SB202190 10μM R03 exp148
Mechanism of Action
Inhibits p38‘± (MAPK14)and p38‘_ (MAPK11) kinase, ATP competitive
- Class / Subclass 1: Signal Transduction / Kinase Inhibitor
Technical Notes
Compound References
- PubChem Name: 4-(4-Fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole
- Synonyms: N/A
- CAS #: 152121-30-7
- PubChem CID: 5169
- IUPAC: 4-[4-(4-fluorophenyl)-5-pyridin-4-yl-1H-imidazol-2-yl]phenol
- INCHI Name: InChI=1S/C20H14FN3O/c21-16-5-1-13(2-6-16)18-19(14-9-11-22-12-10-14)24-20(23-18)15-3-7-17(25)8-4-15/h1-12,25H,(H,23,24)
- INCHI Key: QHKYPYXTTXKZST-UHFFFAOYSA-N
- Molecular Weight: 331.3
- Canonical SMILES: C1=CC(=CC=C1C2=NC(=C(N2)C3=CC=NC=C3)C4=CC=C(C=C4)F)O
- Isomeric SMILES: N/A
- Molecular Formula: C20H14FN3O
Compound Supplier
- Supplier Name: Selleck Chemicals
- Catalog #: S1077
- Lot #: 01
Compound Characterization
- HRMS (ESI-TOF) m/z: (M+H)+ Calcd for C20H14FN3O 332.11937; found 332.11933
Dose Response Curve
- Platform ID: SB202190
- Min: 4.3648; Max: 53.7816
| IC | Concentration (µM) |
|---|---|
| IC10 | N/A |
| IC20 | 2.7330 |
| IC30 | 7.9975 |
| IC40 | 19.2844 |
| IC50 | 43.2506 |
| IC60 | N/A |
| IC70 | N/A |
| IC80 | N/A |
| IC90 | N/A |
Screen Summary
- Round: 03
- Dose: 10µM
- Days of incubation: 8
- Doublings: 6.9
- Numbers of reads: 10145836
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 |
|---|---|---|---|---|---|---|
| 2/0 | Scores |