Assay Detail
Binding
CHEMBL3707946
Review assay metadata, readout intent, target linkage, and publication context from the same page.
In Vitro Assay: Chinese hamster ovary (CHO) cells expressing the human orexin-1 receptor and the human orexin-2 receptor, respectively, are grown in culture medium (Ham F-12 with L-Glutamine) containing 300 ug/ml G418, 100 U/ml penicillin, 100 ug/ml streptomycin and 10% heat inactivated fetal calf serum (FCS). The cells are seeded at 20'000 cells/well into 384-well black clear bottom sterile plates (Greiner). The seeded plates are incubated overnight at 37 C. in 5% CO2.Human orexin-A as an agonist is prepared as 1 mM stock solution in MeOH: water (1:1), diluted in HBSS containing 0.1% bovine serum albumin (BSA), NaHCO3: 0.375 g/l and 20 mM HEPES for use in the assay at a final concentration of 3 nM.Antagonists are prepared as 10 mM stock solution in DMSO, then diluted in 384-well plates using DMSO followed by a transfer of the dilutions into in HBSS containing 0.1% bovine serum albumin (BSA), NaHCO3: 0.375 g/l and 20 mM HEPES. On the day of the assay, 50 ul of staining buffer.
59
Total Activities
59
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Binding |
| Organism | Homo sapiens |
| Confidence | 9 — Direct single protein target |
| Curated By | Autocuration |
Publication
Proline sulfonamide derivatives as orexin receptor antagonists
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 59 | 7.51 | 8.70 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL3667555 | — | — | 1 | 8.70 |
| CHEMBL3667559 | — | — | 1 | 8.70 |
| CHEMBL3667562 | — | — | 1 | 8.70 |
| CHEMBL3667554 | — | — | 1 | 8.52 |
| CHEMBL3667558 | — | — | 1 | 8.52 |
| CHEMBL3667560 | — | — | 1 | 8.52 |
| CHEMBL3667595 | — | — | 1 | 8.40 |
| CHEMBL3597952 | ACT-462206 | 1.0 | 1 | 8.30 |
| CHEMBL3667581 | — | — | 1 | 8.10 |
| CHEMBL3667551 | — | — | 1 | 8.10 |
| CHEMBL3667565 | — | — | 1 | 8.05 |
| CHEMBL3667557 | — | — | 1 | 8.05 |
| CHEMBL3667561 | — | — | 1 | 8.00 |
| CHEMBL3667549 | — | — | 1 | 8.00 |
| CHEMBL3667580 | — | — | 1 | 7.92 |
| CHEMBL3667598 | — | — | 1 | 7.85 |
| CHEMBL3667574 | — | — | 1 | 7.80 |
| CHEMBL3667556 | — | — | 1 | 7.77 |
| CHEMBL3667568 | — | — | 1 | 7.77 |
| CHEMBL3667586 | — | — | 1 | 7.75 |
| CHEMBL3667600 | — | — | 1 | 7.72 |
| CHEMBL3667570 | — | — | 1 | 7.72 |
| CHEMBL3667564 | — | — | 1 | 7.70 |
| CHEMBL3667604 | — | — | 1 | 7.66 |
| CHEMBL3667590 | — | — | 1 | 7.60 |
| CHEMBL3667589 | — | — | 1 | 7.58 |
| CHEMBL3667585 | — | — | 1 | 7.58 |
| CHEMBL3667553 | — | — | 1 | 7.57 |
| CHEMBL3667584 | — | — | 1 | 7.55 |
| CHEMBL3667571 | — | — | 1 | 7.54 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL3667555 | — | IC50 | = | 2.0 | nM | 8.70 |
| CHEMBL3667562 | — | IC50 | = | 2.0 | nM | 8.70 |
| CHEMBL3667559 | — | IC50 | = | 2.0 | nM | 8.70 |
| CHEMBL3667554 | — | IC50 | = | 3.0 | nM | 8.52 |
| CHEMBL3667558 | — | IC50 | = | 3.0 | nM | 8.52 |
| CHEMBL3667560 | — | IC50 | = | 3.0 | nM | 8.52 |
| CHEMBL3667595 | — | IC50 | = | 4.0 | nM | 8.40 |
| CHEMBL3597952 | ACT-462206 | IC50 | = | 5.0 | nM | 8.30 |
| CHEMBL3667581 | — | IC50 | = | 8.0 | nM | 8.10 |
| CHEMBL3667551 | — | IC50 | = | 8.0 | nM | 8.10 |
| CHEMBL3667565 | — | IC50 | = | 9.0 | nM | 8.05 |
| CHEMBL3667557 | — | IC50 | = | 9.0 | nM | 8.05 |
| CHEMBL3667561 | — | IC50 | = | 10.0 | nM | 8.00 |
| CHEMBL3667549 | — | IC50 | = | 10.0 | nM | 8.00 |
| CHEMBL3667580 | — | IC50 | = | 12.0 | nM | 7.92 |
| CHEMBL3667598 | — | IC50 | = | 14.0 | nM | 7.85 |
| CHEMBL3667574 | — | IC50 | = | 16.0 | nM | 7.80 |
| CHEMBL3667556 | — | IC50 | = | 17.0 | nM | 7.77 |
| CHEMBL3667568 | — | IC50 | = | 17.0 | nM | 7.77 |
| CHEMBL3667586 | — | IC50 | = | 18.0 | nM | 7.75 |
| CHEMBL3667600 | — | IC50 | = | 19.0 | nM | 7.72 |
| CHEMBL3667570 | — | IC50 | = | 19.0 | nM | 7.72 |
| CHEMBL3667564 | — | IC50 | = | 20.0 | nM | 7.70 |
| CHEMBL3667604 | — | IC50 | = | 22.0 | nM | 7.66 |
| CHEMBL3667590 | — | IC50 | = | 25.0 | nM | 7.60 |
| CHEMBL3667589 | — | IC50 | = | 26.0 | nM | 7.58 |
| CHEMBL3667585 | — | IC50 | = | 26.0 | nM | 7.58 |
| CHEMBL3667553 | — | IC50 | = | 27.0 | nM | 7.57 |
| CHEMBL3667584 | — | IC50 | = | 28.0 | nM | 7.55 |
| CHEMBL3667571 | — | IC50 | = | 29.0 | nM | 7.54 |
| CHEMBL3667566 | — | IC50 | = | 31.0 | nM | 7.51 |
| CHEMBL3667593 | — | IC50 | = | 32.0 | nM | 7.50 |
| CHEMBL3667578 | — | IC50 | = | 34.0 | nM | 7.47 |
| CHEMBL3667597 | — | IC50 | = | 36.0 | nM | 7.44 |
| CHEMBL3667567 | — | IC50 | = | 37.0 | nM | 7.43 |
| CHEMBL3667579 | — | IC50 | = | 38.0 | nM | 7.42 |
| CHEMBL3667569 | — | IC50 | = | 47.0 | nM | 7.33 |
| CHEMBL3667552 | — | IC50 | = | 47.0 | nM | 7.33 |
| CHEMBL3667588 | — | IC50 | = | 49.0 | nM | 7.31 |
| CHEMBL3667587 | — | IC50 | = | 58.0 | nM | 7.24 |
| CHEMBL3667577 | — | IC50 | = | 68.0 | nM | 7.17 |
| CHEMBL3667599 | — | IC50 | = | 82.0 | nM | 7.09 |
| CHEMBL3667594 | — | IC50 | = | 92.0 | nM | 7.04 |
| CHEMBL3667573 | — | IC50 | = | 98.0 | nM | 7.01 |
| CHEMBL3667591 | — | IC50 | = | 101.0 | nM | 7.00 |
| CHEMBL3667550 | — | IC50 | = | 104.0 | nM | 6.98 |
| CHEMBL3667605 | — | IC50 | = | 106.0 | nM | 6.97 |
| CHEMBL3667603 | — | IC50 | = | 108.0 | nM | 6.97 |
| CHEMBL3667576 | — | IC50 | = | 128.0 | nM | 6.89 |
| CHEMBL3667583 | — | IC50 | = | 136.0 | nM | 6.87 |