Compounds of formula (I): wherein R1, R2, n and m are as defined in the specification, processes for their production, their uses and pharmaceutical compositions containing them.
[EN] SUBSTITUTED TOLYL FUNGICIDES<br/>[FR] FONGICIDES À BASE DE TOLYLE SUBSTITUÉ
申请人:DU PONT
公开号:WO2014066120A1
公开(公告)日:2014-05-01
Disclosed are compounds of Formula 1, including all stereoisomers, N-oxides, and salts thereof, wherein A, Q, R1 and R2 are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula 1 and methods for controlling plant disease caused by a fungal pathogen comprising applying an effective amount of a compound or a composition of the invention.
The present invention provides fungicidal 4-substituted-3-phenyl[(heterocyclylmethoxy)imino]methyl}-1,2,4-oxadiazol-5(4H)-one derivatives of formula (I)
wherein A represents a pyridyl or thiazole group and X1, Y1 to Y5 represent independently different substituents.
CLASS- AND ISOFORM-SPECIFIC HDAC INHIBITORS AND USES THEREOF
申请人:President and Fellows of Harvard College
公开号:US20150307444A1
公开(公告)日:2015-10-29
HDAC inhibitors of the general formula (I) and (II) and pharmaceutically acceptable salts thereof, as described herein, are useful as inhibitors of histone deacetylases or other deacetylases, and thus are useful for the treatment of various diseases and disorders associated with acetylase/deacetylase activity as described herein (e.g., cancer). In certain embodiments, the compounds of the invention selectively target either a class or isoform of the HDAC family. Another aspect of the invention provides an assay for determining the inhibitory effect of a test compound on an HDAC protein comprising: incubating the HDAC protein with a substrate of general formula (IIIc) in the presence of a test compound; and determining the activity of the HDAC protein.