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2-Amino-5-[(4-hydroxyphenyl)methylidene]-1,3-thiazol-4-one

HCID 520459
NotesReactions
Basic informationNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Substructure searchFind similar structures

Basic information

CAS
299953-00-7
Standard SMILES
NC1=NC(=O)C(=Cc2ccc(O)cc2)S1
InChIKey
YBHQCJILTOVLHD-UHFFFAOYSA-N
Molecular formula
C10H8N2O2S
Average molar mass
220.25 g/mol
Monoisotopic mass
220.03064868

Names & identifiers

Preferred name
2-Amino-5-[(4-hydroxyphenyl)methylidene]-1,3-thiazol-4-one
IUPAC
2-amino-5-[(4-hydroxyphenyl)methylidene]-1,3-thiazol-4-one
English name
MRN-ATM Pathway Inhibitor, Mirin
Molecular formula
C10H8N2O2S
Molecular weight
220.25

Names & synonyms

MRN-ATM Pathway Inhibitor, Mirin2-amino-5-[(4-hydroxyphenyl)methylidene]-1,3-thiazol-4-one2-amino-5-[(4-hydroxyphenyl)methylidene]-4,5-dihydro-1,3-thiazol-4-oneSCHEMBL21296287SCHEMBL25307633SCHEMBL305538862-Amino-5-[(4-hydroxyphenyl)methylidene]-1,3-thiazol-4(5H)-oneMirin >=98% (HPLC), powderMirin, MRN-ATM complex inhibitor5-(4-Hydroxybenzylidene)-2-iminothiazolidin-4-one(E)-5-(4-hydroxybenzylidene)-2-iminothiazolidin-4-one4(5H)-Thiazolone, 2-amino-5-[(4-hydroxyphenyl)methylene]-
Show more names
(5E)-5-(4-Hydroxybenzylidene)-2-imino-1,3-thiazolidin-4-one

Database identifiers

CAS
299953-00-7
PubChem CID
520459
DTXSID
DTXSID20334359

Properties

Computed structural properties

XLogP
1.5
Topological polar surface area
101 Ų
Hydrogen bond donors
2
Hydrogen bond acceptors
3
Rotatable bonds
1
Heavy atoms
15
Formal charge
0
Complexity
330

Physicochemical properties

Melting point
295 · 295-297 °C(Solv: ethanol (64-17-5))
Boiling point
441.6 · 441.6±55.0 °C(Predicted)
Density
1.49 · 1.49±0.1 g/cm3(Predicted)
storage temp.
2 · 2-8°C
solubility
10 mg/mL · DMSO: >10mg/mL
pka
9.15 · 9.15±0.30(Predicted)
form
Reddish orange powder
color
red to orange
Sensitive
Moisture Sensitive
Stability
2 years · Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
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
SMILES
NC1=NC(=O)C(\S1)=C\c2ccc(O)cc2
UNSPSC Code
12352200 · 12352200
NACRES
77 · NA.77

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

Safety data

wgk
3
risk_code
36
Signal word
Warning
Symbol(GHS)
GHS07
hazard_code
Xi
safety_code
26
Storage Class
11 - Combustible Solids
Hazard statements
H315-H319-H335
Precautionary statements
P261-P280a-P304+P340-P305+P351+P338-P405-P501a

Chemistry & industry

Applications · 3 items

DescriptionMirin is an inhibitor of the Mre11/Rad50/Nbs1 (MRN) complex, which functions as a DNA damage sensor and activates the DNA repair enzyme ataxia-telangiectasia mutated kinase (ATM). It inhibits phosphorylation of H2AX induced by DNA containing dsDNA breaks (DSBs), indicating decreased ATM activation, with an IC50 value of 66 μM in X. laevis cell-free extracts. Mirin (100 μM) also inhibits the exonuclease activity of Mre11 in a cell-free assay. It induces cell cycle arrest at the G2 phase in TOSA4 cells and inhibits homology-dependent repair in HEK293 cells in a concentration-dependent manner. Nanoparticle-encapsulated mirin (50 mg/kg) reduces tumor growth in an LA-N-5 mouse xenograft model.

UsesThe Mre11-Rad50-Nbs1 (MRN) complex acts as a DNA damage sensor, maintains genome stability during DNA replication, and activates and recruits ataxia-telangiectasia mutated (ATM) to damaged DNA. The genes that encode the MRN proteins are all essential for cell viability, so functional studies of MRN cannot involve deletion of these genes. Mirin is an inhibitor of MRN, inhibiting MRN-dependent phosphorylation of histone H2AX (IC50 = 66 μM). Through its effects on MRN, mirin prevents activation of ATM. Inhibition of MRN centers on the ability of mirin to block the nuclease activity of Mre11, rather than altering DNA-binding or MRN complex formation. In cells, mirin induces G2 arrest, abolishes the radiation-induced G2/M checkpoint, and prevents homology-directed repair of DNA damage.[Cayman Chemical]

UsesMirin has been used:as a small molecule inhibitor of meiotic recombination 11 (MRE11), in the pre-treatment of HCT116 wildtype cells before irradiationas Mre11 inhibitior in BSC-1 cells infected with simian virus 40in 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)

Upstream & downstream products

Upstream raw materials

Pseudothiohydantoin4-Hydroxybenzaldehyde

Suppliers21 total

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Compound notes

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On this pageBasic informationNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Symbol(GHS)
7 · GHS07
Signal word
Warning
Hazard statements
315 · H315-H319-H335
Precautionary statements
261 · P261-P280a-P304+P340-P305+P351+P338-P405-P501a
Hazard Codes
Xi
Risk Statements
36 · 36
Safety Statements
26 · 26
WGK Germany
3 · 3
Storage Class
11 · 11 - Combustible Solids
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