Milciclib 2μM R08 exp502
Mechanism of Action
Inhibits CDK2, also TRKA, CDK1, CDK4
- Class / Subclass 1: Cell Cycle / Cyclin Dependent Kinase Inhibitor
- Class / Subclass 2: Signal Transduction / Kinase Inhibitor
Technical Notes
Compound References
- PubChem Name: Milciclib
- Synonyms: PHA-848125
- CAS #: 802539-81-7
- PubChem CID: 16718576
- IUPAC: N,1,4,4-tetramethyl-8-[4-(4-methylpiperazin-1-yl)anilino]-5H-pyrazolo[4,3-h]quinazoline-3-carboxamide
- INCHI Name: InChI=1S/C25H32N8O/c1-25(2)14-16-15-27-24(29-20(16)22-19(25)21(23(34)26-3)30-32(22)5)28-17-6-8-18(9-7-17)33-12-10-31(4)11-13-33/h6-9,15H,10-14H2,1-5H3,(H,26,34)(H,27,28,29)
- INCHI Key: RXZMYLDMFYNEIM-UHFFFAOYSA-N
- Molecular Weight: 460.6
- Canonical SMILES: CC1(CC2=CN=C(N=C2C3=C1C(=NN3C)C(=O)NC)NC4=CC=C(C=C4)N5CCN(CC5)C)C
- Isomeric SMILES: N/A
- Molecular Formula: C25H32N8O
Compound Supplier
- Supplier Name: Med Chem Express
- Catalog #: HY-10424
- Lot #: 05417
Compound Characterization
- HRMS (ESI-TOF) m/z: (M+H)+ Calcd for C25H32N8O 461.27718; found 461.2785
Dose Response Curve
- Platform ID: Milciclib
- Min: -12.0561; Max: 94.9848
| IC | Concentration (µM) |
|---|---|
| IC10 | 0.3312 |
| IC20 | 0.6400 |
| IC30 | 0.9915 |
| IC40 | 1.4200 |
| IC50 | 1.9730 |
| IC60 | 2.7430 |
| IC70 | 3.9270 |
| IC80 | 6.0840 |
| IC90 | 11.7500 |
Screen Summary
- Round: 08
- Dose: 2µM
- Days of incubation: 8
- Doublings: 0.3
- Numbers of reads: 16227722
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 |
|---|---|---|---|---|---|---|
| 23/45 | Scores |