406234-86-4

Usage

Chemical structure

A pyrazole derivative with a cyclohexylmethyl group attached to the nitrogen atom and an iodine atom at the 4-position of the pyrazole ring.

Potential applications

Medicinal chemistry and pharmaceutical research

Biological activity

May exhibit biological activity related to its structure

Safety precautions

Handle with care and follow proper safety protocols due to potential reactivity and toxicity

Research status

Further research is needed to fully understand its properties and potential uses

Upstream product

• 3469-69-0 4-iodopyrazole 
• 2550-36-9 Cyclohexylmethyl bromide 

Relevant academic research and scientific papers

Structure-affinity relationships of the affinity of 2-pyrazolyl adenosine analogues for the adenosine A2A receptor

The structure-affinity relationships of two novel 2-substituted adenosine series containing a substituted pyrazole attached at the N-1 or C-4 position for the adenosine (ADO) A2A receptor are described. Compounds in the 2-(N-1-pyrazolyl) adenos

N-acylsulfonamide apoptosis promoters

N-Benzoyl arylsulfonamides having the formula are BCL-Xl inhibitors and are useful for promoting apoptosis. Also disclosed are BCL-Xl inhibiting compositions and methods of promoting apoptosis in a mammal.

N-Acylsulfonamide apoptosis promoters

N-Benzoyl arylsulfonamides having the formula Are BCL-X1 inhibitors and are useful for promoting apoptosis. Also disclosed are BCL-X1 inhibiting compositions and methods of promoting apoptosis in a mammal.