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ChemicalBook--->CAS DataBase List--->1558598-41-6

1558598-41-6

1558598-41-6 Structure

1558598-41-6 Structure
IdentificationBack Directory
[Name]

PFM01
[CAS]

1558598-41-6
[Synonyms]

PFM01
PFM01 >=98% (HPLC)
(5Z)-5-[(4-Hydroxyphenyl)methylene]-3-(2-methylpropyl)-2-thioxo-4-thiazolidinone
[Molecular Formula]

C14H15NO2S2
[MDL Number]

MFCD02220972
[MOL File]

1558598-41-6.mol
[Molecular Weight]

293.4
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

Soluble in DMSO
[form ]

powder
[color ]

white to beige
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319
[Precautionary statements ]

P301+P312+P330-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

PFM01(1558598-41-6)1HNMR
Hazard InformationBack Directory
[Biochem/physiol Actions]

PFM01 is a cell-permeable N-alkylated Mirin (Sigma Cat. No. 475954) derivative that selectively inhibits against MRE11 endo-, but not exo-, nuclease activity. PFM01 targets MRE11 at a site near the dimer interface, distinct from that occupied by Mirin and PFM39 to allow disruption of the ssDNA-binding groove and selective inhibition against MRE11 endo-, but not exo-, nuclease activity. While both endonuclease and exonuclease activities are required for MRE11-mediated homologous recombination (HR) repair, only FM01 (100 μM), but not the exonuclease inhibitors Mirin (500 μM) and PFM39 (100 μM), rescues G2-phase double-strand break (DSB) repair defect in HR protein BRCA2-deficient HSC62-hTERT fibroblasts following ionizing irradiation (IR) by blocking HR initiation and thereby allowing non-homologous end joining (NHEJ) to proceed.
[storage]

Store at -20°C
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