1. Cell Cycle/DNA Damage
  2. G-quadruplex DNA/RNA Synthesis
  3. PhpC

PhpC is a G-quadruplex (G4)-DNA/RNA disruptor. PhpC disrupts DNA and RNA G4 structures and promotes G4 helicase activity. PhpC effectively enhancing the activity of Taq polymerase. PhpC modulates G-quadruplexs (G4s) both in vitro and in cells.

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PhpC

PhpC Chemical Structure

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Based on 1 publication(s) in Google Scholar

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Description

PhpC is a G-quadruplex (G4)-DNA/RNA disruptor. PhpC disrupts DNA and RNA G4 structures and promotes G4 helicase activity. PhpC effectively enhancing the activity of Taq polymerase. PhpC modulates G-quadruplexs (G4s) both in vitro and in cells[1][2][3].

In Vitro

PhpC enhances the reverse transcription of RNA containing rMYC G4 while exerting a significant inhibitory effect on the reverse transcription of rhTELO, r5YEY, and rTBA[3].
PhpC promotes the in vitro translation of G4-containing RNA[3].
PhpC inhibits the cell viability of HEK293FT cells, with an IC50 value of 25.7 μM[3].
PhpC (5-20 μM; 24 h) induces an increase in the DNA damage marker γH2AX, indicating that it can induce DNA damage[3].
PhpC (25-100 μM; 24 h) leads to a gradual increase in the transcript level of mature miR-3196 in A549 cells[4].
PhpC can recognize and bind to the regions forming G4s (rG4)-3196 sequence, disrupting its native G4 conformation and leading to a structural transition[4].
In HeLa cells, the immunofluorescence (IF) analyses demonstrats that 100 µM PhpC reduces G4 levels significantly while it has no effect on the metabolic activity[5].
PhpC (90 µM, 48 h) significantly decreases the abundance of NRAS G4 in MCF7 cells[6].
PhpC (90 μM; 72 h) shows no significant effects against LINC01589 and MELTF-AS1, while PhpC triggers a significant decrease against UXT-AS1 and NRAS in HT-29 cells[7].
PhpC modulates the G4 landscapes in a focused manner, altering only the translational activity in astrocytes with the upregulation of 295 proteins mostly involved in RNA transactions[8].

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

RT-PCR[4]

Cell Line: A549 cells
Concentration: 25 μM, 50 μM, 100 μM
Incubation Time: 24 h
Result: Effectively enhanced the levels of miR-3196 in cells.
Clinical Trial
Molecular Weight

356.38

Formula

C18H20N4O4

Appearance

Solid

Color

Light yellow to yellow

SMILES

NCCOC1=CC=CC(C2=CC3=CN(C(N=C3N2)=O)CC(OCC)=O)=C1

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

4°C, sealed storage, away from moisture and light

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)

Purity & Documentation

Purity: 98.00%

References
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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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PhpC
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HY-164421
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