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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
Structure of INDANAZOLINE

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)

HIDE SMILES / InChI

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

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
[Pharmacokinetic study on N-(2-imidazolin-2-yl)-N-(4-indanyl)amine (indanazoline), a new rhinologic drug].
1980
[Toxicity studies on N-(2-imidazolinew-2-yl)-N-(4-indanyl)amine monohydrochloride (indanazoline), a ne rhinologic drug].
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
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:09:55 GMT 2023
Edited
by admin
on Fri Dec 15 16:09:55 GMT 2023
Record UNII
L0U38EHD86
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
INDANAZOLINE
INN   MI   WHO-DD  
INN  
Official Name English
INDANAZOLINE [MI]
Common Name English
2-(4-INDANYLAMINO)-2-IMIDAZOLINE
Systematic Name English
Indanazoline [WHO-DD]
Common Name English
indanazoline [INN]
Common Name English
Classification Tree Code System Code
WHO-ATC R01AA15
Created by admin on Fri Dec 15 16:09:55 GMT 2023 , Edited by admin on Fri Dec 15 16:09:55 GMT 2023
NCI_THESAURUS C29709
Created by admin on Fri Dec 15 16:09:55 GMT 2023 , Edited by admin on Fri Dec 15 16:09:55 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL2104824
Created by admin on Fri Dec 15 16:09:55 GMT 2023 , Edited by admin on Fri Dec 15 16:09:55 GMT 2023
PRIMARY
INN
4733
Created by admin on Fri Dec 15 16:09:55 GMT 2023 , Edited by admin on Fri Dec 15 16:09:55 GMT 2023
PRIMARY
DRUG CENTRAL
3298
Created by admin on Fri Dec 15 16:09:55 GMT 2023 , Edited by admin on Fri Dec 15 16:09:55 GMT 2023
PRIMARY
EPA CompTox
DTXSID40193521
Created by admin on Fri Dec 15 16:09:55 GMT 2023 , Edited by admin on Fri Dec 15 16:09:55 GMT 2023
PRIMARY
PUBCHEM
65979
Created by admin on Fri Dec 15 16:09:55 GMT 2023 , Edited by admin on Fri Dec 15 16:09:55 GMT 2023
PRIMARY
FDA UNII
L0U38EHD86
Created by admin on Fri Dec 15 16:09:55 GMT 2023 , Edited by admin on Fri Dec 15 16:09:55 GMT 2023
PRIMARY
RXCUI
27492
Created by admin on Fri Dec 15 16:09:55 GMT 2023 , Edited by admin on Fri Dec 15 16:09:55 GMT 2023
PRIMARY RxNorm
MERCK INDEX
m6242
Created by admin on Fri Dec 15 16:09:55 GMT 2023 , Edited by admin on Fri Dec 15 16:09:55 GMT 2023
PRIMARY Merck Index
CAS
40507-78-6
Created by admin on Fri Dec 15 16:09:55 GMT 2023 , Edited by admin on Fri Dec 15 16:09:55 GMT 2023
PRIMARY
EVMPD
SUB08166MIG
Created by admin on Fri Dec 15 16:09:55 GMT 2023 , Edited by admin on Fri Dec 15 16:09:55 GMT 2023
PRIMARY
NCI_THESAURUS
C65908
Created by admin on Fri Dec 15 16:09:55 GMT 2023 , Edited by admin on Fri Dec 15 16:09:55 GMT 2023
PRIMARY
MESH
C027634
Created by admin on Fri Dec 15 16:09:55 GMT 2023 , Edited by admin on Fri Dec 15 16:09:55 GMT 2023
PRIMARY
SMS_ID
100000083368
Created by admin on Fri Dec 15 16:09:55 GMT 2023 , Edited by admin on Fri Dec 15 16:09:55 GMT 2023
PRIMARY
DRUG BANK
DB13827
Created by admin on Fri Dec 15 16:09:55 GMT 2023 , Edited by admin on Fri Dec 15 16:09:55 GMT 2023
PRIMARY
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SALT/SOLVATE -> PARENT
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