Details
Stereochemistry | ACHIRAL |
Molecular Formula | C12H15N3 |
Molecular Weight | 201.2676 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C1CC2=C(C1)C(NC3=NCCN3)=CC=C2
InChI
InChIKey=KUCWWEPJRBANHL-UHFFFAOYSA-N
InChI=1S/C12H15N3/c1-3-9-4-2-6-11(10(9)5-1)15-12-13-7-8-14-12/h2,4,6H,1,3,5,7-8H2,(H2,13,14,15)
Molecular Formula | C12H15N3 |
Molecular Weight | 201.2676 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Indanazoline, an imidazoline derivative, (E-VA-16, as monohydrochloride active substance of Farial) is a nasal decongestant. As a nasal spray it can be used for the treatment of acute, chronic and allergic rhinitis. It is characterized by a pronounced vasoconstrictive action after local or intravenous application. This is due to a direct action of the compound on alpha-adrenergic receptors. When applied systemically Indanazoline being a peripherally acting alpha-sympathomimetic induces a rise in blood pressure and a reduction of heart rate and exerts antiphlogistic, spasmolytic, hyperglycemic and diuretic actions. When given by the intranasal route the substance influences blood pressure and heart rate only at concentrations considerably higher than those intended for use in therapy. After enteral administration the effective doses also markedly exceed the single therapeutic doses. There was no evidence of side-effects restricting the use of the drug as compared to other imidazoline derivatives.
Approval Year
PubMed
Title | Date | PubMed |
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[Pharmacology of N-(2-imidazolin-2-yl)-N-(4-indanyl)amino (indanazoline), a new vasoconstrictive imidazoline compound]. | 1980 |
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[Synthesis of N-(2-imidazolin-2-yl)-N-(4-indanyl)amine (indanazoline) (author's transl)]. | 1980 |
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[On the decongesting effect of the novel imidazole derivative N-(2-imidazolin-2-yl)-N-(4-indanyl)amine (indanazoline) (author's transl)]. | 1980 |
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[Pharmacokinetic study on N-(2-imidazolin-2-yl)-N-(4-indanyl)amine (indanazoline), a new rhinologic drug]. | 1980 |
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[Toxicity studies on N-(2-imidazolinew-2-yl)-N-(4-indanyl)amine monohydrochloride (indanazoline), a ne rhinologic drug]. | 1980 |
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[On the galenical development of a nose spray from N-(2-imidazolin-2-yl)-N-(4-indanyl)amine monohydrochloride (indanazoline) (author's transl)]. | 1980 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6159902
10 min after application of Indanazoline the stream volume increased significantly thus evidencing decongestion of the nasal mucosa.
Route of Administration:
Nasal
Substance Class |
Chemical
Created
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admin
on
Edited
Fri Dec 15 16:09:55 GMT 2023
by
admin
on
Fri Dec 15 16:09:55 GMT 2023
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Record UNII |
L0U38EHD86
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Record Status |
Validated (UNII)
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Record Version |
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WHO-ATC |
R01AA15
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NCI_THESAURUS |
C29709
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CHEMBL2104824
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L0U38EHD86
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27492
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m6242
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40507-78-6
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SUB08166MIG
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C65908
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C027634
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DB13827
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Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |