PKMYT1-IN-3
PKMYT1-IN-3 (compound 8ma) is a potent and selective PKMYT1 inhibitor with an IC50 value of 16.5 nM. PKMYT1-IN-3 has antitumor activity.
For research use only. We do not sell to patients.
- Formula: C24H26FN5O2
- Molecular Weight:435.49
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
IC50 & Target
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PKMYT1 16.5 nM (IC50) |
Cellular Effect
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| HCC1569 | EC50 |
116.8 nM
Compound: 8ma
|
Inhibition of colony formation in CCNE1-amplified human HCC1569 cells incubated for 14 days by crystal violet staining based microplate reader assay
Inhibition of colony formation in CCNE1-amplified human HCC1569 cells incubated for 14 days by crystal violet staining based microplate reader assay
|
[PMID: 39163619] |
| HCC1569 | IC50 |
0.25 μM
Compound: 8ma
|
Antiproliferative activity against human HCC1569 cells incubated for 48 to 96 hrs by CCK-8 assay
Antiproliferative activity against human HCC1569 cells incubated for 48 to 96 hrs by CCK-8 assay
|
[PMID: 39163619] |
| ZR-75-1 | EC50 |
>5 μM
Compound: 8ma
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Inhibition of colony formation in human ZR-75-1 cells incubated for 14 days by crystal violet staining based microplate reader assay
Inhibition of colony formation in human ZR-75-1 cells incubated for 14 days by crystal violet staining based microplate reader assay
|
[PMID: 39163619] |
| ZR-75-1 | IC50 |
4.96 μM
Compound: 8ma
|
Antiproliferative activity against human ZR-75-1 cells incubated for 48 to 96 hrs by CCK-8 assay
Antiproliferative activity against human ZR-75-1 cells incubated for 48 to 96 hrs by CCK-8 assay
|
[PMID: 39163619] |
Chemical Information
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Molecular Weight 435.49
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Formula C24H26FN5O2
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SMILES
CC1=CC=C(C(C)=C1C2=C(C(C(N)=O)=CC(C3=CC(N4CC[C@H](C4)N)=NC(F)=C3)=C2)N)O
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Protocols
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Cell Cytotoxicity Assay
Cytotoxicity assays are usually based on the assessment of cell membrane damage, which can also be indirectly detected by measuring cell viability. Detection methods include MTT assay, CKK-8 assay, LDH assay and ATP assay, etc.
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Subcutaneous Cell-Line-Derived Xenograft
Subcutaneous cell-line-derived xenograft (CDX) models are established by implanting cultured human cancer cell lines into immunodeficient mice, where the injected cells form localized tumors that can be monitored in vivo as a measure of tumorigenic potential, growth kinetics, and treatment response. These models are widely used in oncology research because they allow reproducible tumor formation and enable comparative assessment of tumor growth between different cell lines or genetic manipulations in a controlled in vivo microenvironment. Subcutaneous implantation of cancer cells in immunodeficient mice is a standard approach for evaluating tumor growth behavior and therapeutic response across multiple cancer types, including prostate, esophageal, pancreatic, and colon cancer models.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)