ChemicalBook--->CAS DataBase List--->864756-35-4

864756-35-4

864756-35-4 Structure

864756-35-4 Structure
IdentificationBack Directory
[Name]

TC-MCH 7c
[CAS]

864756-35-4
[Synonyms]

TC-MCH 7c
4-(4-Fluoro-benzyloxy)-1-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-1H-pyridin-2-one
4-[(4-Fluorophenyl)methoxy]-1-[4-[2-(1-pyrrolidinyl)ethoxy]phenyl]-2(1H)-pyridinone
[Molecular Formula]

C24H25FN2O3
[MOL File]

864756-35-4.mol
[Molecular Weight]

408.47
Chemical PropertiesBack Directory
[Melting point ]

124-126 °C
[Boiling point ]

606.3±55.0 °C(Predicted)
[density ]

1.27±0.1 g/cm3(Predicted)
[storage temp. ]

Store at RT
[solubility ]

Soluble to 100 mM in 1eq. HCl and to 50 mM in DMSO
[form ]

Powder
[pka]

9.60±0.20(Predicted)
[color ]

Light yellow to yellow
Hazard InformationBack Directory
[Uses]

TC-MCH 7c is a potent melanin-concentrating hormone 1 receptor antagonist.
[in vivo]

TC-MCH 7c (oral; 3-30 mg/kg; once-daily for 1.5 months) exhibits excellent body weight reduction in a dose-dependent manner in DIO mice model[1].
TC-MCH 7c (oral; 3-30 mg/kg) with 30 mg/kg has plasma concentrations of 5.1, 1.8, and 0.7 μM at 2, 15, and 24 hours, respectively[2].

Animal Model:C57BL/6J DIO mice[1]
Dosage:3, 10 and 30 mg/kg
Administration:Oral; once-daily for 1.5 months
Result:Exhibited excellent body weight reduction in a dose-dependent manner.
Animal Model:Diet-induced obesity mice[2]
Dosage:3, 10 and 30 mg/kg (Pharmacokinetic Analysis)
Administration:Oral
Result:Plasma concentrations at 2, 15, and 24 hours were 5.1, 1.8, and 0.7 μM, respectively.
[storage]

Store at RT
Spectrum DetailBack Directory
[Spectrum Detail]

TC-MCH 7c(864756-35-4)1HNMR
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