Assay ID | Title | Year | Journal | Article |
AID1411481 | Selectivity ratio of IC50 for human NaV1.8 to IC50 for human NaV1.3 | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1246035 | Selectivity ratio of IC50 for human NaV1.5 channel to IC50 for human NaV1.3 channel | 2015 | Journal of medicinal chemistry, Sep-24, Volume: 58, Issue:18
| Voltage-Gated Sodium Channels: Structure, Function, Pharmacology, and Clinical Indications. |
AID1246058 | Inhibition of human TTX-sensitive NaV1.3 channel expressed in HEK293 cells by patch clamp electrophysiology assay | 2015 | Journal of medicinal chemistry, Sep-24, Volume: 58, Issue:18
| Voltage-Gated Sodium Channels: Structure, Function, Pharmacology, and Clinical Indications. |
AID1411474 | Inhibition of human NaV1.8 | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1246064 | Inhibition of human NaV1.8 channel by patch clamp electrophysiology assay | 2015 | Journal of medicinal chemistry, Sep-24, Volume: 58, Issue:18
| Voltage-Gated Sodium Channels: Structure, Function, Pharmacology, and Clinical Indications. |
AID1411470 | Inhibition of human NaV1.5 | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1411486 | Lipophilicity, log D of the compound | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1411465 | Inhibition of human NaV1.3 expressed in HEK cells by electrophysiological method | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1246037 | Selectivity ratio of IC50 for human NaV1.5 channel to IC50 for human NaV1.7 channel | 2015 | Journal of medicinal chemistry, Sep-24, Volume: 58, Issue:18
| Voltage-Gated Sodium Channels: Structure, Function, Pharmacology, and Clinical Indications. |
AID1246060 | Inhibition of human NaV1.2 channel by patch clamp electrophysiology assay | 2015 | Journal of medicinal chemistry, Sep-24, Volume: 58, Issue:18
| Voltage-Gated Sodium Channels: Structure, Function, Pharmacology, and Clinical Indications. |
AID1411480 | Selectivity ratio of IC50 for human NaV1.7 to IC50 for human NaV1.3 | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1411467 | Inhibition of human NaV1.1 | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1246063 | Inhibition of human NaV1.6 channel by patch clamp electrophysiology assay | 2015 | Journal of medicinal chemistry, Sep-24, Volume: 58, Issue:18
| Voltage-Gated Sodium Channels: Structure, Function, Pharmacology, and Clinical Indications. |
AID1411466 | Inhibition of rat NaV1.3 by electrophysiological method | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1411483 | Inhibition of CYP2C9 (unknown origin) at 3 uM by high throughput assay relative to control | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1411479 | Selectivity ratio of IC50 for human NaV1.6 to IC50 for human NaV1.3 | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1411485 | Efflux ratio of permeability across basolateral to apical over apical to basolateral side in RRCK cells expressing MDR1 | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1411477 | Selectivity ratio of IC50 for human NaV1.4 to IC50 for human NaV1.3 | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1411476 | Selectivity ratio of IC50 for human NaV1.2 to IC50 for human NaV1.3 | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1246036 | Selectivity ratio of IC50 for human NaV1.5 channel to IC50 for human NaV1.6 channel | 2015 | Journal of medicinal chemistry, Sep-24, Volume: 58, Issue:18
| Voltage-Gated Sodium Channels: Structure, Function, Pharmacology, and Clinical Indications. |
AID1246059 | Inhibition of human NaV1.1 channel by patch clamp electrophysiology assay | 2015 | Journal of medicinal chemistry, Sep-24, Volume: 58, Issue:18
| Voltage-Gated Sodium Channels: Structure, Function, Pharmacology, and Clinical Indications. |
AID1246061 | Inhibition of human NaV1.4 channel by patch clamp electrophysiology assay | 2015 | Journal of medicinal chemistry, Sep-24, Volume: 58, Issue:18
| Voltage-Gated Sodium Channels: Structure, Function, Pharmacology, and Clinical Indications. |
AID1246065 | Inhibition of human NaV1.7 channel expressed in HEK293 cells by patch clamp electrophysiology assay | 2015 | Journal of medicinal chemistry, Sep-24, Volume: 58, Issue:18
| Voltage-Gated Sodium Channels: Structure, Function, Pharmacology, and Clinical Indications. |
AID1411482 | Clearance in human liver microsomes | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1411468 | Inhibition of human NaV1.2 | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1411472 | Inhibition of human NaV1.7 | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1411478 | Selectivity ratio of IC50 for human NaV1.5 to IC50 for human NaV1.3 | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1246062 | Inhibition of human NaV1.5 channel expressed in HEK293 cells by patch clamp electrophysiology assay | 2015 | Journal of medicinal chemistry, Sep-24, Volume: 58, Issue:18
| Voltage-Gated Sodium Channels: Structure, Function, Pharmacology, and Clinical Indications. |
AID1411471 | Inhibition of human NaV1.6 | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1411484 | Aqueous solubility of compound | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1411473 | Inhibition of rat NaV1.7 | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1411475 | Selectivity ratio of IC50 for human NaV1.1 to IC50 for human NaV1.3 | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1411469 | Inhibition of human NaV1.4 | 2017 | MedChemComm, Jun-01, Volume: 8, Issue:6
| The discovery of a potent Na |
AID1246034 | Selectivity ratio of IC50 for human NaV1.5 channel to IC50 for human NaV1.1 channel | 2015 | Journal of medicinal chemistry, Sep-24, Volume: 58, Issue:18
| Voltage-Gated Sodium Channels: Structure, Function, Pharmacology, and Clinical Indications. |
AID1347164 | 384 well plate NINDS Rhodamine confirmatory 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. |
AID1347158 | ZIKV-mCherry secondary 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. |
AID1347156 | DAPI mCherry counterscreen 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. |
AID1347153 | Confirmatory 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. |
AID1347149 | Furin counterscreen 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. |
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. |
AID1347163 | 384 well plate NINDS AMC confirmatory 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. |
AID1347168 | HepG2 cells viability 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. |
AID1347161 | Confirmatory 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. |
AID1347167 | Vero cells viability 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. |
AID1347169 | Tertiary RLuc qRT-PCR qHTS assay 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. |
AID1347157 | Confirmatory screen GU Rhodamine qHTS for Zika virus inhibitors qHTS | 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. |
AID1347152 | Confirmatory screen NINDS 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. |
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. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |