4-Nitroquinoline-1-oxide 0.5μM R08 exp446
Mechanism of Action
UV mimetic, metabolized to electrohpile that forms stable quinolone monoadducts
- Class / Subclass 1: DNA Damage, Repair and Replication / Helix-Distorting Adduct
Technical Notes
Compound References
- PubChem Name: 4-Nitroquinoline N-oxide
- Synonyms: N/A
- CAS #: 56-57-5
- PubChem CID: 5955
- IUPAC: 4-nitro-1-oxidoquinolin-1-ium
- INCHI Name: InChI=1S/C9H6N2O3/c12-10-6-5-9(11(13)14)7-3-1-2-4-8(7)10/h1-6H
- INCHI Key: YHQDZJICGQWFHK-UHFFFAOYSA-N
- Molecular Weight: 190.16
- Canonical SMILES: C1=CC=C2C(=C1)C(=CC=[N+]2[O-])[N+](=O)[O-]
- Isomeric SMILES: N/A
- Molecular Formula: C9H6N2O3
Compound Supplier
- Supplier Name: Enamine
- Catalog #: N300-100463
- Lot #: R284185
Compound Characterization
- HRMS (ESI-TOF) m/z: (M+H)+ Calcd for C9H6N2O3 191.04512; found 191.04473
Dose Response Curve
- Platform ID: 4NQO
- Min: -1.1393; Max: 99.8617
| IC | Concentration (µM) |
|---|---|
| IC10 | 0.2569 |
| IC20 | 0.3742 |
| IC30 | 0.4805 |
| IC40 | 0.5898 |
| IC50 | 0.7118 |
| IC60 | 0.8591 |
| IC70 | 1.0550 |
| IC80 | 1.3540 |
| IC90 | 1.9730 |
Screen Summary
- Round: 08
- Dose: 500nM
- Days of incubation: 8
- Doublings: 3.8
- Numbers of reads: 19213659
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 |
|---|---|---|---|---|---|---|
| 6/3 | Scores |