Assay ID | Title | Year | Journal | Article |
AID1296008 | Cytotoxic Profiling of Annotated Libraries Using Quantitative High-Throughput Screening | 2020 | SLAS discovery : advancing life sciences R & D, 01, Volume: 25, Issue:1
| Cytotoxic Profiling of Annotated and Diverse Chemical Libraries Using Quantitative High-Throughput Screening. |
AID1346987 | P-glycoprotein substrates identified in KB-8-5-11 adenocarcinoma cell line, qHTS therapeutic library screen | 2019 | Molecular pharmacology, 11, Volume: 96, Issue:5
| A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. |
AID1346986 | P-glycoprotein substrates identified in KB-3-1 adenocarcinoma cell line, qHTS therapeutic library screen | 2019 | Molecular pharmacology, 11, Volume: 96, Issue:5
| A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. |
AID1181765 | Induction of apoptosis in human Caco2 cells assessed as vital cells at 0.05 uM after 24 hrs by Annexin V/propidium iodide staining-based flow cytometric analysis (Rvb = 96.67 +/- 1.02%) | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID346585 | Antiproliferative activity against human NCI-H460 cells after short term exposure for 1 hr measured after 72 hrs in drug-free medium | 2009 | Journal of medicinal chemistry, Feb-26, Volume: 52, Issue:4
| Semisynthesis, biological activity, and molecular modeling studies of C-ring-modified camptothecins. |
AID1181753 | Permeability from apical to basolateral side in human Caco2 cells at 10 to 50 uM after 15 to 90 mins by HPLC analysis | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1175655 | Antiproliferative activity against human KB cells after 48 hrs by CCK8 assay | 2015 | Bioorganic & medicinal chemistry, Jan-01, Volume: 23, Issue:1
| Synthesis of novel 10-hydroxycamptothecin derivatives utilizing topotecan hydrochloride as ortho-quinonemethide precursor. |
AID1181766 | Induction of apoptosis in human Caco2 cells assessed as vital cells at 0.5 uM after 24 hrs by Annexin V/propidium iodide staining-based flow cytometric analysis (Rvb = 96.67 +/- 1.02%) | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181764 | Cytotoxicity against human MDA-MB-231 cells after 24 hrs by MTT assay | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181770 | Induction of apoptosis in human Caco2 cells assessed as early apoptotic cells at 0.5 uM after 24 hrs by Annexin V/propidium iodide staining-based flow cytometric analysis (Rvb = 0.72 +/- 0.03%) | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181774 | Induction of apoptosis in human Caco2 cells assessed as late apoptotic cells at 0.5 uM after 24 hrs by Annexin V/propidium iodide staining-based flow cytometric analysis (Rvb = 2.20 +/- 0.77%) | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181759 | Efflux ratio of effective permeability from basolateral to apical side over apical to basolateral side in human Caco2 cells at 10 to 50 uM after 15 to 90 mins by HPLC analysis | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181763 | Cytotoxicity against human Jurkat cells after 24 hrs by MTT assay | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181787 | Induction of apoptosis in human HeLa cells assessed as inhibition of DNA synthesis after 24 hrs by BrdU staining-based ELISA | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1175657 | Antiproliferative activity against human SGC7901 cells after 48 hrs by CCK8 assay | 2015 | Bioorganic & medicinal chemistry, Jan-01, Volume: 23, Issue:1
| Synthesis of novel 10-hydroxycamptothecin derivatives utilizing topotecan hydrochloride as ortho-quinonemethide precursor. |
AID185063 | In vitro No effect conc (NOEC) with respect to elevated levels of alanine aminotransferase (ALT) using primary hepatocytes of rat | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Design and optimization of 20-O-linked camptothecin glycoconjugates as anticancer agents. |
AID1175656 | Antiproliferative activity against human HCT8 cells after 48 hrs by CCK8 assay | 2015 | Bioorganic & medicinal chemistry, Jan-01, Volume: 23, Issue:1
| Synthesis of novel 10-hydroxycamptothecin derivatives utilizing topotecan hydrochloride as ortho-quinonemethide precursor. |
AID1181761 | Cytotoxicity against human Caco2 cells after 24 hrs by MTT assay | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181771 | Induction of apoptosis in human Caco2 cells assessed as early apoptotic cells at 0.05 uM after 48 hrs by Annexin V/propidium iodide staining-based flow cytometric analysis (Rvb = 0.72 +/- 0.03%) | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181784 | Induction of apoptosis in human MDA-MB-231 cells assessed as inhibition of DNA synthesis at 0.8 to 1.6 uM after 24 hrs by BrdU staining-based ELISA | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID59935 | In vitro No effect conc (NOEC) with respect to elevated levels of Lactate dehydrogenase (LDH) using primary hepatocytes of dog | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Design and optimization of 20-O-linked camptothecin glycoconjugates as anticancer agents. |
AID89956 | In vitro No effect conc (NOEC) with respect to elevated levels of alanine aminotransferase (ALT) using primary hepatocytes of human | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Design and optimization of 20-O-linked camptothecin glycoconjugates as anticancer agents. |
AID59936 | In vitro No effect conc (NOEC) with respect to elevated levels of alanine aminotransferase (ALT) using primary hepatocytes of dog | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Design and optimization of 20-O-linked camptothecin glycoconjugates as anticancer agents. |
AID185064 | In vitro No effect conc (NOEC) with respect to elevated levels of aspartate aminotransferase (AST) using primary hepatocytes of rat | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Design and optimization of 20-O-linked camptothecin glycoconjugates as anticancer agents. |
AID1181773 | Induction of apoptosis in human Caco2 cells assessed as late apoptotic cells at 0.05 uM after 24 hrs by Annexin V/propidium iodide staining-based flow cytometric analysis (Rvb = 2.20 +/- 0.77%) | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181775 | Induction of apoptosis in human Caco2 cells assessed as late apoptotic cells at 0.05 uM after 48 hrs by Annexin V/propidium iodide staining-based flow cytometric analysis (Rvb = 2.20 +/- 0.77%) | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181746 | Induction of apoptosis in human MDA-MB-231 cells assessed as p53 phosphorylation at Ser15 by Western blotting analysis | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181783 | Induction of apoptosis in human HeLa cells assessed as inhibition of DNA synthesis at 0.8 to 1.6 uM after 24 hrs by BrdU staining-based ELISA | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181769 | Induction of apoptosis in human Caco2 cells assessed as early apoptotic cells at 0.05 uM after 24 hrs by Annexin V/propidium iodide staining-based flow cytometric analysis (Rvb = 0.72 +/- 0.03%) | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID89957 | In vitro No effect conc (NOEC) with respect to elevated levels of aspartate aminotransferase (AST) using primary hepatocytes of human | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Design and optimization of 20-O-linked camptothecin glycoconjugates as anticancer agents. |
AID1181762 | Cytotoxicity against human A375 cells after 24 hrs by MTT assay | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID185062 | In vitro No effect conc (NOEC) with respect to elevated levels of Lactate dehydrogenase (LDH) using primary hepatocytes of rat | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Design and optimization of 20-O-linked camptothecin glycoconjugates as anticancer agents. |
AID89955 | In vitro No effect conc (NOEC) with respect to elevated levels of Lactate dehydrogenase (LDH) using primary hepatocytes of human | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Design and optimization of 20-O-linked camptothecin glycoconjugates as anticancer agents. |
AID247909 | In vitro cytotoxicity against Bel7402 cell line (human liver cancer) using MTT assay | 2004 | Bioorganic & medicinal chemistry letters, Aug-02, Volume: 14, Issue:15
| Synthesis and cytotoxicity of water soluble quaternary salt derivatives of camptothecin. |
AID1181785 | Induction of apoptosis in human A375 cells assessed as inhibition of DNA synthesis after 24 hrs by BrdU staining-based ELISA | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181747 | Effective permeability from apical to basolateral side in human Caco2 cells at 50 uM after 15 to 90 mins by HPLC analysis | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181745 | Induction of apoptosis in human HeLa cells assessed as p53 phosphorylation at Ser15 by Western blotting analysis | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181760 | Cytotoxicity against human HeLa cells after 24 hrs by MTT assay | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181789 | Induction of apoptosis in human A375 cells assessed as p53 phosphorylation at Ser15 by Western blotting analysis | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181782 | Induction of apoptosis in human Caco2 cells assessed as inhibition of DNA synthesis at 0.8 to 1.6 uM after 24 hrs by BrdU staining-based ELISA | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181772 | Induction of apoptosis in human Caco2 cells assessed as early apoptotic cells at 0.5 uM after 48 hrs by Annexin V/propidium iodide staining-based flow cytometric analysis (Rvb = 0.72 +/- 0.03%) | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181754 | Permeability from basolateral to apical side in human Caco2 cells at 10 to 50 uM after 15 to 90 mins by HPLC analysis | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID59937 | In vitro No effect conc (NOEC) with respect to elevated levels of aspartate aminotransferase (AST) using primary hepatocytes of dog | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Design and optimization of 20-O-linked camptothecin glycoconjugates as anticancer agents. |
AID1181781 | Induction of apoptosis in human A375 cells assessed as inhibition of DNA synthesis at 0.8 to 1.6 uM after 24 hrs by BrdU staining-based ELISA | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID248361 | In vitro cytotoxicity against KB cell line (human epidermoid carcinoma of the nasopharynx) using MTT assay | 2004 | Bioorganic & medicinal chemistry letters, Aug-02, Volume: 14, Issue:15
| Synthesis and cytotoxicity of water soluble quaternary salt derivatives of camptothecin. |
AID1181767 | Induction of apoptosis in human Caco2 cells assessed as vital cells at 0.05 uM after 48 hrs by Annexin V/propidium iodide staining-based flow cytometric analysis (Rvb = 96.67 +/- 1.02%) | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181786 | Induction of apoptosis in human Caco2 cells assessed as inhibition of DNA synthesis after 24 hrs by BrdU staining-based ELISA | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID247865 | In vitro cytotoxicity against HCT-8 cell line (human colon cancer) using MTT assay | 2004 | Bioorganic & medicinal chemistry letters, Aug-02, Volume: 14, Issue:15
| Synthesis and cytotoxicity of water soluble quaternary salt derivatives of camptothecin. |
AID1181776 | Induction of apoptosis in human Caco2 cells assessed as late apoptotic cells at 0.5 uM after 48 hrs by Annexin V/propidium iodide staining-based flow cytometric analysis (Rvb = 2.20 +/- 0.77%) | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID56574 | In vitro fragmentation of DNA in the presence of excess calf thymus topoisomerase. | 1995 | Journal of medicinal chemistry, Mar-31, Volume: 38, Issue:7
| Synthesis, topoisomerase I inhibitory activity, and in vivo evaluation of 11-azacamptothecin analogs. |
AID1181788 | Induction of apoptosis in human MDA-MB-231 cells assessed as inhibition of DNA synthesis after 24 hrs by BrdU staining-based ELISA | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181779 | Induction of apoptosis in human Caco2 cells assessed as necrotic cells at 0.05 uM after 48 hrs by Annexin V/propidium iodide staining-based flow cytometric analysis (Rvb = 0.41 +/- 0.02%) | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1175654 | Antiproliferative activity against human HepG2 cells after 48 hrs by CCK8 assay | 2015 | Bioorganic & medicinal chemistry, Jan-01, Volume: 23, Issue:1
| Synthesis of novel 10-hydroxycamptothecin derivatives utilizing topotecan hydrochloride as ortho-quinonemethide precursor. |
AID20719 | Aqueous solubility determined in pH 5 acetate buffer | 1995 | Journal of medicinal chemistry, Mar-31, Volume: 38, Issue:7
| Synthesis, topoisomerase I inhibitory activity, and in vivo evaluation of 11-azacamptothecin analogs. |
AID1181744 | Induction of apoptosis in human Caco2 cells assessed as p53 phosphorylation at Ser15 by Western blotting analysis | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181768 | Induction of apoptosis in human Caco2 cells assessed as vital cells at 0.5 uM after 48 hrs by Annexin V/propidium iodide staining-based flow cytometric analysis (Rvb = 96.67 +/- 1.02%) | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181778 | Induction of apoptosis in human Caco2 cells assessed as necrotic cells at 0.5 uM after 24 hrs by Annexin V/propidium iodide staining-based flow cytometric analysis (Rvb = 0.41 +/- 0.02%) | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181780 | Induction of apoptosis in human Caco2 cells assessed as necrotic cells at 0.5 uM after 48 hrs by Annexin V/propidium iodide staining-based flow cytometric analysis (Rvb = 0.41 +/- 0.02%) | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181758 | Effective permeability in Wistar rat small intestine assessed as absorption rate coefficient at 50 uM measured after 5 mins in every 5 min interval up to 30 mins | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID1181757 | Effective permeability in Wistar rat small intestine at 50 uM measured after 5 mins in every 5 min interval up to 30 mins | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID121133 | Delay in tumor growth in mice to 500% volume of day 1 relative to control at dose 54 mg/kg. | 1995 | Journal of medicinal chemistry, Mar-31, Volume: 38, Issue:7
| Synthesis, topoisomerase I inhibitory activity, and in vivo evaluation of 11-azacamptothecin analogs. |
AID1181777 | Induction of apoptosis in human Caco2 cells assessed as necrotic cells at 0.05 uM after 24 hrs by Annexin V/propidium iodide staining-based flow cytometric analysis (Rvb = 0.41 +/- 0.02%) | 2014 | European journal of medicinal chemistry, Aug-18, Volume: 83 | A promising camptothecin derivative: Semisynthesis, antitumor activity and intestinal permeability. |
AID651635 | Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression | | | |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2006 | Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
| Microsphere-based protease assays and screening application for lethal factor and factor Xa. |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1
| High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2006 | Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
| Microsphere-based protease assays and screening application for lethal factor and factor Xa. |
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1
| High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID1745850 | Viability Counterscreen for Confirmatory qHTS for Inhibitors of ATXN expression | | | |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2006 | Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
| Microsphere-based protease assays and screening application for lethal factor and factor Xa. |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1
| High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID1745847 | CMV-Luciferase Counterscreen for Inhibitors of ATXN expression | | | |
AID1745846 | Firefly Luciferase Counterscreen for Inhibitors of ATXN expression | | | |
AID1745848 | Confirmatory qHTS for Inhibitors of ATXN expression | | | |
AID1745849 | Viability Counterscreen for CMV-Luciferase Assay of Inhibitors of ATXN expression | | | |
AID1745845 | Primary qHTS for Inhibitors of ATXN expression | | | |
AID1347108 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh41 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347089 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for TC32 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347092 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for A673 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347083 | qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: Viability assay - alamar blue signal for LASV Primary Screen | 2020 | Antiviral research, 01, Volume: 173 | A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity. |
AID1347115 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for NB-EBc1 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347113 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for LAN-5 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347414 | qHTS to identify inhibitors of the type 1 interferon - major histocompatibility complex class I in skeletal muscle: Secondary screen by immunofluorescence | 2020 | ACS chemical biology, 07-17, Volume: 15, Issue:7
| High-Throughput Screening to Identify Inhibitors of the Type I Interferon-Major Histocompatibility Complex Class I Pathway in Skeletal Muscle. |
AID1347102 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh18 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347140 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Orthogonal 3D viability screen for MG 63 (6-TG R) cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347096 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for U-2 OS cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347095 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for NB-EBc1 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347101 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for BT-12 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347136 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Orthogonal 3D viability screen for SJ-GBM2 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347099 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for NB1643 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347103 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for OHS-50 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347114 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for DAOY cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347097 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Saos-2 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347407 | qHTS to identify inhibitors of the type 1 interferon - major histocompatibility complex class I in skeletal muscle: primary screen against the NCATS Pharmaceutical Collection | 2020 | ACS chemical biology, 07-17, Volume: 15, Issue:7
| High-Throughput Screening to Identify Inhibitors of the Type I Interferon-Major Histocompatibility Complex Class I Pathway in Skeletal Muscle. |
AID1347137 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Orthogonal 3D viability screen for Daoy cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347110 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for A673 cells) | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347154 | Primary screen GU AMC qHTS for Zika virus inhibitors | 2020 | Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
| Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors. |
AID1347082 | qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: LASV Primary Screen - GLuc reporter signal | 2020 | Antiviral research, 01, Volume: 173 | A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity. |
AID1347121 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for control Hh wild type fibroblast cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347139 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Orthogonal 3D viability screen for TC32 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347425 | Rhodamine-PBP qHTS Assay for Modulators of WT P53-Induced Phosphatase 1 (WIP1) | 2019 | The Journal of biological chemistry, 11-15, Volume: 294, Issue:46
| Physiologically relevant orthogonal assays for the discovery of small-molecule modulators of WIP1 phosphatase in high-throughput screens. |
AID1347094 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for BT-37 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347141 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Orthogonal 3D viability screen for RD cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347090 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for DAOY cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347424 | RapidFire Mass Spectrometry qHTS Assay for Modulators of WT P53-Induced Phosphatase 1 (WIP1) | 2019 | The Journal of biological chemistry, 11-15, Volume: 294, Issue:46
| Physiologically relevant orthogonal assays for the discovery of small-molecule modulators of WIP1 phosphatase in high-throughput screens. |
AID1347104 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for RD cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347105 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for MG 63 (6-TG R) cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347124 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for RD cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347107 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh30 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1508630 | Primary qHTS for small molecule stabilizers of the endoplasmic reticulum resident proteome: Secreted ER Calcium Modulated Protein (SERCaMP) assay | 2021 | Cell reports, 04-27, Volume: 35, Issue:4
| A target-agnostic screen identifies approved drugs to stabilize the endoplasmic reticulum-resident proteome. |
AID1347106 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for control Hh wild type fibroblast cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347138 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Orthogonal 3D caspase screen for TC32 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347117 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for BT-37 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347100 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for LAN-5 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347116 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for SJ-GBM2 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347135 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Orthogonal 3D viability screen for SK-N-SH cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347112 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for BT-12 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347123 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Rh41 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347086 | qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lymphocytic Choriomeningitis Arenaviruses (LCMV): LCMV Primary Screen - GLuc reporter signal | 2020 | Antiviral research, 01, Volume: 173 | A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity. |
AID1347126 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Rh30 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347125 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Rh18 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347119 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for MG 63 (6-TG R) cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347118 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for TC32 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347109 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for NB1643 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347128 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for OHS-50 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347091 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SJ-GBM2 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347412 | qHTS assay to identify inhibitors of the type 1 interferon - major histocompatibility complex class I in skeletal muscle: Counter screen cell viability and HiBit confirmation | 2020 | ACS chemical biology, 07-17, Volume: 15, Issue:7
| High-Throughput Screening to Identify Inhibitors of the Type I Interferon-Major Histocompatibility Complex Class I Pathway in Skeletal Muscle. |
AID1347122 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for U-2 OS cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347129 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for SK-N-SH cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347093 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-MC cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347127 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Saos-2 cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347111 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for SK-N-MC cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347098 | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-SH cells | 2018 | Oncotarget, Jan-12, Volume: 9, Issue:4
| Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing. |
AID1347411 | qHTS to identify inhibitors of the type 1 interferon - major histocompatibility complex class I in skeletal muscle: primary screen against the NCATS Mechanism Interrogation Plate v5.0 (MIPE) Libary | 2020 | ACS chemical biology, 07-17, Volume: 15, Issue:7
| High-Throughput Screening to Identify Inhibitors of the Type I Interferon-Major Histocompatibility Complex Class I Pathway in Skeletal Muscle. |
AID504749 | qHTS profiling for inhibitors of Plasmodium falciparum proliferation | 2011 | Science (New York, N.Y.), Aug-05, Volume: 333, Issue:6043
| Chemical genomic profiling for antimalarial therapies, response signatures, and molecular targets. |
AID540299 | A screen for compounds that inhibit the MenB enzyme of Mycobacterium tuberculosis | 2010 | Bioorganic & medicinal chemistry letters, Nov-01, Volume: 20, Issue:21
| Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis. |
AID588519 | A screen for compounds that inhibit viral RNA polymerase binding and polymerization activities | 2011 | Antiviral research, Sep, Volume: 91, Issue:3
| High-throughput screening identification of poliovirus RNA-dependent RNA polymerase inhibitors. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |