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Details

Stereochemistry ACHIRAL
Molecular Formula C9H15NO3
Molecular Weight 185.2203
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PROPAZONE

SMILES

CCCC1(CCC)OC(=O)NC1=O

InChI

InChIKey=BVTOXVHDKWVNBF-UHFFFAOYSA-N
InChI=1S/C9H15NO3/c1-3-5-9(6-4-2)7(11)10-8(12)13-9/h3-6H2,1-2H3,(H,10,11,12)

HIDE SMILES / InChI

Molecular Formula C9H15NO3
Molecular Weight 185.2203
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
In Utero Exposure to a Cardiac Teratogen Causes Reversible Deficits in Postnatal Cardiovascular Function, But Altered Adaptation to the Burden of Pregnancy.
2015-11
Maternal rat serum concentrations of dimethadione do not explain intra-litter differences in the incidence of dimethadione-induced birth defects, including novel findings in foetal lung.
2014-12-04
In utero dimethadione exposure causes postnatal disruption in cardiac structure and function in the rat.
2014-12
Alterations in mouse embryo intracellular pH by DMO during culture impair implantation and fetal growth.
2010-08
Acidic and basic solutions dissolve protein plugs made of lithostathine complicating choledochal cyst/pancreaticobiliary maljunction.
2009-07
Review of levetiracetam, with a focus on the extended release formulation, as adjuvant therapy in controlling partial-onset seizures.
2009
Glucose loading precipitates focal lactic acidosis in the vulnerable medial thalamus of thiamine-deficient rats.
2008-03
Polytherapy with hERG-blocking antiepileptic drugs: increased risk for embryonic cardiac arrhythmia and teratogenicity.
2007-08
Embryonic cardiac arrhythmia and generation of reactive oxygen species: common teratogenic mechanism for IKr blocking drugs.
2007-07
Pharmacological evidence that stalk cell differentiation involves increases in the intracellular Ca(2+) and H(+) concentrations in Dictyostelium discoideum.
2007-04
Thoracic skeletal defects and cardiac malformations: a common epigenetic link?
2006-12
Interactive effects of cadmium and all-trans-retinoic acid on the induction of forelimb ectrodactyly in C57BL/6 mice.
2006-01
Discriminative power of an assay for automated in vitro screening of teratogens.
2004-08
Disruption of bovine oocytes and preimplantation embryos by urea and acidic pH.
2003-04
Embryonic arrhythmia by inhibition of HERG channels: a common hypoxia-related teratogenic mechanism for antiepileptic drugs?
2002-05
Selection of test chemicals for the ECVAM international validation study on in vitro embryotoxicity tests. European Centre for the Validation of Alternative Methods.
2002-04-25
The clinical importance of the trimethadione tolerance test as a method for quantitative assessment of hepatic functional reserve in patients with biliary atresia.
2001-12
Na(+)-dependent pH regulation by the amitochondriate protozoan parasite Giardia intestinalis.
2001-08-03
Altering intracellular pH disrupts development and cellular organization in preimplantation hamster embryos.
2001-06
Trimethadione N-demethylation by rat liver CYP2E1 in vitro.
1996-07
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 22:53:06 GMT 2025
Edited
by admin
on Mon Mar 31 22:53:06 GMT 2025
Record UNII
3Q181RIU8E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
5,5-DIPROPYL-2,4-OXAZOLIDINEDIONE
MI  
Preferred Name English
PROPAZONE
Common Name English
2,4-OXAZOLIDINEDIONE, 5,5-DIPROPYL-
Systematic Name English
5,5-DIPROPYL-2,4-OXAZOLIDINEDIONE [MI]
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID20275778
Created by admin on Mon Mar 31 22:53:06 GMT 2025 , Edited by admin on Mon Mar 31 22:53:06 GMT 2025
PRIMARY
CAS
512-12-9
Created by admin on Mon Mar 31 22:53:06 GMT 2025 , Edited by admin on Mon Mar 31 22:53:06 GMT 2025
PRIMARY
MERCK INDEX
m707
Created by admin on Mon Mar 31 22:53:06 GMT 2025 , Edited by admin on Mon Mar 31 22:53:06 GMT 2025
PRIMARY Merck Index
PUBCHEM
79876
Created by admin on Mon Mar 31 22:53:06 GMT 2025 , Edited by admin on Mon Mar 31 22:53:06 GMT 2025
PRIMARY
FDA UNII
3Q181RIU8E
Created by admin on Mon Mar 31 22:53:06 GMT 2025 , Edited by admin on Mon Mar 31 22:53:06 GMT 2025
PRIMARY