Date published: 2025-10-18

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Pyridostatin (CAS 1085412-37-8)

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Alternate Names:
4-(2-aminoethoxy)-N2,N6-bis[4-(2-aminoethoxy)-2-quinolinyl]-2,6-pyridinedicarboxamide, trifluoroacetate salt
CAS Number:
1085412-37-8
Molecular Weight:
596.64
Molecular Formula:
C31H32N8O5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Pyridostatin is a synthetic small molecule that uniquely targets and stabilizes G-quadruplexes (G4s), complex nucleic acid structures formed by guanine-rich sequences of DNA and RNA. These G-quadruplexes are prevalent in the regulatory regions of genes and telomeres, playing critical roles in DNA replication, transcription, and genomic stability. By binding to these G4 structures, Pyridostatin disrupts the normal function of these regulatory elements, leading to a halt in the replication and transcription processes that are essential for cell division and growth. This mechanism of action positions Pyridostatin as a powerful tool in molecular biology and genetics research, enabling scientists to explore the functional implications of G-quadruplex stabilization in genomic regulation and stability. Its ability to selectively interact with these complex structures without affecting other DNA or RNA forms makes it invaluable for studies focused on understanding the molecular underpinnings of genomic regulation and the potential role of G-quadruplexes in genetic diseases and aging.


Pyridostatin (CAS 1085412-37-8) References

  1. Small-molecule-induced DNA damage identifies alternative DNA structures in human genes.  |  Rodriguez, R., et al. 2012. Nat Chem Biol. 8: 301-10. PMID: 22306580
  2. Pyridostatin analogues promote telomere dysfunction and long-term growth inhibition in human cancer cells.  |  Müller, S., et al. 2012. Org Biomol Chem. 10: 6537-46. PMID: 22790277
  3. Stabilization of G-quadruplex DNA and inhibition of Bcl-2 expression by a pyridostatin analog.  |  Feng, Y., et al. 2016. Bioorg Med Chem Lett. 26: 1660-3. PMID: 26923693
  4. Molecular recognition of a carboxy pyridostatin toward G-quadruplex structures: Why does it prefer RNA?  |  Rocca, R., et al. 2017. Chem Biol Drug Des. 90: 919-925. PMID: 28459507
  5. The G-quadruplex DNA stabilizing drug pyridostatin promotes DNA damage and downregulates transcription of Brca1 in neurons.  |  Moruno-Manchon, JF., et al. 2017. Aging (Albany NY). 9: 1957-1970. PMID: 28904242
  6. Submolecular dissection reveals strong and specific binding of polyamide-pyridostatin conjugates to human telomere interface.  |  Mandal, S., et al. 2019. Nucleic Acids Res. 47: 3295-3305. PMID: 30820532
  7. Dimers formed with the mixed-type G-quadruplex binder pyridostatin specifically recognize human telomere G-quadruplex dimers.  |  Ma, TZ., et al. 2020. Org Biomol Chem. 18: 920-930. PMID: 31922164
  8. Catching Common Cold Virus with a Net: Pyridostatin Forms Filaments in Tris Buffer That Trap Viruses-A Novel Antiviral Strategy?  |  Real-Hohn, A., et al. 2020. Viruses. 12: PMID: 32635420
  9. Oxidative probing of the G4 DNA structure induced in double-stranded DNA by molecular crowding or pyridostatin.  |  Beniaminov, A., et al. 2021. Biochimie. 191: 33-36. PMID: 34418485
  10. G-quadruplex binder pyridostatin as an effective multi-target ZIKV inhibitor.  |  Zou, M., et al. 2021. Int J Biol Macromol. 190: 178-188. PMID: 34461156
  11. Anti-tumoural activity of the G-quadruplex ligand pyridostatin against BRCA1/2-deficient tumours.  |  Groelly, FJ., et al. 2022. EMBO Mol Med. 14: e14501. PMID: 35107878
  12. G-quadruplex inducer/stabilizer pyridostatin targets SUB1 to promote cytotoxicity of a transplatinum complex.  |  Hou, Y., et al. 2022. Nucleic Acids Res. 50: 3070-3082. PMID: 35258624
  13. Structural Basis of Pyridostatin and Its Derivatives Specifically Binding to G-Quadruplexes.  |  Liu, LY., et al. 2022. J Am Chem Soc. 144: 11878-11887. PMID: 35749293

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Pyridostatin, 10 mg

sc-476422
10 mg
$250.00