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JNJ-42165279 covalently inactivates the FAAH enzyme but is highly selective with regard to other enzymes, ion channels, transporters, and receptors. JNJ-42165279 (10 μM) exhibits high selectivity against a panel of 50 receptors, enzymes, transporters, and ion-channels, at which concentration it does not produce >50% inhibition of binding to any of the targets. Fortunately, JNJ-42165279 (10 μM) also does not inhibit CYPs (1A2, 2C8, 2C9, 2C19, 2D6, 3A4) or hERG.
Pack Size | Price | Availability | Quantity |
---|---|---|---|
2 mg | $38 | In Stock | |
5 mg | $59 | In Stock | |
10 mg | $88 | In Stock | |
25 mg | $173 | In Stock | |
50 mg | $259 | In Stock | |
100 mg | $382 | In Stock | |
200 mg | $539 | In Stock | |
1 mL x 10 mM (in DMSO) | $69 | In Stock |
Description | JNJ-42165279 covalently inactivates the FAAH enzyme but is highly selective with regard to other enzymes, ion channels, transporters, and receptors. JNJ-42165279 (10 μM) exhibits high selectivity against a panel of 50 receptors, enzymes, transporters, and |
Targets&IC50 | FAAH (rat):313 ± 28 nM, FAAH (human):70 ± 8 nM |
Alias | JNJ42165279 |
Molecular Weight | 410.8 |
Formula | C18H17ClF2N4O3 |
Cas No. | 1346528-50-4 |
Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
Solubility Information | DMSO: 45 mg/mL (109.54 mM) | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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