JH-RE-06 T15611
Specifications
| 1mg/5mg/10mg/25mg/50mg/100mg |
Bioactivity:
JH-RE-06 disrupts mutagenic translesion synthesis (TLS) by preventing the recruitment of mutagenic POL_. JH-RE-06 is an effective REV1-REV7 interface inhibitor (IC50=0.78 _M; Kd=0.42 _M), which targets REV1 that interacts with the REV7 subunit of POL_. JH
CAS nr:
1361227-90-8
Purity:
98%
Molecular Weight:
468,72
SMILES:
O=C1C(C(CC(C)C)=O)=C(NC2=CC=C(Cl)C=C2Cl)NC3=C1C([N+]([O-])=O)=CC=C3Cl
Formula:
C20H16Cl3N3O4
Pathway:
DNA Damage/DNA Repair,Cell Cycle/Checkpoint
Target:
DNA/RNA Synthesis,DNA/RNA Synthesis
