Ozolinone

Nowadays, Ozolinone is a topic that has captured the attention of people from all over the world. With its impact on society, economy and culture, Ozolinone has generated growing interest in its study and analysis. From its historical origins to its relevance in the modern world, Ozolinone has left a lasting mark on different aspects of everyday life. In this article, we will further explore the importance and influence of Ozolinone, as well as its implications for the future.

Ozolinone
Skeletal formula of ozolinone
Space-filling model of oxolinone
Clinical data
Routes of
administration		Oral
ATC code
  • None
Legal status
Legal status
  • In general: uncontrolled
Identifiers
  • (2Z)-2-(3-methyl-4-oxo-5-piperidin-1-yl-1,3-thiazolidin-2-ylidene)acetic acid
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
CompTox Dashboard (EPA)
ECHA InfoCard100.054.876 Edit this at Wikidata
Chemical and physical data
FormulaC11H16N2O3S
Molar mass256.32 g·mol−1
3D model (JSmol)
  • O=C(O)/C=C1/N(C)C(=O)C(S1)N2CCCCC2

Ozolinone is a loop diuretic which was never marketed.[1][2][3]

It is an active metabolite of etozoline.[2]

See also

References

  1. ^ Dictionary of organic compounds. London: Chapman & Hall. 1996. ISBN 0-412-54090-8.
  2. ^ a b Greven J, Heidenreich O (October 1978). "Effects of ozolinone, a diuretic active metabolite of etozoline, on renal function. I. Clearance studies in dogs". Naunyn-Schmiedeberg's Archives of Pharmacology. 304 (3): 283–7. doi:10.1007/bf00507970. PMID 714186. S2CID 20878253.
  3. ^ Greven J, Beckers M, Defrain W, Meywald K, Heidenreich O (March 1980). "Studies with the optically active isomers of the new diuretic drug ozolinone. II. Inhibition by d-ozolinone of furosemide-induced diuresis". Pflügers Archiv: European Journal of Physiology. 384 (1): 61–4. doi:10.1007/bf00589515. PMID 7189867. S2CID 13461213.


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