Etodroxizine

Etodroxizine

Clinical data
ATC code	None
Legal status
Legal status	BR: Class C1 (Other controlled substances) [1]
Identifiers
IUPAC name 2-[2-(2-{4-[(4-Chlorophenyl)(phenyl)methyl]-1-piperazinyl}ethoxy)ethoxy]ethanol
CAS Number	17692-34-1
PubChem CID	63345
ChemSpider	57011
UNII	CI1S3XAK7O
ChEMBL	ChEMBL2104263
CompTox Dashboard (EPA)	DTXSID30864793
Chemical and physical data
Formula	C23H31ClN2O3
Molar mass	418.96 g·mol−1
3D model (JSmol)	Interactive image
SMILES c1ccc(cc1)C(c2ccc(cc2)Cl)N3CCN(CC3)CCOCCOCCO
InChI InChI=1S/C23H31ClN2O3/c24-22-8-6-21(7-9-22)23(20-4-2-1-3-5-20)26-12-10-25(11-13-26)14-16-28-18-19-29-17-15-27/h1-9,23,27H,10-19H2 Key:VUFOCTSXHUWGPW-UHFFFAOYSA-N

Etodroxizine (INN; brand names Vesparax, Drimyl, Indunox, and Isonox) is a first-generation antihistamine of the diphenylmethylpiperazine group which is used as a sedative/hypnotic drug in Europe and South Africa. ^{[2] [3] [4] [5]}

See also

• Hydroxyzine
• Pipoxizine

References

1. Anvisa (2023-03-31). "RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 784 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese). Diário Oficial da União (published 2023-04-04). Archived from the original on 2023-08-03. Retrieved 2023-08-16.
2. Index Nominum 2000: International Drug Directory. Taylor & Francis. January 2000. pp. 418–. ISBN   978-3-88763-075-1.
3. William Andrew Publishing (22 October 2013). Pharmaceutical Manufacturing Encyclopedia, 3rd Edition. Elsevier. pp. 1525–. ISBN   978-0-8155-1856-3.
4. Wolffgramm J, Lechner J, Coper H (1988). "Interaction of two barbiturates and an antihistamine on body temperature and motor performance of mice". Arzneimittelforschung. 38 (7): 885–91. PMID   2905131.
5. Maurer H, Pfleger K (1988). "Identification and differentiation of alkylamine antihistamines and their metabolites in urine by computerized gas chromatography-mass spectrometry". J Chromatogr. 430 (1): 31–41. doi:10.1016/s0378-4347(00)83131-x. PMID   2905706.