Discovery of a Full-Color-Tunable Fluorescent Core Framework through Direct CH (Hetero)arylation of N-Heterocycles
作者:Bo Liu、Zhi Wang、Ningjie Wu、Mingliang Li、Jingsong You、Jingbo Lan
DOI:10.1002/chem.201103329
日期:2012.2.6
coverage of emission wavelengths in the visible region (405–616 nm) with large Stokes shifts in C3‐Indo‐Fluor may be straightforwardly and succinctly achieved by the palladium‐catalyzed direct CHarylation of indolizines at the C3 position of the pyrrole ring (see figure). The fluorophores have successfully marked A375 cells.
POHJAHLA E., ACTA CHEM. SCAND. <ACSA-A4>, 1975, B29, NO 10, 1079-1084
作者:POHJAHLA E.
DOI:——
日期:——
INDOLIZINE DERIVATIVES AS PHOSPHOINOSITIDE 3-KINASES INHIBITORS
申请人:Chiesi Farmaceutici S.p.A.
公开号:EP3157920B1
公开(公告)日:2019-08-07
US9527869B2
申请人:——
公开号:US9527869B2
公开(公告)日:2016-12-27
[EN] INDOLIZINE DERIVATIVES AS PHOSHOINOSITIDE 3-KINASES INHIBITORS<br/>[FR] DÉRIVÉS D'INDOLIZINE SERVANT D'INHIBITEURS DES PHOSHOINOSITIDE 3-KINASES
申请人:CHIESI FARMA SPA
公开号:WO2015193263A1
公开(公告)日:2015-12-23
The invention relates to compounds inhibiting phosphoinositide 3-kinases (PI3K), to pharmaceutical compositions comprising them and therapeutic use thereof in the treatment of disorders associated with PI3K enzymes.