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clomipramine and Leishmaniasis, Cutaneous

clomipramine has been researched along with Leishmaniasis, Cutaneous in 1 studies

Clomipramine: A tricyclic antidepressant similar to IMIPRAMINE that selectively inhibits the uptake of serotonin in the brain. It is readily absorbed from the gastrointestinal tract and demethylated in the liver to form its primary active metabolite, desmethylclomipramine.
clomipramine : A dibenzoazepine that is 10,11-dihydro-5H-dibenzo[b,f]azepine which is substituted by chlorine at position 3 and in which the hydrogen attached to the nitrogen is replaced by a 3-(dimethylamino)propyl group. One of the more sedating tricyclic antidepressants, it is used as the hydrochloride salt for the treatment of depression as well as obsessive-compulsive disorder and phobias.

Leishmaniasis, Cutaneous: An endemic disease that is characterized by the development of single or multiple localized lesions on exposed areas of skin that typically ulcerate. The disease has been divided into Old and New World forms. Old World leishmaniasis is separated into three distinct types according to epidemiology and clinical manifestations and is caused by species of the L. tropica and L. aethiopica complexes as well as by species of the L. major genus. New World leishmaniasis, also called American leishmaniasis, occurs in South and Central America and is caused by species of the L. mexicana or L. braziliensis complexes.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Braga, SF1
Alves, ÉV1
Ferreira, RS1
Fradico, JR1
Lage, PS1
Duarte, MC1
Ribeiro, TG1
Júnior, PA1
Romanha, AJ1
Tonini, ML1
Steindel, M1
Coelho, EF1
de Oliveira, RB1

Other Studies

1 other study available for clomipramine and Leishmaniasis, Cutaneous

ArticleYear
Synthesis and evaluation of the antiparasitic activity of bis-(arylmethylidene) cycloalkanones.
    European journal of medicinal chemistry, 2014, Volume: 71

    Topics: Animals; Antiprotozoal Agents; Cell Line; Chagas Disease; Fibroblasts; Humans; Leishmania mexicana;

2014