Assay ID | Title | Year | Journal | Article |
AID724074 | Therapeutic index, ratio of ED50 for human Jurkat cells to IC50 for Plasmodium falciparum Nigeria infected in human erythrocytes | 2013 | Journal of medicinal chemistry, Jan-24, Volume: 56, Issue:2
| New bis-thiazolium analogues as potential antimalarial agents: design, synthesis, and biological evaluation. |
AID675865 | Antimalarial activity against Plasmodium vinckei petteri 279BY infected in ip dosed Swiss mouse assessed as reduction in parasitemia administered QD for 4 days measured on day 5 | 2012 | Journal of medicinal chemistry, May-24, Volume: 55, Issue:10
| Disulfide prodrugs of albitiazolium (T3/SAR97276): synthesis and biological activities. |
AID675864 | Antiplasmodial activity against Plasmodium falciparum assessed as inhibition of [3H]hypoxanthine incorporation after 48 hrs | 2012 | Journal of medicinal chemistry, May-24, Volume: 55, Issue:10
| Disulfide prodrugs of albitiazolium (T3/SAR97276): synthesis and biological activities. |
AID447918 | Antimalarial activity against Plasmodium vinckei petteri 279BY infected in Swiss mice (Mus musculus) assessed as reduction in parasitaemia level at 10 mg/kg, intraperitoneal measured after 4 days | 2009 | Bioorganic & medicinal chemistry letters, Sep-01, Volume: 19, Issue:17
| N-substituted bis-C-alkyloxadiazolones as dual effectors: efficient intermediates to amidoximes or amidines and prodrug candidates of potent antimalarials. |
AID489741 | Antimalarial activity against Plasmodium vinckei infected in intraperitoneally dosed mice (Mus musculus) | 2010 | Bioorganic & medicinal chemistry letters, Jul-01, Volume: 20, Issue:13
| Exploration of potential prodrug approach of the bis-thiazolium salts T3 and T4 for orally delivered antimalarials. |
AID675867 | Ratio of ED50 for Plasmodium vinckei petteri 279BY infected in ip dosed Swiss mouse to ED50 for Plasmodium venckei petteri 279BY infected in po dosed Swiss mouse | 2012 | Journal of medicinal chemistry, May-24, Volume: 55, Issue:10
| Disulfide prodrugs of albitiazolium (T3/SAR97276): synthesis and biological activities. |
AID724076 | Antimalarial activity against Plasmodium vinckei petteri 279BY infected in Swiss mouse administered as ip qd for 4 days measured on day 5 | 2013 | Journal of medicinal chemistry, Jan-24, Volume: 56, Issue:2
| New bis-thiazolium analogues as potential antimalarial agents: design, synthesis, and biological evaluation. |
AID675866 | Antimalarial activity against Plasmodium vinckei petteri 279BY infected in po dosed Swiss mouse assessed as reduction in parasitemia administered QD for 4 days measured on day 5 | 2012 | Journal of medicinal chemistry, May-24, Volume: 55, Issue:10
| Disulfide prodrugs of albitiazolium (T3/SAR97276): synthesis and biological activities. |
AID516719 | Antimalarial activity against Plasmodium falciparum | 2010 | Bioorganic & medicinal chemistry letters, Oct-01, Volume: 20, Issue:19
| Reverse-benzamidine antimalarial agents: design, synthesis, and biological evaluation. |
AID367721 | Antimalarial activity after 48 hrs against chloroquine-sensitive Plasmodium falciparum Nigerian by [3H]hypoxanthine uptake | 2009 | Bioorganic & medicinal chemistry letters, Feb-01, Volume: 19, Issue:3
| Design and synthesis of amidoxime derivatives for orally potent C-alkylamidine-based antimalarial agents. |
AID447917 | Antimalarial activity against chloroquine-sensitive Plasmodium falciparum Nigerian | 2009 | Bioorganic & medicinal chemistry letters, Sep-01, Volume: 19, Issue:17
| N-substituted bis-C-alkyloxadiazolones as dual effectors: efficient intermediates to amidoximes or amidines and prodrug candidates of potent antimalarials. |
AID447919 | Antimalarial activity against Plasmodium vinckei petteri 279BY infected peroral daily dosed Swiss mice (Mus musculus) assessed as reduction in parasitaemia level measured after 4 days | 2009 | Bioorganic & medicinal chemistry letters, Sep-01, Volume: 19, Issue:17
| N-substituted bis-C-alkyloxadiazolones as dual effectors: efficient intermediates to amidoximes or amidines and prodrug candidates of potent antimalarials. |
AID724075 | Cytotoxicity against human Jurkat cells after 24 hrs by [3H]thymidine incorporation assay | 2013 | Journal of medicinal chemistry, Jan-24, Volume: 56, Issue:2
| New bis-thiazolium analogues as potential antimalarial agents: design, synthesis, and biological evaluation. |
AID1552381 | Antimalarial activity against Plasmodium falciparum infected in erythrocytes | 2019 | Bioorganic & medicinal chemistry letters, 08-15, Volume: 29, Issue:16
| Evaluation of amidoxime derivatives as prodrug candidates of potent bis-cationic antimalarials. |
AID489742 | Antimalarial activity against Plasmodium vinckei infected in perorally dosed mice (Mus musculus) | 2010 | Bioorganic & medicinal chemistry letters, Jul-01, Volume: 20, Issue:13
| Exploration of potential prodrug approach of the bis-thiazolium salts T3 and T4 for orally delivered antimalarials. |
AID724077 | Antiplasmodial activity against Plasmodium falciparum Nigeria infected in human erythrocytes assessed as incorporation of [3H]hypoxanthine after 48 hrs | 2013 | Journal of medicinal chemistry, Jan-24, Volume: 56, Issue:2
| New bis-thiazolium analogues as potential antimalarial agents: design, synthesis, and biological evaluation. |
AID489740 | Antiplasmodial activity against Plasmodium falciparum | 2010 | Bioorganic & medicinal chemistry letters, Jul-01, Volume: 20, Issue:13
| Exploration of potential prodrug approach of the bis-thiazolium salts T3 and T4 for orally delivered antimalarials. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |