92190-35-7

Upstream product

• 493-72-1 5-phenyl-cyclohexane-1,3-dione 
• 64-19-7 acetic acid 
• 75-36-5 acetyl chloride 

Downstream Products

• 2057-01-4 2-acetyl-5-phenylcyclohexane-1,3-dione 
• 17799-39-2 5-phenyl-[1,1'-bi(cyclohexan)]-1-en-3-one 

Relevant academic research and scientific papers

Tetrahydroindazole inhibitors of CDK2/cyclin complexes

Over 50 tetrahydroindazoles were synthesized after 7-bromo-3,6,6-trimethyl-1-(pyridin-2-yl)-5,6,7,7a-tetrahydro-1H-indazol-4(3aH)-one (3) was identified as a hit compound in a high throughput screen for inhibition of CDK2 in complex with cyclin A. The activity of the most promising analogues was evaluated by inhibition of CDK2 enzyme complexes with various cyclins. Analogues 53 and 59 showed 3-fold better binding affinity for CDK2 and 2- to 10-fold improved inhibitory activity against CDK2/cyclin A1, E, and O compared to screening hit 3. The data from the enzyme and binding assays indicate that the binding of the analogues to a CDK2/cyclin complex is favored over binding to free CDK2. Computational analysis was used to predict a potential binding site at the CDK2/cyclin E1 interface.