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Details

Stereochemistry ACHIRAL
Molecular Formula C14H19N3O
Molecular Weight 245.3202
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of XILOBAM

SMILES

CN1CCCC1=NC(=O)NC2=C(C)C=CC=C2C

InChI

InChIKey=PAXRPWSXCPTPCA-UHFFFAOYSA-N
InChI=1S/C14H19N3O/c1-10-6-4-7-11(2)13(10)16-14(18)15-12-8-5-9-17(12)3/h4,6-7H,5,8-9H2,1-3H3,(H,16,18)

HIDE SMILES / InChI

Molecular Formula C14H19N3O
Molecular Weight 245.3202
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Xilobam, a pyrrolidinylidene urea analog was developed as a muscle relaxant. Experiments on animal have shown that this compound was not sedating or anxiolytic in man. Information about the current use of xilobam is not available.

Approval Year

PubMed

PubMed

TitleDatePubMed
Recent advances in biotransformation of CNS and cardiovascular agents.
2000-11
Metabolism of xilobam in laboratory animals and man.
1994-07
Xilobam: analysis, determination of decomposition products, and assessment of stability.
1981-07
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:40:30 GMT 2025
Edited
by admin
on Mon Mar 31 18:40:30 GMT 2025
Record UNII
Q53S20XGPU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
xilobam [INN]
Preferred Name English
XILOBAM
INN   USAN  
USAN   INN  
Official Name English
XILOBAM [USAN]
Common Name English
UREA, N-(2,6-DIMETHYLPHENYL)-N-(1-METHYL-2-PYRROLIDINYLIDENE)-
Common Name English
MCN-3113
Code English
1-(1-Methyl-2-pyrrolidinylidene)-3-(2,6-xylyl)urea
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29696
Created by admin on Mon Mar 31 18:40:30 GMT 2025 , Edited by admin on Mon Mar 31 18:40:30 GMT 2025
Code System Code Type Description
INN
4064
Created by admin on Mon Mar 31 18:40:30 GMT 2025 , Edited by admin on Mon Mar 31 18:40:30 GMT 2025
PRIMARY
SMS_ID
100000079358
Created by admin on Mon Mar 31 18:40:30 GMT 2025 , Edited by admin on Mon Mar 31 18:40:30 GMT 2025
PRIMARY
CAS
50528-97-7
Created by admin on Mon Mar 31 18:40:30 GMT 2025 , Edited by admin on Mon Mar 31 18:40:30 GMT 2025
PRIMARY
MESH
C017798
Created by admin on Mon Mar 31 18:40:30 GMT 2025 , Edited by admin on Mon Mar 31 18:40:30 GMT 2025
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NCI_THESAURUS
C152933
Created by admin on Mon Mar 31 18:40:30 GMT 2025 , Edited by admin on Mon Mar 31 18:40:30 GMT 2025
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FDA UNII
Q53S20XGPU
Created by admin on Mon Mar 31 18:40:30 GMT 2025 , Edited by admin on Mon Mar 31 18:40:30 GMT 2025
PRIMARY
EVMPD
SUB00112MIG
Created by admin on Mon Mar 31 18:40:30 GMT 2025 , Edited by admin on Mon Mar 31 18:40:30 GMT 2025
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EPA CompTox
DTXSID3046164
Created by admin on Mon Mar 31 18:40:30 GMT 2025 , Edited by admin on Mon Mar 31 18:40:30 GMT 2025
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ChEMBL
CHEMBL382769
Created by admin on Mon Mar 31 18:40:30 GMT 2025 , Edited by admin on Mon Mar 31 18:40:30 GMT 2025
PRIMARY
PUBCHEM
39689
Created by admin on Mon Mar 31 18:40:30 GMT 2025 , Edited by admin on Mon Mar 31 18:40:30 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY