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ChemicalBook--->CAS DataBase List--->392338-13-5

392338-13-5

392338-13-5 Structure

392338-13-5 Structure
IdentificationBack Directory
[Name]

A-331440 L-TARTARIC ACID SALT
[CAS]

392338-13-5
[Synonyms]

A 331440
A331440 free base
A-331440 L-tartrate hydrate
A-331440 L-TARTARIC ACID SALT
4-[4-[3-[(3R)-3-(dimethylamino)pyrrolidin-1-yl]propoxy]phenyl]benzonitrile
(R)-4'-(3-(3-(diMethylaMino)pyrrolidin-1-yl)propoxy)biphenyl-4-carbonitrile
[1,1'-Biphenyl]-4-carbonitrile, 4'-[3-[(3R)-3-(dimethylamino)-1-pyrrolidinyl]propoxy]-
4′-[3-[3(R)-Dimethylamino-1-pyrrolidinyl]propoxy]-[1,1-biphenyl]-4′-carbonitrile L-tartrate hydrate
[Molecular Formula]

C22H27N3O
[MDL Number]

MFCD07363908
[MOL File]

392338-13-5.mol
[Molecular Weight]

349.47
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

H2O: insoluble
[form ]

solid
[color ]

white to off-white
[Water Solubility ]

H2O: ≥10mg/mL
Safety DataBack Directory
[Safety Statements ]

22-24/25
[WGK Germany ]

3
Hazard InformationBack Directory
[Biological Activity]

Histamine affects homeostatic mechanismsincluding food and water consumptionby acting on central nervous system (CNS) receptors. Presynaptic histamine H3 receptors regulate release of histamine and other neurotransmittersand histamine H3 receptor antagonists enhance neurotransmitter release. A-331440 [4μ-[3-(3(R)-(dimethylamino)-pyrrolidin-1-yl)-propoxy]-biphenyl-4-carbonitrile] is a histamine H3 receptor antagonist which binds potently and selectively to both human and r at histamine H3 receptors (Ki<=25 nM). Mice were stabilized on a high-f at diet (45 kcal % lard) prior to 28-day oral b.i.d. dosing for measurement of obesity-related parameters. A-331440 administered at 0.5 mg/kg had no significant effect on weightwhereas 5 mg/kg decreased weight comparably to dexfenfluramine (10 mg/kg). A-331440 administered at 15 mg/kg reduced weight to a level comparable to mice on the low-f at diet. The two higher doses reduced
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