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Details

Stereochemistry ACHIRAL
Molecular Formula C13H21N4O3.Cl
Molecular Weight 316.784
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CICLOSIDOMINE HYDROCHLORIDE

SMILES

[Cl-].O=C(NC1=C[N+](=NO1)N2CCOCC2)C3CCCCC3

InChI

InChIKey=KWILRBFYPCZOID-UHFFFAOYSA-N
InChI=1S/C13H20N4O3.ClH/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;1H

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

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
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 17:57:46 GMT 2025
Edited
by admin
on Mon Mar 31 17:57:46 GMT 2025
Record UNII
644XF6791D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NEOPRES
Preferred Name English
CICLOSIDOMINE HYDROCHLORIDE
MART.   MI  
Common Name English
CICLOSIDOMINE HYDROCHLORIDE [MART.]
Common Name English
CICLOSIDOMINE HYDROCHLORIDE [MI]
Common Name English
PR-G 138-CL
Code English
1,2,3-OXADIAZOLIUM, 5-((CYCLOHEXYLCARBONYL)AMINO)-3-(4-MORPHOLINYL)-, CHLORIDE (1:1)
Systematic Name English
PR-G-138-CL
Code English
Code System Code Type Description
FDA UNII
644XF6791D
Created by admin on Mon Mar 31 17:57:46 GMT 2025 , Edited by admin on Mon Mar 31 17:57:46 GMT 2025
PRIMARY
PUBCHEM
71587080
Created by admin on Mon Mar 31 17:57:46 GMT 2025 , Edited by admin on Mon Mar 31 17:57:46 GMT 2025
PRIMARY
MERCK INDEX
m649
Created by admin on Mon Mar 31 17:57:46 GMT 2025 , Edited by admin on Mon Mar 31 17:57:46 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID50180846
Created by admin on Mon Mar 31 17:57:46 GMT 2025 , Edited by admin on Mon Mar 31 17:57:46 GMT 2025
PRIMARY
MESH
C045064
Created by admin on Mon Mar 31 17:57:46 GMT 2025 , Edited by admin on Mon Mar 31 17:57:46 GMT 2025
PRIMARY
CAS
26209-07-4
Created by admin on Mon Mar 31 17:57:46 GMT 2025 , Edited by admin on Mon Mar 31 17:57:46 GMT 2025
PRIMARY
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