101335-99-3

Usage

InChI:InChI=1/C18H22O2S/c19-18(20)12-5-4-10-16-13-14-17(21-16)11-6-9-15-7-2-1-3-8-15/h1-3,7-8,13-14H,4-6,9-12H2,(H,19,20)

Upstream product

• 501-52-0 3-Phenylpropionic acid 
• 101336-00-9 methyl 5-[5-(1-oxo-3-phenylpropyl)-thien-2-yl]-valerate 
• 40027-94-9 3-phenyl-1-(2-thienyl)propan-1-one 
• 29908-27-8 2-(3-phenylpropyl)thiophene 
• 1026420-25-6 5-Oxo-5-[5-(3-phenyl-propyl)-thiophen-2-yl]-pentanoic acid 

Downstream Products

• 1026170-72-8 1-Morpholin-4-yl-5-[5-(3-phenyl-propyl)-thiophen-2-yl]-pentan-1-one 
• 101336-01-0 5-<5-(3-phenylpropyl)-2-thienyl>pentanoic acid sodium salt 
• 101336-13-4 5-<5-(3-phenylpropyl)-2-thienyl>pentanoic acid ethyl ester 

Relevant academic research and scientific papers

Amino derivatives of phenyl alkyl thiophene as inhibitors of bone resorption. Structure-activity relationship

Metabolism of arachidonic acid through the 5-lipoxygenase (LO) pathway generates compounds that stimulate osteoclastic bone resorption; since LO metabolites might play a role in bone loss due to excessive resorption it was tried to develop a series of antiresorptive agents starting from an already known LO inhibitor. Of the 35 compounds synthesized, 11 strongly inhibited (10 μmol/l) retinoic acid-induced bone resorption in cultured mouse calvariae; they were also tested for their effect on LO activity using rat peritoneal neutrophils, but no correlation could be drawn between inhibition of LO and bone resorption. Other pathways, still to be identified, must therefore be targeted by these compounds even though LO inhibition might contribute to their effects on bone. Two compounds selected for further studies were found active on parathyroid hormone-induced osteolysis, while they had no effect on basal resorption; they must, therefore, act at some key point in the process of activation of osteoclastic resorption. This series of compounds may represent a new way for the treatment of bone loss due to excessive resorption.

Omega-aryl-alkylthienyl-compounds and process for the treatment of chronically inflammatory processes in humans

The invention relates to new ω-aryl-alkylthienyl compounds having the Formula I STR1 i.e. omega-aryl-alkyl thienyl alkanoic acids and, respectively, omega-aryl-alkyl thienyl alkenoic acids, the alkali metal salts of such acids and certain esters thereof.