- HISTONE ACETYLTRANSFERASE (HAT) INHIBITOR AND USE THEREOF
-
The present invention relates to a histone acetyltransferase (HAT) inhibitor. Provided are a compound represented by general formula I, a pharmaceutically acceptable salt, a stereoisomer, an enantiomer, a diastereomer, an atropisomer, a racemate, a polymorph, a solvate or an isotope-labeled compound (including deuterium substitution) thereof, a preparation method therefor, a pharmaceutical composition comprising the same, and use thereof in the treatment of various HAT-related diseases or conditions.
- -
-
Paragraph 0091; 0094
(2021/02/25)
-
- Enantioselective synthesis of 2,3-disubstituted indanones via Pd-catalyzed intramolecular asymmetric allylic alkylation of ketones
-
A Pd-catalyzed intramolecular asymmetric allylic alkylation (AAA) reaction with "hard" carbanions has been developed for the first time, affording 2,3-disubstituted indanones with high diastereo- and enantioselectivities. The transformation of these produ
- Li, Xiao-Hui,Zheng, Bao-Hui,Ding, Chang-Hua,Hou, Xue-Long
-
supporting information
p. 6086 - 6089
(2014/01/06)
-
- BENZIMIDAZOLE INHIBITORS OF LEUKOTRIENE PRODUCTION
-
The present invention relates to compounds of formula (I) and pharmaceutically acceptable salt thereof, wherein R1-R7 are as defined herein. The invention also relates to pharmaceutical compositions comprising these compounds, method
- -
-
Page/Page column 137
(2011/06/25)
-
- 1,6 - SUBSTITUTED (3R,6R) -3- (2,3-DIHYDRO-1H-INDEN-2-YL)-2,5-PIPERAZINEDIONE DERIVATIVES AS OXYTOCIN RECEPTOR ANTAGONISTS FOR THE TREATMENT OF PRE-TERM LABOUR, DYSMENORRHEA AND ENDOMETRIOSIS
-
The present invention relates to compound S of Formula (I).
- -
-
Page/Page column 50
(2008/06/13)
-