FP-4
FP-4 is a PROTAC degrader targeting TLR4, with a DC50 of 2.5 μM. FP-4 mediates CRBN-dependent TLR4 ubiquitination and proteasomal degradation through the TLR4/MD-2 interface, and inhibits TLR4/MyD88-NF-κB inflammatory signaling and the downstream expression of TNF-α, ICAM-1, and VCAM-1. FP-4 reduces intracellular reactive oxygen species (ROS) and promotes endothelial cell migration. FP-4 ameliorates endothelial injury in LPS-treated zebrafish larvae and restores the number of intersegmental vessels. FP-4 can be used for research on vascular endothelial injury and LPS-induced vascular endothelial injury.
(Pink: TLR4 ligand (HY-N0060); Blue: Cereblon ligand (HY-41547); Black: linker (HY-140208)).
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- No. CAS: 3071170-20-9
- Fòrmula: C27H28N4O8
- Peso molecular:536.53
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Almacenamiento:
Please store the product under the recommended conditions in the Certificate of Analysis.
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Actividad biológica
Descripciòn
IC50 & Target
[1]|
TLR4 2.5 μM (DC50) |
MD-2 |
NF-κB |
MyD88 |
TNF-α |
ICAM-1 |
VCAM-1 |
In Vitro
FP-4 (10 μM; 24 h) suppresses TLR4/MyD88-NF-κB pathway proteins and adhesion molecules in LPS-stimulated HUVECs[1].
FP-4 (0.1-40 μM; 24 h) degrades TLR4 in LPS-stimulated HUVECs with DC50 = 2.5 μM and Dmax = 50.4%[1].
FP-4 (10 μM; 2-48 h) degrades TLR4 in LPS-stimulated HUVECs beginning at 6 h and peaking at 48 h[1].
FP-4 (10 μM)-induced TLR4 degradation in HUVECs is CRBN-dependent[1].
FP-4 (0-50 μM) protects TLR4 from Pronase E digestion in HUVEC lysates in a concentration-dependent manner[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:HUVECs
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Concentration:10 μM
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Incubation Time:24 h
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Result:Had the strongest TLR4-degrading activity in this screening and significantly reduced TLR4 levels compared with the model group.\nSignificantly reduced TLR4, MyD88, p-p65/p65, TNF-α, ICAM-1, and VCAM-1 levels compared with the model group.
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Cell Line:HUVECs
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Concentration:10 μM
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Incubation Time:24 h
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Result:Reduced IL-6, IL-1β, and TNF-α mRNA expression compared with the model group.
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Tg(fli:EGFP) (transgenic larvae)[1]
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Dosage:0.5 μM (FP-4-L); 1 μM (FP-4-M); 2 μM (FP-4-H)
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Administration:immersion; once at 12 h after initial LPS exposure; 24 h
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Result:At 0.5 μM, endothelial fluorescence showed little difference from the model group.
At 1 μM and 2 μM, endothelial-cell fluorescence intensity increased relative to the model group.
ISV number was restored in a dose-dependent manner, with the 2 μM group showing efficacy comparable to the Dexamethasone (HY-14648) positive control.
In zebrafish, TLR4, MyD88, TNF-α, p-p65/p65, ICAM-1, and VCAM-1 protein levels were reduced relative to the model group.
- RNA extraction experimental
- Scratch/Wound-Healing Migration Assay
- ROS/oxidative-stress fluorescent staining
- Cell migration
- Neural Crest/Neuronal Cell Migration Explant Assay
- Research Protocol for Inflammation-related Diseases
- Zigmond Chamber Chemotaxis Assay
- Under-Agarose Cell Migration Assay
- Transwell/Boyden Chamber Migration Assay
- 3D Collagen/Hydrogel Matrix Migration Assay
- Cell-Exclusion Zone Migration Assay
- Dunn/Insall Chamber Chemotaxis Assay
- Endothelial Cell Migration/Angiogenic Sprouting Assay
Chemical Information
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No. CAS 3071170-20-9
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Peso molecular 536.53
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Fòrmula C27H28N4O8
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SMILES
O=C(NCCOCCNC1=CC=CC(C(N2C(CC3)C(NC3=O)=O)=O)=C1C2=O)/C=C/C4=CC=C(O)C(OC)=C4
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Envío
Room temperature in continental US; may vary elsewhere.
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Almacenamiento
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureza y Documentación
Referencias
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Keywords
- FP-4
- 3071170-20-9
- FP4
- FP 4
- PROTACs
- Toll-like Receptor (TLR)
- MyD88
- NF-κB
- TNF Receptor
- Reactive Oxygen Species (ROS)
- PROTAC
- Nuclear factor-κB
- Nuclear factor-kappaB
- Tumor Necrosis Factor Receptor
- TNFR
- CRBN
- ICAM-1
- MyD88-NF-κB signaling
- TLR4
- TLR4/MD-2 interface
- TNF-α
- VCAM-1
- endothelial cell migration
- proteasomal degradation
- ubiquitination
- Inhibitor
- inhibitor
- inhibit