ChemicalBook--->CAS DataBase List--->347887-36-9

347887-36-9

347887-36-9 Structure

347887-36-9 Structure
IdentificationBack Directory
[Name]

Fedovapagon
[CAS]

347887-36-9
[Synonyms]

Fedovapagon
1,2-Pyrrolidinedicarboxamide, N2,N2-dimethyl-N1-[[2-methyl-4-[(2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl)carbonyl]phenyl]methyl]-, (2S)-
[Molecular Formula]

C27H34N4O3
[MDL Number]

MFCD19443737
[MOL File]

347887-36-9.mol
[Molecular Weight]

462.58
Chemical PropertiesBack Directory
[Boiling point ]

740.0±60.0 °C(Predicted)
[density ]

1.203±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: ≥ 125 mg/mL (270.22 mM)
[form ]

Solid
[pka]

13.38±0.40(Predicted)
[color ]

Off-white to light yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
Hazard InformationBack Directory
[Uses]

Fedovapagon is a potent, nonpeptidic vasopressin V2 receptor agonists.
[in vivo]

Fedovapagon (1 mg/kg, oral administration) inhibits urine output with 81% inhibition rate in rats[1].

Animal Model:Brattleboro rats[1]
Dosage:1 mg/kg, 3 mg/kg
Administration:Oral administration
Result:Reduced urine volume with almost full inhibition of urine output for 2 h.
Returned the urine to normal levels 5 h after dosing.
[IC 50]

V2 Receptor; V2 Receptor: 24 nM (EC50)
Spectrum DetailBack Directory
[Spectrum Detail]

Fedovapagon(347887-36-9)1HNMR
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