160937-99-5

Upstream product

• 5468-77-9 2-bromo-N,N-dimethylethanamide 
• 2627-86-3 (S)-1-phenyl-ethylamine 

Downstream Products

• 180344-13-2 N¹-<1(S)-(cyclohexylmethyl)-2(R),3(S)-dihydroxy-5-methylhexyl>-N⁴-<2-(dimethylamino)-2-oxoethyl>-N⁴-<1(S)-phenylethyl>-2(R)-<<(2,2,2-trichloroethoxy)carbonyl>amino>-4-thiazolylmethylbutanediamide 
• 160938-17-0 N-dimethylcarbamoylmethyl-N-(1-phenyl-ethyl)-2-[2-(2,2,2-trichloro-ethoxycarbonylamino)-thiazol-4-ylmethyl]-succinamic acid 
• 160447-15-4 N¹-(1-cyclohexylmethyl-2,3-dihydroxy-5-methyl-hexyl)-N⁴-dimethylcarbamoylmethyl-N⁴-(1-phenyl-ethyl)-2-(1-trityl-1H-imidazol-4-ylmethyl)-succinamide 
• 180344-14-3 3-<4-<<2-(dimethylamino)-2-oxoethyl><1(S)-phenylethyl>amino>-1,4-dioxo-2(R)-<<2-<<(2,2,2-trichloroethoxy)carbonyl>amino>-4-thiazolyl>methyl>butyl>-4(S)-(1-methylethyl)-2-oxazolidinone 

Relevant academic research and scientific papers

Effects of thionation and fluorination on cis-trans isomerization in tertiary amides: An investigation of N -alkylglycine (Peptoid) rotamers

Peptoids constitute a class of peptidomimetics with potential as protease resistant, biologically active ligands. To harness the full potential of such compounds, however, detailed predictive insight into their propensity to adopt well-defined secondary s

Discovery of non-peptidic P2-P3 butanediamide renin inhibitors with high oral efficacy

A new series of non-peptidic renin inhibitors having a 2-substituted butanediamide moiety at the P2 and P3 positions has been identified. The optimized inhibitors have IC50 values of 0.8 to 1.4nM and 2.5 to 7.6nM in plasma renin assays at pH 6.0 and 7.4, respectively. When evaluated in the normotensive cynomolgus monkey model, two of the most potent inhibitors were orally active at a dose as low as 3mg/kg. These potent renin inhibitors are characterized by oral bioavailabilities of 40 and 89% in the cynomolgus monkey. Inhibitor 3z (BILA 2157 BS) was selected as candidate for pre-development. Copyright (C) 1999 Elsevier Science Ltd.