U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C12H15N3.ClH
Molecular Weight 237.729
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of INDANAZOLINE HYDROCHLORIDE

SMILES

Cl.C1CC2=C(C1)C(NC3=NCCN3)=CC=C2

InChI

InChIKey=GZVYIVIJAOMGJT-UHFFFAOYSA-N
InChI=1S/C12H15N3.ClH/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);1H

HIDE SMILES / InChI
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

PubMed

TitleDatePubMed
[Pharmacology of N-(2-imidazolin-2-yl)-N-(4-indanyl)amino (indanazoline), a new vasoconstrictive imidazoline compound].
1980
[Synthesis of N-(2-imidazolin-2-yl)-N-(4-indanyl)amine (indanazoline) (author's transl)].
1980
[On the decongesting effect of the novel imidazole derivative N-(2-imidazolin-2-yl)-N-(4-indanyl)amine (indanazoline) (author's transl)].
1980
[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

10 min after application of Indanazoline the stream volume increased significantly thus evidencing decongestion of the nasal mucosa.
Route of Administration: Nasal
Name Type Language
INDANAZOLINE HYDROCHLORIDE
MART.   MI   WHO-DD  
Common Name English
INDANAZOLINE HYDROCHLORIDE [MI]
Common Name English
Indanazoline hydrochloride [WHO-DD]
Common Name English
INDANAZOLIN HYDROCHLORIDE
Common Name English
INDANAZOLINE HCL
Common Name English
INDANAZOLINE HYDROCHLORIDE [MART.]
Common Name English
2-(4-INDANYLAMINO)-2-IMIDAZOLINE HYDROCHLORIDE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29709
Created by admin on Fri Dec 15 17:24:14 GMT 2023 , Edited by admin on Fri Dec 15 17:24:14 GMT 2023
Code System Code Type Description
EVMPD
SUB02661MIG
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PRIMARY
CAS
40507-80-0
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PRIMARY
PUBCHEM
162014
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DRUG BANK
DBSALT002561
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NCI_THESAURUS
C97700
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PRIMARY
CAS
56601-85-5
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SUPERSEDED
RXCUI
292036
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MESH
C027634
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EPA CompTox
DTXSID20960910
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ECHA (EC/EINECS)
254-945-0
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SMS_ID
100000086981
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MERCK INDEX
m6242
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PRIMARY Merck Index
FDA UNII
Z364A90IV8
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