1. Epigenetics TGF-beta/Smad Apoptosis Cell Cycle/DNA Damage MAPK/ERK Pathway
  2. PKC Apoptosis Caspase PARP p38 MAPK JNK
  3. ICA-1S

ICA-1S is a specific PKC-ι inhibitor. ICA-1S can inhibit MAPK/JNK signaling pathway and downregulate the levels of c-Jun and TNF-α. ICA-1S inhibits the proliferation of breast cancer cells. ICA-1S induces apoptosis of breast cancer cells. ICA-1S can be used in breast cancer-related research.

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

ICA-1S

ICA-1S Chemical Structure

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Description

ICA-1S is a specific PKC-ι inhibitor. ICA-1S can inhibit MAPK/JNK signaling pathway and downregulate the levels of c-Jun and TNF-α. ICA-1S inhibits the proliferation of breast cancer cells. ICA-1S induces apoptosis of breast cancer cells. ICA-1S can be used in breast cancer-related research[1].

In Vitro

ICA-1S (2.5-30 μM; 120 h) potently inhibits the proliferation of BT-549 and MCF-7 breast cancer cells, with IC50 values of 10 μM and 20 μM respectively after 5 days of treatment[1].
Treatment with ICA-1S (10-20 μM; 120 h) at the IC50 concentration for 5 days induces apoptosis in BT-549 (via upregulation of cleaved Caspase 3 and cleaved PARP) and MCF-7 (via upregulation of cleaved PARP) breast cancer cells[1].
ICA-1S (10-20 μM (MCF-7); 120 h) downregulates the levels of PKC-ι and PKC-ζ in BT-549 and MCF-7 breast cancer cells, but exerts no such effect on MCF-7 cells[1].
ICA-1S (10-20 μM; 120 h) inhibits the oncogenic MAPK/JNK pathway and reduces the levels of phosphorylated and total pathway proteins, c-Jun, and TNF-α in BT-549 and MCF-7 breast cancer cells[1].
ICA-1S (10-20 μM; 120 h) reduces c-Jun mRNA levels by 50% in BT-549 breast cancer cells[1].

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

Cell Proliferation Assay[1]

Cell Line: BT-549, MCF-7 breast cancer cell lines
Concentration: 2.5 μM, 5 μM, 10 μM, 20 μM, 30 μM
Incubation Time: 120 h, with treatments every 24 h
Result: Significantly reduced cell proliferation in both cell lines.
Achieved an IC50 of 10 μM, resulting in 45% inhibition for BT-549 cells.
Achieved an IC50 of 20 μM, resulting in 43% inhibition for MCF-7 cells.

Real Time qPCR[1]

Cell Line: BT-549, MCF-7 breast cancer cell lines
Concentration: 10 μM (BT-549); 20 μM (MCF-7)
Incubation Time: 120 h
Result: Reduced c-Jun mRNA levels by 50% in BT-549 cells compared to untreated controls.
Had no significant effect on c-Jun mRNA levels in MCF-7 cells.
Molecular Weight

240.26

Formula

C10H16N4O3

SMILES

O=C(C1=C(N)N([C@H]2[C@H](O)[C@@H](O)[C@H](C)C2)C=N1)N

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Room temperature in continental US; may vary elsewhere.

Storage

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

Purity & Documentation
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Help & FAQs
  • 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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ICA-1S
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HY-183252
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