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5-Bromoindirubin is a synthetic small molecule belonging to the indirubin family of compounds. It is structurally characterized as a brominated derivative of indirubin and has the chemical formula C16H9BrN2O2. The compound acts primarily as an inhibitor of cyclin-dependent kinase 2 (CDK2), with an IC50 value of approximately 80 nM[1]. This mechanism suggests potential utility in modulating cell cycle progression and proliferation. Preclinical research indicates that derivatives of 5-bromoindirubin exhibit anticancer activity by inhibiting cell cycle-related kinases such as CDKs and glycogen synthase kinase‑3β[3][5]. While it has been explored for its anticancer properties and structure–activity relationships in experimental settings, there are currently no approved indications or advanced clinical trials for this compound.
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