Patents
Patents for A61K 31 - Medicinal preparations containing organic active ingredients (785,912)
07/2008
07/31/2008US20080182906 Therapy for diabetic retinopathy
07/31/2008US20080182905 Using (4,5,6,7-tetrahydro-5,5,8,8-tetramethylnaphthalen-2-yl)carbamoyl benzoic acid
07/31/2008US20080182904 Antidepressants; psychological disorders
07/31/2008US20080182903 Weight control; sexual disorders; stomach blotting; gastrointestinal disorders; anticholesterol agents
07/31/2008US20080182902 Sphingolipids in Treatment and Prevention of Steatosis and of Steatosis or of Hepatotoxicity and its Sequelae
07/31/2008US20080182901 Crystalline acid of lipoxin A4 analogs and method of making
07/31/2008US20080182900 Method of treatment of virus infections using shikonin compounds
07/31/2008US20080182899 Adrenergic receptor antagonist and enzyme inhibitors; antidepressant; anxiolytic agents
07/31/2008US20080182898 Treatment of metabolic syndrome with norfluoxetine
07/31/2008US20080182897 Crystalline potassium salt of lipoxin A4 analogs
07/31/2008US20080182896 Use of metal chelates in human or animal feeding
07/31/2008US20080182895 Identification and characterization of hcv replicon variants with reduced susceptibility to hcv-796, and methods related thereto
07/31/2008US20080182894 Efficiency; determine , calibration nutrients needed for therapy
07/31/2008US20080182893 Prevention, therapy atherosclerosis; prevent plaque destabilization; using ienzyme modified soquercitrin
07/31/2008US20080182892 Treatment of interstitial cystitis using (6aR, 10aR)-delta-8-tetrahydrocannabinol-11-oic acids
07/31/2008US20080182891 Chromane and chromene derivatives and uses thereof
07/31/2008US20080182890 Methods of using low-dose doxepin for the improvement of sleep
07/31/2008US20080182889 Prodrugs of excitatory amino acids
07/31/2008US20080182888 Novel Crystalline Compounds
07/31/2008US20080182887 atorvastatin, atorvastatin lactone less than 0.5% by weight of atorvastatin, and carrier comprising 0.5% - 3.0% by weight of tromethamine and an additional stabilizer (antioxident) to prevent degradation of atorvastatin; storage stability
07/31/2008US20080182885 Modified Azole Compounds As Antifungal and Antibacterial Agents
07/31/2008US20080182883 e.g. 1-Benzyl-3-pentyl-2-[6-(1H-tetraazol-5-ylmethoxy)-2-naphthyl]-1H-indole; stroke associated with or resulting from atrial fibrillation; thrombolytic agents for prohylaxis of cardiovascular disorders
07/31/2008US20080182882 E.g., N-(5-chloro-2-methylbenzyl)-N'-hydroxy-4-(hydroxymethyl)-1,2,5-oxadiazole-3-carboximidamide; inhibiting immunosuppression; treating cancer, viral infection, depression, neurodegenerative disorder, trauma, age-related cataracts, organ transplant rejection, or autoimmune disease
07/31/2008US20080182881 TNF-alpha production inhibitors
07/31/2008US20080182880 5-[[4-[2-(5-ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-2,4-]thiazolidinedione; physical form of pioglitazone; sulfonylureas, metformin, or the alpha -glucosidase inhibitors, peroxisome proliferator-activated receptor-gamma agonist; antidiabetic, hypoglycemic agent; insulin resistance
07/31/2008US20080182879 e.g. 6-hydroxy-2-[3-(4-tert-butylphenyl)-1,2,4-oxadiazol-5-yl]chromone; tyrosine kinase inhibitors, anticarcinogenic and antiinflammatory agent; cerebral, genito-urinary tract, lymphatic system, stomach, laryngeal, pancreatic, breast or lung tumor; rheumatoid arthritis, psoriasis, contact dermatitis
07/31/2008US20080182878 benzothienyl containing amido-derivatives, antibacterial agent; quorum sensing regulated virulence factors; inhibiting biofilm formation; virulence gene expression blocking agent, disinfectants, antifouling coatings
07/31/2008US20080182877 Rimonabant forms and methods of making the same
07/31/2008US20080182876 Histamine H3-Receptor Ligands and Their Therapeutic Application
07/31/2008US20080182875 N-(2-Hydroxyethyl)-N-Methyl-4-(Quinolin-8-yl(1-(Thiazol-4-ylmethyl)Piperidin-4-ylidene)Methyl)Benzamide
07/31/2008US20080182874 e.g. 1-[6-Chloro-5-[(tricyclo[3.3.1.13,7]dec-1-ylacetyl)amino]-2-quinolinyl]-4piperidinecarboxylic acid; adamantyl-containing purinergic receptor P2X7 antagonists; antiinflammatory agent, immune or cardiovascular diseases; asthma, chronic obstructive pulmonary disease, rheumatoid arthritis
07/31/2008US20080182873 Process for the manufacture of hmg-coa reductase inhibitors
07/31/2008US20080182872 e.g. 2-(3-fluoro-4-hydroxyphenyl)-7-vinyl-1,3-benzoxazol-5-ol or 3-(3-fluoro-4-hydroxy-phenyl)-7-hydroxy-naphthalene-1-carbonitrile; estrogen receptor beta selective modulator; antiinflammatory agent; induced by peritonitis or intravenous bacteremia during sepsis, or by oxygen toxicity;
07/31/2008US20080182871 e.g. 3-(3-methoxyphenyl)isoquinolin-1-amine; antiproliferative and antigrowth agent; breast tumors, prostate tumors, colon tumors, ovary tumors, kidney tumors, pancreas tumors, glioblastoma and melanoma.
07/31/2008US20080182870 PYRIDO(3,2-d)PYRIMIDINES USEFUL FOR TREATING VIRAL INFECTIONS
07/31/2008US20080182868 Novel chemical compounds
07/31/2008US20080182867 Administering one or more rapamycin derivatives (including rapamycin and 40-O-(2-hydroxy)ethyl-rapamycin); lymphocytic leukemia, lymphoma, Epstein-Barr virus, inhibiting graft rejection and metastasis; drug screening
07/31/2008US20080182866 Tetra-Cyclic Carboline Derivatives Useful in the Inhibition of Angiogenesis
07/31/2008US20080182865 combination of at least one selective histone deacetylase inhibitor and kinase inhibitor with anti-EGFR activity (gefitinib, erlotinib, lapatinib, sutent, vandetanib, or sorafenib); anticarcinogenic agent; non-small cell lung, breast, skin, bladder, colon, prostate, uterine, cervical, ovarian cancer
07/31/2008US20080182864 2-(1-Aroylaminoalkyl)-3-(alkylaryl)-7-(halo- or cyano)quinazolinone derivatives, e.g., 2-[1'-(N,N-dimethylethylenediamino)propyl]-3-benzylquinazolin-4-one; mitotic kinesin spindle protein inhibitors; disrupting mitosis; modulating mitotic spindle formation; restenosis
07/31/2008US20080182863 e.g. 4-[2-(5-Chloro-2-fluoro-phenyl)-7-(2-dimethylamino-ethylamino)-pyrido-[2,3-d]pyrimidin-4-ylamino]-nicotinic acid; viricide; transforming growth factor-beta inhibitor; hepatitis C infection; fibroproliferative conditions: fibrosis, glomerulonephritis, diabetic nephropathy, and certain cancers
07/31/2008US20080182862 e.g. 1-(isoquinolin-1-yl)-N3-(2-(pyrrolidin-1-ylmethyl)benzo[d]oxazol-5-yl)-1H-1,2,4-triazole-3,5-diamine; protein tyrosine kinase receptor Axl inhibitor; bioassay; antiinflammatory, anticarcinogenic agent, anticoagulant; rheumatoid arthritis, vascular disease, diabetic retinopathy, osteoporosis
07/31/2008US20080182861 Inhibitors of diacylglycerol o-acyltransferase type 1 enzyme
07/31/2008US20080182860 Pyrimidine Compounds as Purine Receptor Antagonist
07/31/2008US20080182859 Small organic molecule regulators of cell proliferation
07/31/2008US20080182858 infectious disorders; antiarrhythmic, antifibrillatory agents; 1-[[[5-(4-chlorophenyl)-2-furanyl]methylene]amino]-3-[4-(4-methyl-1-piperazinyl)butyl]-2,4-imidazolidinedione dihydrochloride; different polymorphic, hydrate and solvate forms of compound are advantageous for the manufacture of compositions
07/31/2008US20080182857 Heat Shock Protein 90 inhibitors; 5-(2,4-dihydroxyphenyl)-4-(naphth-1-yl)-4H-1,2,4-triazole-3-thiol; incorrect protein folding or aggregation; hydrazonederivatives react with dimiadazole cabonyl/thiocarbonyl derivatives; hydrazines derivatives react with isocyanate or isothiocyanates; tumors, cancer
07/31/2008US20080182856 Novel crystalline forms of aripiprazole
07/31/2008US20080182855 Antibacterial Quinoline Derivatives
07/31/2008US20080182854 4-Amino-5-Cyanopyrimidine Derivatives
07/31/2008US20080182853 suppressing neuronal death; sudden loss of oxygen and/or energy loss, and degenerative diseases, such as Alzheimer's disease; Parkinson's disease; ischemic states
07/31/2008US20080182852 Anthranilamide inhibitors of aurora kinase
07/31/2008US20080182851 Acetylene derivatives as stearoyl coa desaturase inhibitors
07/31/2008US20080182850 3-(heteroaryl)alanine derivatives-inhibitors of leukocyte adhesion mediated by vla-4
07/31/2008US20080182849 Certain Heterocyclic Substituted Imidazo[1,2-A]Pyrazin-8-Ylamines And Methods Of Inhibition Of Bruton's Tyrosine Kinase By Such Compounds
07/31/2008US20080182848 anxiety; insomnia; high yielding; optically resolving eszopiclone using a multi-column continuous process or a simulated moving bed process; stationary phase used in chiral chromatography process is a derivative of tris(3,5-dimethylphenyl carbamate), or a derivative of tris- alpha -methylbenzylcarbamate
07/31/2008US20080182847 Anticancer agents; potent Deoxycytidine kinase inhibitors; inhibit thymidine kinase; inhibit uridine kinase; N-[3-(4-amino-5-fluoro-2-oxo-2H-pyrimidin-1-yl)-cyclopentyl]-3-bromo-benzenesulfonamide
07/31/2008US20080182846 Preventives or remedies for Alzheimer's disease, or amyloid protein fibril-formation inhibitors, which include a nitrogen-containing heteroaryl compound
07/31/2008US20080182845 Method of preventing or treating organ, hematopoietic stem cell or bone marrow transplant rejection
07/31/2008US20080182844 7-Substituted Aza-Indazoles, Compositions Containing Same, Production Method and Use Thereof
07/31/2008US20080182843 Mitotic Kinesin Inhibitors
07/31/2008US20080182842 L-alanine derivatives as a5beta1 antagonists
07/31/2008US20080182841 Sustained release bioadhesive carrier such as polycarbophil; coronary antiarrhythmic; local anesthetic; calcium channel blocker; autocoid; antiprostaglandin; nonsteroidal antiinflammatory; cyclooxygenase, thromboxane or leukotriene inhibitor; infertility
07/31/2008US20080182840 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
07/31/2008US20080182839 LFA1 related immune and/or inflammatory disorders; interactions with leukointegrins; such as fused nitrogen heterocyclic secondary amine derivatives
07/31/2008US20080182838 (5-{5-[4-(2-Bromo-5-fluorophenoxy)piperidin-1-yl]pyrazin-2-yl}-2H-tetrazol-2-yl)acetic acid; metabolic disorders,antidiabetic, hypoglycemic agent; obesity, insulin resistance, liver steatosis, atherosclerosis, neurological disease, dyslipidemia, hyperlipidemia, low HDL, and high LDL
07/31/2008US20080182837 New chemical compounds
07/31/2008US20080182836 Cephalosporin compounds comprising a C3 thio-methyl moiety substituted with N-containing heterocyclic group, and a C7 thiourea acetamido group, their preparations and uses thereof
07/31/2008US20080182835 Cobalt attached/coordinated to 6 same or different ligands including a N-based ligand donor atom that is ammonia, primary amine or secondary amine, or salt; does not have free cobalt(III) coordination sites and does not hydrolyze oligonucleotides; complex may be bound to an oligonucleotide
07/31/2008US20080182834 less toxic than the unassociated metal complex by hindering reactions in the blood stream; antitumor agents; platinum, palladium, gold amine inclusion compounds
07/31/2008US20080182832 orphan nuclear Receptor agonists; chenodeoxycholic acid, ursodeoxycholic acid or cholic acid derivatives; atherosclerosis, arteriosclerosis, dyslipidemia, hypercholesterolemia, and hypertriglyceridemia.atherosclerosis, arteriosclerosis, hypercholestremia, and hyperlipidemia
07/31/2008US20080182831 e.g. Cyanomethyl (6 alpha ,11 beta ,16 alpha ,17 alpha )-17-({[(1,1-dimethylethyl)oxy]carbonyl}oxy)-6,9-difluoro-11-hydroxy-16-methyl-3-oxoandrosta-1,4-diene-17-carboxylate; glucocorticoid receptor agonists of the androstane series; with other beta 2-adrenoreceptor agonist; asthma, rhinitis, eczema
07/31/2008US20080182830 Agent for Treatment and Prevention of Endometriosis and Uterine Adenomyosis
07/31/2008US20080182829 8Beta-Hydrocarbyl-Substituted Estratrienes As Selectively Active Estrogens
07/31/2008US20080182828 dominant estrogenic activity phase of three daily doses of an estrogen equivalent to 1 mg per day of 17 beta -estradiol per day and a dominant progestagenic activity phase of a combination of an estrogen and a progestogen equivalent to 90 mu g per day of norgestimate; hot flushes
07/31/2008US20080182827 mixture of sustained release oral minocycline hydrochloride (tetracyclin) antibiotic, and fast dissolving carrier, and slow dissolving carrier (encapsulates said intragranular fast dissolving carrier) at ratio of about 0.3 to 0.5; dosage form comprises a coating; once-a-day dosing regimen
07/31/2008US20080182826 Method for the treatment of acne
07/31/2008US20080182825 oral dosage form antiacne agent containing minocycline antibiotic; lactose monohydrate as fast dissolving carrier; e.g. polyvinyl pyrrolidone, hydroxypropylmethyl cellulose as slow dissolving carrier; fewer side effects; sustained release
07/31/2008US20080182824 e.g. N-methyl-N-propargyl-4-hydroxybenzyl amine; monoamine oxidase inhibitors; are mediated via a peripheral (i.e., non-CNS) mechanism; antidiabetic agent, metabolic disordes, obesity, insulin resistance
07/31/2008US20080182823 E.g., polyethylene glycol-linked alendronate or pamidronate; osteoporosis, osteopenia, urolithiasis, hypercalcemia, Paget's disease, bone metastasis, multiple myeloma, or neoplastic bone lesion
07/31/2008US20080182822 Liquid Pharmaceutical Compositions Comprising a Bisphosphonate Compound
07/31/2008US20080182821 Anti-Inflammatory and/or Analgesic Composition For the Intestine Comprising Branched Maltodextrins
07/31/2008US20080182820 Mixtures of sulfated oligosaccharides
07/31/2008US20080182819 Chitosan compositions and methods for using chitosan compositions in the treatment of health disorders
07/31/2008US20080182818 Th1 CELL DIFFERENTIATION ACCELERATOR
07/31/2008US20080182817 Cyanocobalamin low viscosity aqueous formulations for intranasal delivery
07/31/2008US20080182816 Utilizing prodrug technique to couple polysaccharides containing galactose with a parent compound through different bridge linkage to derive conjugates; polysaccharide component protects 5-fluorouracil(5-FU) from absorption in the upper gastrointestinal tract, delivers the 5-FU to colorectal area
07/31/2008US20080182815 Act against several infective agents, and most notably Bacillus spp. and Staphylococcus spp., including infection caused by methicillin-resistant Staphylococcus aureus (MRSA)
07/31/2008US20080182814 Beta-L-2'-deoxynucleosides for the treatment of resistant HBV strains and combination therapies
07/31/2008US20080182813 UNIVERSAL TARGET SEQUENCES FOR siRNA GENE SILENCING
07/31/2008US20080182812 Disease model animals of metabolic syndrome and a method of screening preventive and therapeutic agents for metabolic syndrome using the same
07/31/2008US20080182811 Activating a metabotropic glutamate receptor by administering one or more kinds of amino acids selected from amino acids other than glutamic acid; use in treating neurological diseases, cardiovascular diseases, surgical diseases, neurosurgical diseases, thoracic surgical diseases, orthopedic diseases
07/31/2008US20080182810 Antisense modulation of acyl coa cholesterol acyltransferase-2 expression
07/31/2008US20080182809 Oligonucleotide sequences which bind biomolecules such as peptides, hydrophobic molecules and extracellular proteins for diagnosing and treating cardiovascular disorders in mammals
07/31/2008US20080182808 Capable of inducing breakdown of mrna enzymes that break down connective tissue; particularly suited for treating degenerative skin disorders; pharmaceutical and cosmetic compositions for topical application and which contain the oligoribonucleotides
07/31/2008US20080182807 gene therapy against tumors and cancer; expression vector includes insert into tumor an effective amount of polynucleotides encoding a functionally active p53, express p53 to first DNA damaging agent, contact tumor cell with first DNA damaging agent, and kill tumor cell
07/31/2008US20080182806 Use of acetylated or esterificated azacytidine, decitabine, or other nucleoside analogs as oral agents for the treatment of tumors or other dysplastic syndromes sensitive to hypomethylating agents
07/31/2008US20080182805 O-GlcNAcase-specific inhibitor and substrate engineered by the extension of the N-Acetyl moiety
07/31/2008US20080182804 Cyanooxime inhibitors of carbonyl reductase and methods of using said inhibitors in treatments involving anthracyclines
07/31/2008US20080182803 extract from Cassia or Senna plants comprises rubrofusarin gentiobioside with egg white, egg membrane, milk whey, yeast/vegetable proteins, soy bean, L-cysteine, L-methionine, and vitamin C; synergistic; intracellular biosynthesis of glutathione stimulator; liver, brain, vision, or immune disorders