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The structural luteolin analog, tetramethoxyflavone (methoxyluteolin), has no phenol groups and is even more potent than luteolin in inhibiting both mast cells and microglia [288,362,509,510,511]
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The STAT News coverage noted that if the FDA ultimately reclassifies the compounds and they are produced by compounding pharmacies, clinicians would have discretion to prescribe them outside the narrow indications under review, meaning a substance reviewed only for ulcerative colitis could legally be prescribed for any purpose a physician deemed appropriate
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