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Details

Stereochemistry RACEMIC
Molecular Formula C11H16N2O3
Molecular Weight 224.2563
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ENALLYLPROPYMAL

SMILES

CC(C)C1(CC=C)C(=O)NC(=O)N(C)C1=O

InChI

InChIKey=AXJXURWWUFZZKN-UHFFFAOYSA-N
InChI=1S/C11H16N2O3/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)

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 ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Metabolism of bucolome in rats. Stability and biliary excretion of bucolome N-glucuronide.
2001 Aug 5
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
17BT2X209M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ENALLYLPROPYMAL
MI  
Common Name English
2,4,6(1H,3H,5H)-PYRIMIDINETRIONE, 1-METHYL-5-(1-METHYLETHYL)-5-(2-PROPEN-1-YL)-
Systematic Name English
NSC-25571
Code English
N-METHYL-5-ALLYL-5-ISOPROPYLBARBITURIC ACID
Systematic Name English
5-ALLYL-5-ISOPROPYL-1-METHYLBARBITURIC ACID
Systematic Name English
ENALLYLPROPYMAL [MI]
Common Name English
NARCONUMAL
Common Name English
Code System Code Type Description
DRUG CENTRAL
3448
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
NSC
25571
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
CAS
1861-21-8
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
WIKIPEDIA
Enallylpropymal
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
ECHA (EC/EINECS)
217-463-1
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
PUBCHEM
95636
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
17BT2X209M
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
EPA CompTox
DTXSID40871852
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
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SALT/SOLVATE -> PARENT
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ACTIVE MOIETY