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Details

Stereochemistry RACEMIC
Molecular Formula C3H5ClN2O6
Molecular Weight 200.535
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLONITRATE

SMILES

[O-][N+](=O)OCC(CCl)O[N+]([O-])=O

InChI

InChIKey=SUAJWTBTMNHVBZ-UHFFFAOYSA-N
InChI=1S/C3H5ClN2O6/c4-1-3(12-6(9)10)2-11-5(7)8/h3H,1-2H2

HIDE SMILES / InChI

Molecular Formula C3H5ClN2O6
Molecular Weight 200.535
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Clonitrate (chloroglyceryl dinitrate) is a derivative of nitroglycerin. The compound is identical with glycerol trinitrate with the exception of the replacement of the nitrate radical on the first carbon atom by an atom of chlorine. Clonitrate is equipotent with glycerine trinitrate in increasing coronary flow in Langendorff rabbit heart and appears to evoke a lesser degree of depressor response. In the 1960s, clonitrate was used in the clinics a vasodilator for the treatment of angina pectoris.

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 16:27:23 GMT 2023
Edited
by admin
on Sat Dec 16 16:27:23 GMT 2023
Record UNII
MIG1YFL8MD
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLONITRATE
INN   MI   USAN  
USAN   INN  
Official Name English
3-CHLORO-1,2-PROPANEDIOL 1,2-DINITRATE
Common Name English
CLONITRATE [USAN]
Common Name English
DYLATE
Brand Name English
DINITROCHLOROHYDRIN
Common Name English
clonitrate [INN]
Common Name English
CLONITRATE [MI]
Common Name English
1,2-PROPANEDIOL, 3-CHLORO-, DINITRATE
Systematic Name English
3-Chloro-1,2-propanediol dinitrate
Systematic Name English
3-CHLOROPROPYLENEGLYCOL DINITRATE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29707
Created by admin on Sat Dec 16 16:27:24 GMT 2023 , Edited by admin on Sat Dec 16 16:27:24 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C80875
Created by admin on Sat Dec 16 16:27:24 GMT 2023 , Edited by admin on Sat Dec 16 16:27:24 GMT 2023
PRIMARY
MERCK INDEX
m1082
Created by admin on Sat Dec 16 16:27:24 GMT 2023 , Edited by admin on Sat Dec 16 16:27:24 GMT 2023
PRIMARY Merck Index
PUBCHEM
17468
Created by admin on Sat Dec 16 16:27:24 GMT 2023 , Edited by admin on Sat Dec 16 16:27:24 GMT 2023
PRIMARY
RXCUI
2372697
Created by admin on Sat Dec 16 16:27:24 GMT 2023 , Edited by admin on Sat Dec 16 16:27:24 GMT 2023
PRIMARY
DRUG CENTRAL
3110
Created by admin on Sat Dec 16 16:27:24 GMT 2023 , Edited by admin on Sat Dec 16 16:27:24 GMT 2023
PRIMARY
CAS
2612-33-1
Created by admin on Sat Dec 16 16:27:24 GMT 2023 , Edited by admin on Sat Dec 16 16:27:24 GMT 2023
PRIMARY
SMS_ID
100000084530
Created by admin on Sat Dec 16 16:27:24 GMT 2023 , Edited by admin on Sat Dec 16 16:27:24 GMT 2023
PRIMARY
INN
1458
Created by admin on Sat Dec 16 16:27:24 GMT 2023 , Edited by admin on Sat Dec 16 16:27:24 GMT 2023
PRIMARY
EPA CompTox
DTXSID10862999
Created by admin on Sat Dec 16 16:27:24 GMT 2023 , Edited by admin on Sat Dec 16 16:27:24 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104377
Created by admin on Sat Dec 16 16:27:24 GMT 2023 , Edited by admin on Sat Dec 16 16:27:24 GMT 2023
PRIMARY
EVMPD
SUB06732MIG
Created by admin on Sat Dec 16 16:27:24 GMT 2023 , Edited by admin on Sat Dec 16 16:27:24 GMT 2023
PRIMARY
DAILYMED
MIG1YFL8MD
Created by admin on Sat Dec 16 16:27:24 GMT 2023 , Edited by admin on Sat Dec 16 16:27:24 GMT 2023
PRIMARY
FDA UNII
MIG1YFL8MD
Created by admin on Sat Dec 16 16:27:24 GMT 2023 , Edited by admin on Sat Dec 16 16:27:24 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY