Skip to main content

MW 211.22 Da, Purity >97%. Negative control for the Src kinase inhibitor PP2 (ab120308). Inhibits EGFR kinase (IC50 = 2.7 μM).

Be the first to review this product! Submit a review

Images

Chemical Structure - PP3, Negative control for PP2 (AB120617), expandable thumbnail
  • Functional Studies - PP3, Negative control for PP2 (AB120617), expandable thumbnail

Publications

Key facts

CAS number
5334-30-5
Purity
> 97%
Form
Solid
Molecular weight
211.22 Da
Molecular formula
C11H9N5
PubChem identifier
4879
Nature
Synthetic

Alternative names

Recommended products

MW 211.22 Da, Purity >97%. Negative control for the Src kinase inhibitor PP2 (ab120308). Inhibits EGFR kinase (IC50 = 2.7 μM).

Key facts

Purity
> 97%
PubChem identifier
4879
Solubility

Soluble in ethanol to 25 mM.

Soluble in DMSO to 100 mM.

Biochemical name
1-Phenyl-1h-pyrazolo[3,4-d]pyrimidin-4-amine
Biological description

Negative control for the Src kinase inhibitor PP2 (ab120308). Inhibits EGFR kinase (IC50 = 2.7 μM).

Canonical SMILES
C1=CC=C(C=C1)N2C3=NC=NC(=C3C=N2)N
InChI
InChI=1S/C11H9N5/c12-10-9-6-15-16(11(9)14-7-13-10)8-4-2-1-3-5-8/h1-7H,(H2,12,13,14)
InChIKey
KKDPIZPUTYIBFX-UHFFFAOYSA-N
IUPAC name
1-phenylpyrazolo[3,4-d]pyrimidin-4-amine

Storage

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C
Storage information
Store under desiccating conditions, The product can be stored for up to 12 months

Supplementary info

This supplementary information is collated from multiple sources and compiled automatically.
Activity summary

EGFR also known as epidermal growth factor receptor is a membrane-bound protein with a mass of approximately 170 kDa. It is expressed in many cell types including epithelial tissues. EGFR has tyrosine kinase activity and plays an important role in the regulation of cell growth and differentiation. PI4K2B PI4 kinase beta also known as PI4KB shares a similar functional landscape. With a mass of about 92 kDa PI4KB localizes mainly in the cytoplasm and trans-Golgi network and participates in phosphatidylinositol (PI) phosphorylation converting PI to phosphatidylinositol 4-phosphate (PI4P). PI4K2A has a function similar to PI4KB in lipid-mediated signaling.

Biological function summary

EGFR participates in signal transduction cascades that promote cellular proliferation and survival. It often forms homodimers or heterodimers with other receptors in the cell membrane upon ligand binding. PI4K2B acting within lipid microdomains regulates membrane trafficking and assignation of signaling proteins to various cell functions. It does not necessarily work alone and could be a component of larger protein complexes that control phosphorylation dynamics. Both PI4KB and PI4K2A have recognized roles in the maintenance of PI4P levels within cells affecting vesicular trafficking.

Pathways

EGFR primarily associates with the MAPK and PI3K-Akt signaling pathways influencing cell cycle progression and apoptosis. Key interactions with proteins such as Src enhance downstream signaling and functional outcomes. PI4K2B and PI4KB integrate into pathways that involve phosphatidylinositol metabolism playing roles alongside proteins such as PIP kinase and serving as important nodes in PI3P-related pathways. These connections influence cellular trafficking and organelle function.

Associated diseases and disorders

EGFR overexpression or mutations relate to cancers notably lung cancer and glioblastoma through altered signaling pathways resulting in unchecked cell division. Its interaction with Src renders it a target for inhibitors like PP2 Src inhibitors in therapeutic investigations. PI4KB dysregulation associates with neurological diseases where disruptions in PI4P balance affect neurodegenerative disease progression. Therefore EGFR and PI4K enzymes are linked to cancer and neurological disorders where their pathways intertwine with disease-specific alterations in protein networks.

Product promise

We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.

In the unlikely event of one of our products not working as expected, you are covered by our product promise.

Full details and terms and conditions can be found here:
Terms & Conditions.

2 product images

  • Chemical Structure - PP3, Negative control for PP2 (ab120617), expandable thumbnail

    Chemical Structure - PP3, Negative control for PP2 (ab120617)

    2D chemical structure image of ab120617, PP3, Negative control for PP2

  • Functional Studies - PP3, Negative control for PP2 (ab120617), expandable thumbnail

    Functional Studies - PP3, Negative control for PP2 (ab120617)

    Anti-E Cadherin antibody [DECMA-1] - Intercellular Junction Marker ab11512 staining E cadherin in SW480 cells treated with PP3 (ab120617), by ICC/IF. No change of E cadherin expression with increased concentration of PP3 is observed, as described in literature, since PP3 is the negative control for PP2.
    The cells were incubated at 37°C for 24h in media containing different concentrations of ab120617 (PP3) in DMSO, fixed with 4% formaldehyde for 10 minutes at room temperature and blocked with PBS containing 10% goat serum, 0.3 M glycine, 1% BSA and 0.1% tween for 2h at room temperature. Staining of the treated cells with Anti-E Cadherin antibody [DECMA-1] - Intercellular Junction Marker ab11512 (5 μg/ml) was performed overnight at 4°C in PBS containing 1% BSA and 0.1% tween. A DyLight 488 anti-rat polyclonal antibody (ab98386) at 1/250 dilution was used as the secondary antibody. Nuclei were counterstained with DAPI and are shown in blue.

Downloads

Product protocols

For this product, it's our understanding that no specific protocols are required. You can:

Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.

For licensing inquiries, please contact partnerships@abcam.com