ChemicalBook--->CAS DataBase List--->372523-75-6

372523-75-6

372523-75-6 Structure

372523-75-6 Structure
IdentificationBack Directory
[Name]

(2S)-1-(3,4-Dihydro-6,7-dimethoxy-2(1H)-isoquinolinyl)-3,3-dimethyl-2-[(4-pyridinylmethyl)amino]-1-butanonehydrochloride
[CAS]

372523-75-6
[Synonyms]

TCS OX2 29
TCS-OX2-29, CID 10408514
(2S)-1-(6,7-DIMETHOXY-3,4-DIHYDRO-1H-ISOQUINOLIN-2-YL)-3,3-DIMETHYL-2-(PYRIDIN-4-YLMETHYLAMINO)BUTAN-1-ONE
1-Butanone, 1-(3,4-dihydro-6,7-dimethoxy-2(1H)-isoquinolinyl)-3,3-dimethyl-2-[(4-pyridinylmethyl)amino]-, (2S)-
(2S)-1-(3,4-Dihydro-6,7-dimethoxy-2(1H)-isoquinolinyl)-3,3-dimethyl-2-[(4-pyridinylmethyl)amino]-1-butanonehydrochloride
[Molecular Formula]

C23H31N3O3
[MOL File]

372523-75-6.mol
[Molecular Weight]

397.51
Chemical PropertiesBack Directory
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[solubility ]

DMSO : 25 mg/mL (62.89 mM; Need ultrasonic)Ethanol : 25 mg/mL (62.89 mM; Need ultrasonic)H2O : < 0.1 mg/mL (insoluble)
[form ]

Powder
[color ]

White to off-white
[Water Solubility ]

H2O: ≥2.0mg/mL, clear
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

TCS OX2 29 is a potent and selective orexin-2 receptor (OX2) antagonist.
[Biological Activity]

TCS OX2 29 or TCS-OX2-29 is a potent and selective orexin 2 receptor (Ox2ROx2-ROx-2-R) antagonist (IC50 = 40 nM/Ox2R>10 μM/Ox1R) with little potency toward 50 other receptorsion channelsand transporters tested (<30% inhibition at 10 μM). TCS OX2 29 is widely used for elucidating various physiological functions mediated by Ox2R both in cultures and in mice and rats in vivo.
[in vivo]

TCS-OX2-29 (5-10 mg/kg; intraperitoneal injection; adult male NMRI mice) treatment suppresses conditioned place preference (CPP) acquisition and expression in both na ve and dependent mice significantly[2].

Animal Model:440 adult male NMRI mice (25-30 g)[2]
Dosage:5 mg/kg and 10 mg/kg
Administration:Intraperitoneal injection (Pharmacokinetic study)
Result:Suppressed conditioned place preference (CPP) acquisition and expression in both na?ve and dependent mice significantly.
[IC 50]

OX2 Receptor
[storage]

Store at -20°C
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