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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T8646 | URB937 | FAAH | |
URB937 is an inhibitor of FAAH and increases anandamide levels(IC50 : 26.8 nM). | |||
TN4910 | Rhoeadine | Others | |
Rhoeadine is a natural product for research related to life sciences. The catalog number is TN4910 and the CAS number is 2718-25-4. | |||
T75540 | Ipomoeassin F | ||
Ipomoeassin F, a selective and potent inhibitor of endoplasmic reticulum (ER) protein translocation, targets the Sec61 complex's pore-forming subunit (Sec61α) at the ER membrane. It inhibits the ER membrane translocation... | |||
T126468 | 7-O-Methylaloeasinol | ||
7-O-Methylaloeasinol is a useful organic compound for research related to life sciences. The catalog number is T126468 and the CAS number is 105317-69-9. | |||
T23204 | PSN 375963 | PSN 375963 hydrochloride | GPR |
PSN 375963 (PSN 375963 hydrochloride) hydrochloride is a synthetic agonist of the endogenous ligand for GPR119. | |||
T29938 | AM-3102 | KDS-5104,AM 3102,Methyl oleoylethanolamide | |
AM-3102 is an OEA analog that stimulates PPARα transcriptional activity and prolongs feeding latency. It is resistant to enzymatic hydrolysis and is as potent as OEA in enhancing transcriptional activity of PPARα and red... | |||
T25366 | Elaidyl-sulfamide | Elaidylsulfamide,ES | |
Elaidyl-sulfamide is a sulfamoyl analogue of oleoylethanolamide (OEA). ES is a lipid mediator of satiety that acts through the PPARα. | |||
T16678 | PSN632408 | Others | |
PSN632408 is an optimized agonist of GPR119 receptors that display similar potency to OEA at both recombinant mouse and human GPR119 receptors (EC50: 5.6 and 7.9 uM, respectively). | |||
T23204L | PSN 375963 hydrochloride(388575-52-8 Free base) | ||
PSN 375963 hydrochloride, a potent GPR119 agonist, demonstrates EC50 values of 8.4 μM and 7.9 μM for human and mouse GPR119, respectively. Its efficacy is comparable to that of the endogenous agonist oleoylethanolamide (... | |||
T60378 | NAAA-IN-2 | ||
NAAA-IN-2 (Compound 9), a potent and selective inhibitor of NAAA, exhibits an IC50 of 50 nM. NAAA, a cysteine amidase, primarily breaks down the endogenous biolipids palmitoylethanolamide (PEA) and oleoylethanolamide (OE... | |||
T60767 | NAAA-IN-1 | ||
NAAA-IN-1 (Compound 1) can be used in the inflammation and pain research. NAAA-IN-1 is a potent and selective NAAA inhibitor (IC 50 = 7 nM). NAAA is a cysteine amidase. NAAA preferentially hydrolyzes the endogenous bioli... | |||
T60432 | NAAA-IN-3 | ||
NAAA-IN-3 (Compound 17a) is a potent and selective NAAA inhibitor with an IC50 of 50 nM. NAAA is a cysteine amidase which preferentially hydrolyzes the endogenous biolipids palmitoylethanolamide (PEA) and oleoylethanola... |