About 7 results found for searched term "FAAH-IN-2" (0.119 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M6169 | FAAH-IN-2 | FAAH |
| FAAH-IN-2 is a potent FAAH (fatty acid amide hydrolase) inhibitor. | ||
| M2783 | JNJ-1661010 | FAAH |
| Takeda-25 | ||
| JNJ-1661010 is a potent and selective FAAH inhibitor with IC50 of 10 nM (rat) and 12 nM (human), exhibits >100-fold selectivity for FAAH-1 when compared to FAAH-2. | ||
| M3525 | PF-3845 | FAAH |
| PF-3845 is a potent, selective and irreversible FAAH inhibitor with Ki of 230 nM, showing negligible activity against FAAH2. | ||
| M4693 | Biochanin-A | FAAH |
| 4-Methylgenistein; Olmelin | ||
| Biochanin A is A naturally occurring fatty acid amide hydrolase (FAAH) inhibitor that inhibits FAAH in mice, rats and humans with FAAH IC50 of 1.8, 1.4 and 2.4 μM, respectively. | ||
| M4890 | JZL 195 | MAGL |
| GTPL8606, KB-78011 | ||
| JZL195 is an effective FAAH and MAGL inhibitor with IC50 of 2 nM and 4 nM, respectively. | ||
| M8950 | JNJ-42165279 | FAAH |
| JNJ-42165279 is a potent and selective FAAH inhibitor with IC50s of 70 ± 8 nM and 313 ± 28 nM for hFAAH and rFAAH, respectively. | ||
| M56682 | URB937 | FAAH |
| URB937 is an orally active and peripherally restricted FAAH inhibitor (IC50=26.8 nM) and increases anandamide levels. | ||
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