Patents
Sitemap › C07 - Organic chemistry › C07D - Heterocyclic compounds › C07D 487 - Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups
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)
11/2010
11/04/2010CA2747420A1 Azaazulene compounds
11/03/2010EP2245033A1 Pyrrolopyrazine kinase inhibitors
11/03/2010EP2245027A1 Hepatitis c virus inhibitors
11/03/2010EP2245014A1 Urea derivatives of benzomorphanes and related scaffolds, medicaments containing such compounds and their use
11/03/2010EP2244701A2 Corroles for neuroprotection and neurorescue
11/03/2010EP2099801B1 Imidazoý1,5-b¨pyridazinamido ligands and their complexes
11/03/2010EP2049544B1 Purinone derivatives as hm74a agonists
11/03/2010EP1846406B1 Maleimide derivatives, pharmaceutical compositions and methods for treatment of cancer
11/03/2010CN1553938B 荧光二酮吡咯并吡咯 Fluorescent diketopyrrolopyrrole
11/03/2010CN101878310A Process for production of pyrrole compound
11/03/2010CN101878217A Agent for prevention and/or treatment of skin diseases
11/03/2010CN101878216A Pyrimidine derivatives as protein kinase inhibitors
11/03/2010CN101878215A Polymorphs of a C-MET/HGFR inhibitor
11/03/2010CN101878204A Novel carboxylic acid 4-phenylazo-phenyl ester derivatives and their use as monoamine neurotransmitter re-uptake inhibitors
11/03/2010CN101343274B Carbazoles alkaloid, preparation and application thereof
11/03/2010CN101318960B Process for synthesizing acetate bicyclo guanidine and catalysis synthesis for poly-lactide and poly-serine morpholine diketone
11/03/2010CN101115760B Pyrrolopyrazoles, potent kinase inhibitors
11/03/2010CN101108850B Single-side bridged chirality metalloporphyrin compound and chiral catalytic system used for unsymmetrical oxidation reaction thereof
11/03/2010CN101098870B Novel fused imidazole derivative
11/02/2010US7825147 Enzyme inhibitors of phosphodiesterases for treatment of AIDS, asthma, arthritis, bronchitis and other disorders
11/02/2010US7825118 4-Amino-3-phenyl-1H-pyrazolo[3,4-d]pyrimidine derivatives; can be covalently bonded to Bruton's tyrosine kinase; autoimmune diseases, lymphoma, leukemia; antiproliferative, anticarcinogenic and antiinflammatory agents
11/02/2010US7825108 in the form of coded data, whilst minimizing visible coloration of the substrate; using a light to heat conversion dye comprising a metal-cyanine
11/02/2010US7824780 Imidazopyrimidine-based compound and organic light-emitting device employing organic layer including the same
11/02/2010US7824698 Lyophilized formulations of Salinosporamide A
11/02/2010CA2545527C Pyrazole derivatives as inhibitors of receptor tyrosyne kinases
11/02/2010CA2497544C Pyrazolo[1,5-a]pyrimidines compounds as cyclin dependent kinase inhibitors
11/02/2010CA2462799C Pyrimidine derivatives
11/02/2010CA2457720C Medicine containing pyrimidine derivative
11/02/2010CA2439784C Pyrazolopyrimidinone derivatives having pde7 inhibiting action
11/02/2010CA2400167C Insecticidal anthranilamides
10/2010
10/28/2010WO2010124047A1 Bisaryl alkynylamides as negative allosteric modulators of metabotropic glutamate receptor 5 (mglur5)
10/28/2010WO2010123956A2 2,5-disubstituted arylsulfonamide ccr3 antagonists
10/28/2010WO2010123919A2 Piperidine inhibitors of janus kinase 3
10/28/2010WO2010123018A1 Diazaspiroalkane derivative
10/28/2010WO2010122777A1 Colored composition, color filter, and color liquid crystal display element
10/28/2010WO2010122578A2 Process for the preparation of sitagliptin and its intermediates
10/28/2010WO2010074480A3 Novel pyrazolodiazepine compounds as a transglutaminase inhibitor, the preparation method thereof and a composition containing the same
10/28/2010WO2010068708A3 3'-azido purine nucleotide prodrugs for treatment of viral infections
10/28/2010WO2010065898A3 Egfr kinase knockdown via electrophilically enhanced inhibitors
10/28/2010WO2009142732A3 Substituted pyridazinone derivatives as histamine-3 (h3) receptor ligands
10/28/2010US20100274018 Process for the resolution of zopiclone and intermediate compounds
10/28/2010US20100274005 Bicyclic pyrazole compounds as antibacterial agents
10/28/2010US20100274004 Bicyclic pirazole compounds as antibacterial agents
10/28/2010US20100274003 Acid addition salts of synthetic intermediates for carbapenem antibiotics and processes for preparing the same
10/28/2010US20100273830 Novel insecticides
10/28/2010US20100273824 Substituted 1,3-dioxanes and their uses
10/28/2010US20100273812 Diazo bicyclic smac mimetics and the uses thereof
10/28/2010US20100273803 Oral Formulations for Tetrapyrrole Derivatives
10/28/2010US20100273802 New purine derivatives having, in particular, anti-proliferative properties, and their biological uses
10/28/2010US20100273801 Betulin derived compounds useful as antibacterial agents
10/28/2010US20100273799 Small molecule inhibitors of mdm2 and the uses thereof
10/28/2010US20100273792 Macrocyclic indoles as hepatitis c virus inhibitors
10/28/2010US20100273788 Fused heterocyclic derivative and use thereof
10/28/2010US20100273786 Tetrahydro-imidaz0[1,5-a]pyrazine derivatives, preparation process and medicinal use thereof
10/28/2010US20100273784 Fused ring heterocycles as potassium channel modulators
10/28/2010US20100273782 2,5-disubstituted arylsulfonamide ccr3 antagonists
10/28/2010US20100273776 Inhibition of alpha-synuclein toxicity
10/28/2010US20100273775 Fungicidal bicyclic pyrazoles
10/28/2010US20100273772 Bisaryl Alkynylamides as Negative Allosteric Modulators of Metabotropic Glutamate Receptor 5 (MGLUR5)
10/28/2010US20100273767 Modulators of 5-ht receptors and methods of use thereof
10/28/2010US20100273754 Organic compounds
10/28/2010US20100273753 Organic compounds
10/28/2010US20100272681 Inhibitors of Serine Proteases
10/28/2010CA2759607A1 Modulators of 5-ht receptors and methods of use thereof
10/28/2010CA2759026A1 Piperidine inhibitors of janus kinase 3
10/28/2010CA2758985A1 2,5-disubstituted arylsulfonamide ccr3 antagonists
10/27/2010EP2243782A2 Two-photon absorption material and application thereof
10/27/2010EP2242756A2 Pyrrolopyrimidines and pyrrolopyridines
10/27/2010EP2111405B1 Intermediates useful in preparing certain pyrrolotriazine compounds and a process for making the intermediates
10/27/2010EP2099761B1 Antibacterial quinoline derivatives
10/27/2010EP1932846B1 Method for producing sulfonyl chloride compound
10/27/2010CN1898246B Process for preparing substituted 5-amino-pyrazolo-[4,3-e]-1,2,4-triazolo-[1,5-c]-pyrimidine
10/27/2010CN1261823B Metal complex used for oxidation and katalysis system
10/27/2010CN101874021A Azaindenofluorenedione derivative, organic electroluminescent device material, and organic electroluminescent device
10/27/2010CN101870700A Method for synthesizing Indiplon
10/27/2010CN101870699A Benzenesulfonyl piperazine derivative and preparation method thereof
10/27/2010CN101870698A Sulfonyl-phenyl imidazo triazine derivative and preparation method
10/27/2010CN101175738B Apoptosis promoters
10/27/2010CN101027306B Method of preparing poly(ADP-ribose) polymerases inhibitors
10/26/2010US7820820 Method of preparation of azaindole derivatives
10/26/2010US7820814 Inhibitors of kinases
10/26/2010US7820682 3-{[(3R)-1-(3,5-dimethoxy-4-methylbenzoyl)-5-(2-phenylethyl)-3-pyrrolidinyl]oxy}benzoic acid methyl ester; treatment of urinary system disease; anticarcinogenic agent, antiarthritic agent, treats proliferative disease, inflammation/immune system disease, Sjogren*s syndrome, brain-related disease
10/26/2010US7820680 HIV integrase inhibitors
10/26/2010US7820675 Benzofuran compounds
10/26/2010US7820668 POLY/ADP-RIBOSE/ POLYMERASE (PARP) inhibitors; for treating neural tissue damage resulting from ischemia and reperfusion injury, depression, arthritis, inflammatory bowel disorders, gout, chronic pain, acute pain, neuropathic pain, renal failure, retinal ischemia, and septic shock; antitumor agents
10/26/2010US7820666 Tetrahydrotriazolopyrazine derivatives and uses thereof
10/26/2010US7820665 phosphatidyl inositol 3-kinase inhibitors such as N-(6-(6-Chloro-5-(3-(difluoromethoxy)phenylsulfonamido)pyridin-3-yl)-3-(pyridin-4-yl)imidazo[1,2-b]pyridazin-2-acetamide
10/26/2010US7820664 N-(2-aylamino)aryl sulfonamides such as N-(7-(4-bromo-2-fluorophenylamino)imidazo[1,2-b]pyridazin-6-yl)-1-(2-hydroxyethyl)cyclopropane-1-sulfonamide; mitogen-activated ERK activating kinase (MEK) inhibitors; antiproliferative, anticarcinogenic, and antiinflammatory agents
10/26/2010US7820662 IGF-1R enzyme inhibitor; antiproliferative, anticarcinogenic, antiinflammatory agent, antiallergen; psoriasis, asthma, disease and conditions of the immune system and central nervous system; better selectivity or potency, reduced toxicity, or fewer side effects
10/26/2010US7820658 such as 2-Amino-4-phenyl-thieno[2,3-d]pyrimidine-6-carboxylic acid ethylamide; veterinary medicine; anticancer agents
10/26/2010US7820650 active mainly against dermatophytes
10/26/2010US7820648 Inhibitors of the FAK (focal adhesion kinase) protein tyrosine kinases, antiproliferative, antitumor; for example 5-{4-[(1-Hydroxy-cyclopentylmethyl)-amino]-5-trifluoromethyl-pyrimidin-2-ylamino}-1,3-dihydro-indol-2-one
10/26/2010US7820644 Substituted porphyrins
10/26/2010US7820640 administering mixture of allopurinol, ebselen and n-acetylcysteine
10/26/2010CA2372058C Hemisynthetic method of ecteinascidins and new intermediates
10/21/2010WO2010120996A1 5,6,7,8-tetrahydropyrido[3,4-d]pyrimidine compounds, their use as mtor kinase and pi3 kinase inhibitors, and their syntheses
10/21/2010WO2010120987A1 Ring fused, ureidoaryl- and carbamoylaryl-bridged morpholino-pyrimidine compounds, their use as mtor kinase and pi3 kinase inhibitors, and their syntheses
10/21/2010WO2010120112A2 Novel compounds of reverse-turn mimetics, method for manufacturing the same and use thereof
10/21/2010WO2010119264A1 Imidazopyrazines for use as kinase inhibitors
10/21/2010WO2010119222A1 Derivatives of n-[(7-aza-bicyclo[2.2.1]hept-1-yl)-aryl-methyl]-benzamide, preparation thereof, and therapeutic use thereof
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