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
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
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 |
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 15:36:55 GMT 2023
by
admin
on
Fri Dec 15 15:36:55 GMT 2023
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Record UNII |
U3P3Y52JKX
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Record Status |
Validated (UNII)
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Record Version |
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253-670-3
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37795-09-8
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DTXSID20958837
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U3P3Y52JKX
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