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Indirubin

Clinical trial

Mechanism of Action

CDK2 inhibition; anti-leukemic via cell cycle arrest; anti-inflammatory through STAT3 inhibition
CDK2/cyclin E inhibition, GSK-3β inhibition, anti-leukemic, anti-inflammatory via AhR (aryl hydrocarbon receptor)
CDK inhibition (cyclin-dependent kinase); anti-inflammatory; antiviral; antileukaemic
Anti-inflammatory; CDK inhibition; anti-leukemic; antiviral via interferon induction
CDK inhibition, anti-leukemic, anti-inflammatory, antiviral

Research Notes

Indirubin gained clinical validation treating chronic myelogenous leukemia in the 1970s-80s with complete remission in a significant proportion of patients.

Historically used in CML treatment in China before imatinib era. CDK inhibition confirmed as mechanism. Anti-psoriatic effects via AhR activation — basis for topical psoriasis use.

Used in traditional Chinese leukaemia treatment; indirubin and analogues are potent CDK2/GSK-3β inhibitors; synthetic analogues in clinical trials for CML and other cancers

Indirubin from Isatis leaf has anti-inflammatory and antiviral properties. Clinical use in China for respiratory viral infections and leukemia.

Antiviral activity against influenza, hepatitis, and SARS-CoV in vitro studies. Same compound as in Qing Dai but at lower concentration in root. Anti-inflammatory via multiple pathways.

Found In 5 Herbs

3D Molecular Structure

Bisindole (indole alkaloid)
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Indirubin

Bisindole (indole alkaloid)Nitrogen-containing compounds with potent pharmacological effects

Representative pattern: C₉H₇N₂O

Atoms
Nitrogen
Carbon
Hydrogen
Oxygen

Live Research

Open on PubMed

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