miltefosine has been researched along with Malaria, Falciparum in 5 studies
miltefosine: hexadecyl phosphocholine derivative of cisplatin; did not substantially activate HIV long terminal repeat; less toxic than cisplatin
miltefosine : A phospholipid that is the hexadecyl monoester of phosphocholine.
Malaria, Falciparum: Malaria caused by PLASMODIUM FALCIPARUM. This is the severest form of malaria and is associated with the highest levels of parasites in the blood. This disease is characterized by irregularly recurring febrile paroxysms that in extreme cases occur with acute cerebral, renal, or gastrointestinal manifestations.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (20.00) | 29.6817 |
2010's | 4 (80.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Tasdemir, D | 1 |
Sanabria, D | 1 |
Lauinger, IL | 1 |
Tarun, A | 1 |
Herman, R | 1 |
Perozzo, R | 1 |
Zloh, M | 1 |
Kappe, SH | 1 |
Brun, R | 3 |
Carballeira, NM | 1 |
Mayence, A | 1 |
Vanden Eynde, JJ | 1 |
Kaiser, M | 2 |
Yarlett, N | 1 |
Huang, TL | 1 |
Bosc, D | 1 |
Mouray, E | 1 |
Cojean, S | 1 |
Franco, CH | 1 |
Loiseau, PM | 1 |
Freitas-Junior, LH | 1 |
Moraes, CB | 1 |
Grellier, P | 1 |
Dubois, J | 1 |
Saccoliti, F | 1 |
Madia, VN | 1 |
Tudino, V | 1 |
De Leo, A | 1 |
Pescatori, L | 1 |
Messore, A | 1 |
De Vita, D | 1 |
Scipione, L | 1 |
Mäser, P | 1 |
Calvet, CM | 1 |
Jennings, GK | 1 |
Podust, LM | 1 |
Costi, R | 1 |
Di Santo, R | 1 |
Choubey, V | 1 |
Maity, P | 1 |
Guha, M | 1 |
Kumar, S | 1 |
Srivastava, K | 1 |
Puri, SK | 1 |
Bandyopadhyay, U | 1 |
5 other studies available for miltefosine and Malaria, Falciparum
Article | Year |
---|---|
2-Hexadecynoic acid inhibits plasmodial FAS-II enzymes and arrests erythrocytic and liver stage Plasmodium infections.
Topics: Alkynes; Antimalarials; Binding Sites; Cell Line, Tumor; Computer Simulation; Erythrocytes; Fatty Ac | 2010 |
Bis(oxyphenylene)benzimidazoles: a novel class of anti-Plasmodium falciparum agents.
Topics: Animals; Antimalarials; Benzimidazoles; Cell Line; Humans; Inhibitory Concentration 50; Malaria, Fal | 2011 |
Highly improved antiparasitic activity after introduction of an N-benzylimidazole moiety on protein farnesyltransferase inhibitors.
Topics: Alkyl and Aryl Transferases; Animals; Antiparasitic Agents; Cell Line; Enzyme Inhibitors; Humans; Im | 2016 |
Biological evaluation and structure-activity relationships of imidazole-based compounds as antiprotozoal agents.
Topics: Animals; Antiprotozoal Agents; Cell Line; Chagas Disease; Female; Humans; Imidazoles; Inhibitory Con | 2018 |
Inhibition of Plasmodium falciparum choline kinase by hexadecyltrimethylammonium bromide: a possible antimalarial mechanism.
Topics: Animals; Antiprotozoal Agents; Cetrimonium; Cetrimonium Compounds; Choline Kinase; Dose-Response Rel | 2007 |