Assay ID | Title | Year | Journal | Article |
AID738714 | Antiproliferative activity against human RKO cells expressing wild type p53 after 5 days by MTS assay | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738697 | Cell cycle arrest at human A549 cells expressing wild type p53 assessed as accumulation at S phase at 5 uM after 48 hrs by propidium iodide staining-based flow cytometric analysis (Rvb = 30.8%) | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738726 | Antiproliferative activity against human PC3 cells harboring p53 mutant at 10 uM after 5 days by MTS assay | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID1118050 | Inhibition of p53 interaction to MDM2 (unknown origin) by surface plasmon resonance assay | 2011 | MedChemComm, , Volume: 2 | The p53-MDM2/MDMX axis - A chemotype perspective. |
AID243263 | Potency against MDM2 (murine double minute-2 gene) binding to p53; Range =100-300 nM | 2005 | Journal of medicinal chemistry, Jul-14, Volume: 48, Issue:14
| p53 Activation by small molecules: application in oncology. |
AID738719 | Cytotoxicity against human PC3 cells harboring p53 mutant assessed as cell viability at 10 uM after 5 days by MTS assay | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738698 | Cell cycle arrest at human A549 cells expressing wild type p53 assessed as accumulation at G2/M phase at 5 uM after 48 hrs by propidium iodide staining-based flow cytometric analysis (Rvb = 11.3%) | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738705 | Cell cycle arrest at human SJSA1 cells expressing wild type p53 assessed as accumulation at G0/G1 phase at 5 uM after 48 hrs by propidium iodide staining-based flow cytometric analysis (Rvb = 53.8%) | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738703 | Cell cycle arrest at human SJSA1 cells expressing wild type p53 assessed as accumulation at S phase at 5 uM after 48 hrs by propidium iodide staining-based flow cytometric analysis (Rvb = 33.2%) | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID754224 | Binding affinity to MDM2 (unknown origin) expressed in Escherichia coli BL21(DE3) after 30 mins by fluorescence polarization assay in presence of P4 peptide | 2013 | Bioorganic & medicinal chemistry, Jul-15, Volume: 21, Issue:14
| Benzimidazole-2-one: a novel anchoring principle for antagonizing p53-Mdm2. |
AID1195730 | Binding affinity to MDM2 (unknown origin) | 2015 | Journal of medicinal chemistry, Feb-12, Volume: 58, Issue:3
| Small-molecule inhibitors of the MDM2-p53 protein-protein interaction (MDM2 Inhibitors) in clinical trials for cancer treatment. |
AID738712 | Cytotoxicity against human A549 cells expressing wild type p53 assessed as cell viability after 5 days by MTS assay | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738707 | Cell cycle arrest at human MDA-MB-435S cells harboring p53 mutant assessed as accumulation at G2/M phase at 10 uM after 48 hrs by propidium iodide staining-based flow cytometric analysis (Rvb = 8.8%) | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738700 | Cell cycle arrest at human SJSA1 cells expressing wild type p53 assessed as accumulation at S phase at 10 uM after 48 hrs by propidium iodide staining-based flow cytometric analysis (Rvb = 33.2%) | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID691697 | Inhibition of MDM2 binding to p53 | 2012 | Bioorganic & medicinal chemistry letters, Oct-15, Volume: 22, Issue:20
| Discovery of novel dihydroimidazothiazole derivatives as p53-MDM2 protein-protein interaction inhibitors: synthesis, biological evaluation and structure-activity relationships. |
AID738715 | Antiproliferative activity against human HepG2 cells expressing wild type p53 after 5 days by MTS assay | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738699 | Cell cycle arrest at human A549 cells expressing wild type p53 assessed as accumulation at G0/G1 phase at 5 uM after 48 hrs by propidium iodide staining-based flow cytometric analysis (Rvb = 57.9%) | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738720 | Cytotoxicity against human MDA-MB-435S cells harboring p53 mutant assessed as cell viability at 10 uM after 5 days by MTS assay | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738979 | Antiproliferative activity against human HeLa cells harboring p53 mutant at 10 uM after 5 days by MTS assay | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738722 | Cell cycle arrest at human MDA-MB-435S cells harboring p53 mutant assessed as accumulation at G0/G1 phase at 5 uM after 48 hrs by propidium iodide staining-based flow cytometric analysis (Rvb = 56.8%) | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738721 | Cytotoxicity against human HeLa cells harboring p53 mutant assessed as cell viability at 10 uM after 5 days by MTS assay | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738702 | Cell cycle arrest at human SJSA1 cells expressing wild type p53 assessed as accumulation at G0/G1 phase at 10 uM after 48 hrs by propidium iodide staining-based flow cytometric analysis (Rvb = 53.8%) | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738709 | Cytotoxicity against human RKO cells expressing wild type p53 assessed as cell viability after 5 days by MTS assay | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738723 | Cell cycle arrest at human MDA-MB-435S cells harboring p53 mutant assessed as accumulation at G2/M phase at 5 uM after 48 hrs by propidium iodide staining-based flow cytometric analysis (Rvb = 8.8%) | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738718 | Cytotoxicity against human SW480 cells harboring p53 mutant assessed as cell viability at 10 uM after 5 days by MTS assay | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738710 | Cytotoxicity against human HepG2 cells expressing wild type p53 assessed as cell viability after 5 days by MTS assay | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738711 | Cytotoxicity against human HCT116 cells expressing wild type p53 assessed as cell viability after 5 days by MTS assay | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738704 | Cell cycle arrest at human SJSA1 cells expressing wild type p53 assessed as accumulation at G2/M phase at 5 uM after 48 hrs by propidium iodide staining-based flow cytometric analysis (Rvb = 13%) | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738701 | Cell cycle arrest at human SJSA1 cells expressing wild type p53 assessed as accumulation at G2/M phase at 10 uM after 48 hrs by propidium iodide staining-based flow cytometric analysis (Rvb = 13%) | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738980 | Cell cycle arrest at human MDA-MB-435S cells harboring p53 mutant assessed as accumulation at G0/G1 phase at 10 uM after 48 hrs by propidium iodide staining-based flow cytometric analysis (Rvb = 56.8%) | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738696 | Cell cycle arrest at human A549 cells expressing wild type p53 assessed as accumulation at G0/G1 phase at 10 uM after 48 hrs by propidium iodide staining-based flow cytometric analysis (Rvb = 57.9%) | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738724 | Cell cycle arrest at human MDA-MB-435S cells harboring p53 mutant assessed as accumulation at S phase at 5 uM after 48 hrs by propidium iodide staining-based flow cytometric analysis (Rvb = 34.4%) | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738713 | Antiproliferative activity against human SJSA1 cells expressing wild type p53 after 5 days by MTS assay | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738725 | Antiproliferative activity against human SW480 cells harboring p53 mutant at 10 uM after 5 days by MTS assay | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738708 | Cytotoxicity against human SJSA1 cells expressing wild type p53 assessed as cell viability after 5 days by MTS assay | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738694 | Cell cycle arrest at human A549 cells expressing wild type p53 assessed as accumulation at S phase at 10 uM after 48 hrs by propidium iodide staining-based flow cytometric analysis (Rvb = 30.8%) | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738706 | Cell cycle arrest at human MDA-MB-435S cells harboring p53 mutant assessed as accumulation at S phase at 10 uM after 48 hrs by propidium iodide staining-based flow cytometric analysis (Rvb = 34.4%) | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738695 | Cell cycle arrest at human A549 cells expressing wild type p53 assessed as accumulation at G2/M phase at 10 uM after 48 hrs by propidium iodide staining-based flow cytometric analysis (Rvb = 11.3%) | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738717 | Antiproliferative activity against human A549 cells expressing wild type p53 after 5 days by MTS assay | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738727 | Antiproliferative activity against human MDA-MB-435S cells harboring p53 mutant at 10 uM after 5 days by MTS assay | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
AID738716 | Antiproliferative activity against human HCT116 cells expressing wild type p53 after 5 days by MTS assay | 2013 | Bioorganic & medicinal chemistry, Apr-15, Volume: 21, Issue:8
| Synthesis and evaluation of an imidazole derivative-fluorescein conjugate. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |