T11255 |
FAAH-IN-1
|
1242441-47-9
|
98%
|
|
FAAH-IN-1 is a fatty acid amide hydrolase (FAAH) inhibitor, with IC50s of 145 nM and 650 nM for rat and human FAAH, respectively.
|
T16847 |
SA 47
|
792236-07-8
|
98%
|
|
SA 47 is a selective and effective inhibitor of fatty acid amide hydrolase and carbamate.
|
T67745 |
CB2R/FAAH modulator-2
|
2876918-68-0
|
98%
|
|
CB2R/FAAH modulator-2 (compound 26) is a dual modulator targeting at CB2R and FAAH. CB2R/FAAH modulator-2 acts as a CB2R agonist and FAAH inhibitor, the Ki value...
|
T12826 |
SA57
|
1346169-63-8
|
98%
|
|
SA57 is a potent, selective inhibitor of FAAH(IC50s of 3.2 nM and 1.9 nM for mouse and human FAAH).
|
T63536 |
Dual FAAH/sEH-IN-1
|
2756099-59-7
|
98%
|
|
Dual FAAH/sEH-IN-1 (compound 3) is a high affinity dual inhibitor of FAAH (fatty acid amide hydrolase) and sEH (soluble epoxide hydrolase), with IC50 values of 7...
|
T67747 |
CB2R/FAAH modulator-3
|
2876918-67-9
|
98%
|
|
CB2R/FAAH modulator-3 (compound 27) is a modulator targeting at CB2R and FAAH. CB2R/FAAH modulator-3 acts as a CB2R agonist and FAAH inhibitor, the Ki values are...
|
T28353 |
PDP-EA
|
861891-72-7
|
98%
|
|
PDP-EA is an activator of fatty acid amide hydrolase(FAAH) and enhances the amidohydrolase activity of FAAH.
|
T16515 |
PF 750
|
959151-50-9
|
98%
|
|
PF 750 is a selective and covalent inhibitor of FAAH. PF 750 shows IC50s varying from 16.2 to 595 nM in different incubation times.
|
T9374 |
AA38-3
|
65815-76-1
|
|
|
AA38-3 inhibites three SHs (ABHD6, ABHD11, and FAAH)
|
T6714 |
URB-597
|
546141-08-6
|
97.84%
|
|
URB597 is an effective, orally bioavailable FAAH inhibitor (IC50: 4.6 nM), and no effect on other cannabinoid-related targets.
|
T2859 |
Biochanin A
|
491-80-5
|
98%
|
|
Biochanin A is an isoflavone derivative isolated from red clover Trifolium pratense with anticarcinogenic properties. Biochanin A is a naturally occurring fatty ...
|
T11256 |
FAAH inhibitor 1
|
326866-17-5
|
98.05%
|
|
FAAH inhibitor 1 is an effective FAAH inhibitor with an IC50 of 18 nM.
|
T15802 |
LY2183240
|
874902-19-9
|
98.17%
|
|
LY2183240 inhibits fatty acid amide hydrolase (FAAH) activity (IC50 = 12.4 nM). LY2183240 is a novel and highly effective blocker of anandamide uptake (IC50 = 27...
|
T5357 |
ARN272
|
488793-85-7
|
98.23%
|
|
ARN272 is a FAAH-like anandamide transporter (FLAT) inhibitor (IC50: 1.8 μM).
|
T7688 |
4-Nonylphenylboronic acid
|
256383-45-6
|
99.13%
|
|
4-Nonylphenylboronic acid is a inhibitor of FAAH.
|
T15268 |
FAAH-IN-2
|
184475-71-6
|
99.18%
|
|
FAAH-IN-2 is a potent inhibitor of FAAH(fatty acid amide hydrolase).
|
T1325 |
Carprofen
|
53716-49-7
|
99.45%
|
|
Carprofen is a propionic acid derivate and nonsteroidal anti-inflammatory drug (NSAID) with anti-inflammatory, analgesic, and antipyretic activities.
|
T8646 |
URB937
|
1357160-72-5
|
99.55%
|
|
URB937 is an inhibitor of FAAH and increases anandamide levels(IC50 : 26.8 nM).
|
T4859 |
1-Monomyristin
|
589-68-4
|
99.58%
|
|
1-Myristoyl-rac-glycerol, a 1-monoglyceride of myristic acid, has antibacterial activity against several Gram-positive bacterial strains. 1-Myristoyl-rac-glycero...
|
T6043 |
PF-3845
|
1196109-52-0
|
99.58%
|
|
PF-3845 is a potent, selective and irreversible FAAH inhibitor with Ki of 230 nM, showing negligible activity against FAAH2.
|