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SML1176

Sigma-Aldrich

Carboxypyridostatin trifluoroacetate salt

≥95% (HPLC)

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Synonym(s):
4-[[[2,6-Bis[[[4-(2-aminoethoxy)-2-quinolinyl]amino]carbonyl]-4-pyridinyl]oxy]methyl]-1H-1,2,3-triazole-1-propanoic acid trifluoroacetate salt, carboxyPDS trifluoroacetate salt
Empirical Formula (Hill Notation):
C35H34N10O7 · xC2HF3O2
CAS Number:
Molecular Weight:
706.71 (free base basis)
UNSPSC Code:
12352200
NACRES:
NA.77

Quality Level

Assay

≥95% (HPLC)

form

powder

storage condition

desiccated

color

white to light brown

solubility

H2O: 25 mg/mL, clear

storage temp.

−20°C

Application

Carboxypyridostatin trifluoroacetate salt has been used in the study of translation, stimulated by DHX36 (DEAH-box helicase 36) binding at G-rich sites in mRNA untranslated regions.

Biochem/physiol Actions

Carboxypyridostatin (carboxyPDS) selectively stabilizes RNA-containg G-quadruplex stuctures. Immunofluorescent staining of carboxyPDS treated cells using an anti G-quadruplex antibody reveals staining only in the cytoplasm and not the nucleus, demonstrating selectivity against DNA G-quadruplex structures.

Other Notes

Light sensitive

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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DHX36 binding at G-rich sites in mRNA untranslated regions promotes translation.
Sauer M, et al.
bioRxiv (2017)
Pauline Herviou et al.
Nature communications, 11(1), 2661-2661 (2020-05-29)
RNA G-quadruplexes (RG4s) are four-stranded structures known to control mRNA translation of cancer relevant genes. RG4 formation is pervasive in vitro but not in cellulo, indicating the existence of poorly characterized molecular machinery that remodels RG4s and maintains them unfolded.

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