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

Details

Stereochemistry ACHIRAL
Molecular Formula C13H9BrN4O3
Molecular Weight 349.14
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of AZUMOLENE

SMILES

BrC1=CC=C(C=C1)C2=CN=C(O2)\C=N\N3CC(=O)NC3=O

InChI

InChIKey=SEGCNGONCZQFDW-OMCISZLKSA-N
InChI=1S/C13H9BrN4O3/c14-9-3-1-8(2-4-9)10-5-15-12(21-10)6-16-18-7-11(19)17-13(18)20/h1-6H,7H2,(H,17,19,20)/b16-6+

HIDE SMILES / InChI

Molecular Formula C13H9BrN4O3
Molecular Weight 349.14
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Azumolene is a direct-acting, skeletal muscle relaxant with structural similarities to dantrolene. It is a muscle relaxant that inhibits the release of calcium from skeletal muscle sarcoplasmic reticulum. Azumolene inhibits a component of store-operated calcium entry (SOCE) coupled to activation of type 1 ryanodine receptor (RyR1) by caffeine and ryanodine, whereas the SOCE component induced by thapsigargin is not affected. Azumolene distinguishes between two mechanisms of cellular signaling to SOCE in skeletal muscle, one that is coupled to and one independent from RyR1. Azumolene is equipotent to dantrolene sodium in blocking pharmacologic-induced muscle contractures and that azumolene is efficacious for treatment/prevention of malignant hyperthermia.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Component of store-operated calcium entry
PubMed

PubMed

TitleDatePubMed
Dantrolene inhibition of ryanodine receptor Ca2+ release channels. Molecular mechanism and isoform selectivity.
2001 Apr 27
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:33:25 GMT 2023
Edited
by admin
on Fri Dec 15 15:33:25 GMT 2023
Record UNII
5U7IO9CV80
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AZUMOLENE
INN  
INN  
Official Name English
1-(((5-(P-BROMOPHENYL)-2-OXAZOLYL)METHYLENE)AMINO)HYDANTOIN
Common Name English
2,4-IMIDAZOLIDINEDIONE, 1-(((5-(4-BROMOPHENYL)-2-OXAZOLYL)METHYLENE)AMINO)-
Systematic Name English
azumolene [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29696
Created by admin on Fri Dec 15 15:33:25 GMT 2023 , Edited by admin on Fri Dec 15 15:33:25 GMT 2023
Code System Code Type Description
EVMPD
SUB05665MIG
Created by admin on Fri Dec 15 15:33:25 GMT 2023 , Edited by admin on Fri Dec 15 15:33:25 GMT 2023
PRIMARY
FDA UNII
5U7IO9CV80
Created by admin on Fri Dec 15 15:33:25 GMT 2023 , Edited by admin on Fri Dec 15 15:33:25 GMT 2023
PRIMARY
ChEMBL
CHEMBL315108
Created by admin on Fri Dec 15 15:33:25 GMT 2023 , Edited by admin on Fri Dec 15 15:33:25 GMT 2023
PRIMARY
INN
5871
Created by admin on Fri Dec 15 15:33:25 GMT 2023 , Edited by admin on Fri Dec 15 15:33:25 GMT 2023
PRIMARY
WIKIPEDIA
Azumolene
Created by admin on Fri Dec 15 15:33:25 GMT 2023 , Edited by admin on Fri Dec 15 15:33:25 GMT 2023
PRIMARY
EPA CompTox
DTXSID20867096
Created by admin on Fri Dec 15 15:33:25 GMT 2023 , Edited by admin on Fri Dec 15 15:33:25 GMT 2023
PRIMARY
PUBCHEM
9568620
Created by admin on Fri Dec 15 15:33:25 GMT 2023 , Edited by admin on Fri Dec 15 15:33:25 GMT 2023
PRIMARY
CAS
64748-79-4
Created by admin on Fri Dec 15 15:33:25 GMT 2023 , Edited by admin on Fri Dec 15 15:33:25 GMT 2023
PRIMARY
MESH
C061387
Created by admin on Fri Dec 15 15:33:25 GMT 2023 , Edited by admin on Fri Dec 15 15:33:25 GMT 2023
PRIMARY
SMS_ID
100000086107
Created by admin on Fri Dec 15 15:33:25 GMT 2023 , Edited by admin on Fri Dec 15 15:33:25 GMT 2023
PRIMARY
NCI_THESAURUS
C72715
Created by admin on Fri Dec 15 15:33:25 GMT 2023 , Edited by admin on Fri Dec 15 15:33:25 GMT 2023
PRIMARY
CHEBI
143225
Created by admin on Fri Dec 15 15:33:25 GMT 2023 , Edited by admin on Fri Dec 15 15:33:25 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY