L-74142 5μM R03 exp131
Mechanism of Action
DRD4 receptor antagonist
- Class / Subclass 1: Signal Transduction / GPCR antagonist
Technical Notes
Compound References
- PubChem Name: 5-(4-Chlorophenyl)-4-methyl-3-(1-(2-phenylethyl)piperidin-4-YL)isoxazole hydrochloride
- Synonyms: N/A
- CAS #: 874882-93-6
- PubChem CID: 24744861
- IUPAC: 5-(4-chlorophenyl)-4-methyl-3-[1-(2-phenylethyl)piperidin-4-yl]-1,2-oxazole;hydrochloride
- INCHI Name: InChI=1S/C23H25ClN2O.ClH/c1-17-22(25-27-23(17)20-7-9-21(24)10-8-20)19-12-15-26(16-13-19)14-11-18-5-3-2-4-6-18;/h2-10,19H,11-16H2,1H3;1H
- INCHI Key: HZRPUQURUAXOHB-UHFFFAOYSA-N
- Molecular Weight: 417.4
- Canonical SMILES: CC1=C(ON=C1C2CCN(CC2)CCC3=CC=CC=C3)C4=CC=C(C=C4)Cl.Cl
- Isomeric SMILES: N/A
- Molecular Formula: C23H26Cl2N2O
Compound Supplier
- Supplier Name: Tocris Bioscience
- Catalog #: 1004
- Lot #: 2A/171873
Compound Characterization
- HRMS (ESI-TOF) m/z: (M+H)+ Calcd for C23H25ClN2O 381.17282; found 381.17493
Dose Response Curve
- Platform ID: L741742
- Min: -5.7324; Max: 58.2869
| IC | Concentration (µM) |
|---|---|
| IC10 | N/A |
| IC20 | 4.3609 |
| IC30 | 5.6579 |
| IC40 | 7.0041 |
| IC50 | 8.5196 |
| IC60 | N/A |
| IC70 | N/A |
| IC80 | N/A |
| IC90 | N/A |
Screen Summary
- Round: 03
- Dose: 5µM
- Days of incubation: 8
- Doublings: 7.1
- Numbers of reads: 12019422
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 |
|---|---|---|---|---|---|---|
| 6/0 | Scores |