CINANSERIN HYDROCHLORIDE
CINANSERIN HYDROCHLORIDE Basic information
- Product Name:
- CINANSERIN HYDROCHLORIDE
- Synonyms:
-
- N-[2-[[3-(DIMETHYLAMINO)PROPYL]THIO]PHENYL]-3-PHENYL-2-PROPENAMIDE
- N-[2-[[3-(DIMETHYLAMINO)PROPYL]THIO]PHENYL]-3-PHENYL-2-PROPENAMIDE HYDROCHLORIDE
- 2'-(3-DIMETHYLAMINOPROPYL-THIO)-CINNAMANILIDE HYDROCHLORIDE
- CINANSERIN
- CINANSERIN HYDROCHLORIDE
- DPTC
- DPTC HYDROCHLORIDE
- Cinanserine
- CAS:
- 1166-34-3
- MF:
- C20H24N2OS
- MW:
- 340.48
- Product Categories:
-
- Serotonin receptor
- Mol File:
- 1166-34-3.mol
CINANSERIN HYDROCHLORIDE Chemical Properties
- 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
CINANSERIN HYDROCHLORIDE Usage And Synthesis
Uses
Serotonin inhibitor.
Uses
A 5-HT antagonist
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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