LMD-009是选择性CCR8非肽激动剂。LMD-009以高效力介导趋化性,肌醇磷酸盐积累和钙释放,EC50为11至87nM。
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LMD-009 is a selective CCR8 nonpeptide agonist. LMD-009 mediates chemotaxis, inositol phosphate accumulation, and calcium release in high potencies with EC50s from 11 to 87 nM[1].
[1]. Jensen PC, et al. Molecular interaction of a potent nonpeptide agonist with the chemokine receptor CCR8. Mol Pharmacol. 2007 Aug;72(2):327-40.
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