摘要:
o-Anisamide derivatives which serve as peroxisome proliferator-activated receptor (PPAR) agonists, in particular human PPAR agonists, and are efficacious in preventing and/or treating metabolic diseases in which they participate (hyperlipemia, diabetes, etc.), acid addition salts thereof and a process for producing the same. Namely, o-anisamide derivatives represented by general formula (1), pharmaceutically acceptable salts thereof and hydrates of the same, wherein R represents carboxy, carboxymethyl, CH2CHXCOY (wherein X represents mercapto or S(O)nMe wherein n is 0, 1 or 2; and Y represents amino or hydroxy).
摘要:
An objective of the present invention is to provide compounds that can effectively suppress the concentration of phosphorus in serum to effectively prevent or treat diseases induced by an increase in concentration of phosphate in serum. The compounds according to the present invention are compounds represented by formula (I) and pharmaceutically acceptable salts and solvates thereof:
wherein A represents an optionally substituted five- to nine-membered unsaturated carbocyclic moiety or a five- to nine-membered unsaturated heterocyclic moiety, and ---- represents a single bond or a double bond, R 5 represents optionally substituted aryl or the like, Z represents - N=CHR 6 R 7 or the like, R 6 and R 7 represent H, optionally substituted alkyl, optionally substituted aryl or the like, R 101 and R 102 together form =O, and R 103 and R 104 represent H, or R 101 and R 104 together from a bond, and R 102 and R 103 together form a bond.
摘要:
This invention provides a process for preparing compounds of formula (1) wherein: X is phenyl optionally substituted with one or more substituents selected from the group consisting of halogen, alkyl of 1-6 carbon atoms, alkoxy of 1-6 carbon atoms, hydroxy, trifluoromethyl, cyano, nitro, carboxy, carboalkoxy of 2-7 carbon atoms, carboalkyl of 2-7 carbon atoms, amino, and alkanoylamino of 1-6 carbon atoms; R and R1 are each, independently, hydrogen, halogen, alkyl of 1-6 carbon atoms, alkoxy of 1-6 carbon atoms, hydroxy, or trifluoromethyl; R2 is hydrogen, alkyl of 1-6 carbon atoms, alkoxy of 1-6 carbon atoms, hydroxy, trifluoromethyl; Y is (2) or (3); R3 is independently hydrogen, alkyl of 1-6 carbon atoms, carboxy, carboalkoxy of 1-6 carbon atoms, phenyl, or carboalkyl of 2-7 carbon atoms; n = 2-4; or a pharmaceutically acceptable salt thereof, with the proviso that each R3 of Y may be the same or different.
摘要:
The present invention provides compounds of the structure: including pharmaceutical compositions thereof and methods of treating sleepiness associated with narcolepsy, obstructive sleep apnoea or shift work disorder; Parkinson's disease; Alzheimer's disease; attention deficit disorder; attention deficit hyperactivity disorder; depression and fatigue therewith.
摘要:
Compounds having a urea structure as the basic structure and carrying sulfur and amide bonds in side chains. It has been found out that these compounds have pharmacological effects, in particular, a TNF-α production inhibitory effect. The above compounds are represented by general formula [I] wherein R1 represents H, alkyl, an aromatic group, R?A-CO-, RC¿-S- or a group of formula [II]; R?2, R3 and R4¿ represent each H, alkyl, alkenyl, cycloalkyl, cycloalkenyl or an aromatic group; R?5 and R6¿ represent each H, alkyl, alkenyl, cycloalkyl, cycloalkenyl or an aromatic group, or R?5 and R6¿ may form together a nonaromatic heterocycle; R7 represents H, alkyl, cycloalkyl, hydroxy, mercapto, phenyl, R?B-O-, RC-S-, RD¿-COS-, RE-OCO-, RF-N(RG)- or -CONHOH; and A?1 and A2¿ represent each an alkylene.
摘要:
A N-biphenylamide compound of the formula (1): wherein R 1 , R 2 , R 3 , R 4 and R 5 independently represent a hydrogen atom, halogen atom or the like, R 6 represents C1-C6 alkyl and the like, R 7 represents a hydrogen atom or C1-C3 alkyl, R 8 represents a hydrogen atom or C1-C3 alkyl, R 9 and R 10 independently represents a halogen atom, C1-C6 alkyl, C1-C6 alkoxy or the like, R 11 , R 12 and R 13 independently represent a hydrogen atom, halogen atom or the like, R 14 , R 15 , R 16 and R 17 independently is a hydrogen atom, halogen atom or the like, X 1 represents an oxygen atom or sulfur atom, X 2 represents an oxygen atom or sulfur atom; has excellent effect aginst plant diseases.
摘要:
The invention relates to a method for producing chiral compounds according to the condition of a 1.4 Michael reaction in addition to a compound of general formula (31) and the use thereof as an antalgic.
摘要:
Phenylalanine derivatives represented by general formula (1) or pharmaceutically acceptable salts thereof: wherein x represents an interatomic bond, -O-, etc.; Y and Z represent each -C(=O)-, etc.; A represents a specific substituted phenyl group, a specific nitrogen-containing heterocycle, etc.; C represents hydrogen, alkly, etc.; D and E represent each alkyl or D and E may be bonded to each other to form a ring, etc.; F and G represent each hydrogen or alkyl, or F and G may be bonded to each otherto form a ring, etc.; n is from 0 to 2; K represents OR7, NR7R8, R7, etc.; and J and J' represent each hydrogen, halogeno, etc. These derivatives and analogs thereof show an α 4 integlin inhibitory activity and are usable as remedies for various diseases relating to α 4 integlin.