110429-24-8

Upstream product

• 529-23-7 o-aminobenzaldehyde 
• 171917-54-7 Methyl 3-(benzyloxy)quinoline-2-carboxylate 
• 100-51-6 benzyl alcohol 

Downstream Products

• 171917-54-7 Methyl 3-(benzyloxy)quinoline-2-carboxylate 
• 174311-16-1 N¹-SES-N⁶-<<3-(benzyloxy)quinolyl>-2-carbonyl>-(D-Ser-Pip-Gly-Sar-NMe-Val)2(serine hydroxyl) dilactone 
• 1515606-02-6 (N-[(3-benzyloxy)quinolyl]-2-carbonyl-D-Ser-(S)-β-L-triisopropylsilyloxy-Pip-Gly-Sar-N-Me-L-Val)₂ 
• 15462-45-0 Methyl 3-hydroxyquinoline-2-carboxylate 

Relevant academic research and scientific papers

Synthesis of key sandramycin analogs: Systematic examination of the intercalation chromophore

The preparation and examination of 2-22 constituting a systematic study of the chromophore of sandramycin (1) are detailed. Fluorescence quenching studies were used to establish binding constants for 1-24 within calf thymus DNA, within a single high affin

Substituted quinoline-2-carboxamides, their preparation and their use as pharmaceuticals, and intermediates

The invention relates to substituted quinoline-2-carboxylic acid amides of the formula I STR1 their preparation and their use, and intermediates which are formed in the preparation of the compounds of the formula I. The compounds according to the inventio

Substituted quinoline-2-carboxamides, their preparation and their use as pharmaceuticals, and intermediates

The invention relates to substituted quinoline-2-carboxylic acid amides of the formula I STR1 their preparation and their use, and intermediates which are formed in the preparation of the compounds of the formula I. The compounds according to the inventio

SUBSTITUTED HETEROCYCLIC CARBOXYAMIDES, THEIR PREPARATION AND THEIR USE AS PHARMACEUTICALS

The invention relates to compounds of the formula I, to a process for their preparation and to their use as pharmaceuticals. In particular, the compounds are used as inhibitors of prolyl-4-hydroxylase and as inhibitors of collagen biosynthesis, as pharmac