The invention relates to malonamide derivatives of formula
wherein each of the variables are as defined herein and to pharmaceutically acceptable acid addition salts, optically pure enantiomers, racemates and diastereomeric mixtures thereof. These compounds are γ-secretase inhibitors and may be used for the treatment of Alzheimer's disease.
[EN] TEAD INHIBITORS AND USES THEREOF<br/>[FR] INHIBITEURS DE TEAD ET LEURS UTILISATIONS
申请人:CEDILLA THERAPEUTICS INC
公开号:WO2022204452A1
公开(公告)日:2022-09-29
The present application relates to compounds of formula (I'), pharmaceutically acceptable compositions thereof, and methods of using the same. The compounds of formula I' are TEAD inhibitors, useful in the treatment of cancer.
Nouvelles méthodes de préparation des 2-F-alkyléthylamines
作者:F. Szönyi、F. Guennouni、A. Cambon
DOI:10.1016/s0022-1139(00)81256-7
日期:1991.11
2-F-Alkylethylamines are difficult to obtain on the laboratory scale and their preparation without the formation of secondary products has never been reported. In this work we demonstrate that it is possible to obtain these compounds univocally and with easy to use methods. The spectral data of these compounds are reported for the first time.
Hydrophobic and oleophobic surface modification using gelling agents derived from amino acids
作者:Anilkumar Raghavanpillai、Vincent A. Franco、Walter E. Meredith
DOI:10.1016/j.jfluchem.2011.10.015
日期:2012.3
series of fluorinated and non-fluorinated organogelators containing urea and amide functionalities was synthesized from readily available amino acid building blocks. These derivatives showed excellent gelation behavior in a variety of organic solvents at low concentrations ranging from 0.5–4 wt%. Gelation in the presence of a fibrous substrate led to a gel-coated surface, which upon drying provided