# | Aladdin ID | Assay Type | Description | Organism | Compounds | Reference | BAO Format | Source | |
---|---|---|---|---|---|---|---|---|---|
1. | ALA646863 | B | Affinity for alpha-1 adrenergic receptor in rat was determined by [3H]- prazosin binding assay | 7 | assay format | Scientific Literature | |||
2. | ALA877791 | F | ED50 value was calculated by mouse electric shock assay (MES). | Mus musculus | 7 | organism-based format | Scientific Literature | ||
3. | ALA753016 | F | In vitro inhibitory concentration against NMDA responses at cloned NR1A/2A receptors expressed in Xenopus oocytes | Rattus norvegicus | 8 | cell-based format | Scientific Literature | ||
4. | ALA752242 | F | In vitro inhibitory concentration against NMDA responses at NR1A/2B receptors expressed in Xenopus oocytes | Rattus norvegicus | 8 | cell-based format | Scientific Literature | ||
5. | ALA752250 | F | In vitro inhibitory concentration against NMDA responses at NR1A/2C receptors expressed in Xenopus oocytes | Rattus norvegicus | 8 | cell-based format | Scientific Literature | ||
6. | ALA815530 | F | Inhibition of voltage -gated K+ currents was measured by whole cell voltage clamp recordings from dissociated rat superior cervical ganglion neurons at 10 uM | Rattus | 7 | organism-based format | Scientific Literature | ||
7. | ALA832427 | B | Inhibition of [3H]-Ro-25-6981 binding to NMDA receptor | 19 | protein complex format | Scientific Literature | |||
8. | ALA828708 | B | Inhibition of NMDA-evoked increased intracellular [Ca2+] in cells expressing NR1/NR2B receptor | 19 | cell-based format | Scientific Literature | |||
9. | ALA834611 | F | In vivo analgesic activity was tested using formalin test in mouse upon i.p. administration | Mus musculus | 2 | organism-based format | Scientific Literature | ||
10. | ALA825873 | F | In vivo analgesic activity was tested using formalin test in mouse upon p.o. administration; IA is inactive | Mus musculus | 2 | organism-based format | Scientific Literature | ||
11. | ALA1614250 | F | PUBCHEM_BIOASSAY: qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization. (Class of assay: confirmatory) [Related pubchem assays: 596 ] | Homo sapiens | 20,446 | assay format | PubChem BioAssays | ||
12. | ALA3215169 | B | PubChem BioAssay. qHTS for Inhibitors of binding or entry into cells for Lassa Virus. (Class of assay: confirmatory) | 3,383 | assay format | PubChem BioAssays | |||
13. | ALA3214913 | B | PubChem BioAssay. qHTS for Inhibitors of binding or entry into cells for Marburg Virus. (Class of assay: confirmatory) | 4,591 | assay format | PubChem BioAssays | |||
14. | ALA4303805 | F | Antiviral activity determined as inhibition of SARS-CoV-2 induced cytotoxicity of Caco-2 cells at 10 uM after 48 hours by high content imaging | Homo sapiens | 5,612 | organism-based format | SARS-CoV-2 Screening Data 2020-21 | ||
15. | ALA4495582 | F | SARS-CoV-2 3CL-Pro protease inhibition percentage at 20µM by FRET kind of response from peptide substrate | Severe acute respiratory syndrome coronavirus 2 | 7,212 | assay format | SARS-CoV-2 Screening Data 2020-21 | ||
16. | ALA4513082 | F | Antiviral activity determined as inhibition of SARS-CoV-2 induced cytotoxicity of VERO-6 cells at 10 uM after 48 hours exposure to 0.01 MOI SARS CoV-2 virus by high content imaging | Chlorocebus sabaeus | 7,212 | organism-based format | SARS-CoV-2 Screening Data 2020-21 | ||
17. | ALA4808149 | B | Enzymatic assay of human HDAC6 with commercial peptide substrate | Homo sapiens | 5,603 | single protein format | Fraunhofer HDAC6 | ||
18. | ALA4808150 | B | Enzymatic assay of human HDAC6 with custom peptide substrate | Homo sapiens | 5,603 | single protein format | Fraunhofer HDAC6 |