Fenethazine

The importance of Fenethazine in today's society is undeniable. Whether as a public figure, as a topic of debate, or as part of history, Fenethazine has left his mark on the lives of many people. In this article we will explore its influence in different aspects, from its impact on popular culture to its contributions in the scientific field. Through in-depth analysis, we will be able to better understand the role Fenethazine has played in the world and the relevance it continues to have today.

Fenethazine
Clinical data
Other namesPhenethazinum, Phenethazine, Phenetazine; RP-3015, SC-1627, WY-1143
Identifiers
  • N,N-Dimethyl-2-phenothiazin-10-ylethanamine
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.007.570 Edit this at Wikidata
Chemical and physical data
FormulaC16H18N2S
Molar mass270.39 g·mol−1
3D model (JSmol)
  • CN(C)CCN1C2=CC=CC=C2SC3=CC=CC=C31
  • InChI=1S/C16H18N2S/c1-17(2)11-12-18-13-7-3-5-9-15(13)19-16-10-6-4-8-14(16)18/h3-10H,11-12H2,1-2H3 checkY
  • Key:PFAXACNYGZVKMX-UHFFFAOYSA-N checkY

Fenethazine (INN) (brand names Anergen, Contralergial, Ethysine, Etisine, Lisergan, Lysergan; former developmental code names RP-3015, SC-1627, WY-1143), or phenethazine, is a first-generation antihistamine of the phenothiazine group. Promethazine and chlorpromazine, were derived from fenethazine. Fenethazine, in turn, was derived from phenbenzamine.

References

  1. ^ Elks J (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 434–. ISBN 978-1-4757-2085-3.
  2. ^ Dörwald FZ (4 February 2013). Lead Optimization for Medicinal Chemists: Pharmacokinetic Properties of Functional Groups and Organic Compounds. John Wiley & Sons. pp. 301–. ISBN 978-3-527-64565-7.
  3. ^ Sneader W (23 June 2005). Drug Discovery: A History. John Wiley & Sons. pp. 404–. ISBN 978-0-471-89979-2.



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