Azosemide

Azosemide

Clinical data
AHFS/Drugs.com	International Drug Names
ATC code	none
Identifiers
IUPAC name 2-chloro-5-(2H-tetrazol-5-yl)-4-[(thiophen-2-ylmethyl)amino]benzenesulfonamide
CAS Number	27589-33-9 N
PubChem CID	2273
DrugBank	DB08961 N
ChemSpider	2186 Y
UNII	MR40VT1L8Z
KEGG	D01323 Y
ChEBI	CHEBI:31248 Y
ChEMBL	ChEMBL1097235 Y
CompTox Dashboard (EPA)	DTXSID7046910
ECHA InfoCard	100.044.121
Chemical and physical data
Formula	C12H11ClN6O2S2
Molar mass	370.83 g·mol−1
3D model (JSmol)	Interactive image
SMILES O=S(=O)(N)c2c(Cl)cc(c(c1n[nH]nn1)c2)NCc3sccc3
InChI InChI=1S/C12H11ClN6O2S2/c13-9-5-10(15-6-7-2-1-3-22-7)8(12-16-18-19-17-12)4-11(9)23(14,20)21/h1-5,15H,6H2,(H2,14,20,21)(H,16,17,18,19) Y Key:HMEDEBAJARCKCT-UHFFFAOYSA-N Y
NY (what is this?)  (verify)

Azosemide is a high-ceiling loop diuretic agent that was brought to market in 1981 by Boehringer Mannheim.^[1][2] As of 2015 it was available as a generic in some Asian countries.^[3]

Azosemide has been found as an adulterant in ketamine.^[4]

1. ^ Sittig M (1988). Pharmaceutical Manufacturing Encyclopedia (PDF). Vol. 1. Noyes Publications. p. 122. ISBN 978-0-8155-1144-1. Archived from the original (PDF) on 2007-10-23.
2. ^ Bormann D (January 1980). "Diuretics". In Hess HJ (ed.). Annual Reports in Medicinal Chemistry. Vol. 15. Academic Press. pp. 100–105 (101). ISBN 978-0-08-058359-4.
3. ^ "International listings for azosemide". Drugs.com. Retrieved 23 July 2015.
4. ^ "Drug Checking Report 2011" (PDF). Energy Control. Archived (PDF) from the original on 20 January 2022. Retrieved 20 January 2022.

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