Assay ID | Title | Year | Journal | Article |
AID1347159 | Primary screen GU Rhodamine qHTS for Zika virus inhibitors: Unlinked NS2B-NS3 protease assay | 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. |
AID1347160 | Primary screen NINDS Rhodamine 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. |
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. |
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. |
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. |
AID108610 | In vitro effective concentration towards human Melanocortin 1 receptor (MC1R) in SPA-based cAMP assay in melanoma cells | 2003 | Journal of medicinal chemistry, Mar-27, Volume: 46, Issue:7
| Discovery of tyrosine-based potent and selective melanocortin-1 receptor small-molecule agonists with anti-inflammatory properties. |
AID109303 | In vitro effective concentration towards human Melanocortin 5 receptor (MC5R) was determined by a SPA-based cAMP assay in melanoma cells | 2003 | Journal of medicinal chemistry, Mar-27, Volume: 46, Issue:7
| Discovery of tyrosine-based potent and selective melanocortin-1 receptor small-molecule agonists with anti-inflammatory properties. |
AID28093 | Cmax value was evaluated in mice by intravenous administration of 6.8 umol/kg dose | 2003 | Journal of medicinal chemistry, Mar-27, Volume: 46, Issue:7
| Discovery of tyrosine-based potent and selective melanocortin-1 receptor small-molecule agonists with anti-inflammatory properties. |
AID108796 | In vitro intrinsic activity against human Melanocortin 3 receptor (MC3R) | 2003 | Journal of medicinal chemistry, Mar-27, Volume: 46, Issue:7
| Discovery of tyrosine-based potent and selective melanocortin-1 receptor small-molecule agonists with anti-inflammatory properties. |
AID108973 | In vitro effective concentration towards human Melanocortin 4 receptor (MC4R) was determined by a SPA-based cAMP assay in melanoma cells | 2003 | Journal of medicinal chemistry, Mar-27, Volume: 46, Issue:7
| Discovery of tyrosine-based potent and selective melanocortin-1 receptor small-molecule agonists with anti-inflammatory properties. |
AID108805 | In vitro inhibitory concentration against human Melanocortin 3 receptor (MC3R) | 2003 | Journal of medicinal chemistry, Mar-27, Volume: 46, Issue:7
| Discovery of tyrosine-based potent and selective melanocortin-1 receptor small-molecule agonists with anti-inflammatory properties. |
AID25237 | AUC value was evaluated in mice by intravenous administration of 6.8 umol/kg dose | 2003 | Journal of medicinal chemistry, Mar-27, Volume: 46, Issue:7
| Discovery of tyrosine-based potent and selective melanocortin-1 receptor small-molecule agonists with anti-inflammatory properties. |
AID109136 | In vitro intrinsic activity against human Melanocortin 4 receptor (MC4R) | 2003 | Journal of medicinal chemistry, Mar-27, Volume: 46, Issue:7
| Discovery of tyrosine-based potent and selective melanocortin-1 receptor small-molecule agonists with anti-inflammatory properties. |
AID30168 | Vss value was determined by intravenous administration of 6.8 umol/kg dose in mice | 2003 | Journal of medicinal chemistry, Mar-27, Volume: 46, Issue:7
| Discovery of tyrosine-based potent and selective melanocortin-1 receptor small-molecule agonists with anti-inflammatory properties. |
AID109430 | In vitro intrinsic activity against human Melanocortin 5 receptor (MC5R) | 2003 | Journal of medicinal chemistry, Mar-27, Volume: 46, Issue:7
| Discovery of tyrosine-based potent and selective melanocortin-1 receptor small-molecule agonists with anti-inflammatory properties. |
AID27772 | MRT value was determined by intravenous administration of 6.8 umol/kg dose in mice | 2003 | Journal of medicinal chemistry, Mar-27, Volume: 46, Issue:7
| Discovery of tyrosine-based potent and selective melanocortin-1 receptor small-molecule agonists with anti-inflammatory properties. |
AID29060 | Half life by intravenous administration of 6.8 umol/kg dose in mice | 2003 | Journal of medicinal chemistry, Mar-27, Volume: 46, Issue:7
| Discovery of tyrosine-based potent and selective melanocortin-1 receptor small-molecule agonists with anti-inflammatory properties. |
AID108615 | In vitro inhibitory concentration against human Melanocortin 1 receptor (MC1R) | 2003 | Journal of medicinal chemistry, Mar-27, Volume: 46, Issue:7
| Discovery of tyrosine-based potent and selective melanocortin-1 receptor small-molecule agonists with anti-inflammatory properties. |
AID27868 | Cl value was determined by intravenous administration of 6.8 umol/kg dose in mice | 2003 | Journal of medicinal chemistry, Mar-27, Volume: 46, Issue:7
| Discovery of tyrosine-based potent and selective melanocortin-1 receptor small-molecule agonists with anti-inflammatory properties. |
AID108620 | In vitro intrinsic activity against human Melanocortin 1 receptor (MC1R) | 2003 | Journal of medicinal chemistry, Mar-27, Volume: 46, Issue:7
| Discovery of tyrosine-based potent and selective melanocortin-1 receptor small-molecule agonists with anti-inflammatory properties. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |