ChemicalBook--->CAS DataBase List--->1166-34-3

1166-34-3

1166-34-3 Structure

1166-34-3 Structure
IdentificationBack Directory
[Name]

CINANSERIN HYDROCHLORIDE
[CAS]

1166-34-3
[Synonyms]

DPTC
CINANSERIN
Cinanserine
DPTC HYDROCHLORIDE
CINANSERIN HYDROCHLORIDE
2'-(3-DIMETHYLAMINOPROPYL-THIO)-CINNAMANILIDE HYDROCHLORIDE
N-[2-[[3-(Dimethylamino)propyl]thio]phenyl]-3-phenylpropenamide
N-[2-[[3-(DIMETHYLAMINO)PROPYL]THIO]PHENYL]-3-PHENYL-2-PROPENAMIDE
2-Propenamide, N-[2-[[3-(dimethylamino)propyl]thio]phenyl]-3-phenyl-
N-[2-[[3-(DIMETHYLAMINO)PROPYL]THIO]PHENYL]-3-PHENYL-2-PROPENAMIDE HYDROCHLORIDE
[Molecular Formula]

C20H24N2OS
[MDL Number]

MFCD00055609
[MOL File]

1166-34-3.mol
[Molecular Weight]

340.48
Chemical PropertiesBack Directory
[Melting point ]

82-83 °C
[Boiling point ]

519.5±50.0 °C(Predicted)
[density ]

1.13±0.1 g/cm3(Predicted)
[RTECS ]

UC6323000
[storage temp. ]

Desiccate at RT
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

13.46±0.70(Predicted)
[color ]

White to Off-White
[Water Solubility ]

Soluble to 50 mM in water
Safety DataBack Directory
[HS Code ]

2930909099
Hazard InformationBack Directory
[Uses]

A 5-HT antagonist
[Uses]

Serotonin inhibitor.
[Definition]

ChEBI: Cinanserin is an aryl sulfide that is (2E)-3-phenyl-N-(2-sulfanylphenyl)prop-2-enamide in which the hydrogen of the thiol group is substituted by a 3-(dimethylamino)propyl group. It is a 5-hydroxytryptamine receptor antagonist and an inhibitor of SARS-CoV replication. It has a role as an EC 3.4.22.69 (SARS coronavirus main proteinase) inhibitor, an antiviral agent and an anticoronaviral agent. It is a tertiary amino compound, a secondary carboxamide, a member of cinnamamides and an aryl sulfide. It is a conjugate base of a cinanserin(1+).
[Biological Activity]

5-HT 2 antagonist.
[in vivo]

Cinanserin (5 mg/kg; i.v.) treatment significantly reduces systemic burn edema levels[1].

Animal Model:Male Wistar rats (250 g) underwent thermal injury[1]
Dosage:5 mg/kg
Administration:Intravenous injection; for 2 hours
Result:Significantly reduced systemic burn edema to shamburn levels, leukocyte-endothelial interactions are significantly reduced by administration of Cinanserin.
[IC 50]

5-HT2 Receptor: 41 nM (Ki); 5-HT1 Receptor: 3500 nM (Ki); SARS-CoV 3CLpro: 49.4 μM (Kd)
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