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

Details

Stereochemistry ACHIRAL
Molecular Formula C14H9Cl2N3O3
Molecular Weight 338.146
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CLODANOLENE

SMILES

ClC1=C(Cl)C=C(C=C1)C2=CC=C(O2)\C=N\N3CC(=O)NC3=O

InChI

InChIKey=HIQONTNPQNNMST-UBKPWBPPSA-N
InChI=1S/C14H9Cl2N3O3/c15-10-3-1-8(5-11(10)16)12-4-2-9(22-12)6-17-19-7-13(20)18-14(19)21/h1-6H,7H2,(H,18,20,21)/b17-6+

HIDE SMILES / InChI

Molecular Formula C14H9Cl2N3O3
Molecular Weight 338.146
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Clodanolene is a skeletal muscle contraction antagonist, closely related to dantrolene sodium. The drug has no measurable direct effect on the peripheral or central nervous systems. In a mouse of muscle spasticity (Straub-tail mouse), clodanolene induced skeletal muscle relaxation more effectively than neuromuscular blocking agents, local anesthetics, or centrally-acting muscle relaxants. Indirect evidence indicates clodanolene acts on caffeine-sensitive calcium stores in the muscle cells.

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:24:58 GMT 2023
Edited
by admin
on Fri Dec 15 15:24:58 GMT 2023
Record UNII
96L9G9BL3X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLODANOLENE
INN   USAN  
USAN   INN  
Official Name English
NSC-186557
Code English
2,4-IMIDAZOLIDINEDIONE, 1-(((5-(3,4-DICHLOROPHENYL)-2-FURANYL)METHYLENE)AMINO)-
Systematic Name English
F-413
Code English
CLODANOLENE [USAN]
Common Name English
clodanolene [INN]
Common Name English
1-[[5-(3,4-Dichlorophenyl)furfurylidene]amino]hydantoin
Systematic Name English
F-605 FREE ACID
Code English
Classification Tree Code System Code
NCI_THESAURUS C29696
Created by admin on Fri Dec 15 15:24:58 GMT 2023 , Edited by admin on Fri Dec 15 15:24:58 GMT 2023
Code System Code Type Description
PUBCHEM
9568463
Created by admin on Fri Dec 15 15:24:58 GMT 2023 , Edited by admin on Fri Dec 15 15:24:58 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106600
Created by admin on Fri Dec 15 15:24:58 GMT 2023 , Edited by admin on Fri Dec 15 15:24:58 GMT 2023
PRIMARY
INN
3981
Created by admin on Fri Dec 15 15:24:58 GMT 2023 , Edited by admin on Fri Dec 15 15:24:58 GMT 2023
PRIMARY
SMS_ID
100000084307
Created by admin on Fri Dec 15 15:24:58 GMT 2023 , Edited by admin on Fri Dec 15 15:24:58 GMT 2023
PRIMARY
MESH
C020999
Created by admin on Fri Dec 15 15:24:58 GMT 2023 , Edited by admin on Fri Dec 15 15:24:58 GMT 2023
PRIMARY
CAS
14796-28-2
Created by admin on Fri Dec 15 15:24:58 GMT 2023 , Edited by admin on Fri Dec 15 15:24:58 GMT 2023
PRIMARY
EVMPD
SUB06689MIG
Created by admin on Fri Dec 15 15:24:58 GMT 2023 , Edited by admin on Fri Dec 15 15:24:58 GMT 2023
PRIMARY
FDA UNII
96L9G9BL3X
Created by admin on Fri Dec 15 15:24:58 GMT 2023 , Edited by admin on Fri Dec 15 15:24:58 GMT 2023
PRIMARY
EPA CompTox
DTXSID70864535
Created by admin on Fri Dec 15 15:24:58 GMT 2023 , Edited by admin on Fri Dec 15 15:24:58 GMT 2023
PRIMARY
NCI_THESAURUS
C80981
Created by admin on Fri Dec 15 15:24:58 GMT 2023 , Edited by admin on Fri Dec 15 15:24:58 GMT 2023
PRIMARY
NSC
186557
Created by admin on Fri Dec 15 15:24:58 GMT 2023 , Edited by admin on Fri Dec 15 15:24:58 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY