U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C7H7N5
Molecular Weight 161.164
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FENAMOLE

SMILES

NC1=NN=NN1C2=CC=CC=C2

InChI

InChIKey=ULIDRMKBVYYVIQ-UHFFFAOYSA-N
InChI=1S/C7H7N5/c8-7-9-10-11-12(7)6-4-2-1-3-5-6/h1-5H,(H2,8,9,11)

HIDE SMILES / InChI

Molecular Formula C7H7N5
Molecular Weight 161.164
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Fenamole is a muscle relaxant. It is effectively inhibits muscle spasms at good levels for a four hours and at significant levels for six hours. Clinical benefits were derived in patients with spasticity-spasm for periods up to 24 hours after a single oral dose. Fenamole is relatively free of adverse side effects particularly in the central nervous system. It is a potent copper chelator. It was once investigated as a potential antirheumatic agent in man.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Palliative
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Synthesis, characterization, and biological evaluation of new tetrazole-based platinum(II) and palladium(II) chlorido complexes--potent cisplatin analogues and their trans isomers.
2013-03
Two derivatives of 5-aminotetrazole: 5-amino-1-phenyltetrazole and 5-amino-1-(1-naphthyl)tetrazole.
2003-12
Patents

Sample Use Guides

In Vivo Use Guide
800 mg single dose
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:49:07 GMT 2025
Edited
by admin
on Mon Mar 31 17:49:07 GMT 2025
Record UNII
K4H264PBQ7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FENAMOLE
INN   USAN  
USAN   INN  
Official Name English
AL 0559
Preferred Name English
NSC-25413
Code English
PAT
Code English
fenamole [INN]
Common Name English
1H-TETRAZOL-5-AMINE, 1-PHENYL-
Systematic Name English
AL-0559
Code English
FENAMOLE [USAN]
Common Name English
P-463
Code English
5-Amino-1-phenyl-1H-tetrazole
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C257
Created by admin on Mon Mar 31 17:49:07 GMT 2025 , Edited by admin on Mon Mar 31 17:49:07 GMT 2025
Code System Code Type Description
NCI_THESAURUS
C80547
Created by admin on Mon Mar 31 17:49:07 GMT 2025 , Edited by admin on Mon Mar 31 17:49:07 GMT 2025
PRIMARY
PUBCHEM
21640
Created by admin on Mon Mar 31 17:49:07 GMT 2025 , Edited by admin on Mon Mar 31 17:49:07 GMT 2025
PRIMARY
EPA CompTox
DTXSID4048694
Created by admin on Mon Mar 31 17:49:07 GMT 2025 , Edited by admin on Mon Mar 31 17:49:07 GMT 2025
PRIMARY
FDA UNII
K4H264PBQ7
Created by admin on Mon Mar 31 17:49:07 GMT 2025 , Edited by admin on Mon Mar 31 17:49:07 GMT 2025
PRIMARY
SMS_ID
100000081262
Created by admin on Mon Mar 31 17:49:07 GMT 2025 , Edited by admin on Mon Mar 31 17:49:07 GMT 2025
PRIMARY
DRUG BANK
DB12506
Created by admin on Mon Mar 31 17:49:07 GMT 2025 , Edited by admin on Mon Mar 31 17:49:07 GMT 2025
PRIMARY
INN
2079
Created by admin on Mon Mar 31 17:49:07 GMT 2025 , Edited by admin on Mon Mar 31 17:49:07 GMT 2025
PRIMARY
ChEMBL
CHEMBL2106224
Created by admin on Mon Mar 31 17:49:07 GMT 2025 , Edited by admin on Mon Mar 31 17:49:07 GMT 2025
PRIMARY
NSC
25413
Created by admin on Mon Mar 31 17:49:07 GMT 2025 , Edited by admin on Mon Mar 31 17:49:07 GMT 2025
PRIMARY
EVMPD
SUB07539MIG
Created by admin on Mon Mar 31 17:49:07 GMT 2025 , Edited by admin on Mon Mar 31 17:49:07 GMT 2025
PRIMARY
ECHA (EC/EINECS)
226-780-4
Created by admin on Mon Mar 31 17:49:07 GMT 2025 , Edited by admin on Mon Mar 31 17:49:07 GMT 2025
PRIMARY
CAS
5467-78-7
Created by admin on Mon Mar 31 17:49:07 GMT 2025 , Edited by admin on Mon Mar 31 17:49:07 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY