ChemicalBook--->CAS DataBase List--->244218-51-7

244218-51-7

244218-51-7 Structure

244218-51-7 Structure
IdentificationBack Directory
[Name]

JTC 801
[CAS]

244218-51-7
[Synonyms]

CS-161
JTC 801
JTC 801 HCl
JTC-801/JTC801
JTC 801 USP/EP/BP
JTC-801 >=98% (HPLC)
JTC-801 hydrochloride
N-(4-Amino-2-methyl-6-quinolinyl)-2-[(4-ethylphenoxy)methyl]benzamidehydrochloride
N-(4-AMino-2-Methyl-quinolin-6-yl)-2-(4-ethyl-phenoxyMethyl)-benzaMide hydrochloride
Benzamide,N-(4-amino-2-methyl-6-quinolinyl)-2-[(4-ethylphenoxy)methyl]-, hydrochloride
N-(4-Amino-2-methyl-6-quinolinyl)-2-[(4-ethylphenoxy)methyl]benzamide monohydrochloride
[Molecular Formula]

C26H25N3O2.ClH
[MDL Number]

MFCD06198707
[MOL File]

244218-51-7.mol
[Molecular Weight]

447.963
Chemical PropertiesBack Directory
[Melting point ]

235℃
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

DMSO: ≥20mg/mL
[form ]

powder
[color ]

tan
[InChIKey]

NQLIYKXNAXKMBL-UHFFFAOYSA-N
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36
[Safety Statements ]

26
[WGK Germany ]

1
Hazard InformationBack Directory
[Uses]

JTC 801 is a novel opioid receptor-like1 (ORL1) receptor antagonist.
[Biological Activity]

High affinity, selective NOP receptor antagonist (K i = 8.2 nM). Displays approximately 12.5-, 129- and 1055-fold selectivity over human μ -, κ - and δ -opioid receptors respectively. In vivo shows anti-nociceptive effects in acute pain models. Orally active.
[storage]

Desiccate at RT
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