81635-83-8

Upstream product

• 930-69-8 sodium thiophenolate 
• 65193-81-9 2,4,6-trimethyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid 2-chloro-ethyl ester ethyl ester 
• 100303-72-8 2-(phenylthio)ethyl-acetylacetate 
• 41867-20-3 ethyl (E)-3-aminobut-2-enoate 
• 75-07-0 acetaldehyde 
• 699-12-7 2-(phenylthio)ethanol 
• 626-34-6 ethyl aminocrotonate 

Relevant academic research and scientific papers

4-ALKYL-1,4-DIHYDROPYRIDINES WITH PAF-ANTAGONIST ACTIVITY

4-alkyl-1,4-dihyropyridines, with PAF-antagonist activity, of formula (I) wherein R is saturated C 1-C 4, R' is saturated C. sub.1-C. sub.6 alkyl which may be interrupted by an oxygen atom, or 2-tetrahydrofurfuryl and R 2 is saturated C 1-C 4 or phenyl, t

4-Alkyl-1,4-dihydropyridines Derivatives as Specific PAF-Acether Antagonists

A new series of 4-alkyl-1,4-dihydropyridines (1,4-DHP) were synthesized and evaluated for their ability to inhibit washed rabbit platelet aggregation induced by PAF-acether (1-O-hexadecyl/octadecyl-2-O-acetyl-sn-glycero-3-phosphorylcholine) and to reverse

Esters of 1,4-dihydropyridine-3- and -3,5-carbothiolic acids

Methods for the preparation of esters of 1,4-dihydropyridine-3- and -3,5-carbothiolic acids were developed, and their structure and reactivity were studied. A comparative analysis was made of the spectroscopic characteristics of sulfur-containing esters of the 1,4-dihydropyridine series and their oxygen analogs. More strongly expressed electron-acceptor properties of the COSAlk groupings as compared with alkoxycarbonyl substituents were observed.