| Cat. No. |
Product Name |
Information |
| PC-63017 |
LY 2318912
|
LY 2318912 is a potent, competitive, small molecule inhibitor of anandamide uptake with IC50 of 7.27 nM, shows high affinity against anandamide transporter binding site with Kd o f7.62 nM. |
| PC-62533 |
SSR 411298
|
SSR411298 is a highly selective, brain penetrant and orally-active inhibitor of FAAH with IC50 of 62.5 nM (mouse brain FAAH). |
| PC-60986 |
ASP 3652
|
A potent, selective, peripherally active and orally available FAAH inhibitor for treatment of chronic prostatitis/chronic pelvic pain syndrome.. |
| PC-60706 |
SA-57
|
A highly potent and selective dual FAAH/MAGL inhibitor with IC50 of 1-3 nM against FAAH, inhibits mouse (IC50=410 nM) and human (IC50=1.4 uM) MAGL. |
| PC-70218 |
FAAH-IN-2
|
A potent, selective, noncovalent FAAH inhibitor with IC50 of 28 nM toward human FAAH and 100 nM toward rat FAAH. |
| PC-60219 |
MK-4409
|
A potent and selective, brain penetrant FAAH inhibitor with IC50 of 11 nM. |
| PC-45666 |
JNJ-42165279
|
JNJ-42165279 is a highly selective inhibitor of fatty acid amide hydrolase (FAAH) with IC50 of 70 nM for hFAAH. |
| PC-42719 |
FAAH inhibitor 1
|
A potent, and selective FAAH inhibitor with IC50 of 18 nM. |
| PC-42721 |
LY2183240
|
A highly potent blocker of anandamide uptake with IC50 of 270 pM in cellular assay. |
