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XL-001 is a novel compound identified through in silico screening and medicinal chemistry modifications. It functions as a highly affine and selective inverse agonist of the cannabinoid receptor type 2 (CB2). This drug has been shown to inhibit CB2-triggered activation of β-catenin and fibrotic injury, and to ameliorate kidney injury, fibrosis, and inflammation in preclinical models of kidney disease, including unilateral ureteral obstruction and ischemia/reperfusion injury. Its development aims to provide a strategy against fibrotic kidney diseases.
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