13033-49-3

Upstream product

• 100-83-4 meta-hydroxybenzaldehyde 
• 75-31-0 isopropylamine 

Downstream Products

• 213891-23-7 N-(3-hydroxybenzyl)isopropylamine 
• 213891-19-1 3-[N-isopropyl-N-(3-hydroxybenzyl)amino]propoxyxanthen-9-one 
• 142677-46-1 1-isopropyl-5-(3-methoxyphenyl)imidazole 
• 142677-47-2 5-(3-isobutoxyphenyl)-1-isopropylimidazole 
• 142677-48-3 5-(3-hexyloxyphenyl)-1-isopropylimidazole 
• 142677-49-4 1-isopropyl-5-(3-octyloxyphenyl)imidazole 
• 142706-10-3 1-isopropyl-5-(3-phenethyloxyphenyl)imidazole 
• 141364-90-1 5-(3-benzyloxyphenyl)-1-isopropylimidazole 
• 142677-51-8 1-isopropyl-5-(3-α-methylbenzyloxyphenyl)imidazole 
• 142677-50-7 5-(3-geranyloxyphenyl)-1-isopropylimidazole 
• 142677-53-0 5-<3-(3-chlorobenzyloxy)phenyl>-1-isopropylimidazole 
• 142677-57-4 5-<3-(4-fluorobenzyloxy)phenyl>-1-isopropylimidazole 
• 142677-54-1 5-<3-(4-chlorobenzyloxy)phenyl>-1-isopropylimidazole 
• 142677-55-2 1-isopropyl-5-<3-(3-methoxybenzyloxy)phenyl>imidazole 

Relevant academic research and scientific papers

Acetylcholinesterase inhibitors: Synthesis and structure-activity relationships of ω-[N-methyl-N-(3-alkylcarbamoyloxyphenyl)- methyl]aminoalkoxyheteroaryl derivatives

Acetylcholinesterase (ACHE) inhibitors are one of the most actively investigated classes of compounds in the search for an effective treatment of Alzheimer's disease. This work describes the synthesis, AChE inhibitory activity, and structure-activity relationships of some compounds related to a recently discovered series of AChE inhibitors: the ω-[N-methyl-N-(3- alkylcarbamoyloxyphenyl)methyl]aminoalkoxyxanthen-9-ones. The influence of structural variations on the inhibitory potency was carefully investigated by modifying different parts of the parent molecule, and a theoretical model of the binding of one representative compound to the enzyme was developed. The biological properties of the series were investigated in some detail by considering not only the activity on isolated enzyme but the selectivity with respect to butyrylcholinesterase (BuChE) and the in vitro inhibitory activity on rat cerebral cortex as well. Some of the newly synthesized derivatives, when tested on isolated and/or AChE-enriched rat brain cortex fraction, displayed a selective inhibitory activity and were more active than physostigmine. In particular, compound 13, an azaxanthone derivative, displayed the best rat cortex AChE inhibition (190-fold higher than physostigmine), as well as a high degree of enzyme selectivity (over 60-fold more selective for AChE than for BuChE). When tested in the isolated enzyme, compound 13 was less active, suggesting some differences either in drug availability/biotransformation or in the inhibitor-sensitive residues of the enzyme when biologically positioned in rat brain membranes.

Synthesis and Insect Growth Regulatory Activity of 1,5-Disubstituted Imidazoles with Non-terpene Chains

1-Isobutyl-5-(4-phenoxyphenyl)imidazole (KK-98), an inhibitor of juvenile hormone (JH) biosynthesis in the cockroach, and related imidazole compounds were evaluated against silkworm, Bombyx mori, for their activity to induce precocious metamorphosis.KK-98