Minaprine
-
Minaprine
structure -
-
CAS No:
25905-77-5
-
Formula:
C17H22N4O
-
Chemical Name:
Minaprine
-
Synonyms:
4-Morpholineethanamine,N-(4-methyl-6-phenyl-3-pyridazinyl)-;N-(4-Methyl-6-phenyl-3-pyridazinyl)-4-morpholineethanamine;Minaprine;Mineprine
- Categories:
-
CAS No:
Description
Minaprine is a reversible inhibitor of MAO-A; weakly inhibit acetylcholinesterase; an antidepressant for treatment of depression.
Solid
Minaprine is a member of pyridazines, a secondary amine and a member of morpholines. It has a role as an antidepressant, a serotonin uptake inhibitor, a dopamine uptake inhibitor, a cholinergic drug and an antiparkinson drug.|Minaprine is a psychotropic drug which has proved to be effective in the treatment of various depressive states. Like most antidepressants minaprine antagonizes behavioral despair. Minaprine is an amino-phenylpyridazine antidepressant reported to be relatively free of cardiotoxicity, drowsiness, and weight gain.
Minaprine Basic Attributes
371.3
298.38
247-329-8
00U7GX0NLM
DTXSID5048477
N - Nervous system
2934999090
Safety Information
NONH for all modes of transport
3
22
36
QE3477830
Xn
P264, P270, P301+P312, P330, P501
H302
|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P301+P312, P330, and P501|Aggregated GHS information provided by 38 companies from 1 notifications to the ECHA C&L Inventory.
Drug Information
For the treatment of depression
Minaprine is an amino-phenylpyridazine antidepressant reported to be relatively free of cardiotoxicity, drowsiness, and weight gain. Similar to other antidepressant treatments, minaprine attenuates the beta-adrenergic receptor function. Studies have also shown that minaprine improves memory consolidation and that repeated drug administration leads to potentiation of this effect. Moreover, the effects of minaprine on memory consolidation are related to its dopaminergic action.
Mood-stimulating drugs used primarily in the treatment of affective disorders and related conditions. Several MONOAMINE OXIDASE INHIBITORS are useful as antidepressants apparently as a long-term consequence of their modulation of catecholamine levels. The tricyclic compounds useful as antidepressive agents (ANTIDEPRESSIVE AGENTS, TRICYCLIC) also appear to act through brain catecholamine systems. A third group (ANTIDEPRESSIVE AGENTS, SECOND-GENERATION) is a diverse group of drugs including some that act specifically on serotonergic systems. (See all compounds classified as Antidepressive Agents.)
Hepatic. Cytochrome P4502D is responsible for the 4-hydroxylation of minaprine to 4-hydroxyminaprine.|Minaprine has known human metabolites that include 4-Hydroxyminaprine.
Minaprine binds to serotonin type 2 receptors and to dopamine D1 and D2 type receptors. It also binds to the serotonin reuptake pump. Therefore, minaprine blocks the reuptake of both dopamine and serotonin. It is also, to a slight degree, cholinomimetic. Thus it may exhibit both mood-brightening and nootropic properties. It also acts as a reversible inhibitor of MAO-A (RIMA).It has also been found to inhibit acetylcholinesterase.
3-(2-morpholino-ethylamino)-4-methyl-6-phenyl pyridazine, dihydrochloride
Computed Properties
Molecular Weight:298.4
XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:298.17936134
Monoisotopic Mass:298.17936134
Topological Polar Surface Area:50.3
Heavy Atom Count:22
Complexity:316
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Latest News on Minaprine
- The world's first uniform international safety standard for plastics and rubber
- The nation's first group standard for meltblown cloth for masks is released
- Several compulsory national standards have been issued
- Japan has seized the right to formulate international standards
- Henan Efforts to Improve the Standardized Management Level of Food Production
Learn More Other Chemicals
-
Fluocinolone
807-38-5
-
2-Propenoic acid, 2-methyl-, methyl ester, polymer with butyl 2-propenoate, 2-ethylhexyl 2-propenoate and 2-propenoic acid
42398-14-1
-
(3S,7R)-N-[(2-fluorophenyl)methyl]-11-hydroxy-7-methyl-9,12-dioxo-4-oxa-1,8-diazatricyclo[8.4.0.03,8]tetradeca-10,13-diene-13-carboxamide
1863916-87-3
-
1,1-Cyclopropanedicarboxylic acid, 1,1-dimethyl ester Formula
6914-71-2
-
(6R,7R)-7-[[2-amino-2-(cyclohexen-1-yl)acetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid Formula
37051-00-6
-
3-Hydroxy-4-Methyl-2(5H)-thiophenone Formula
34876-35-2
-
10-Methoxy-5H-dibenz[b,f]azepine-5-carbonyl chloride Structure
28721-08-6
-
3,7-Dihydro-3,7-dimethyl-1-(2-propen-1-yl)-1H-purine-2,6-dione Structure
2530-99-6
-
What is 1-[4-[4-(2,3-Dichlorophenyl)piperazin-1-yl]butyl]-7-hydroxy-3,4-dihydrocarbostyril
1797983-65-3
-
What is 3,5-DIIODO-4'-(4-HYDROXYPHENOXY)BENZOICACID
2055-97-2