3,4-DIHYDROQUINAZOLINE DERIVATIVE AND COMBINATION COMPRISING THE SAME
申请人:UNIVERSITY-INDUSTRY COOPERATION GROUP OF KYUNG HEE UNIVERSITY
公开号:US20170081291A1
公开(公告)日:2017-03-23
A 3,4-dihydroquinazoline derivative or a pharmaceutically acceptable salt thereof and a composition containing the same are provided. The 3,4-dihydroquinazoline derivative or a pharmaceutically acceptable salt thereof show activities of blocking an intracellular influx of calcium ions acting as a secondary signal essential to the proliferation and growth of cancer cells, thereby inducing the cell cycle arrest of cancer cells, and eventually reinforcing the efficacy of existing anti-cancer drugs. A combination comprising the above compound and another anti-cancer drug is also provided.
[EN] SUNSCREEN COMPOSITIONS CONTAINING A COMBINATION OF A LINEAR ULTRAVIOLET RADIATION-ABSORBING POLYETHER AND OTHER ULTRAVIOLET-SCREENING COMPOUNDS<br/>[FR] COMPOSITIONS DE PROTECTION SOLAIRE CONTENANT UNE COMBINAISON D'UN POLYÉTHER LINÉAIRE ABSORBANT LES RAYONNEMENTS ULTRAVIOLETS ET D'AUTRES COMPOSÉS DE PROTECTION CONTRE LES ULTRAVIOLETS
申请人:JOHNSON & JOHNSON CONSUMER INC
公开号:WO2017218390A1
公开(公告)日:2017-12-21
Sunscreen composition including a combination of a linear ultraviolet radiation absorbing polyether that includes a covalently bound UV-chromophore, and at least one non-polymeric UV-screening compounds.
Quinoline-derived amide modulators of vanilloid VR1 receptor
申请人:——
公开号:US20040192728A1
公开(公告)日:2004-09-30
This invention is directed to vanilloid receptor VR1 ligands. More particularly, this invention relates to quinoline-derived amides that are potent antagonists or agonists of VR1 which are useful for the treatment and prevention of inflammatory and other pain conditions in mammals.
QUINOLINE-DERIVED AMIDE MODULATORS OF VANILLOID VR1 RECEPTOR
申请人:Codd Ellen
公开号:US20080300236A1
公开(公告)日:2008-12-04
This invention is directed to vanilloid receptor VR1 ligands. More particularly, this invention relates to quinoline-derived amides that are potent antagonists or agonists of VR1 which are useful for the treatment and prevention of inflammatory and other pain conditions in mammals.