GSK626616 14μM R08 exp485
Mechanism of Action
Inhibits DYRK3, prevents stress granule dissolution, mTORC1 release
- Class / Subclass 1: Signal Transduction / Kinase Inhibitor
Technical Notes
Compound References
- PubChem Name: 4(5H)-Thiazolone, 2-((2,6-dichlorophenyl)amino)-5-(6-quinoxalinylmethylene)-, (5Z)-
- Synonyms: N/A
- CAS #: 1025821-33-3
- PubChem CID: 135416229
- IUPAC: (5Z)-2-(2,6-dichlorophenyl)imino-5-(quinoxalin-6-ylmethylidene)-1,3-thiazolidin-4-one
- INCHI Name: InChI=1S/C18H10Cl2N4OS/c19-11-2-1-3-12(20)16(11)23-18-24-17(25)15(26-18)9-10-4-5-13-14(8-10)22-7-6-21-13/h1-9H,(H,23,24,25)/b15-9-
- INCHI Key: RJPNRXFBYZVRIB-DHDCSXOGSA-N
- Molecular Weight: 401.3
- Canonical SMILES: C1=CC(=C(C(=C1)Cl)N=C2NC(=O)C(=CC3=CC4=NC=CN=C4C=C3)S2)Cl
- Isomeric SMILES: C1=CC(=C(C(=C1)Cl)N=C2NC(=O)/C(=C/C3=CC4=NC=CN=C4C=C3)/S2)Cl
- Molecular Formula: C18H10Cl2N4OS
Compound Supplier
- Supplier Name: Tocris Bioscience
- Catalog #: 6638
- Lot #: 1A/216989
Compound Characterization
- HRMS (ESI-TOF) m/z: (M+H)+ Calcd for C18H10Cl2N4OS 401.00251; found 401.00255
Dose Response Curve
- Platform ID: GSK626616
- Min: -3.2829; Max: 99.0208
| IC | Concentration (µM) |
|---|---|
| IC10 | 8.4010 |
| IC20 | 11.1700 |
| IC30 | 13.4900 |
| IC40 | 15.7500 |
| IC50 | 18.1600 |
| IC60 | 20.9400 |
| IC70 | 24.4500 |
| IC80 | 29.5400 |
| IC90 | 39.2700 |
Screen Summary
- Round: 08
- Dose: 14µM
- Days of incubation: 8
- Doublings: 1.9
- Numbers of reads: 16240671
Screen Results
| Sensitive/Resistant hits (FDR<0.05) | CRANKS | Score Plot | Top 30 Genes | Screen Similarity | Top 30 Sensitive GO terms | Top 30 Resistant GO terms |
|---|---|---|---|---|---|---|
| 22/93 | Scores |