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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 May
Patents

Patents

Sample Use Guides

1 mg/kg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:26:22 GMT 2023
Edited
by admin
on Fri Dec 15 15:26:22 GMT 2023
Record UNII
644XF6791D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CICLOSIDOMINE HYDROCHLORIDE
MART.   MI  
Common Name English
CICLOSIDOMINE HYDROCHLORIDE [MART.]
Common Name English
CICLOSIDOMINE HYDROCHLORIDE [MI]
Common Name English
NEOPRES
Brand 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 Fri Dec 15 15:26:22 GMT 2023 , Edited by admin on Fri Dec 15 15:26:22 GMT 2023
PRIMARY
PUBCHEM
71587080
Created by admin on Fri Dec 15 15:26:22 GMT 2023 , Edited by admin on Fri Dec 15 15:26:22 GMT 2023
PRIMARY
MERCK INDEX
m649
Created by admin on Fri Dec 15 15:26:22 GMT 2023 , Edited by admin on Fri Dec 15 15:26:22 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID50180846
Created by admin on Fri Dec 15 15:26:22 GMT 2023 , Edited by admin on Fri Dec 15 15:26:22 GMT 2023
PRIMARY
MESH
C045064
Created by admin on Fri Dec 15 15:26:22 GMT 2023 , Edited by admin on Fri Dec 15 15:26:22 GMT 2023
PRIMARY
CAS
26209-07-4
Created by admin on Fri Dec 15 15:26:22 GMT 2023 , Edited by admin on Fri Dec 15 15:26:22 GMT 2023
PRIMARY
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