PW507 is a potent, brain-penetrant and selective sigma 1 receptor (S1R) antagonist with a Ki of 7.5 nM for human S1R. PW507 displays a low binding affinity to S2R and hERG. PW507 can be used for the study of painful diabetic neuropathy (PDN)[1].
Molecular Weight:
334.89
CAS Number:
[2573850-59-4]
Formula:
C18H27ClN4
Target:
Sigma Receptor
Application Notes:
Reference compound
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