91944-98-8

Upstream product

• 300-87-8 3,5-dimethyl-1,2-oxazole 
• 91944-99-9 4-<(6-bromohexyl)-oxy>benzonitrile 
• 629-03-8 1 ,6-dibromohexane 
• 100-42-5 styrene 
• 7439-93-2 lithium 
• 767-00-0 4-cyanophenol 

Downstream Products

• 91945-32-3 1-(4-{[7-(3-methyl-5-isoxazolyl)heptyl]oxy}phenyl)ethanone 
• 98360-44-2 ethyl 4-<<7-(3-methyl-5-isoxazolyl)heptyl>oxy>benzenecarboximidate hydrochloride 
• 91945-23-2 5-[7-(4-ethoxycarbonylphenoxy)heptyl]-3-methylisoxazole 
• 91945-35-6 3-methyl-5-[7-(4-carboxamidophenoxy)heptyl]isoxazole 
• 91945-17-4 4-<<7-(3-methyl-5-isoxazolyl)heptyl>oxy>benzoic acid 
• 112270-41-4 (S)-5-{7-[4-(4,5-Dihydro-4-propyl-2-oxazolyl)phenoxy]heptyl}-3-methylisoxazole 
• 98034-32-3 3-Methyl-5-{7-[4-(4-methyl-4,5-dihydro-oxazol-2-yl)-phenoxy]-heptyl}-isoxazole 
• 98033-63-7 5-{7-[4-(4,5-dihydro-5-methoxymethyl-2-oxazolyl)phenoxy]heptyl}-3-methylisoxazole 
• 98033-97-7 5-{7-[4-(4,5-dihydro-5-hydroxymethyl-2-oxazolyl)phenoxy]heptyl}-3-methylisoxazole 
• 120666-36-6 5-(7-(4-(4,5-dihydro-4-methyl-2-oxazolyl)phenoxy)heptyl)-3-methylisoxazole 
• 98033-99-9 (2-{4-[7-(3-Methyl-isoxazol-5-yl)-heptyloxy]-phenyl}-4,5-dihydro-oxazol-4-yl)-methanol 
• 98054-14-9 5-{7-[4-(4,4-Dimethyl-4,5-dihydro-oxazol-2-yl)-phenoxy]-heptyl}-3-methyl-isoxazole 
• 87495-31-6 disoxaril 

Relevant academic research and scientific papers

Di-heterocyclic compounds and their use as antiviral agents

Compounds of the formulas: STR1 wherein Het is an oxazole or oxazine moiety; X is O, S or SO, n is an integer from 3 to 9, Y is an aliphatic bridge; and the various R groups represent hydrogen or various substituents as described herein, are useful as antiviral agents, especially against picornaviruses. N-(Chloroalkyl)amide intermediates for the compounds of Formula I are also active as antiviral agents. Related compounds outside the scope of the above formulas are also disclosed.

[[(4,5-Dihydro-2-oxazolyl)phenoxy]alkyl]isoxazoles. Inhibitors of picornavirus uncoating

A series of [[(4,5-dihydro-2-oxazolyl)phenoxy]alkyl]isoxazoles has been synthesized and evaluated as antipicornavirus agents. The effect of alkyl groups in the 4- and 5-position of the oxazoline ring, as well as the alkyl chain length, on antiviral activi

Isoxazoles with antipicornavirus activity

The synthesis and evaluation of a series of 3,5-disubstituted isoxazoles as antipicornavirus agents have led to the discovery of several compounds effective in vitro against rhinovirus type 2 and poliovirus type 2. Compound 32 was found more effective tha