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Details

Stereochemistry RACEMIC
Molecular Formula C12H13NO.C4H6O5
Molecular Weight 321.3252
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NAFOMINE MALATE

SMILES

OC(CC(O)=O)C(O)=O.CC1=C(CON)C2=CC=CC=C2C=C1

InChI

InChIKey=VZJYMJIBQDNNRI-UHFFFAOYSA-N
InChI=1S/C12H13NO.C4H6O5/c1-9-6-7-10-4-2-3-5-11(10)12(9)8-14-13;5-2(4(8)9)1-3(6)7/h2-7H,8,13H2,1H3;2,5H,1H2,(H,6,7)(H,8,9)

HIDE SMILES / InChI

Molecular Formula C4H6O5
Molecular Weight 134.0874
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula C12H13NO
Molecular Weight 187.2377
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including: https://www.google.ch/patents/US6323236

Nafomine is the muscle relaxant. It was tested on lower extremity spasms in spinal cord injuries.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Effects of nafomine malate on lower extremity spasms in spinal cord injuries (a preliminary study).
1971
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:37:38 UTC 2023
Edited
by admin
on Fri Dec 15 18:37:38 UTC 2023
Record UNII
6GY9OKU6VW
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NAFOMINE MALATE
USAN  
USAN  
Official Name English
BUTANEDIOIC ACID, HYDROXY-, COMPD. WITH O-((2-METHYL-1-NAPHTHALENYL)METHYL)HYDROXYLAMINE (1:1)
Common Name English
NAFOMINE MALATE [USAN]
Common Name English
Malic acid compound with O-[(2-methyl-1-naphthyl)methyl]hydroxylamine (1:1)
Systematic Name English
Code System Code Type Description
CAS
23247-36-1
Created by admin on Fri Dec 15 18:37:38 UTC 2023 , Edited by admin on Fri Dec 15 18:37:38 UTC 2023
PRIMARY
FDA UNII
6GY9OKU6VW
Created by admin on Fri Dec 15 18:37:38 UTC 2023 , Edited by admin on Fri Dec 15 18:37:38 UTC 2023
PRIMARY
NCI_THESAURUS
C166937
Created by admin on Fri Dec 15 18:37:38 UTC 2023 , Edited by admin on Fri Dec 15 18:37:38 UTC 2023
PRIMARY
ChEMBL
CHEMBL2110690
Created by admin on Fri Dec 15 18:37:38 UTC 2023 , Edited by admin on Fri Dec 15 18:37:38 UTC 2023
PRIMARY
PUBCHEM
31748
Created by admin on Fri Dec 15 18:37:38 UTC 2023 , Edited by admin on Fri Dec 15 18:37:38 UTC 2023
PRIMARY
EPA CompTox
DTXSID60945928
Created by admin on Fri Dec 15 18:37:38 UTC 2023 , Edited by admin on Fri Dec 15 18:37:38 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
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ACTIVE MOIETY