CGP52608 is a selective agonist for the RZR/ROR receptor, known for its anti-tumor activity, and has almost no affinity for the cell surface G-protein coupled melatonin receptor. CGP52608 can inhibit the growth of mouse 16/C breast cancer cells. CGP52608 can induce the formation of vesicles in diatoms[1][2].
Molecular Weight:
244.34
CAS Number:
[87958-67-6]
Formula:
C8H12N4OS2
Target:
Melatonin Receptor
Application Notes:
MCE Product type: Reference compound
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