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1623481-80-0

1623481-80-0 Structure

1623481-80-0 Structure
IdentificationBack Directory
[Name]

ML381(VU0488130)
[CAS]

1623481-80-0
[Synonyms]

ML381
VU0488130
VU-0488130
VU 0488130
ML381(VU0488130)
ML381 (VU0488130) Fumarate
3-Isoxazolecarboxamide, 5-[(3-acetylphenoxy)methyl]-N-methyl-N-[(1S)-1-(2-pyridinyl)ethyl]-
ML381(VU0488130) ?5-[(3-Acetylphenoxy)methyl]-N-methyl-N-[(1S)-1-pyridin-2-ylethyl]-1,2-oxazole-3-carboxamide
[Molecular Formula]

C21H21N3O4
[MDL Number]

MFCD34597614
[MOL File]

1623481-80-0.mol
[Molecular Weight]

379.41
Chemical PropertiesBack Directory
[Boiling point ]

598.7±50.0 °C(Predicted)
[density ]

1.231±0.06 g/cm3(Predicted)
[form ]

Oil
[pka]

4.12±0.12(Predicted)
[color ]

Colorless to light yellow
Hazard InformationBack Directory
[Uses]

ML381 (VU0488130) is a highly selective, central nervous system penetrant mAChR M5 orthogonal antagonist (IC50 = 450 nM; Ki = 340 nM). ML381 is unstable in rat plasma and can be mainly used as a molecular probe for in vitro and electrophysiological studies[1][2].
[in vivo]

ML381 (0.2 mg/kg; i.v.; single) possesses an overall acceptable DMPK profile for pharmacodynamic studies in rat, with the exception of poor metabolic stability and a potential for amide hydrolysis in plasma; as such, ML381 is best suited to use as an in vitro/electrophysiological probe[1].

Animal Model:Sprague-Dawley rat[1].
Dosage:0.2 mg/kg
Administration:Intravenous injection; single.
Result:1.19Pharmacokinetic Parameters of ML381 in Sprague-Dawley rat[1].
IV (0.2 mg/kg)
Hepatic microsomal CLint (mL min-1 kg-1)770
Predicted CLhep (mL min-1 kg-1)64
fubrain0.14
Cbrain/Cplasma (Kp*)0.58
*Kp value was determined at 0.25 h following a 0.2 mg/kg IV dose (n=2).
[References]

[1] Gentry PR, et al. Discovery, synthesis and characterization of a highly muscarinic acetylcholine receptor (mAChR)-selective M5-orthosteric antagonist, VU0488130 (ML381): a novel molecular probe. ChemMedChem. 2014 Aug;9(8):1677-82. DOI:10.1002/cmdc.201402051
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