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Details

Stereochemistry RACEMIC
Molecular Formula C11H15N2O3.Na
Molecular Weight 246.2382
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ENALLYLPROPYMAL SODIUM

SMILES

[Na+].CC(C)C1(CC=C)C(=O)[N-]C(=O)N(C)C1=O

InChI

InChIKey=FWUAYRKNHAUSPM-UHFFFAOYSA-M
InChI=1S/C11H16N2O3.Na/c1-5-6-11(7(2)3)8(14)12-10(16)13(4)9(11)15;/h5,7H,1,6H2,2-4H3,(H,12,14,16);/q;+1/p-1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.98976928
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C11H16N2O3
Molecular Weight 224.2563
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Identification of the UDP-glucuronosyltransferase responsible for bucolome N-glucuronide formation in rats.
2010-11
Hydrogen-bond motifs in N-monosubstituted derivatives of barbituric acid: 5-allyl-5-isopropyl-1-methylbarbituric acid (enallylpropymal) and 1,5-di(but-2-enyl)-5-ethylbarbituric acid.
2010-01
Risks and benefits of combined use of bucolome and warfarin in anticoagulation therapy.
2010
Interferon-alpha is a predisposing risk factor for carbamazepine-induced hyponatremia: A case of syndrome of inappropriate antidiuresis caused by interferon-alpha therapy.
2008-11-30
Influences of haemodialysis on the binding sites of human serum albumin: possibility of an efficacious administration plan using binding inhibition.
2008-07
The effect of bucolome, a CYP2C9 inhibitor, on the pharmacokinetics of losartan.
2008
[Intraluminal ureteral hematoma complicating anticoagulant therapy].
2005-07
Usefulness of coadministration of bucolome in warfarin therapy: pharmacokinetic and pharmacodynamic analysis using outpatient prescriptions.
2005-04-11
Bucolome, a potent binding inhibitor for furosemide, alters the pharmacokinetics and diuretic effect of furosemide: potential for use of bucolome to restore diuretic response in nephrotic syndrome.
2005-04
Metabolism of bucolome in rats. Stability and biliary excretion of bucolome N-glucuronide.
2001-08-05
The stereoselective effects of bucolome on the pharmacokinetics and pharmacodynamics of racemic warfarin.
2001-04
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 22:42:30 GMT 2025
Edited
by admin
on Mon Mar 31 22:42:30 GMT 2025
Record UNII
2N3C21X38F
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ENALLYLPROPYMAL SODIUM
Common Name English
ENALLYLPROPYMAL SODIUM SALT
MI  
Preferred Name English
ENALLYLPROPYMAL SODIUM SALT [MI]
Common Name English
2,4,6(1H,3H,5H)-PYRIMIDINETRIONE, 1-METHYL-5-(1-METHYLETHYL)-5-(2-PROPEN-1-YL)-, SODIUM SALT (1:1)
Common Name English
Code System Code Type Description
CAS
59005-68-4
Created by admin on Mon Mar 31 22:42:30 GMT 2025 , Edited by admin on Mon Mar 31 22:42:30 GMT 2025
PRIMARY
MERCK INDEX
m716
Created by admin on Mon Mar 31 22:42:30 GMT 2025 , Edited by admin on Mon Mar 31 22:42:30 GMT 2025
PRIMARY Merck Index
PUBCHEM
91667971
Created by admin on Mon Mar 31 22:42:30 GMT 2025 , Edited by admin on Mon Mar 31 22:42:30 GMT 2025
PRIMARY
FDA UNII
2N3C21X38F
Created by admin on Mon Mar 31 22:42:30 GMT 2025 , Edited by admin on Mon Mar 31 22:42:30 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE