Details
Stereochemistry | ACHIRAL |
Molecular Formula | C14H16N2O |
Molecular Weight | 228.2896 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC1=C(CC2=NCCN2)C3=C(O1)C=CC=C3
InChI
InChIKey=QZRIKRJFJVVUSF-UHFFFAOYSA-N
InChI=1S/C14H16N2O/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)
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 |
DescriptionSources: https://patents.google.com/patent/GB1333471A/en
Sources: https://patents.google.com/patent/GB1333471A/en
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
Edited
Fri Dec 15 16:10:40 GMT 2023
by
admin
on
Fri Dec 15 16:10:40 GMT 2023
|
Record UNII |
TR7Y641235
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Code | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C29709
Created by
admin on Fri Dec 15 16:10:40 GMT 2023 , Edited by admin on Fri Dec 15 16:10:40 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
100000083735
Created by
admin on Fri Dec 15 16:10:40 GMT 2023 , Edited by admin on Fri Dec 15 16:10:40 GMT 2023
|
PRIMARY | |||
|
TR7Y641235
Created by
admin on Fri Dec 15 16:10:40 GMT 2023 , Edited by admin on Fri Dec 15 16:10:40 GMT 2023
|
PRIMARY | |||
|
CHEMBL2106000
Created by
admin on Fri Dec 15 16:10:40 GMT 2023 , Edited by admin on Fri Dec 15 16:10:40 GMT 2023
|
PRIMARY | |||
|
3134
Created by
admin on Fri Dec 15 16:10:40 GMT 2023 , Edited by admin on Fri Dec 15 16:10:40 GMT 2023
|
PRIMARY | |||
|
37681-00-8
Created by
admin on Fri Dec 15 16:10:40 GMT 2023 , Edited by admin on Fri Dec 15 16:10:40 GMT 2023
|
PRIMARY | |||
|
SUB06815MIG
Created by
admin on Fri Dec 15 16:10:40 GMT 2023 , Edited by admin on Fri Dec 15 16:10:40 GMT 2023
|
PRIMARY | |||
|
C007141
Created by
admin on Fri Dec 15 16:10:40 GMT 2023 , Edited by admin on Fri Dec 15 16:10:40 GMT 2023
|
PRIMARY | |||
|
C79706
Created by
admin on Fri Dec 15 16:10:40 GMT 2023 , Edited by admin on Fri Dec 15 16:10:40 GMT 2023
|
PRIMARY | |||
|
37808
Created by
admin on Fri Dec 15 16:10:40 GMT 2023 , Edited by admin on Fri Dec 15 16:10:40 GMT 2023
|
PRIMARY | |||
|
DTXSID50191114
Created by
admin on Fri Dec 15 16:10:40 GMT 2023 , Edited by admin on Fri Dec 15 16:10:40 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |