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

Details

Stereochemistry ACHIRAL
Molecular Formula C13H20N4O3
Molecular Weight 280.3229
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CICLOSIDOMINE

SMILES

O=C([N-]C1=C[N+](=NO1)N2CCOCC2)C3CCCCC3

InChI

InChIKey=AJPLPOWGYORUIF-UHFFFAOYSA-N
InChI=1S/C13H20N4O3/c18-13(11-4-2-1-3-5-11)14-12-10-17(15-20-12)16-6-8-19-9-7-16/h10-11H,1-9H2

HIDE SMILES / InChI

Molecular Formula C13H21N4O3
Molecular Weight 281.3308
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Ciclosidomine is morpholine derivative and nitric oxide donors developed for vascular diseases treatment.

Approval Year

PubMed

PubMed

TitleDatePubMed
Solution stability of ciclosidomine.
1987-05
Patents

Patents

Sample Use Guides

1 mg/kg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:31:38 GMT 2025
Edited
by admin
on Mon Mar 31 18:31:38 GMT 2025
Record UNII
S7P608OW2O
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PR-G 138-CL FREE BASE
Preferred Name English
CICLOSIDOMINE
INN   MI  
INN  
Official Name English
ciclosidomine [INN]
Common Name English
SYDNONE IMINE, N-(CYCLOHEXYLCARBONYL)-3-(4-MORPHOLINYL)-
Systematic Name English
CICLOSIDOMINE [MI]
Common Name English
PR-G-138-CL FREE BASE
Code English
1,2,3-OXADIAZOLIUM, 5-((CYCLOHEXYLCARBONYL)AMINO)-3-(4-MORPHOLINYL)-, INNER SALT
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29707
Created by admin on Mon Mar 31 18:31:38 GMT 2025 , Edited by admin on Mon Mar 31 18:31:38 GMT 2025
NCI_THESAURUS C45845
Created by admin on Mon Mar 31 18:31:38 GMT 2025 , Edited by admin on Mon Mar 31 18:31:38 GMT 2025
Code System Code Type Description
FDA UNII
S7P608OW2O
Created by admin on Mon Mar 31 18:31:38 GMT 2025 , Edited by admin on Mon Mar 31 18:31:38 GMT 2025
PRIMARY
EVMPD
SUB06249MIG
Created by admin on Mon Mar 31 18:31:38 GMT 2025 , Edited by admin on Mon Mar 31 18:31:38 GMT 2025
PRIMARY
MESH
C045064
Created by admin on Mon Mar 31 18:31:38 GMT 2025 , Edited by admin on Mon Mar 31 18:31:38 GMT 2025
PRIMARY
ChEMBL
CHEMBL2104476
Created by admin on Mon Mar 31 18:31:38 GMT 2025 , Edited by admin on Mon Mar 31 18:31:38 GMT 2025
PRIMARY
PUBCHEM
71972
Created by admin on Mon Mar 31 18:31:38 GMT 2025 , Edited by admin on Mon Mar 31 18:31:38 GMT 2025
PRIMARY
DRUG CENTRAL
3709
Created by admin on Mon Mar 31 18:31:38 GMT 2025 , Edited by admin on Mon Mar 31 18:31:38 GMT 2025
PRIMARY
CAS
66564-16-7
Created by admin on Mon Mar 31 18:31:38 GMT 2025 , Edited by admin on Mon Mar 31 18:31:38 GMT 2025
PRIMARY
EPA CompTox
DTXSID40216744
Created by admin on Mon Mar 31 18:31:38 GMT 2025 , Edited by admin on Mon Mar 31 18:31:38 GMT 2025
PRIMARY
MERCK INDEX
m649
Created by admin on Mon Mar 31 18:31:38 GMT 2025 , Edited by admin on Mon Mar 31 18:31:38 GMT 2025
PRIMARY Merck Index
SMS_ID
100000081305
Created by admin on Mon Mar 31 18:31:38 GMT 2025 , Edited by admin on Mon Mar 31 18:31:38 GMT 2025
PRIMARY
INN
4547
Created by admin on Mon Mar 31 18:31:38 GMT 2025 , Edited by admin on Mon Mar 31 18:31:38 GMT 2025
PRIMARY
NCI_THESAURUS
C77149
Created by admin on Mon Mar 31 18:31:38 GMT 2025 , Edited by admin on Mon Mar 31 18:31:38 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY