摘要:
Melanin concentrating hormone antagonists containing compounds of the general formula (I) or salts thereof are useful as preventive or therapeutic drugs for obesity and so on wherein Ar1 is an optionally substituted cyclic group; X and Y are each independently a spacer having a C¿1-6? main chain; Ar is an optionally substituted fused polycyclic aromatic ring; R?1 and R2¿ are each independently hydrogen or an optionally substituted hydrocarbon group, or alternatively R?1 and R2¿ together with the nitrogen atom adjacent thereto may form a nitrogenous heterocycle, or R2 together with the nitrogen atom adjacent thereto and Y may form an optionally substituted nitrogenous heterocycle, or R2 together with the nitrogen atom adjacent thereto, Y, and Ar may form a fused ring.
摘要:
Compounds of formula (1) and the pharmaceutically acceptable salts and esters thereof wherein X and Y are as defined in the specification, are effective inhibitors of the binding of VCAM-1 to VLA-4 in vivo and are useful in treating inflammation in inflammatory diseases in which such binding acts to bring on the inflammation.
摘要:
Selective IgE production inhibitors which contain substances inhibiting the production of IgE in the process of the differentiation of matured B cells into antibody-producing cells and the production of the antibody thereby while not or scarcely inhibiting the production of IgG, IgM and/or IgA to be produced simultaneously with IgE; compounds represented by general formula (I); a process for producing the same; and drugs containing the same. In said formula R to R represent each hydrogen, halogeno, lower alkyl, lower alkoxy, etc.; X represents O-, -CH2-, -NR - or -S(O)p-; and Y represents lower alkyl or lower alkenyl.
worin n eine Zahl von 1 bis 4 bedeutet, A und D gleich oder verschieden sind und unabhängig voneinander je für einen Rest der Formeln
oder für ein Isomerengemisch aus den beiden Resten Formel
stehen und E einen Rest der Formel
bedeutet, wobei R für ein Wasserstoffatom oder einen Rest der Formel -CO-NH-A-NH₂ oder -CO-NH-D-NH₂ steht, R₁ für einen Rest der Formel -CO-NH-A-NH₂ oder -CO-NH-D-NH₂ steht und m eine Zahl von 2 bis 12 bedeutet, eignen sich zum Härten von Epoxidharzen, vorzugsweise für die Kalthärtung.
摘要:
Novel dinitro and diamino compounds having the formula: wherein A is selected from the group consisting of SO₂, O, S, CO, C₁ to C₆ alkyl, perfluoroalkyl or perfluoroarylalkyl having from 1 to 10 carbon atoms, and a carbon-carbon bond directly linking the two aromatic groups, R is selected from the group consisting of hydrogen, hydroxy and C₁ to C₄ alkoxy, and R′ is selected from the group consisting of NO₂ and NH₂. In the most preferred embodiment, the A linking group is selected from hexafluoroisopropylidene or 1-phenyl-2,- 2,2-trifluoroethane, and R is hydroxy. The compounds of the present invention, where R′ is NH₂, may be used as crosslinking agents for epoxy resins and for unsaturated elastomers, or as a reactant monomer with an organic diacid or dianhydride co-reactant monomer in the preparation of polyamide, polyimide, polyamide-imide and polybenzoxazole polymers having superior thermal and mechanical properties.
摘要:
The present invention relates to a compound of formula (I), wherein L is –C(O)NH-, -NHC(O)-, -S(O)2NH-, -NH- or -NHC(O)NH-; Ar is phenyl, benzyl, naphthyl or heteroaryl, selected from the group consisting of pyridinyl, pyrazolyl, pyrimidinyl, isoxazolyl or pyrazinyl, wherein Ar may be optionally substituted by one, two or three R1; R1 is hydrogen, lower alkyl, lower alkoxy, halogen, cyano, cycloalkyl, NHC(O)-lower alkyl, lower alkoxy substituted by halogen, lower alkyl substituted by halogen, or is phenyl optionally substituted by one or two halogen atoms, CF3O or lower alkyl, or is furanyl, thiazolyl or thiophenyl, optionally substituted by halogen or lower alkyl; X is CH or O; R is hydrogen or halogen; or a pharmaceutically suitable acid addition salt thereof, all racemic mixtures, all their corresponding enantiomers and/or optical isomers, which may be used for the treatment of depression, anxiety disorders, bipolar disorder, attention deficit hyperactivity disorder (ADHD), stress-related disorders, psychotic disorders, schizophrenia, neurological diseases, Parkinson's disease, neurodegenerative disorders, Alzheimer's disease, epilepsy, migraine, hypertension, substance abuse, metabolic disorders, eating disorders, diabetes, diabetic complications, obesity, dyslipidemia, disorders of energy consumption and assimilation, disorders and malfunction of body temperature homeostasis, disorders of sleep and circadian rhythm, and cardiovascular disorders.
摘要:
The present invention relates to substituted N-biphenyl-3-acetylamino-benzamides and N-[3-(acetylamino)phenyl]-biphenyl-carboxamides of general formula (I) as described and defined herein, to methods of preparing said compounds, to intermediate compounds useful for preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular of a hyperproliferative disorder, as a sole agent or in combination with other active ingredients.