# | Aladdin ID | Assay Type | Description | Organism | Compounds | Reference | BAO Format | Source | |
---|---|---|---|---|---|---|---|---|---|
1. | ALA1794438 | B | PUBCHEM_BIOASSAY: Counterscreen for inhibitors of TLR9-MyD88 binding: fluorescence-based cell-based high throughput dose response assay to identify non-selective inhibitors of the beta-lactamase enzyme (BLA). (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID504734, AID504750, AID540250, AID540251] | 235 | cell-based format | PubChem BioAssays | |||
2. | ALA1614376 | B | PubChem BioAssay. FRET-based counterscreen for selective VIM-2 inhibitors: dose response biochemical high throughput screening assay to identify epi-absorbance assay artifacts. (Class of assay: confirmatory) | Pseudomonas aeruginosa | 123 | single protein format | PubChem BioAssays | ||
3. | ALA1613916 | B | PubChem BioAssay. Epi-absorbance-based dose response assay for common IMP-1 and VIM-2 inhibitors: biochemical high throughput screening assay to identify inhibitors of VIM-2 metallo-beta-lactamase. (Class of assay: confirmatory) | Pseudomonas aeruginosa | 93 | single protein format | PubChem BioAssays | ||
4. | ALA1614210 | B | PubChem BioAssay. Epi-absorbance-based dose response biochemical high throughput screening assay for selective inhibitors of VIM-2 metallo-beta-lactamase. (Class of assay: confirmatory) | Pseudomonas aeruginosa | 123 | single protein format | PubChem BioAssays | ||
5. | ALA1737906 | U | PubChem BioAssay. Late stage results from the probe development efforts to identify selective inhibitors of VIM-2 metallo-beta-lactamase: probe results. (Class of assay: other) Panel member name: VIM-2 Ki Assay | 1 | assay format | PubChem BioAssays | |||
6. | ALA1737908 | U | PubChem BioAssay. Late stage results from the probe development efforts to identify selective inhibitors of VIM-2 metallo-beta-lactamase: probe results. (Class of assay: other) Panel member name: Nitrocefin-based IMP1 Inhibition Counterscreen | 1 | assay format | PubChem BioAssays | |||
7. | ALA1737909 | U | PubChem BioAssay. Late stage results from the probe development efforts to identify selective inhibitors of VIM-2 metallo-beta-lactamase: probe results. (Class of assay: other) Panel member name: Nitrocefin-based VIM2 Inhibition Assay | 1 | assay format | PubChem BioAssays | |||
8. | ALA1737945 | F | PubChem BioAssay. Late stage assay provider results from the probe development efforts to identify selective inhibitors of VIM-2 metallo-beta-lactamase: VIM-2-transformed E. coli growth inhibition in the presence of imipenem (synergy). (Class of assay: confirmatory) | Pseudomonas aeruginosa | 1 | assay format | PubChem BioAssays | ||
9. | ALA1738439 | U | PubChem BioAssay. Late stage results from the probe development efforts to identify selective inhibitors of VIM-2 metallo-beta-lactamase: Prior art results. (Class of assay: screening) Panel member name: Nitrocefin-based VIM2 Inhibition Assay | 1 | assay format | PubChem BioAssays | |||
10. | ALA1738440 | U | PubChem BioAssay. Late stage results from the probe development efforts to identify selective inhibitors of VIM-2 metallo-beta-lactamase: Prior art results. (Class of assay: screening) Panel member name: Nitrocefin-based IMP1 Inhibition Counterscreen | 1 | assay format | PubChem BioAssays | |||
11. | ALA1738441 | U | PubChem BioAssay. Late stage results from the probe development efforts to identify selective inhibitors of VIM-2 metallo-beta-lactamase: Prior art results. (Class of assay: screening) Panel member name: VIM-2 Ki Assay | 1 | assay format | PubChem BioAssays | |||
12. | ALA2114720 | F | PubChem BioAssay. Late stage counterscreen results from the probe development effort to identify common IMP-1 and VIM-2 inhibitors: Epi-absorbance-based biochemical dose response assay for inhibitors of TEM-1 metallo-beta-lactamase. (Class of assay: confirmatory) | Pseudomonas aeruginosa | 6 | assay format | PubChem BioAssays | ||
13. | ALA2114772 | F | PubChem BioAssay. Counterscreen for inhibitors of the interaction of nucleotide-binding oligomerization domain containing 2 (NOD2) and receptor-interacting serine-threonine kinase 2 (RIPK2): Fluorescence-based cell-based high throughput dose response assay to identify non-selective inhibitors of the beta-lactamase enzyme (BLA). (Class of assay: confirmatory) | Pseudomonas aeruginosa | 232 | cell-based format | PubChem BioAssays |