Cinanserin je antagonist 5-HT2A i 5-HT2C receptora koji je otkriven tokom 1960-tih.[1]

Cinanserin
IUPAC ime
(2E)-N-(2-{[3-(dimetilamino)propil]tio}fenil)-3-fenilakrilamid
Identifikatori
CAS broj1166-34-3 ДаY
ATC kodnone
PubChemCID 5475158
ChemSpider4584027
UNIIKI6J9OY7A3 ДаY
Hemijski podaci
FormulaC20H24N2OS
Molarna masa340,482 g/mol
  • CN(C)CCCSC1=CC=CC=C1NC(=O)\C=C\C2=CC=CC=C2
  • InChI=1S/C20H24N2OS/c1-22(2)15-8-16-24-19-12-7-6-11-18(19)21-20(23)14-13-17-9-4-3-5-10-17/h3-7,9-14H,8,15-16H2,1-2H3,(H,21,23)/b14-13+ ДаY
  • Key:RSUVYMGADVXGOU-BUHFOSPRSA-N ДаY

Preparat cinanserina je efektivan protiv atipične pneumonije (SARS).[2]

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Reference уреди

  1. ^ Neuman RS, Zebrowska G (1992). „Serotonin (5-HT2) receptor mediated enhancement of cortical unit activity”. Canadian Journal of Physiology and Pharmacology. 70 (12): 1604—9. PMID 1301238. 
  2. ^ Lili Chen; Chunshan Gui; Xiaomin Luo; Qingang Yang; Stephan Günther; Elke Scandella; Christian Drosten; Donglu Bai; Xichang He; Burkhard Ludewig; Jing Chen; Haibin Luo; Yiming Yang; Yifu Yang; Jianping Zou; Volker Thiel; Kaixian Chen; Jianhua Shen; Xu Shen; Hualiang Jiang (2005). „Cinanserin Is an Inhibitor of the 3C-Like Proteinase of Severe Acute Respiratory Syndrome Coronavirus and Strongly Reduces Virus Replication In Vitro”. J. Virol. 79: 7095—7103. Архивирано из оригинала 11. 08. 2020. г. Приступљено 16. 11. 2012. 

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