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TMPyP4 tosylate

Catalog #: 4253
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TMPyP4 tosylate | CAS No. 36951-72-1 | Telomerase Inhibitors
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Description: Inhibitor of human telomerase

Chemical Name: 5,10,15,20-Tetrakis(1-methylpyridinium-4-yl)porphyrin tetra(p-toluenesulfonate)

Purity: ≥95%

Product Details
Citations (1)
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Biological Activity Technical Data Background Product Datasheets Calculators

Biological Activity

TMPyP4 tosylate is a cationic porphyrin; inhibits human telomerase. Stacks with G tetrads to stabilize quadruplex DNA. Inhibits cell proliferation and induces cell death in three myeloma cell lines. Activity results in telomere shortening at concentrations between 1 and 5 μM.

Technical Data

M.Wt:
1363.6
Formula:
C72H66N8O12S4
Solubility:
Soluble to 50 mM in water
Purity:
≥95%
Storage:
Store at +4°C
CAS No:
36951-72-1

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.

Background References

  1. Effect of telomere and telomerase interactive agents on human tumor and normal cell lines.
    Rha et al.
    Clin.Cancer Res., 2000;6:987
  2. Telomerase inhibition and cell growth arrest by G-quadruplex interactive agent in multiple myeloma.
    Shammas et al.
    Mol.Cancer Ther., 2003;2:825
  3. Cationic porphyrins as telomerase inhibitors: the interaction of tetra-(N-methyl-4-pyridyl)porphine with quadruplex DNA.
    Wheelhouse et al.
    J.Am.Chem.Soc., 1998;120:3261
  4. Quadruplex-interactive agents as telomerase inhibitors: synthesis of porphyrins and structure-activity relationship for the inhibition of telomerase.
    Shi et al.
    J.Med.Chem., 2001;474:4509

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Citation for TMPyP4 tosylate

The citations listed below are publications that use Tocris products. Selected citations for TMPyP4 tosylate include:

1 Citation: Showing 1 - 1

  1. Mitochondrial clearance and maturation of autophagosomes are compromised in LRRK2 G2019S familial Parkinson's disease patient fibroblasts.
    Authors: Ole Et al.
    Hum Mol Genet  2019;28:3232-3243

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