1146783-07-4

Upstream product

• 1146763-80-5 4-chloro-1-(4-chlorophenyl)-2-methyl-5-(2,4,6-trifluorophenyl)-1H-imidazole 
• 124-41-4 sodium methylate 
• 1192241-83-0 (4-chlorophenyl)-[1-(2,4,6-trifluorophenyl)meth-(E)-ylidene]amine 
• 1192241-84-1 1-(4-chlorophenyl)-5-(2,4,6-trifluorophenyl)-1H-imidazole 
• 58551-83-0 2,4,6-trifluorobenzaldehyde 
• 106-47-8 4-chloro-aniline 
• 1193347-97-5 4-chloro-1-(4-chlorophenyl)-5-(2,6-difluoro-4-methoxyphenyl)-1H-imidazole 
• 74-88-4 methyl iodide 
• 1416326-85-6 (4-chlorophenylamino)-(2,4,6-trifluorophenyl)acetonitrile 

Relevant academic research and scientific papers

Multitargeted Imidazoles: Potential Therapeutic Leads for Alzheimer's and Other Neurodegenerative Diseases

Alzheimer's disease (AD) is a complex, multifactorial disease in which different neuropathological mechanisms are likely involved, including those associated with pathological tau and Aβ species as well as neuroinflammation. In this context, the development of single multitargeted therapeutics directed against two or more disease mechanisms could be advantageous. Starting from a series of 1,5-diarylimidazoles with microtubule (MT)-stabilizing activity and structural similarities with known NSAIDs, we conducted structure-Activity relationship studies that led to the identification of multitargeted prototypes with activities as MT-stabilizing agents and/or inhibitors of the cyclooxygenase (COX) and 5-lipoxygenase (5-LOX) pathways. Several examples are brain-penetrant and exhibit balanced multitargeted in vitro activity in the low μM range. As brain-penetrant MT-stabilizing agents have proven effective against tau-mediated neurodegeneration in animal models, and because COX-and 5-LOX-derived eicosanoids are thought to contribute to Aβ plaque deposition, these 1,5-diarylimidazoles provide tools to explore novel multitargeted strategies for AD and other neurodegenerative diseases.

Synthesis and fungicidal activity of tubulin polymerisation promoters. Part 3: Imidazoles

A novel class of experimental fungicides has been discovered, which consists of special tetrasubstituted imidazoles. They are highly active against important phytopathogens, such as Botrytis cinerea (grey mould), Uncinula necator (grape powdery mildew), M

FUNGICIDAL SUBSTITUTED AZOLES

Disclosed are compounds of Formula 1, including all geometric and stereoisomers, N-oxides, and salts thereof, wherein J is Q2 or R1;X is N, CR2 or CQ3;Y is N or CR3;Z is N or CR4; andQ1, Q2, Q3, R1 R2 and R3 are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula 1 and methods for controlling plant disease caused by a fungal pathogen comprising applying an effective amount of a compound or a composition of the invention.

FUNGICIDAL MIXTURES

Disclosed is a fungicidal composition comprising (a) at least one compound selected from the compounds of Formula 1, N-oxides, and salts thereof, wherein R1, R2, Q1 and Q2 are as defined in the disclosure; and (b) at least one additional fungicidal compound. Also disclosed is a method for controlling plant diseases caused by fungal plant pathogens comprising applying to the plant or portion thereof, or to the plant seed, a fungicidally effective amount of a compound of Formula 1, an N-oxide, or salt thereof (e.g., as a component in the aforesaid composition). Also disclosed is a composition comprising: (a) at least one compound selected from the compounds of Formula 1 described above, N-oxides, and salts thereof; and at least one invertebrate pest control compound or agent.

NOVEL IMIDAZOLE DERIVATIVES HAVING MICROBIOCIDAL ACTIVITY

The present invention relates to novel imidazole derivatives of formula I as active ingredients which have microbiocidal activity, in particular fungicidal activity wherein (I) wherein R1 is halogen, C1-C4alkyl or C1

FUNGICIDAL SUBSTITUTED AZOLES

Disclosed are compounds of Formula (1), including all geometric and stereoisomers, N-oxides, and salts thereof, wherein J is Q2or R1; X is N, CR2or CQ3; Y is N or CR3; Z is N or CR4; and Q