Fig. 1 · Structure

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WZ8040

Cat. No. A10992 CAS 1214265-57-2

EGFR Inhibitor

WZ8040 is a novel EGFR inhibitors that suppress the growth of EGFR-T790M-containing cell lines and inhibit EGFR phosphorylation.

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Biological Activity

Target & Activity

Target Activity Value
EGFR (T790M)

Cellular Effect

Cell Line Activity Value Description Reference
BaF3 IC50 2 nM Antiproliferative activity against gefitinib sensitive mouse BA/F3 cells expressing EGFR exon 19 del E746_A750 activating mutant after 72 hrs by MTS assay [PMID: 26882288]
BaF3 IC50 32 nM Antiproliferative activity against mouse BA/F3 cells expressing wild type EGFR after 72 hrs by MTS assay [PMID: 26882288]
BaF3 IC50 9 nM Antiproliferative activity against gefitinib resistant mouse BA/F3 cells expressing EGFR L858R/T790M double mutant after 72 hrs by MTS assay [PMID: 26882288]
NCI-H1975 IC50 9 nM Antiproliferative activity against gefitinib resistant human NCI-H1975 cells expressing EGFR L858R/T790M double mutant after 72 hrs by MTS assay [PMID: 26882288]

In Vitro Studies

WZ8040 was evaluated in L. mexicana promastigotes cultivated in the presence of test compounds. The reported result was a dose–response curve for promastigote viability. [1]

Literature-reported observations and conditions; not Adooq-tested protocols or general treatment recommendations.

WZ8040 in L. mexicana promastigotes

Cell-based study · L. mexicana (strain MNYC/BZ/62/M379) promastigotes [1]

L. mexicana promastigotes were cultivated in the presence of WZ8040. A dose–response curve was reported for promastigote viability.

Measured endpoints — not treatment concentrations
EndpointReported resultReference
promastigote viabilityReported result Dose–response curve for WZ8040 in Leishmania promastigotes.[1]

Literature-Reported Treatment Conditions

Exposure duration
cells were cultivated in the presence of test compounds for 24 h and incubated with 10% AlamarBlue™ Cell Viability Reagent (ThermoFisher) for 24 h
Method
cells were cultivated in the presence of test compounds
Vehicle
1% DMSO
Reported limits
Not stated in the sentences used: dose.
Methods and source locations

Compound reported in the paper: WZ8040

Literature evidence for the named compound in the stated model; no Adooq product-use or lot-performance claim.

Methods > Leishmania Cell Culture & Genetic Manipulation (S31, S35, S36); Figure 6 legend (S100)

promastigote viability: promastigote viability; comparator: Untreated cells (1% DMSO) — Methods > Leishmania Cell Culture & Genetic Manipulation (S35); Figure 6 legend (S100)

Specifications

Manufacturer Adooq Bioscience
Actions Inhibitor
CAS Number 1214265-57-2
Applications EGFR Inhibitor
Formula C24H25ClN6OS
Molecular Weight 481
SMILES
CN1CCN(CC1)C2=CC=C(C=C2)NC3=NC=C(C(=N3)SC4=CC=CC(=C4)NC(=O)C=C)Cl

Storage & Solubility

In Vitro Solubility

Reported Solubility

SolventReported Solubility
DMSO 86 mg/mL (178.79 mM)
Water Insoluble
Ethanol 3 mg/mL (6.23 mM)

Preparing Stock Solutions

Stock preparation is unavailable for this product molecular weight.

Calculated stock concentrations do not establish solvent solubility. Refer to the reported solubility data for experimental guidance.

Storage

Store powder at -20°C, keep desiccated.
In powder form, the chemical is stable for 36 months.
In solution, store at -20°C and use within 1 month to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

Research References

  1. [1] Catta-Preta CMC, Ramos PZ, Carnielli JBT, et al. Discovery and Characterization of Cell-Permeable Inhibitors of Leishmania mexicana CLK1 Using an In-Cell Target Engagement Assay. ACS Infect Dis (2025). PMID: 40994280 DOI: 10.1021/acsinfecdis.5c00610 Source material

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