Page last updated: 2024-11-06
droprenylamine
Description
Droprenylamine is a potent and selective inhibitor of the enzyme monoamine oxidase-A (MAO-A). MAO-A is an enzyme that breaks down neurotransmitters such as serotonin, norepinephrine, and dopamine in the brain. Inhibition of MAO-A can lead to increased levels of these neurotransmitters, which can have a variety of effects on mood, cognition, and behavior. Droprenylamine has been studied as a potential treatment for depression, anxiety, and other psychiatric disorders. Its mechanism of action, selectivity, and potential therapeutic applications make it an area of ongoing research. However, it is important to note that droprenylamine is not currently approved for use in humans and further research is needed to assess its safety and efficacy.'
droprenylamine: secondary amine structurally related to prenylamine; RN given refers to parent cpd; synonym MG 8926 refers to HCl; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
Cross-References
ID Source | ID |
PubMed CID | 65470 |
CHEMBL ID | 2106278 |
CHEBI ID | 135426 |
SCHEMBL ID | 123362 |
MeSH ID | M0061819 |
Synonyms (31)
Synonym |
D03915 |
57653-27-7 |
valcor (tn) |
droprenilamine (usan/inn) |
droprenylamine |
droprenilamine |
CHEBI:135426 |
n-(1-cyclohexylpropan-2-yl)-3,3-diphenylpropan-1-amine |
(+-)-n-(3,3-diphenylpropyl)-alpha-methylcyclohexaneethylamine |
droprenilamina [inn-spanish] |
droprenilaminum |
droprenilamine [usan:inn] |
31ipx0zd7r , |
benzenepropanamine, n-(2-cyclohexyl-1-methylethyl)-gamma-phenyl-, (+-)- |
m.g. 8926 [as hydrochloride] |
droprenilamina |
valcor |
unii-31ipx0zd7r |
droprenilaminum [inn-latin] |
CHEMBL2106278 |
m.g. 8926 free base |
SCHEMBL123362 |
mg-8926 free base |
droprenilamine [mi] |
droprenilamine [inn] |
(+/-)-n-(3,3-diphenylpropyl)-.alpha.-methylcyclohexaneethylamine |
benzenepropanamine, n-(2-cyclohexyl-1-methylethyl)-.gamma.-phenyl-, (+/-)- |
droprenilamine [usan] |
Q27256057 |
DTXSID10866639 |
AKOS040751643 |
Drug Classes (1)
Class | Description |
diarylmethane | Any compound containing two aryl groups connected by a single C atom. |
[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 (5)
Timeframe | Studies, This Drug (%) | All Drugs % |
pre-1990 | 4 (80.00) | 18.7374 |
1990's | 1 (20.00) | 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 (20.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 4 (80.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |