875155-09-2

Upstream product

• 31601-41-9 N-(4-methoxy-2-methylphenyl)acetamide 
• 196194-97-5 N-(4-methoxy-2-methyl-5-nitrophenyl)acetamide 
• 196194-98-6 2-acetamido-5-methoxy-4-nitrobenzoic acid 
• 74-88-4 methyl iodide 
• 102-50-1 2-methyl-4-methoxyaniline 
• 67-56-1 methanol 
• 875155-08-1 2-acetylamino-5-fluoro-4-nitro-benzoic acid methyl ester 

Downstream Products

• 875155-10-5 2-amino-5-methoxy-4-nitro-benzoic acid methyl ester 
• 1378949-37-1 methyl 2-acetamido-4-amino-5-methoxybenzoate 

Relevant academic research and scientific papers

Double-sided α-helix mimetics

The design and synthesis of substituted bis- and tris-benzamides is reported in which the projection of side-chain residues on both sides of an α-helix is reproduced. The scaffold is conformationally constrained by a series of intramolecular hydrogen bonds, allowing for spatial and angular mimicry of the i, i+2, i+4 and i+6 side-chains in the case of the bis-benzamide, and may be extended to higher-order oligomers.

QUINAZOLINE DERIVATIVES

The present invention relates to 1H-Quinazoline-2,4-dione derivatives of formula (I) wherein the substituents are defined as in the specification, their preparation, their use as pharmaceuticals, and pharmaceutical compositions containing them.