3,4-Dihydro-6,7-isoquinolinediol acts as a selective β2-adrenergic receptor (β2-AR) agonist, exhibiting an EC50 of 106.9 μM in CH-K1/GA1S cells. In addition to its agonistic activity, it demonstrates anti-inflammatory properties by inhibiting nitric oxide production in lipopolysaccharide-stimulated mouse macrophage RAW 264.7 cells. This compound is suitable for research applications exploring β2-AR signaling and its implications in inflammation.
3,4-Dihydro-6,7-isoquinolinediol acts as a selective β2-adrenergic receptor (β2-AR) agonist, exhibiting an EC50 of 106.9 μM in CH-K1/GA1S cells. In addition to its agonistic activity, it demonstrates anti-inflammatory properties by inhibiting nitric oxide production in lipopolysaccharide-stimulated mouse macrophage RAW 264.7 cells. This compound is suitable for research applications exploring β2-AR signaling and its implications in inflammation.
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