Fenethazine

This article will address the topic of Fenethazine, which has sparked great interest and debate in contemporary society. Fenethazine is a topic that has marked a before and after in the way we understand the current world, since it has generated divided opinions and has provoked various controversies. Throughout this writing, we will delve into the different aspects related to Fenethazine, analyzing its implications, repercussions and possible solutions. Likewise, various points of view will be presented to achieve a complete and enriching understanding of Fenethazine.

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.[1] Promethazine and chlorpromazine, were derived from fenethazine.[2] Fenethazine, in turn, was derived from phenbenzamine.[3]

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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