LHF418
LHF418 is a SOS1 PROTAC degrader that induces the degradation of the target protein SOS1 by recruiting cereblon. LHF418 promotes the formation of the SOS1-PROTAC-CRBN ternary complex and induces SOS1 degradation in a cereblon- and proteasome-dependent manner. LHF418 inhibits EGF-induced ERK1/2 phosphorylation and the clonogenic growth of KRAS-mutant cancer cells. LHF418 can be used in studies related to SOS1-targeted protein degradation and KRAS-driven tumors.
(Pink: SOS1 ligand (HY-161452); Blue: Cereblon ligand (HY-A0003); Black: linker (HY-B0704)).
For research use only. We do not sell to patients.
- Formula: C46H52F3N7O7
- Molecular Weight:871.94
-
Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
All PROTACs Isoforms
More
Biological Activity
Description
IC50 & Target
[1]|
SOS1 209.4 nM (DC50) |
Cellular Effect
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| A549 | DC50 |
209.4 nM
|
SOS1 degradation in A549 human lung cancer cells assessed by immunoblotting assay after 24 h incubation.
SOS1 degradation in A549 human lung cancer cells assessed by immunoblotting assay after 24 h incubation.
|
38489998 |
| HPAF-II | DC50 |
353.9 nM
|
SOS1 degradation in HPAF-II human pancreatic cancer cells assessed by immunoblotting assay after 24 h incubation.
SOS1 degradation in HPAF-II human pancreatic cancer cells assessed by immunoblotting assay after 24 h incubation.
|
38489998 |
| MIA PaCa-2 | DC50 |
539.7 nM
|
SOS1 degradation in MIA-PACA2 human pancreatic cancer cells assessed by immunoblotting assay after 24 h incubation.
SOS1 degradation in MIA-PACA2 human pancreatic cancer cells assessed by immunoblotting assay after 24 h incubation.
|
38489998 |
In Vitro
LHF418 (10 nM-10 μM; 24 h) degrades SOS1 in a dose-dependent manner in A549 cells, with a DC50 of 209.4 nM and a Dmax of > 80%; at high concentrations of 20 μM and 30 μM, a hook effect occurs, and SOS1 degradation is incomplete[1].
LHF418 (3 μM; 0-72 h) reduces SOS1 protein levels in A549 cells in a time-dependent manner, with a T1/2 of 22.51 h fitted to the time curve; SOS1 levels decrease significantly at 24 h and continue to decline for at least 72 h[1].
LHF418 (10 nM-10 μM; 24 h) induces SOS1 degradation in KRASG12D-bearing HPAF-II cells, with a DC50 of 353.9 nM[1].
LHF418 (10 nM-10 μM; 24 h) induces SOS1 degradation in MIA-PACA2 cells carrying KRASG12C, with a DC50 of 539.7 nM[1].
LHF418 produces the highest maximum luminescence signal among the compared PROTACs in the AlphaScreen assay containing GST-SOS1 (100 nM) and His-CRBN (10 nM), which supports the formation of a strong SOS1-PROTAC-CRBN ternary complex[1].
SOS1 degradation induced by LHF418 (1 μM; 24 h) in A549 cells is blocked by the SOS1 warhead BI3406 (HY-125817) (10 μM; 1 h pre-exposure) or the CRBN ligand Lenalidomide (HY-A0003) (10 μM; 1 h pre-exposure)[1].
In A549 cells, the SOS1 degradation induced by LHF418 (1 μM; 24 h) is completely blocked by MG132 (HY-13259) (1 μM; 1 h pre-exposure) or MLN4924 (HY-70062) (0.5 μM; 1 h pre-exposure), whereas Bafilomycin (1 μM; 1 h pre-exposure) fails to restore SOS1 levels. These findings support that SOS1 degradation depends on the CRBN/ubiquitin-proteasome system rather than the lysosomal autophagy pathway[1].
LHF418 (10 nM-10 μM; 24 h) reduces SOS1 protein levels in A549 cells, but does not decrease SOS2 or GSPT1 protein levels even at the highest concentration of 10 μM[1].
LHF418 (10 nM-10 μM; 24 h; EGF 5 ng/mL, 1 h) inhibits EGF-induced ERK1/2 phosphorylation concomitant with a reduction in SOS1 levels in serum-starved A549 cells[1].
LHF418 (300 nM-30 μM; 14 days) inhibits the colony formation of MIA-PACA2 cells, and colony formation further decreases with increasing concentration[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Cell Line:A549
-
Concentration:10 nM-10 μM
-
Incubation Time:24 h
-
Result:Dose-dependently degraded SOS1.
Produced a DC50 of 209.4 nM.
Reached a Dmax of >80%.
Showed incomplete SOS1 degradation at 20 and 30 μM, consistent with a hook effect.
-
Cell Line:A549
-
Concentration:3 μM
-
Incubation Time:0-72 h
-
Result:Time-dependently reduced SOS1 protein levels.
Produced a fitted time-course T1/2 of 22.51 h.
Clearly reduced SOS1 at 24 h.
Maintained reduced SOS1 levels through 72 h.
-
Cell Line:HPAF-II (KRASG12D); MIA-PACA2 (KRASG12C)
-
Concentration:10 nM-10 μM
-
Incubation Time:24 h
-
Result:Degraded SOS1 with a DC50 of 353.9 nM.
Degraded SOS1 with a DC50 of 539.7 nM.
-
Cell Line:A549 cells
-
Concentration:LHF418: 1 μM; BI3406: 10 μM; Lenalidomide: 10 μM
-
Incubation Time:Competitor pre-exposure: 1 h; LHF418: 24 h
-
Result:SOS1 degradation was blocked by the SOS1 warhead BI3406.
SOS1 degradation was blocked by the CRBN ligand Lenalidomide.
-
Cell Line:A549 cells
-
Concentration:LHF418: 1 μM; MG132: 1 μM; MLN4924: 0.5 μM; Bafilomycin: 1 μM
-
Incubation Time:Modulator pre-exposure: 1 h; LHF418: 24 h
-
Result:SOS1 degradation was completely blocked by MG132.
SOS1 degradation was completely blocked by MLN4924.
SOS1 degradation was not rescued by Bafilomycin.
-
Cell Line:A549 cells
-
Concentration:10 nM-10 μM
-
Incubation Time:24 h
-
Result:Reduced SOS1 protein levels.
Did not reduce SOS2 protein levels at concentrations up to 10 μM.
Did not reduce GSPT1 protein levels at concentrations up to 10 μM.
-
Cell Line:A549 cells
-
Concentration:10 nM-10 μM
-
Incubation Time:24 h; EGF 5 ng/mL for 1 h
-
Result:Reduced SOS1 protein levels.
Suppressed EGF-induced ERK1/2 phosphorylation.
-
Cell Line:MIA-PACA2
-
Concentration:300 nM, 1 μM, 3 μM, 10 μM, 30 μM
-
Incubation Time:14 days
-
Result:Suppressed colony formation.
Produced progressively fewer colonies with increasing concentration.
Chemical Information
-
Molecular Weight 871.94
-
Formula C46H52F3N7O7
-
SMILES
NC1=CC([C@@H](C)CC2=NC(C)=NC3=C2C=C(O[C@@H]4CN(C(CCCCCCCC(NC5=C6C(C(N(C7CCC(NC7=O)=O)C6)=O)=CC=C5)=O)=O)CC4)C(OC)=C3)=CC(C(F)(F)F)=C1
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)