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In Vitro and In Vivo leishmanicidal activities of natural and synthetic quinoids
The activities of various compounds isolated from plants traditionally used against leishmaniasis in populations from the tablelands of the Guyanas have been examined and similar synthetic compounds such as quinol and quinone acetates showed increased activity in experimental cutaneous leish maniasis in mice.
Iron chelators as antimalarial agents: in vitro activity of dicatecholate against Plasmodium falciparum.
- B. Pradines, J. Rolain, D. Parzy
- Medicine, BiologyThe Journal of antimicrobial chemotherapy
- 1 August 2002
A potent antimalarial effect of FR160 (R = C9H19) on five different strains of P. falciparum in vitro is demonstrated, which could explain why FR160 antagonized the effects of artesunate and dihydroartemisinin.
In vitro activity of iron-binding compounds against Senegalese isolates of Plasmodium falciparum.
In vitro activities of FR160, a synthetic catecholate siderophore, and two iron-binding agents, desferrioxamine and doxycycline, were evaluated against Plasmodium falciparum isolates and could be a rationale partner to use in combination with doxy cycline.
Incorporation of fatty acids into cuticular hydrocarbons of male and female Drosophila melanogaster.
Sex pheromones of rice moth,Corcyra cephalonica Stainton
Wing-gland extracts or synthetic compounds were shown to be attractive to females by inducing walking and this pheromone was identified as a blend of (E,E) and (Z,E)-farnesal.
In Vitro Potentiation of Antibiotic Activities by a Catecholate Iron Chelator against Chloroquine-Resistant Plasmodium falciparum
- B. Pradines, F. Ramiandrasoa, D. Parzy
- Medicine, ChemistryAntimicrobial Agents and Chemotherapy
- 1 January 2002
ABSTRACT FR160, a catechol iron chelator, and tetracyclines or norfloxacin exert in vitro additive or synergistic activity against a chloroquine-resistant Plasmodium falciparum clone. FR160 shows…
Synthesis and in vitro antibacterial activity of catechol-spiramycin conjugates.
- H. Poras, G. Kunesch, J. Barrière, N. Berthaud, A. Andremont
- Chemistry, BiologyThe Journal of antibiotics
- 25 August 1998
The preliminary biological evaluation of these novel conjugates under standard and iron depleted conditions has shown that their antibacterial activity was comparable to that of spiramycin 1 and neospiramycin 2.
Effect of cinnamoyl putrescines on in vitro cell multiplication and differentiation of tobacco explants
- Claude Martin, G. Kunesch, J. Martin-Tanguy, J. Negrel, M. Paynot, M. Carré
- BiologyPlant Cell Reports
- 1 May 1985
Hydroxycinnamoyl putrescines promote the cell multiplication of leaf discs of a tobacco mutant, RMB7, cultivated in vitro on the Murashige and Skoog medium and their possible role in plant metabolism is discussed.
Kinetics and Thermodynamics of Complex Formation between FeIII and Two Synthetic Chelators of the Dicatecholspermidine Family