69739-62-4Relevant academic research and scientific papers
Beyond the BET Family: Targeting CBP/p300 with 4-Acyl Pyrroles
Hügle, Martin,Lucas, Xavier,Ostrovskyi, Dmytro,Regenass, Pierre,Gerhardt, Stefan,Einsle, Oliver,Hau, Mirjam,Jung, Manfred,Breit, Bernhard,Günther, Stefan,Wohlwend, Daniel
, p. 12476 - 12480 (2017/09/13)
Bromodomain and extra-terminal domain (BET) inhibitors are widely used both as chemical tools to study the biological role of their targets in living organisms and as candidates for drug development against several cancer variants and human disorders. However, non-BET bromodomains such as those in p300 and CBP are less studied. XDM-CBP is a highly potent and selective inhibitor for the bromodomains of CBP and p300 derived from a pan-selective BET BRD-binding fragment. Along with X-ray crystal-structure analysis and thermodynamic profiling, XDM-CBP was used in screenings of several cancer cell lines in vitro to study its inhibitory potential on cancer cell proliferation. XDM-CBP is demonstrated to be a potent and selective CBP/p300 inhibitor that acts on specific cancer cell lines, in particular malignant melanoma, breast cancer, and leukemia.
Catalytic asymmetric intermolecular bromoesterification of unfunctionalized olefins
Li, Lijun,Su, Cunxiang,Liu, Xiaoqin,Tian, Hua,Shi, Yian
, p. 3728 - 3731 (2014/08/05)
An asymmetric intermolecular bromoesterification of unfunctionalized olefins catalyzed by (DHQD)2PHAL is described. Optically active bromoesters can be obtained with up to 92% ee.
Intramolecular Aromatic Cyclizations of Alkenyliodonium Tetrafluoroborates
Ochiai, Masahito,Takaoka, Yoshikazu,Sumi, Kenzo,Nagao, Yoshimitsu
, p. 1382 - 1384 (2007/10/02)
1,2-Dihydronaphthalene and 2H-chromene derivatives have been synthesized by thermal intramolecular cyclizations of alkenyliodonium tetrafluoroborates under mild reaction conditions.
