-(2S-(1-tetrahydro-pyrimid-2-onyl)-3-methyl butanoyl)amino-1,6-diphenylhexane; HIV therapy
10/09/2007US7279578 Use as orexin receptor antagonists, depression; anxiety; addictions; obsessive compulsive disorder; affective neurosis; depressive neurosis; anxiety neurosis; dysthymic disorder; behaviour disorder; mood disorder; sexual dysfunction; psychosexual dysfunction; schizophrenia; manic depression; delerium
10/09/2007US7279498 Substituted aryl amides as IP antagonists
10/09/2007US7279497 Benzopyran derivatives substituted with secondary amines including imidazole, their preparation and pharmaceutical compositions containing them
10/09/2007US7279478 Cathepsin cysteine protease inhibitors
10/09/2007US7279477 Cardiovascular disease, diabetes, acidosis, cancer, obesity; such as 1-butyl-3,3-dimethyl-1-(4-(2,2,2-trifluoro-1-hydroxy-1-trifluoromethyl -ethyl)-phenyl)-thiourea
10/09/2007US7279470 Compounds and uses thereof for decreasing activity of hormone-sensitive lipase
10/09/2007US7279444 for controlling undesirable plants
10/09/2007US7279324 Nucleic acid encoding G-protein coupled receptor with modified DRY motif
10/09/2007CA1341557C Novel triazole and imidazole compounds
10/04/2007WO2007111263A1 Nitrogen-containing heterocyclic derivative and organic electroluminescent device using same
10/04/2007WO2007110363A1 Novel guanidine derivatives and their medical use
10/04/2007WO2007110337A1 Pyridine and pyrimidine derivatives as mglur2 antagonists
10/04/2007WO2007085556A3 Use of 4-imidazole derivatives for cns disorders
10/04/2007US20070232664 Iron binding agents
10/04/2007US20070232590 3-Cylcoalkylbenzazepines as Histamine H3 Antagonists
10/04/2007US20070231647 Proton Conductor and Fuel Cell Using the Same
10/04/2007CA2646732A1 Pyridine and pyrimidine derivatives as mglur2 antagonists
10/04/2007CA2644369A1 Amide derivatives and their application for the treatment of g protein related diseases
10/03/2007EP1838800A1 Compositions, redox couples and uses thereof
10/03/2007EP1838679A1 Imidazole derivatives as enzyme reverse transcriptase modulators
10/03/2007EP1838304A2 Heterocyclic aspartyl protease inhibitors
10/03/2007EP1663232B1 1-(2-amino-benzoyl)-piperazine derivatives as glycine uptake inhibitors for the treatment of psychoses
10/03/2007EP1587813B1 Phosphonium and imidazolium salts and methods of their preparation
10/03/2007CN101048381A Novel imidazolidine derivative and use thereof
10/03/2007CN101048375A Amino, amino acid or peptide conjugates of retinoic acid
10/03/2007CN101048340A 分离气体的方法 Method of separating gases
10/03/2007CN101048139A Compositions for controlled delivery of pharmaceutically active compounds
10/03/2007CN100340556C Novel aryllimidazole derivatives, preparation and therapeutic used thereof
10/03/2007CN100340550C Method for preparing prochloraz
10/02/2007US7276522 dextrorotatory and levo-rotatory enantiomers; specific to alpha2B adrenergic receptors
09/2007
09/30/2007CA2541444A1 Process for preparing n,n'-carbonyldiazoles
09/27/2007WO2007109175A1 N-hydroxylsulfonamide derivatives as new physiologically useful nitroxyl donors
09/27/2007WO2007107356A1 Method for preparing doped organic semiconductor materials and formulation utilized therein
09/27/2007WO2007107311A2 Organic sulphinic acid derivatives
09/27/2007US20070225497 Chiral Tertiary Aminoalkylnaphthols
09/27/2007US20070225347 Imidazole Derivatives
09/27/2007US20070224263 Aminoalkylphosphonates and related compounds as Edg receptor agonists
09/27/2007DE102006013260A1 Organische Sulfinsäurederivate Organic sulfinic acid derivatives
09/26/2007EP1837926A1 Heterocyclic radicals or diradicals and their dimers, oligomers, polymers, di-spiro and polycyclic derivatives as well as their use in organic semiconductor materials and electronic devices.
09/26/2007EP1837330A1 Benzamide inhibitors of the P2X7 receptor
09/26/2007EP1837329A1 Novel heteroaryl derivative
09/26/2007EP1302461B1 Tnf-alpha production inhibitors
09/26/2007CN101044120A Unsubstituted and substituted 4-benzyl-1,3-dihydro-imidazole-2-thiones acting as specific or selective alpha2 adrenergic agonists and methods for using the same
09/26/2007CN101041673A Triimine radical metaphosphate acid ion containing liquid and synthesizing method
09/26/2007CN101041669A Non nucleoside reverse transcriptase inhibitors
09/26/2007CN101041638A Chirality amine containing imidazole sulfur ether structure and preparation method and usage thereof
09/26/2007CN101041637A Chirality amine protonic acid salt containing imidazole sulfur ether structure and preparation method and usage thereof
09/26/2007CN101041636A Method for synthesizing heterocyclic ketenes amine condensation derivatives
09/26/2007CN101041635A Method for synthesizing ketenes amine condensation derivatives
09/26/2007CN100339710C Mass spectrometer for biological samples
09/26/2007CN100339369C Type-Y second order non-linear optical chromophore containing imidazolyl heterocycle and its synthesis process
09/26/2007CN100339368C Process for preparing substituted imidazole derivates and intermediates used in the process
09/26/2007CN100339079C Substituted imidazolidines, process for their preparation, and their use as a medicament or diagnostic, and medicament comprising them
09/25/2007US7273878 Difluoroalkene derivative, pest control agent containing the same, and intermediate therefor
09/25/2007US7273863 Benzophenones as inhibitors of reverse transcriptase
09/25/2007CA2256516C Peptides
09/25/2007CA2251401C Process for the preparation of formylimidazoles
09/20/2007WO2007106022A2 A new crystalline form g of (5s) -5- [4- (5-chloro-pyridin-2- yloxy) -piperidine-1-sulfonylmethyl] - 5 -methyl -imidazolidine - 2,4-dione (i) and intermediates thereof.
09/20/2007WO2007106021A1 Process to prepare sulfonyl chloride derivatives
09/20/2007WO2007104696A1 Antimalarial agents having polyaromatic structure
09/20/2007WO2007104144A1 Compounds, ionic liquids, molten salts and uses thereof
09/20/2007WO2007085557A3 Use of substituted 2-imidazole of imidazoline derivatives
09/20/2007WO2007011910A3 Chiral amine-catalyzed asymmetric addition of carbon-centered nucleophiles to imines
09/20/2007US20070219379 Ionic Liquid and Process for Producing the Same
09/20/2007US20070219378 Method for Producing Sodium Fosphenytoin
09/20/2007US20070219163 2-amino-2-[5-(4-octyl-phenyl)-1H-imidazol-2-yl]-propan-1-ol or phosphate, sphingosine-1-phosphate (S1P) receptor modulators; agonists; antagonists; G protein coupled receptors; cell proliferation endothelial cells chemotaxis; antitumor agents; wound healing agents;platelet aggregation
09/20/2007CA2644345A1 A new crystalline form g of (5s) -5- [4- (5-chloro-pyridin-2- yloxy) -piperidine-1-sulfonylmethyl] - 5 -methyl -imidazolidine - 2,4-dione (i) and intermediates thereof.
09/20/2007CA2644016A1 Process to prepare sulfonyl chloride derivatives
09/19/2007EP1833802A2 1,2-diphenyl-imidazole derivatives and their use as cb1 receptor ligands
09/19/2007EP1833801A2 Intermediate compounds for the preparation of angiotensin ii receptor antagonists
09/19/2007EP1833796A1 Indenyl derivatives and use thereof for the treatment of neurological disorders
09/19/2007EP1833758A1 Method for separating gas
09/19/2007EP1198456B1 Potassium channel openers
09/19/2007CN101039916A Imidazole derivatives as large conductance calcium activated K channel openers
09/19/2007CN101039913A Method for producing high-purity quaternary ammonium compounds
09/19/2007CN100338077C Combretastatin A-4 phosphate prodrug, mono-and di-organic amine salt, mono-and di-amino acids salts, and mono-and di-amino acid ester salt
09/19/2007CN100338074C Heterocyclic compounds and cerebral function improvers containing same as active
09/19/2007CN100338039C Ornidazole optical antimer preparation and purification method
09/18/2007US7271271 Imidazolo-related compounds, compositions and methods for their use
09/18/2007US7271270 High affinity small molecule C5a receptor modulators
09/18/2007US7271189 1H-imidazole derivatives as cannabinoid receptor modulators
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