| Assay ID | Title | Year | Journal | Article |
|---|
| AID504812 | Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | 2010 | Endocrinology, Jul, Volume: 151, Issue:7
| A small molecule inverse agonist for the human thyroid-stimulating hormone receptor. |
| 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. |
| 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. |
| 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. |
| AID651635 | Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression | | | |
| AID1745845 | Primary qHTS for Inhibitors of ATXN expression | | | |
| AID504810 | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | 2010 | Endocrinology, Jul, Volume: 151, Issue:7
| A small molecule inverse agonist for the human thyroid-stimulating hormone receptor. |
| AID654127 | Growth inhibition of human NCI-H460 cells after 48 hrs by sulforhodamine B assay | 2012 | Bioorganic & medicinal chemistry, Apr-15, Volume: 20, Issue:8
| Free radical scavenging and antiproliferative properties of Biginelli adducts. |
| AID654130 | Growth inhibition of human HT-29 cells after 48 hrs by sulforhodamine B assay | 2012 | Bioorganic & medicinal chemistry, Apr-15, Volume: 20, Issue:8
| Free radical scavenging and antiproliferative properties of Biginelli adducts. |
| AID654128 | Growth inhibition of human PC3 cells after 48 hrs by sulforhodamine B assay | 2012 | Bioorganic & medicinal chemistry, Apr-15, Volume: 20, Issue:8
| Free radical scavenging and antiproliferative properties of Biginelli adducts. |
| AID654126 | Growth inhibition of human 786-0 cells after 48 hrs by sulforhodamine B assay | 2012 | Bioorganic & medicinal chemistry, Apr-15, Volume: 20, Issue:8
| Free radical scavenging and antiproliferative properties of Biginelli adducts. |
| AID654125 | Growth inhibition of human NCI-ADR-RES cells after 48 hrs by sulforhodamine B assay | 2012 | Bioorganic & medicinal chemistry, Apr-15, Volume: 20, Issue:8
| Free radical scavenging and antiproliferative properties of Biginelli adducts. |
| AID654124 | Growth inhibition of human U251 cells after 48 hrs by sulforhodamine B assay | 2012 | Bioorganic & medicinal chemistry, Apr-15, Volume: 20, Issue:8
| Free radical scavenging and antiproliferative properties of Biginelli adducts. |
| AID654115 | Antioxidant activity assessed as scavenging of DPPH at 160 uM after 30 mins by spectrophotometry | 2012 | Bioorganic & medicinal chemistry, Apr-15, Volume: 20, Issue:8
| Free radical scavenging and antiproliferative properties of Biginelli adducts. |
| AID654129 | Growth inhibition of human OVCAR3 cells after 48 hrs by sulforhodamine B assay | 2012 | Bioorganic & medicinal chemistry, Apr-15, Volume: 20, Issue:8
| Free radical scavenging and antiproliferative properties of Biginelli adducts. |
| AID1153368 | Inhibition pig alpha-amylase at 50 to 300 ug/ml pretreated for 30 mins followed by addition of 1% starch for 10 mins by spectrometer | 2014 | Bioorganic & medicinal chemistry letters, Jul-01, Volume: 24, Issue:13
| Graphite catalyzed solvent free synthesis of dihydropyrimidin-2(1H)-ones/thiones and their antidiabetic activity. |
| [information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |