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Merck

M9948

Sigma-Aldrich

Mirin

≥98% (HPLC), powder

Synonym(e):

5-(4-Hydroxybenzylidene)-2-iminothiazolidin-4-one

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About This Item

Empirische Formel (Hill-System):
C10H8N2O2S
CAS-Nummer:
Molekulargewicht:
220.25
MDL-Nummer:
UNSPSC-Code:
12352200
PubChem Substanz-ID:
NACRES:
NA.77

Qualitätsniveau

Assay

≥98% (HPLC)

Form

powder

Lagerbedingungen

desiccated

Farbe

red to orange

Löslichkeit

DMSO: >10 mg/mL

Lagertemp.

2-8°C

SMILES String

NC1=NC(=O)C(\S1)=C\c2ccc(O)cc2

InChI

1S/C10H8N2O2S/c11-10-12-9(14)8(15-10)5-6-1-3-7(13)4-2-6/h1-5,13H,(H2,11,12,14)/b8-5-

InChIKey

YBHQCJILTOVLHD-YVMONPNESA-N

Angaben zum Gen

human ... MRE11A(4361)

Anwendung

Mirin has been used:
  • as a small molecule inhibitor of meiotic recombination 11 (MRE11), in the pre-treatment of HCT116 wildtype cells before irradiation
  • as Mre11 inhibitior in BSC-1 cells infected with simian virus 40
  • in the pre-treatment of W12E cells for quantification of human papilloma virus (HPV) episome levels and to potentiate the effect of polyamide-25 (PA-25)

Biochem./physiol. Wirkung

Mirin causes cell cycle arrest at G1 phase. Mirin sensitizes virus to antiviral polyamides (AVP). In human papilloma virus (HPV) episomes, mirin promotes damage by forming double stranded DNA breaks. It aids in reducing the inhibitory concentration (IC50s) of AVP.
Mirin is an inhibitor of the Mre11-Rad50-Nbs1 complex. It disrupts nuclease activity of Mre11 and thus, the ability to repair DNA double strand breaks.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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