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ChemicalBook--->CAS DataBase List--->515141-51-2

515141-51-2

515141-51-2 Structure

515141-51-2 Structure
IdentificationBack Directory
[Name]

GW 803430
[CAS]

515141-51-2
[Synonyms]

GW 3430
GW 803430
GW-803430A
GW-803430 >=98% (HPLC)
Thieno[3,2-d]pyrimidin-4(3H)-one, 6-(4-chlorophenyl)-3-[3-methoxy-4-[2-(1-pyrrolidinyl)ethoxy]
6-(4-Chlorophenyl)-3-[3-methoxy-4-[2-(1-pyrrolidinyl)ethoxy]phenyl]-thieno[3,2-d]pyrimidin-4(3H)-one
6-(4-chloro-phenyl)-3-[3-methoxy-4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-3H-thieno[3,2-d]pyrimidin-4-one
Thieno[3,2-d]pyrimidin-4(3H)-one, 6-(4-chlorophenyl)-3-[3-methoxy-4-[2-(1-pyrrolidinyl)ethoxy]phenyl]-
[Molecular Formula]

C25H24ClN3O3S
[MDL Number]

MFCD09970889
[MOL File]

515141-51-2.mol
[Molecular Weight]

481.99
Chemical PropertiesBack Directory
[Boiling point ]

677.7±65.0 °C(Predicted)
[density ]

1.37±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

DMSO: ≥4mg/mL at warmed to 60°C
[form ]

powder
[pka]

9.52±0.20(Predicted)
[color ]

white to beige
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H319
[Precautionary statements ]

P264-P270-P280-P301+P312-P305+P351+P338-P337+P313
[Hazard Codes ]

Xn
[Risk Statements ]

22-36
[Safety Statements ]

26
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

GW 803430 is a melanin-concentrating hormone receptor 1( MCH1) antagonist for treatment of obesity and depression.
[Biochem/physiol Actions]

GW-803430 antagonizes central MCHR1 and produces anxiolytic, anti-depressant and anti-obesity effects in rats and mice. It also controls the alcohol-seeking behavior in rats and is a promising treatment for alcohol use-related disorders.
[in vivo]

GW-803430 (0.3, 3, and 15 mg/kg; oral administration; once daily) causes a sustained dose-dependent weight loss relative to vehicle controls[1].
GW-803430 is a suitable compound for its good pharmacokinetic properties (bioavailability=31%, t1/2=11 h) and brain penetration (6:1 brain:plasma concentration) in mice[1].

Animal Model:High fat diet-induced obese AKR/J mice[1]
Dosage:0.3, 3, and 15 mg/kg
Administration:Orally, qd,12 days
Result:Caused a sustained dose-dependent weight loss of -6.2%, -12.1%, and -13.1%, respectively, relative to vehicle controls.
[storage]

Store at -20°C
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