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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 May
Patents

Patents

Sample Use Guides

1 mg/kg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:34:17 GMT 2023
Edited
by admin
on Fri Dec 15 16:34:17 GMT 2023
Record UNII
S7P608OW2O
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CICLOSIDOMINE
INN   MI  
INN  
Official Name English
ciclosidomine [INN]
Common Name English
PR-G 138-CL FREE BASE
Code 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 Fri Dec 15 16:34:18 GMT 2023 , Edited by admin on Fri Dec 15 16:34:18 GMT 2023
NCI_THESAURUS C45845
Created by admin on Fri Dec 15 16:34:18 GMT 2023 , Edited by admin on Fri Dec 15 16:34:18 GMT 2023
Code System Code Type Description
FDA UNII
S7P608OW2O
Created by admin on Fri Dec 15 16:34:18 GMT 2023 , Edited by admin on Fri Dec 15 16:34:18 GMT 2023
PRIMARY
EVMPD
SUB06249MIG
Created by admin on Fri Dec 15 16:34:18 GMT 2023 , Edited by admin on Fri Dec 15 16:34:18 GMT 2023
PRIMARY
MESH
C045064
Created by admin on Fri Dec 15 16:34:18 GMT 2023 , Edited by admin on Fri Dec 15 16:34:18 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104476
Created by admin on Fri Dec 15 16:34:18 GMT 2023 , Edited by admin on Fri Dec 15 16:34:18 GMT 2023
PRIMARY
PUBCHEM
71972
Created by admin on Fri Dec 15 16:34:18 GMT 2023 , Edited by admin on Fri Dec 15 16:34:18 GMT 2023
PRIMARY
DRUG CENTRAL
3709
Created by admin on Fri Dec 15 16:34:18 GMT 2023 , Edited by admin on Fri Dec 15 16:34:18 GMT 2023
PRIMARY
CAS
66564-16-7
Created by admin on Fri Dec 15 16:34:18 GMT 2023 , Edited by admin on Fri Dec 15 16:34:18 GMT 2023
PRIMARY
EPA CompTox
DTXSID40216744
Created by admin on Fri Dec 15 16:34:18 GMT 2023 , Edited by admin on Fri Dec 15 16:34:18 GMT 2023
PRIMARY
MERCK INDEX
m649
Created by admin on Fri Dec 15 16:34:18 GMT 2023 , Edited by admin on Fri Dec 15 16:34:18 GMT 2023
PRIMARY Merck Index
SMS_ID
100000081305
Created by admin on Fri Dec 15 16:34:18 GMT 2023 , Edited by admin on Fri Dec 15 16:34:18 GMT 2023
PRIMARY
INN
4547
Created by admin on Fri Dec 15 16:34:18 GMT 2023 , Edited by admin on Fri Dec 15 16:34:18 GMT 2023
PRIMARY
NCI_THESAURUS
C77149
Created by admin on Fri Dec 15 16:34:18 GMT 2023 , Edited by admin on Fri Dec 15 16:34:18 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY