1. Anti-infection Cell Cycle/DNA Damage PI3K/Akt/mTOR Epigenetics Cytoskeleton
  2. Parasite DNA/RNA Synthesis AMPK Clathrin
  3. NEU-4438

NEU-4438 is an antimalarial agent. NEU-4438 inhibits DNA synthesis, reduces AMPK-γ, and increases Clathrin heavy chain. NEU-4438 exhibits antiparasitic activity against Trypanosoma brucei. NEU-4438 reduces trypanosome tissue burden in a chronic HAT mouse model.

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NEU-4438

NEU-4438 Chemical Structure

CAS No. : 2306305-57-5

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Description

NEU-4438 is an antimalarial agent. NEU-4438 inhibits DNA synthesis, reduces AMPK-γ, and increases Clathrin heavy chain. NEU-4438 exhibits antiparasitic activity against Trypanosoma brucei. NEU-4438 reduces trypanosome tissue burden in a chronic HAT mouse model[1].

IC50 & Target[1]

Trypanosoma

 

In Vitro

NEU-4438 (serial dilutions; 6 h, then 48 h in drug-free medium) induces delayed trypanocidality in bloodstream Trypanosoma brucei brucei Lister427 cells, with a DC50 of 334 nM after 6 h treatment followed by 48 h in drug-free medium[1].
NEU-4438 (150-1013 nM; 6 h) dose-dependently reduces AMPK-γ protein levels and increases clathrin heavy chain levels in bloodstream Trypanosoma brucei cells expressing Myc-tagged versions of these proteins, with maximal effects at 1013 nM (DC90) after 6 h treatment[1].
NEU-4438 (150 nM; 6 h, then 1 h EdU labeling) inhibits nuclear DNA synthesis in bloodstream Trypanosoma brucei brucei Lister427 cells, as shown by a reduction in EdU-positive cells and decreased nuclear EdU signal intensity[1].

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

Western Blot Analysis[1]

Cell Line: bloodstream Trypanosoma brucei cells expressing Myc-tagged AMPK-γ and clathrin heavy chain
Concentration: 159 nM (DCC25); 1474 nM (DCC90)
Incubation Time: 6 h
Result: Reduced AMPK-γ protein levels 0.54-fold at DCC25 and 0.86-fold at DCC90 compared to vehicle-treated cells.
Increased clathrin heavy chain levels 0.19-fold at DCC25 and 0.36-fold at DCC90 nM compared to vehicle-treated cells.

Immunofluorescence[1]

Cell Line: bloodstream Trypanosoma brucei brucei Lister427 cells
Concentration: 150 nM
Incubation Time: 6 h
Result: Increased the fraction of trypanosomes with one basal body (1BB) and decreased the proportion of cells with two basal bodies (2BB), with a statistically significant difference in population distribution compared to vehicle-treated cells (p = 2.8×10-2, Pearson’s Chi-square test).
In Vivo

NEU-4438 (120-150 mg/kg; daily; days 1-7 post-infection) achieves greater than 100-fold reduction in median trypanosome tissue load in a mouse model of chronic HAT by day 7 post-infection, though the dosing regimen does not produce a cure by day 14[1].

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

Animal Model: Swiss-Webster (Hsd:ND4) (female, 8-10 weeks old, 20-25 g, infected with 5×104 bioluminescent T. brucei AnTat1.1 AmLuc via inoculation)[1]
Dosage: 150 mg/kg (days 1-4 post-infection); 120 mg/kg (days 5-7 post-infection)
Administration: daily; days 1-7 post-infection
Result: Produced a 3.92-fold reduction in trypanosome tissue bioluminescence signal on day 3 post-infection (p = 6.8×10-3).
Reduced median total trypanosome tissue flux greater than 100-fold, with undetectable tissue infection in 3 out of 4 treated mice on day 7 post-infection.
Left detectable parasites in tissues of 2 out of 4 treated mice on day 14 post-infection.
Molecular Weight

426.52

Formula

C24H26N8

CAS No.
SMILES

CN1CCN(C2=NC=C(C3=CC(N(C)C=C/4)=C(C=C3)C4=N\C5=NC=CN=C5)C=N2)CCC1

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Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
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    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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NEU-4438
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HY-125188
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