1. Apoptosis NF-κB MAPK/ERK Pathway Immunology/Inflammation
  2. RIP kinase NF-κB p38 MAPK TNF Receptor Interleukin Related
  3. RIPK1-IN-32

RIPK1-IN-32 is a RIPK inhibitor with anti-inflammatory activity. RIPK1-IN-32 inhibits nitric oxide (NO) release with an IC50 of 3.26 μM. RIPK1-IN-32 significantly alleviates acute liver injury associated with sepsis through the RIPK1/NF-κB/MAPK pathway, therefore preventing the nuclear translocation of p65 and c-fos, which results in reduced expression of TNF-α and IL-6. RIPK1-IN-32 can be used for the study of acute liver injury and sepsis.

For research use only. We do not sell to patients.

RIPK1-IN-32

RIPK1-IN-32 Chemical Structure

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Description

RIPK1-IN-32 is a RIPK inhibitor with anti-inflammatory activity. RIPK1-IN-32 inhibits nitric oxide (NO) release with an IC50 of 3.26 μM. RIPK1-IN-32 significantly alleviates acute liver injury associated with sepsis through the RIPK1/NF-κB/MAPK pathway, therefore preventing the nuclear translocation of p65 and c-fos, which results in reduced expression of TNF-α and IL-6. RIPK1-IN-32 can be used for the study of acute liver injury and sepsis[1].

IC50 & Target[1]

NF-κB

 

IL-6

 

RIPK1

 

In Vitro

RIPK1-IN-32 (Compound 12) (0-25 μM, 45-63 ℃) significantly inhibits the thermal degradation of RIPK1 in RAW264.7 macrophages[1].
RIPK1-IN-32 (2.5 μM) significantly diminishes p65 and c-fos nuclear translocation in RAW264.7 macrophages[1].
RIPK1-IN-32 (0.625-2.5 μM, 8 h) notably reduces d the levels of IL-6 and TNF-α in RAW 264.7 cells[1].
RIPK1-IN-32 (0.625-2.5 μM, 8 h) effectively hinders the LPS (HY-D1056B3)-induced activation of the RIPK1/NF-κB/MAPK pathway[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

ELISA Assay[1]

Cell Line: LPS-stimulated RAW 264.7 macrophages
Concentration: 0.625, 1.25, 2.5 μM
Incubation Time: 8 h, including 1 μg/mL LPS for 6 hours
Result: Significantly diminished the contents of IL-6 and TNF-α.

Western Blot Analysis[1]

Cell Line: LPS-stimulated RAW 264.7 macrophages
Concentration: 0.625, 1.25, 2.5 μM
Incubation Time: 8 h, including 1 μg/mL LPS for 6 hours
Result: Resulted in notable decreases in the levels of RIPK1, p-p65, and p-IκB suggesting an inhibition of NF-κB signaling.
Found to lower the protein levels of p-p38, p-ERK, and p-JNK which aligns with the suppression of MAPK signaling.
In Vivo

RIPK1-IN-32 (Compound 12) (1.25-5 mg/kg, i.v., single dose) provides considerable protective benefits against LPS-induced injuries in the liver, lung and kidney of mice subjected to sepsis[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: LPS injection into the tail vein to create a sepsis model established in Male BALB/c mice (18-20 g)[1]
Dosage: 1.25, 2.5 and 5 mg/kg
Administration: Intravenous injection (i.v.), single dose
Result: Markedly alleviated LPS-induced ALI.
Decreased the serum levels of ALT and AST.
Significantly diminished the contents of IL-6 and TNF-α.
Attenuated the damage to lung tissue and markedly lessened the pathological alterations noted in the kidneys subsequent.
Decreased in liver concentrations of RIPK1, p-p65, P-IκB, p-p38, p-ERK, and p-JNK.
Molecular Weight

754.05

Formula

C42H59NO7S2

SMILES

[H][C@@]12CC[C@@]([C@]3(C)[C@@](C4=C(C(O[C@H]4C3)=O)CC/C=C(C)/C)([H])C[C@H]5O)(C)[C@@]5([C@]1(CC[C@H]([C@H]2C)OC(CCSSCCC(NOCC6=CC=CC=C6)=O)=O)C)[H]

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
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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RIPK1-IN-32
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HY-175007
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