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

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
The stereoselective effects of bucolome on the pharmacokinetics and pharmacodynamics of racemic warfarin.
2001 Apr
Metabolism of bucolome in rats. Stability and biliary excretion of bucolome N-glucuronide.
2001 Aug 5
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 Apr
Usefulness of coadministration of bucolome in warfarin therapy: pharmacokinetic and pharmacodynamic analysis using outpatient prescriptions.
2005 Apr 11
[Intraluminal ureteral hematoma complicating anticoagulant therapy].
2005 Jul
The effect of bucolome, a CYP2C9 inhibitor, on the pharmacokinetics of losartan.
2008
Influences of haemodialysis on the binding sites of human serum albumin: possibility of an efficacious administration plan using binding inhibition.
2008 Jul
Interferon-alpha is a predisposing risk factor for carbamazepine-induced hyponatremia: A case of syndrome of inappropriate antidiuresis caused by interferon-alpha therapy.
2008 Nov 30
Risks and benefits of combined use of bucolome and warfarin in anticoagulation therapy.
2010
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 Jan
Identification of the UDP-glucuronosyltransferase responsible for bucolome N-glucuronide formation in rats.
2010 Nov
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 09:32:21 UTC 2023
Edited
by admin
on Sat Dec 16 09:32:21 UTC 2023
Record UNII
2N3C21X38F
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ENALLYLPROPYMAL SODIUM
Common Name English
ENALLYLPROPYMAL SODIUM SALT [MI]
Common Name English
ENALLYLPROPYMAL SODIUM SALT
MI  
Systematic 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 Sat Dec 16 09:32:21 UTC 2023 , Edited by admin on Sat Dec 16 09:32:21 UTC 2023
PRIMARY
MERCK INDEX
m716
Created by admin on Sat Dec 16 09:32:21 UTC 2023 , Edited by admin on Sat Dec 16 09:32:21 UTC 2023
PRIMARY Merck Index
PUBCHEM
91667971
Created by admin on Sat Dec 16 09:32:21 UTC 2023 , Edited by admin on Sat Dec 16 09:32:21 UTC 2023
PRIMARY
FDA UNII
2N3C21X38F
Created by admin on Sat Dec 16 09:32:21 UTC 2023 , Edited by admin on Sat Dec 16 09:32:21 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE