Page last updated: 2024-11-06
indanazoline
Description
Indanazoline is a sympathomimetic amine that acts as an α-adrenergic agonist. Its synthesis involves several steps, starting with the condensation of 2-indanone with ethyl cyanoacetate followed by a series of reactions. Indanazoline has been studied for its potential therapeutic applications, particularly in the treatment of nasal congestion, hypotension, and glaucoma. It exerts vasoconstrictive effects, leading to nasal decongestion and an increase in blood pressure. However, its clinical use is limited due to its adverse effects such as headache, insomnia, and tachycardia. Further research is ongoing to investigate its potential in other areas, including its role in neuroprotection and its ability to modulate the immune system.'
indanazoline: RN given refers to parent cpd; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
Cross-References
ID Source | ID |
PubMed CID | 65979 |
CHEMBL ID | 2104824 |
CHEBI ID | 134863 |
SCHEMBL ID | 151815 |
MeSH ID | M0089655 |
Synonyms (31)
Synonym |
indanazolin |
CHEBI:134863 |
indanazoline |
n-(2,3-dihydro-1h-inden-4-yl)-4,5-dihydro-1h-imidazol-2-amine |
40507-78-6 |
D08075 |
indanazoline (inn) |
unii-l0u38ehd86 |
1h-imidazol-2-amine, n-(2,3-dihydro-1h-inden-4-yl)-4,5-dihydro- |
l0u38ehd86 , |
indanazolina [spanish] |
2-(4-indanylamino)-2-imidazoline |
indanazolina [inn-spanish] |
indanazoline [inn] |
indanazolinum |
indanazolina |
indanazolinum [latin] |
indanazolinum [inn-latin] |
n-(2-imidazolin-2-yl)-n-(4-indanyl)amine |
CHEMBL2104824 |
indanazoline [who-dd] |
indanazoline [mi] |
SCHEMBL151815 |
(4,5-dihydro-1h-imidazol-2-yl)-4-indanylamine |
DTXSID40193521 |
AKOS027378075 |
HY-U00075 |
CS-6599 |
FT-0710425 |
DB13827 |
Q27282563 |
Research Excerpts
Dosage Studied
Drug Classes (1)
Class | Description |
indanes | |
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Research
Studies (7)
Timeframe | Studies, This Drug (%) | All Drugs % |
pre-1990 | 7 (100.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Study Types
Publication Type | This drug (%) | All Drugs (%) |
Trials | 1 (14.29%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 6 (85.71%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |