摘要:
The invention relates to (hetero)aryl cyclopropylamine compounds, including particularly the compounds of formula (I) as described and defined herein, and their use in therapy, including, e.g ., in the treatment or prevention of cancer, a neurological disease or condition, or a viral infection.
摘要:
Disclosed is an N-substituted phenyl glycine (dabigatran etexilate intermediate) preparation method unreported in any document, the method comprising: utilizing cheap and easily available substituted aniline (1) as raw material to condense with glyoxylic acid to form an imine, while conducting hydrogenation reduction to obtain N-(substituted phenyl) glycine. The synthetic route is not reported in any document, and the raw material is cheap and easily available; in addition, the present invention has simple unit operation and low device requirement, and is suitable for large-scale industrial production.
摘要:
The present disclosure relates generally, but not exclusively, to compounds and their use as enzyme interacting agents, in particular, agents which interact with one or more enzymes in the sphingolipid biosynthesis pathway. The disclosure further relates to the use of such compounds as research tools, use in therapy, to compositions and agents comprising said compounds, and to methods of treatment using said compounds.
摘要:
It is intended to provide compounds represented by the following general formula (I) which have a high affinity for human thyroid hormone receptors, in particular, human thyroid hormone receptor β, medicinal compositions containing the same, and use thereof: (I) wherein W represents O, S(O)m, CH2, etc.; R1 represents halogeno, lower alkyl, halo(lower alkyl), CN, etc.; R2 represents hydrogen, halogeno, lower alkyl, etc.; R3 represents hydroxy, etc.; R4 represents hydrogen, halogeno, alkyl, halo(lower alkyl), substituted alkyl, aryl, aralkyl, alkoxy, substituted alkoxy, alkanoyl, aroyl, -CONR7(R8), -S(O)mR9, -SO2NR7(R8), etc.; R5 represents hydrogen, halogeno, alkyl, substituted alkyl, etc.; and A represents -N(R6)CO-A1-COR10, etc.
摘要:
The present invention relates to non-steroidal ligands for use in nuclear receptor-based inducible gene expression system, and a method to modulate exogenous gene expression in which an ecdysone receptor complex comprising: a DNA binding domain; a ligand binding domain; a transactivation domain; and a ligand is contacted with a DNA construct comprising: the exogenous gene and a response element; wherein the exogenous gene is under the control of the response element and binding of the DNA binding domain to the response element in the presence of the ligand results in activation or suppression of the gene.