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Details

Stereochemistry MIXED
Molecular Formula C9H18N2O2
Molecular Weight 186.2514
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CAPURIDE

SMILES

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

InChI

InChIKey=HLSLSXBFTXUKCY-UHFFFAOYSA-N
InChI=1S/C9H18N2O2/c1-4-6(3)7(5-2)8(12)11-9(10)13/h6-7H,4-5H2,1-3H3,(H3,10,11,12,13)

HIDE SMILES / InChI

Molecular Formula C9H18N2O2
Molecular Weight 186.2514
Charge 0
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Capuride is a a central nervous systemactive urea derivative of valnoctic acid patented by pharmaceutical company Abbott Laboratories as sedative therapeutic compound with a duration of hypnotic effect similar to that of the short‐acting barbiturates.

CNS Activity

Sources: Epilepsia (2010), 51, (3), 323-32.

Approval Year

PubMed

PubMed

TitleDatePubMed
Potent anticonvulsant urea derivatives of constitutional isomers of valproic acid.
2007 Dec 13
Anticonvulsant profile and teratogenic evaluation of potent new analogues of a valproic acid urea derivative in NMRI mice.
2009 Oct
Evaluation of stereoselective anticonvulsant, teratogenic, and pharmacokinetic profile of valnoctylurea (capuride): a chiral stereoisomer of valproic acid urea derivative.
2010 Mar
Patents

Patents

Sample Use Guides

400 mg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:09:09 GMT 2023
Edited
by admin
on Fri Dec 15 15:09:09 GMT 2023
Record UNII
3FO9QT93IS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CAPURIDE
INN   MI   USAN  
USAN   INN  
Official Name English
(2-Ethyl-3-methylvaleryl)urea
Systematic Name English
PENTANAMIDE, N-(AMINOCARBONYL)-2-ETHYL-3-METHYL-
Systematic Name English
NSC-27690
Code English
NSC-27178
Code English
CAPURIDE [MI]
Common Name English
MCN-X-94
Code English
capuride [INN]
Common Name English
CAPURIDE [USAN]
Common Name English
CAPURID
Common Name English
PACINOX
Brand Name English
Classification Tree Code System Code
NCI_THESAURUS C29756
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
Code System Code Type Description
MERCK INDEX
m619
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY Merck Index
DRUG CENTRAL
485
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
CHEBI
134831
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
PUBCHEM
231285
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
NSC
27690
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
CAS
5579-13-5
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
SMS_ID
100000081606
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
ChEMBL
CHEMBL392861
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
FDA UNII
3FO9QT93IS
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
MESH
C004646
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
INN
1650
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
NSC
27178
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
EPA CompTox
DTXSID5022728
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
EVMPD
SUB06082MIG
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
NCI_THESAURUS
C83587
Created by admin on Fri Dec 15 15:09:09 GMT 2023 , Edited by admin on Fri Dec 15 15:09:09 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY