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ChemicalBook--->CAS DataBase List--->1802326-66-4

1802326-66-4

1802326-66-4 Structure

1802326-66-4 Structure
IdentificationBack Directory
[Name]

JNJ 63533054
[CAS]

1802326-66-4
[Synonyms]

CS-2223
JNJ 63533054
JNJ-63533054 (JNJ63533054
JNJ-63533054 >=98% (HPLC)
3-Chloro-N-[2-oxo-2-[[(1S)-1-phenylethyl]amino]ethyl]benzamide
Benzamide, 3-chloro-N-[2-oxo-2-[[(1S)-1-phenylethyl]amino]ethyl]-
[Molecular Formula]

C17H17ClN2O2
[MDL Number]

MFCD29924732
[MOL File]

1802326-66-4.mol
[Molecular Weight]

316.78
Chemical PropertiesBack Directory
[Boiling point ]

559.7±45.0 °C(Predicted)
[density ]

1.224±0.06 g/cm3(Predicted)
[storage temp. ]

room temp
[solubility ]

Soluble in DMSO (up to 35 mg/ml).
[form ]

powder
[pka]

12.77±0.46(Predicted)
[color ]

white to beige
[optical activity]

[α]/D -89 to -99°, c = 1 in ethanol
[Stability:]

Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 2 months.
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319
[Precautionary statements ]

P264-P270-P280-P301+P312-P302+P352-P305+P351+P338
Hazard InformationBack Directory
[Description]

JNJ-63533054 (1802326-66-4) is a potent and selective brain-penetrant GPR139 agonist (EC50=16 nM) an orphan G-protein-coupled receptor expressed in the CNS.1?Tritium-labeled JNJ-63533054 binds to cell membranes expressing GPR139 and can be displaced by putative endogenous ligands.2?Decreases compulsive-like alcohol drinking and hyperalgesia in alcohol-dependent rodents.3?Suppresses morphine intake in a mouse self-administration model.4
[Uses]

JNJ 63533054 is a potent and selective agonist of hGPR139 with an EC50 = 16 nM.
[Biochem/physiol Actions]

JNJ-63533054 is a potent and selective agonist of the orphan receptor hGPR139, a GPCR receptor expressed in the brain in circumventricular regions of the habenula and septum. JNJ-63533054 has an EC50 value of 16 nM, crosses the blood-brain barrier, and is orally available.
[storage]

Store at RT
[References]

1) Dvorak?et al.?(2015),?Identification and SAR of Glycine Benzamides as Potent Agonists for the GPR139 Receptor;?ACS Med. Chem. Lett.,?6?1015 2) Liu?et al. (2015),?GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids L-Tryptophan and L-Phenylalanine; Mol. Pharmacol.,?88?911 3) Kononoff?et al.?(2018),?Systemic and Intra-Habenular Activation of the Orphan G Protein-Coupled Receptor GPR139 Decreases Compulsive-Like Alcohol Drinking and Hyperalgesia in Alcohol-Dependent Rats;?eNeuro,?5?ENEURO 0153-18 2018 4) Wang?et al.?(2019),?Genetic behavioral screen identifies an orphan anti-opioid system; Science,?365?1267
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