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A synthetic small molecule belonging to the hypoxanthine class of purines, characterized by a cyclohexylmethoxy group at the purine C6 position and an anilino (phenylamino) group at C2. It acts as an ATP competitive inhibitor of cyclin-dependent kinase 2 (CDK2), a key regulator of cell cycle progression. The compound has been studied primarily in preclinical settings as a tool compound for probing CDK function and selectivity, but it is not approved for clinical use and has no known therapeutic indications[1][8]. Its mechanism involves binding to the ATP site of CDK2, thereby inhibiting its kinase activity.
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