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Details

Stereochemistry ACHIRAL
Molecular Formula C14H16N2O.ClH
Molecular Weight 264.751
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of COUMAZOLINE HYDROCHLORIDE

SMILES

Cl.CCC1=C(CC2=NCCN2)C3=C(O1)C=CC=C3

InChI

InChIKey=YDDYHDKRIBOHOT-UHFFFAOYSA-N
InChI=1S/C14H16N2O.ClH/c1-2-12-11(9-14-15-7-8-16-14)10-5-3-4-6-13(10)17-12;/h3-6H,2,7-9H2,1H3,(H,15,16);1H

HIDE SMILES / InChI

Molecular Formula C14H16N2O
Molecular Weight 228.2896
Charge 0
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

Coumazoline is a vasoconstrictor developed as a nasal decongestant by a French corporation Labez. Intravenous administration of the compound to dogs lead to a marked and prolonged drop in the temperature of the gingival mucosa. In rats, coumazoline caused slowing of the dye diffusion on the surface of the skin. The compound did not influence the ciliary motility, as was measured on an isolated guinea pig trachea.

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:36:55 GMT 2023
Edited
by admin
on Fri Dec 15 15:36:55 GMT 2023
Record UNII
U3P3Y52JKX
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
COUMAZOLINE HYDROCHLORIDE
Common Name English
1H-IMIDAZOLE, 2-((2-ETHYL-3-BENZOFURANYL)METHYL)-4,5-DIHYDRO-, HYDROCHLORIDE (1:1)
Systematic Name English
L5818
Code English
L-5818
Code English
1H-IMIDAZOLE, 2-((2-ETHYL-3-BENZOFURANYL)METHYL)-4,5-DIHYDRO-, MONOHYDROCHLORIDE
Systematic Name English
2-((2-ETHYLBENZOFURAN-3-YL)METHYL)-2-IMIDAZOLINE
Systematic Name English
Code System Code Type Description
PUBCHEM
16205103
Created by admin on Fri Dec 15 15:36:55 GMT 2023 , Edited by admin on Fri Dec 15 15:36:55 GMT 2023
PRIMARY
ECHA (EC/EINECS)
253-670-3
Created by admin on Fri Dec 15 15:36:55 GMT 2023 , Edited by admin on Fri Dec 15 15:36:55 GMT 2023
PRIMARY
CAS
37795-09-8
Created by admin on Fri Dec 15 15:36:55 GMT 2023 , Edited by admin on Fri Dec 15 15:36:55 GMT 2023
PRIMARY
EPA CompTox
DTXSID20958837
Created by admin on Fri Dec 15 15:36:55 GMT 2023 , Edited by admin on Fri Dec 15 15:36:55 GMT 2023
PRIMARY
FDA UNII
U3P3Y52JKX
Created by admin on Fri Dec 15 15:36:55 GMT 2023 , Edited by admin on Fri Dec 15 15:36:55 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY