摘要:
Triphenylmethane derivatives of the formula (I) are disclosed. The compounds are inhibitors of the mitotic kinesin KSP and are useful in the treatment of cellular proliferative diseases, such as cancer, hyperplasias, restenosis, cardiac hypertrophy, immune disorders and inflammation
摘要:
Compounds of the formulae (I, II or III) wherein: R1, R2, R3 and R4 which may be the same or different, are selected from the group consisting of hydrogen, alkyl of 1-6 carbons, cycloalkyl of 3 to 6 carbons, alkenyl of 2-6 carbons, or together represent methylene groups -(CH2)n- where n is a whole number from 1 to 6, provided that R1 and R2 or R3 and R4 are not both hydrogen.
摘要:
La présente invention concerne des composés dérivés de 1, 3-diphénylpropane substitués, possédant des propriétés d'agonistes PPAR, les compositions pharmaceutiques les comprenant ainsi que leurs applications thérapeutiques, notamment dans les domaines de la santé humaine et animale.
摘要:
The invention relates to substituted phenoxyacetic acids (I) as useful pharmaceutical compounds for treating respiratory disorders, pharmaceutical compositions containing them, and processes for their preparation.
摘要:
Compounds of Formula (IA) and Formula (IB) wherein R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 are as defined herein for Formula (IA) or Formula (IB), or a tautomer, prodrug, solvate,or salt thereof; pharmaceutical compositions containing such compounds, and methods of modulating the glucocorticoid receptor function and methods of treating disease-states or conditions mediated by the glucocorticoid receptor function or characterized by inflammatory, allergic, or proliferative processes in a patient using these compounds.
摘要:
The invention provides for a non-steroidal compound having the formula [I], wherein R and 'R are OH, optionally independently etherified or esterified; Z is -CH2- or -CH2CH2-; R is H, halogen, CF3, or (1C-4C)alkyl; R , R and R are independently H, halogen, -CF3, -OCF3, (1C-8C)Alkyl, hydroxy, (1C-8C)alkyloxy, aryloxy, aryl(1C-8C)alkyl, halo(1C-8C)alkyl, -O(CH2)mX, wherein X is halogen or phenyl and m = 2-4; -O(CH2)mNRaRb, -S(CH2)mNRaRb or -(CH2)mNRaRb, wherein m = 2-4 and Ra, Rb are independently (1C-8C)alkyl, (2C-8C)alkenyl, (2C-8C)alkynyl, or aryl, optionally substituted with halogen, -CF3, -OCF3, -CN, -NO2, -OH, (1C-8C)alkoxy, aryloxy, carboxyl, (1C-8C)alkylthio, carboxylate, (1C-8C)alkyl, aryl, aryl(1C-8C)alkyl, halo(1C-8C)alkyl or Ra and Rb form a 3-8 membered ring structure, optionally substituted with halogen, -CF3, -OCF3, -CN, -NO2, hydroxy, hydroxy(1C-4C)alkyl, (1C-8C)alkoxy, aryloxy, (1C-8C)alkylthio, carboxyl, carboxylate, (1C-8C)alkyl, aryl, aryl(1C-8C)alkyl, halo(1C-8C)alkyl. The compounds can be used for the preparation of a medicine, in particular for use in estrogen-receptor-related treatments.
摘要:
3-Arylphenyl sulfide derivatives represented by general formula (I) and insecticides and miticides containing these derivatives as the active ingredient, wherein R represents C2-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, etc.; B0 to B2 and B3 represent each hydrogen, halogeno, cyano, C1-4 haloalkyl, etc.; n is 0, 1 or 2; and Ar represents a phenyl, thiophene or pyrazole ring, etc.
摘要:
Biphenyl derivatives represented by general formula (1), or salts thereof which have excellent anti-inflammatory, antipyric/analgesic and antiarthritic effects and thus are useful as medicines, wherein R represents lower alkyl, aryl or amino; R represents aryl or -Z-R (wherein R represents alkyl, alkenyl, alkylsulfonyl, aryl, etc; and Z represents oxygen, sulfur, imino, etc.); R and R represent each hydroen, halogeno, cyano, azido, nitro, amino, carboxy, hydroxy, acyl, alkoxycarbonyl, alkyl, alkenyl, alkoxy, alkylthio, etc.; and n is 0, 1 or 2.
摘要翻译:由通式(1)表示的联苯衍生物或其盐具有优异的抗炎,止痛/镇痛作用和抗关节炎作用,因此可用作药物,其中R 1表示低级烷基,芳基或氨基; R 2表示芳基或-Z-R 5(其中R 5表示烷基,烯基,烷基磺酰基,芳基等; Z表示氧,硫,亚氨基等); R 3和R 4各自表示各个氢,卤代,氰基,叠氮基,硝基,氨基,羧基,羟基,酰基,烷氧基羰基,烷基,烯基,烷氧基,烷硫基等。 n为0,1或2。