The present invention provides 5-membered heterocycle compounds represented by the following general formula (I):
The present compounds have a superior acid secretion inhibitory effect, and shows an antiulcer activity and the like.
[EN] PIPERIDINES AS MENIN INHIBITORS<br/>[FR] PIPÉRIDINES EN TANT QU'INHIBITEURS DE MÉNINE
申请人:UNIV MICHIGAN
公开号:WO2017192543A1
公开(公告)日:2017-11-09
The present disclosure provides compounds represented by Formula (I): (Formula(I)) and the pharmaceutically acceptable salts, hydrates, and solvates thereof, wherein R2, R3a, R3b, A, G, X, and Y are as defined as set forth in the specification. The present disclosure also provides compounds of Formula (I) for use to treat a condition or disorder responsive to menin inhibition such as cancer.
Disclosed is a compound represented by formula (1) or a pharmacologically acceptable salt thereof (In the formula, A represents a group that is represented by formula (A-1); R
1a
and R
1b
may be the same or different and each independently represents a C
1-6
alkyl group which may be substituted by one to three halogen atoms; m and n each independently represents an integer of 0-5; X
1
represents a hydroxyl group or an aminocarbonyl group; Z
1
represents a single bond or the like; and R
2
represents an optionally substituted C
1-6
alkyl group, an optionally substituted C
6-10
aryl group or the like.)
Quinoline derivatives as neurokinin receptor antagonists
申请人:Carling William Robert
公开号:US20090054440A1
公开(公告)日:2009-02-26
The present invention relates to substituted quinoline hydrazides of Formula (I): wherein R
1
, R
2
, R
3
, R
4
, R
5
, X, Y and Z are defined herein, pharmaceutical compositions comprising them and their use in treating diseases mediated by neurokinin-2 and/or neurokinin-3 (NK-3) receptors. These compounds can thus be used in methods of treatment to suppress and treat such disorders.
Selected compounds are effective for treatment of diseases, such as cell proliferation or apoptosis mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable derivatives thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving stroke, cancer and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.