Mirin

Modify Date: 2024-01-02 17:45:53

Mirin Structure
Mirin structure
Common Name Mirin
CAS Number 1198097-97-0 Molecular Weight 220.248
Density 1.5±0.1 g/cm3 Boiling Point 441.6±55.0 °C at 760 mmHg
Molecular Formula C10H8N2O2S Melting Point 298 °C
MSDS Chinese Flash Point 220.8±31.5 °C

 Use of Mirin


Mirin is a small-molecule inhibitor of MRN (Mre11, Rad50, and Nbs1) complex.Target: in vitro: Mirin was shown to block Mre11 exonuclease activity and MRN-dependent ATM activation, and to inhibit the ionizing radiation-induced G2/M checkpoint and homologous recombination in mammalian cells. Mirin inhibition of ATM activation is independent of Mre11 nuclease inhibition since the M(HN)RN and M(HL/DV)RN mutant complexes are inhibited equivalently to the wild-type enzyme despite the fact that they are nuclease-deficient. The effects of Mirin have been ascribed to its effects on Mre11 nuclease activity, but as we show here, Mirin is inhibitory of MRN function independent of the nuclease activity of the complex. [2] Addition of the Mre11 inhibitor Mirin to egg extracts and mammalian cells reduces RCC1 association with mitotic chromosomes. HeLa cells expressing Histone H2B-EYFP were treated with Mirin (25 or 50 μM), and mitotic progression was immediately monitored using live cell imaging. Although Mirin-treated cells were able to congress chromosomes to the metaphase plate with similar kinetics as untreated cells, a significant fraction of Mirin-treated cells paused for extended periods of time in a metaphase-like stage without anaphase onset . [1]

 Names

Name (Z)-5-(4-hydroxybenzylidene)-2-imino-4-oxo-thiazolidine
Synonym More Synonyms

 Mirin Biological Activity

Description Mirin is a small-molecule inhibitor of MRN (Mre11, Rad50, and Nbs1) complex.Target: in vitro: Mirin was shown to block Mre11 exonuclease activity and MRN-dependent ATM activation, and to inhibit the ionizing radiation-induced G2/M checkpoint and homologous recombination in mammalian cells. Mirin inhibition of ATM activation is independent of Mre11 nuclease inhibition since the M(HN)RN and M(HL/DV)RN mutant complexes are inhibited equivalently to the wild-type enzyme despite the fact that they are nuclease-deficient. The effects of Mirin have been ascribed to its effects on Mre11 nuclease activity, but as we show here, Mirin is inhibitory of MRN function independent of the nuclease activity of the complex. [2] Addition of the Mre11 inhibitor Mirin to egg extracts and mammalian cells reduces RCC1 association with mitotic chromosomes. HeLa cells expressing Histone H2B-EYFP were treated with Mirin (25 or 50 μM), and mitotic progression was immediately monitored using live cell imaging. Although Mirin-treated cells were able to congress chromosomes to the metaphase plate with similar kinetics as untreated cells, a significant fraction of Mirin-treated cells paused for extended periods of time in a metaphase-like stage without anaphase onset . [1]
Related Catalog
References

[1]. Rozier L, et al. The MRN-CtIP pathway is required for metaphase chromosome alignment. Mol Cell. 2013 Mar 28;49(6):1097-107.

[2]. Lee JH, et al. Ataxia telangiectasia-mutated (ATM) kinase activity is regulated by ATP-driven conformational changes in the Mre11/Rad50/Nbs1 (MRN) complex. J Biol Chem. 2013 May 3;288(18):12840-51.

[3]. Garner KM, et al. Corrected structure of Mirin, a small-molecule inhibitor of the Mre11-Rad50-Nbs1 complex. Nat Chem Biol. 2009 Mar;5(3):129-30.

 Chemical & Physical Properties

Density 1.5±0.1 g/cm3
Boiling Point 441.6±55.0 °C at 760 mmHg
Melting Point 298 °C
Molecular Formula C10H8N2O2S
Molecular Weight 220.248
Flash Point 220.8±31.5 °C
Exact Mass 220.030655
PSA 98.48000
LogP 1.36
Vapour Pressure 0.0±1.1 mmHg at 25°C
Index of Refraction 1.718

 Synonyms

5-(4-Hydroxy-benzylidene)-2-imino-thiazolidin-4-one
4(5H)-Thiazolone, 2-amino-5-[(4-hydroxyphenyl)methylene]-, (5Z)-
(5Z)-2-Amino-5-(4-hydroxybenzylidene)-1,3-thiazol-4(5H)-one
4-Thiazolidinone, 5-(p-hydroxybenzylidene)-2-imino-
Lu AA 47070
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