54-84-2

Cinanserin hydrochloride Chemical Structure
54-84-2

Chemical Structure

Cinanserin hydrochloride

Synonym(s): SQ 10643

  • CAS No.: 54-84-2
  • Formula:C20H25ClN2OS
  • Molecular Weight:376.94

IUPAC Name: N-(2-((3-(dimethylamino)propyl)thio)phenyl)cinnamamide hydrochloride

InChIKey: LXGJPDKYMJJWRB-IERUDJENSA-N

SMILES: O=C(NC1=CC=CC=C1SCCCN(C)C)/C=C/C2=CC=CC=C2.[H]Cl

Biological Activity: Cinanserin hydrochloride (SQ 10643) is a potent, selective and highly affinity 5-HT2 receptor antagonist with a Ki of 41 nM. Cinanserin hydrochloride has a much higher binding affinity for the 5-HT2 than for the 5-HT1 receptor (Ki of 3500 nM). Cinanserin is also an inhibitor of 3C-like proteinase of severe acute respiratory syndrome coronavirus and strongly reduces virus replication in vitro[1][2][3].

Cat. No. Product Name Purity Description Pricing
HY-100943
Cinanserin hydrochloride 99.48% Cinanserin hydrochloride (SQ 10643) is a potent, selective and highly affinity 5-HT2 receptor antagonist with a Ki of 41 nM. Cinanserin hydrochloride has a much higher binding affinity for the 5-HT2 than for the 5-HT1 receptor (Ki of 3500 nM). Cinanserin is also an inhibitor of 3C-like proteinase of severe acute respiratory syndrome coronavirus and strongly reduces virus replication in vitro.
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HY-100943R
Cinanserin hydrochloride (Standard) ≥98% Cinanserin (hydrochloride) (Standard) is the analytical standard of Cinanserin (hydrochloride) (HY-100943). This product is intended for research and analytical applications. Cinanserin hydrochloride (SQ 10643) is a potent, selective and highly affinity 5-HT2 receptor antagonist with a Ki of 41 nM. Cinanserin hydrochloride has a much higher binding affinity for the 5-HT2 than for the 5-HT1 receptor (Ki of 3500 nM). Cinanserin is also an inhibitor of 3C-like proteinase of severe acute respiratory syndrome coronavirus and strongly reduces virus replication in vitro.
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References