Page last updated: 2024-10-25

desipramine and Malignant Melanoma

desipramine has been researched along with Malignant Melanoma in 2 studies

Desipramine: A tricyclic dibenzazepine compound that potentiates neurotransmission. Desipramine selectively blocks reuptake of norepinephrine from the neural synapse, and also appears to impair serotonin transport. This compound also possesses minor anticholinergic activity, through its affinity to muscarinic receptors.
desipramine : A dibenzoazepine consisting of 10,11-dihydro-5H-dibenzo[b,f]azepine substituted on nitrogen with a 3-(methylamino)propyl group.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kuzu, OF1
Gowda, R1
Noory, MA1
Robertson, GP1
Kato, Y1
Ozawa, S1
Tsukuda, M1
Kubota, E1
Miyazaki, K1
St-Pierre, Y1
Hata, R1

Other Studies

2 other studies available for desipramine and Malignant Melanoma

ArticleYear
Modulating cancer cell survival by targeting intracellular cholesterol transport.
    British journal of cancer, 2017, Aug-08, Volume: 117, Issue:4

    Topics: Administration, Intravenous; Administration, Oral; Animals; Antidepressive Agents, Tricyclic; Antips

2017
Acidic extracellular pH increases calcium influx-triggered phospholipase D activity along with acidic sphingomyelinase activation to induce matrix metalloproteinase-9 expression in mouse metastatic melanoma.
    The FEBS journal, 2007, Volume: 274, Issue:12

    Topics: Animals; Calcium; Calcium Channel Blockers; Calcium Channels; Cell Line, Tumor; Chelating Agents; De

2007