摘要:
The present invention provides a compound of formula (I): said compound is inhibitor of MMP-2, and/or MMP-8, and/or MMP-9, and/or MMP-12 and/or MMP-13, and thus can be employed for the treatment of a disorder or disease characterized by abnormal activity of MMP-2, and/or MMP-8, and/or MMP-9, and/or MMP-12 and/or MMP-13. Accordingly, the compound of formula (I) can be used in treatment of disorders or diseases mediated by MMP-2, and/or MMP-8, and/or MMP-9, and/or MMP-12, and/or MMP-13. Finally, the present invention also provides a pharmaceutical composition.
摘要:
Aryl sulfone compounds of formula (I) and (II) are described and have therapeutic utility, particularly in the treatment of diabetes, obesity and related conditions and disorders.
摘要:
The present invention provides compounds that are effective in treating central nervous system disorders and maintaining normal brain function. Methods of making and using the compounds are also provided.
摘要:
Verwendung von aminosubstituierten Hydroxybenzophenonen der allgemeinen Formel I,
in der die Variablen die in der Beschreibung erläuterte Bedeutung haben, als photostabile UV-Filter in kosmetischen und pharmazeutischen Zubereitungen zum Schutz der menschlichen Haut oder menschlicher Haare gegen Sonnenstrahlen, allein oder zusammen mit an sich für kosmetische und pharmazeutische Zubereitungen bekannten, im UV-Bereich absorbierenden Verbindungen.
摘要:
Compounds of formula (I) [in which: A and B are terminal groups; R1 represents a group of formula (II) or (III); R2 is alkyl or aryl; Z is a group -(CHR3)n , where R3 is hydrogen, hydroxy or alkyl, and n is a number from 0 to 6; Y is carbonyl or a group -CH2-; Q represents a residue of a dihydroxy compound; and x is a number from 1 to 100] are useful sensitisers for use with Type II photoinitiators in the formulation of printing inks and other energy curable coatings.
摘要:
A compound represented by the general formula (I) [wherein ring A represents an optionally substituted 5- to 8-membered ring; ring B represents a further optionally substituted 4- to 10-membered ring; ring C represents a further optionally substituted benzene ring; X1 represents carbon; X2 represents carbon, oxygen, etc.; W represents nitrogen, etc.; Y11 represents a group represented by the formula CR2R3' (wherein R2 represents hydrogen, cyano, nitro, etc. and R3' represents hydrogen, cyano, nitro, etc.); Y21 represents a group represented by the formula CR4R5' (wherein R4 represents hydrogen, cyano, nitro, etc. and R5' represents hydrogen, cyano, nitro, etc.), etc.; R1 represents an electron-attracting group; and the symbol ... represents a single bond or double bond]. The compound is useful as an androgen receptor modulator. Also provided is a salt of the compound.
摘要翻译:由通式(I)表示的化合物[其中环A表示任选取代的5-至8-元环; 环B表示另外任选取代的4-至10-元环; 环C表示另一个任选取代的苯环; X1代表碳; X2代表碳,氧等; W代表氮等; Y11表示式CR2R3'(其中R2表示氢,氰基,硝基等,R3'表示氢,氰基,硝基等)表示的基团。 Y 21表示式CR 4 R 5'(式中,R 4表示氢,氰基,硝基等,R 5'表示氢,氰基,硝基等)表示的基团等。 R1表示吸电子基团; 符号表示单键或双键]。 该化合物可用作雄激素受体调节剂。 还提供了该化合物的盐。
摘要:
The invention provides novel alkoxyaminochalcone derivatives and analogues thereof. Use of the compounds, or compositions comprising them, as pharmaceutically active agents, in particular against bacterial and parasitic infections, is also disclosed. The invention further relates to a method for detecting inhibitory effects against e.g., bacteria, parasites, fungi, and helminths. The chalcones of the invention carry amino substituents and exhibit enhanced biological effects combined with improved metabolic and physicochemical properties, making the compounds useful as drug substances, in particular as antiparasitic, bacteriostatic, and bacteriocidal agents.
摘要:
The invention provides novel diamino-functionalised chalcone derivatives and analogues thereof. Use of the compounds, or compositions comprising them, as pharmaceutically active agents, in particular against bacterial and parasitic infections, is also disclosed. The invention further relates to a method for detecting inhibitory effects against e.g., bacteria, parasites, fungi, and helminths. The chalcones of the invention carry amino substituents and exhibit enhanced biological effects combined with improved metabolic and physicochemical properties, making the compounds useful as drug substances, in particular as antiparasitic and bacteriostatic agents.