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ChemicalBook--->CAS DataBase List--->118290-26-9

118290-26-9

118290-26-9 Structure

118290-26-9 Structure
IdentificationBack Directory
[Name]

N-[2-[2-[(Dipropylamino)methyl]-1-piperidinyl]ethyl]-5,6-dihydro-6-oxo-11H-pyrido[2,3-b][1,4]benzodiazepine-11-carboxamide
[CAS]

118290-26-9
[Synonyms]

AF-DX 384 Free Base
AF-DX-384; AF-DX384
N-[2-[2-[(dipropylamino)methyl]piperidin-1-yl]ethyl]-6-oxo-5H-pyrido[2,3-b][1,4]benzodiazepine-11-carboxamide
N-[2-[2-[(Dipropylamino)methyl]-1-piperidinyl]ethyl]-5,6-dihydro-6-oxo-11H-pyrido[2,3-b][1,4]benzodiazepine-11-carboxamide
11H-Pyrido[2,3-b][1,4]benzodiazepine-11-carboxamide, N-[2-[2-[(dipropylamino)methyl]-1-piperidinyl]ethyl]-5,6-dihydro-6-oxo-
[Molecular Formula]

C27H38N6O2
[MDL Number]

MFCD00884624
[MOL File]

118290-26-9.mol
[Molecular Weight]

478.63
Chemical PropertiesBack Directory
[Boiling point ]

618.4±55.0 °C(Predicted)
[density ]

1.144±0.06 g/cm3(Predicted)
[storage temp. ]

room temp
[solubility ]

DMSO: soluble10mg/mL, clear (warmed)
[form ]

powder
[pka]

11.55±0.20(Predicted)
[color ]

white to beige
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack Directory
[Description]

AF-DX 384 is an antagonist of M2 and M4 muscarinic acetylcholine receptors (Kis = 6.03 and 10 nM, respectively). It is selective for M2 and M4 over M1, M3, and M5 receptors (Kis = 30.9, 66.07, and 537.03 nM, respectively). AF-DX 384 increases acetylcholine release in the hippocampus and cortex of young and aged rats in vivo when infused locally at a concentration of 1 μM and in the cortex when administered intraperitoneally at a dose of 5 mg/kg. It reverses deficits in novel object recognition and passive avoidance in aged rats, as well as in young rats with impairments induced by scopolamine .
[Uses]

AF-DX 384 is a potent mAChR M2/mAChR M4??selective antagonist.
[Definition]

ChEBI: N-[2-[2-[(dipropylamino)methyl]-1-piperidinyl]ethyl]-6-oxo-5H-pyrido[2,3-b][1,4]benzodiazepine-11-carboxamide is a benzodiazepine.
[storage]

Store at RT
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