Catenarin, an anthraquinone compound, inhibits CCR5 - and CXCR4 -mediated chemotaxis. Catenarin reduces the phosphorylation of mitogen-activated protein kinases ( p38 and JNK ) and their upstream kinases ( MKK6 and MKK7 ), and calcium mobilization. Catenarin shows anti-inflammatory effect and suppresses leukocyte migration in the diabetes. Catenarin exhibits significant inhibitory effects against Gram-positive bacteria. Catenarin prevents type 1 diabetes (T1D) in nonobese diabetic mice [1][2] .
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