Assay ID | Title | Year | Journal | Article |
AID31885 | Binding affinity to adenosine A1 receptor in rat brain membranes by measuring displacement of specific [3H]PIA as radioligand. | 1995 | Journal of medicinal chemistry, Mar-31, Volume: 38, Issue:7
| Search for new purine- and ribose-modified adenosine analogues as selective agonists and antagonists at adenosine receptors. |
AID300104 | Antimalarial activity against chloroquine, pyrimethamine and cycloguanil-resistant Plasmodium falciparum VS1 after 24 hrs | 2007 | Bioorganic & medicinal chemistry, Aug-15, Volume: 15, Issue:16
| Anti-malarial activity of N6-modified purine analogues. |
AID595466 | Antiproliferative activity against doxorubicin-sensitive human K562 cells after 72 hrs by MTS assay | 2011 | European journal of medicinal chemistry, May, Volume: 46, Issue:5
| Synthesis and biological activity of novel N6-substituted and 2,N6-disubstituted adenine ribo- and 3'-C-methyl-ribonucleosides as antitumor agents. |
AID595461 | Antiproliferative activity against human MCF7 cells after 72 hrs by MTS assay | 2011 | European journal of medicinal chemistry, May, Volume: 46, Issue:5
| Synthesis and biological activity of novel N6-substituted and 2,N6-disubstituted adenine ribo- and 3'-C-methyl-ribonucleosides as antitumor agents. |
AID595465 | Inhibition of human recombinant ribonucleotide reductase p53R2/M1 expressed in Escherichia coli BL21 (DE3) after 30 mins by [3H]CDP reduction method | 2011 | European journal of medicinal chemistry, May, Volume: 46, Issue:5
| Synthesis and biological activity of novel N6-substituted and 2,N6-disubstituted adenine ribo- and 3'-C-methyl-ribonucleosides as antitumor agents. |
AID25507 | HPLC capacity factor (k') | 1985 | Journal of medicinal chemistry, Nov, Volume: 28, Issue:11
| Dog coronary artery adenosine receptor: structure of the N6-alkyl subregion. |
AID300102 | Antimalarial activity against drug-sensitive Plasmodium falciparum 3D7 after 24 hrs | 2007 | Bioorganic & medicinal chemistry, Aug-15, Volume: 15, Issue:16
| Anti-malarial activity of N6-modified purine analogues. |
AID1694546 | Displacement of FITC-geldanamycin from GRP94 (unknown origin) after 24 hrs by fluorescence polarization assay | 2021 | ACS medicinal chemistry letters, Mar-11, Volume: 12, Issue:3
| Biological Evaluation of 5'-( |
AID1694549 | Displacement of FITC-geldanamycin from HSP90alpha (unknown origin) at 50 uM after 24 hrs by fluorescence polarization assay relative to control | 2021 | ACS medicinal chemistry letters, Mar-11, Volume: 12, Issue:3
| Biological Evaluation of 5'-( |
AID228918 | Molar potency ratio was evaluated | 1985 | Journal of medicinal chemistry, Nov, Volume: 28, Issue:11
| Dog coronary artery adenosine receptor: structure of the N6-alkyl subregion. |
AID33337 | Binding affinity determined by displacement of specific binding of [125I]N-(4-amino-3-iodophenethyl)-adenosine in membranes of CHO cells stably transfected with the rat adenosine A3 receptor | 1995 | Journal of medicinal chemistry, Mar-31, Volume: 38, Issue:7
| Search for new purine- and ribose-modified adenosine analogues as selective agonists and antagonists at adenosine receptors. |
AID300105 | Cytotoxicity against human KB cells | 2007 | Bioorganic & medicinal chemistry, Aug-15, Volume: 15, Issue:16
| Anti-malarial activity of N6-modified purine analogues. |
AID300106 | Selectivity index, ratio of CC50 for human KB cells to IC50 for Plasmodium falciparum 3D7 | 2007 | Bioorganic & medicinal chemistry, Aug-15, Volume: 15, Issue:16
| Anti-malarial activity of N6-modified purine analogues. |
AID1694547 | Displacement of FITC-geldanamycin from HSP90alpha (unknown origin) after 24 hrs by fluorescence polarization assay | 2021 | ACS medicinal chemistry letters, Mar-11, Volume: 12, Issue:3
| Biological Evaluation of 5'-( |
AID521783 | Antiviral activity against Poliovirus G64S infected in HeLaS3 cells at 2 mM after 6 hrs | 2008 | Antimicrobial agents and chemotherapy, Mar, Volume: 52, Issue:3
| Lethal mutagenesis of picornaviruses with N-6-modified purine nucleoside analogues. |
AID595464 | Inhibition of human recombinant ribonucleotide reductase M2/M1 expressed in Escherichia coli BL21 (DE3) after 30 mins by [3H]CDP reduction method | 2011 | European journal of medicinal chemistry, May, Volume: 46, Issue:5
| Synthesis and biological activity of novel N6-substituted and 2,N6-disubstituted adenine ribo- and 3'-C-methyl-ribonucleosides as antitumor agents. |
AID595459 | Antiproliferative activity against human HeLa cells after 72 hrs by MTS assay | 2011 | European journal of medicinal chemistry, May, Volume: 46, Issue:5
| Synthesis and biological activity of novel N6-substituted and 2,N6-disubstituted adenine ribo- and 3'-C-methyl-ribonucleosides as antitumor agents. |
AID595460 | Antiproliferative activity against human K562 cells after 72 hrs by MTS assay | 2011 | European journal of medicinal chemistry, May, Volume: 46, Issue:5
| Synthesis and biological activity of novel N6-substituted and 2,N6-disubstituted adenine ribo- and 3'-C-methyl-ribonucleosides as antitumor agents. |
AID521786 | Antiviral activity against Coxsackievirus infected in compound pre-treated HeLaS3 cells assessed as reduction in viral titer at 0.5 mM after 6 hrs relative to control | 2008 | Antimicrobial agents and chemotherapy, Mar, Volume: 52, Issue:3
| Lethal mutagenesis of picornaviruses with N-6-modified purine nucleoside analogues. |
AID521785 | Antiviral activity against Poliovirus infected in compound pre-treated HeLaS3 cells assessed as reduction in viral titer at 0.5 mM after 6 hrs relative to control | 2008 | Antimicrobial agents and chemotherapy, Mar, Volume: 52, Issue:3
| Lethal mutagenesis of picornaviruses with N-6-modified purine nucleoside analogues. |
AID595462 | Antiproliferative activity against human HT-29 cells after 72 hrs by MTS assay | 2011 | European journal of medicinal chemistry, May, Volume: 46, Issue:5
| Synthesis and biological activity of novel N6-substituted and 2,N6-disubstituted adenine ribo- and 3'-C-methyl-ribonucleosides as antitumor agents. |
AID595463 | Antiproliferative activity against human Caco2 cells after 72 hrs by MTS assay | 2011 | European journal of medicinal chemistry, May, Volume: 46, Issue:5
| Synthesis and biological activity of novel N6-substituted and 2,N6-disubstituted adenine ribo- and 3'-C-methyl-ribonucleosides as antitumor agents. |
AID300107 | Selectivity index, ratio of CC50 for human KB cells to IC50 for Plasmodium falciparum K1 | 2007 | Bioorganic & medicinal chemistry, Aug-15, Volume: 15, Issue:16
| Anti-malarial activity of N6-modified purine analogues. |
AID521781 | Cytotoxicity against human HeLaS3 cells assessed cell viability at 0.05 after 24 hrs by Alamar blue assay | 2008 | Antimicrobial agents and chemotherapy, Mar, Volume: 52, Issue:3
| Lethal mutagenesis of picornaviruses with N-6-modified purine nucleoside analogues. |
AID1694548 | Displacement of FITC-geldanamycin from GRP94 (unknown origin) at 50 uM after 24 hrs by fluorescence polarization assay relative to control | 2021 | ACS medicinal chemistry letters, Mar-11, Volume: 12, Issue:3
| Biological Evaluation of 5'-( |
AID33792 | Binding affinity to adenosine A2A receptor in rat striatal membranes by measuring displacement of specific [3H]-CGS- 21680 as radioligand | 1995 | Journal of medicinal chemistry, Mar-31, Volume: 38, Issue:7
| Search for new purine- and ribose-modified adenosine analogues as selective agonists and antagonists at adenosine receptors. |
AID300103 | Antimalarial activity against chloroquine,pyrimethamine-resistant Plasmodium falciparum K1 after 24 hrs | 2007 | Bioorganic & medicinal chemistry, Aug-15, Volume: 15, Issue:16
| Anti-malarial activity of N6-modified purine analogues. |
AID300108 | Selectivity index, ratio of CC50 for human KB cells to IC50 for Plasmodium falciparum VS1 | 2007 | Bioorganic & medicinal chemistry, Aug-15, Volume: 15, Issue:16
| Anti-malarial activity of N6-modified purine analogues. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |