Page last updated: 2024-08-25

tebuquine and Malaria

tebuquine has been researched along with Malaria in 6 studies

*Malaria: A protozoan disease caused in humans by four species of the PLASMODIUM genus: PLASMODIUM FALCIPARUM; PLASMODIUM VIVAX; PLASMODIUM OVALE; and PLASMODIUM MALARIAE; and transmitted by the bite of an infected female mosquito of the genus ANOPHELES. Malaria is endemic in parts of Asia, Africa, Central and South America, Oceania, and certain Caribbean islands. It is characterized by extreme exhaustion associated with paroxysms of high FEVER; SWEATING; shaking CHILLS; and ANEMIA. Malaria in ANIMALS is caused by other species of plasmodia. [MeSH]

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19903 (50.00)18.7374
1990's1 (16.67)18.2507
2000's1 (16.67)29.6817
2010's1 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Johnson, J; Kesten, SJ; Werbel, LM1
Cook, PD; Elslager, EF; Hung, JH; Johnson, JL; Kesten, SJ; McNamara, DJ; Ortwine, DF; Werbel, LM; Worth, DF1
Gerena, L; Hudson, TH; Kyle, DE; Lin, AJ; Miroshnikova, OV1
Acosta, ME; Charris, JE; Gamboa, N; López, SE; Romero, AH; Salazar, J1
Peters, W; Robinson, BL2

Other Studies

6 other study(ies) available for tebuquine and Malaria

ArticleYear
Synthesis and antimalarial effects of 4-[(7-chloro-4-quinolinyl)amino]-2-[(diethylamino)methyl] -6-alkylphenols and their N omega-oxides.
    Journal of medicinal chemistry, 1987, Volume: 30, Issue:5

    Topics: Aminoquinolines; Animals; Chemical Phenomena; Chemistry; Cyclic N-Oxides; Malaria; Mice; Phenols; Plasmodium berghei; Structure-Activity Relationship

1987
Synthesis, antimalarial activity, and quantitative structure-activity relationships of tebuquine and a series of related 5-[(7-chloro-4-quinolinyl)amino]-3-[(alkylamino)methyl] [1,1'-biphenyl]-2-ols and N omega-oxides.
    Journal of medicinal chemistry, 1986, Volume: 29, Issue:6

    Topics: Aminoquinolines; Animals; Antimalarials; Drug Resistance; Malaria; Mice; Regression Analysis; Structure-Activity Relationship

1986
Synthesis and antimalarial activity of new isotebuquine analogues.
    Journal of medicinal chemistry, 2007, Feb-22, Volume: 50, Issue:4

    Topics: Animals; Antimalarials; Biphenyl Compounds; Drug Resistance; Magnetic Resonance Spectroscopy; Malaria; Mice; Plasmodium berghei; Plasmodium falciparum; Quinolines; Structure-Activity Relationship

2007
Synthesis, β-hematin inhibition studies and antimalarial evaluation of dehydroxy isotebuquine derivatives against Plasmodium berghei.
    Bioorganic & medicinal chemistry, 2015, Aug-01, Volume: 23, Issue:15

    Topics: Aminoquinolines; Animals; Antimalarials; Chloroquine; Drug Evaluation, Preclinical; Hemeproteins; Malaria; Male; Mice; Mice, Inbred BALB C; Plasmodium berghei; Structure-Activity Relationship

2015
The chemotherapy of rodent malaria, XXXVII. The in vivo action of two Mannich bases, WR 194,965 and WR 228,258 and an 8-aminoquinoline WR 225,448.
    Annals of tropical medicine and parasitology, 1984, Volume: 78, Issue:6

    Topics: Aminoquinolines; Animals; Antimalarials; Blood; Butylated Hydroxytoluene; Chemical Phenomena; Chemistry; Dose-Response Relationship, Drug; Malaria; Male; Mice; Plasmodium

1984
The chemotherapy of rodent malaria. XLVII. Studies on pyronaridine and other Mannich base antimalarials.
    Annals of tropical medicine and parasitology, 1992, Volume: 86, Issue:5

    Topics: Aminoquinolines; Amodiaquine; Animals; Antimalarials; Drug Resistance; Malaria; Mannich Bases; Mice; Naphthyridines; Plasmodium berghei; Plasmodium yoelii

1992