MRS 2578

MRS 2578 Basic information
Product Name:MRS 2578
Synonyms:N,N''-1,4-BUTANEDIYLBIS[N'-(3-ISOTHIOCYANATOPHENYL)THIOUREA];MRS 2578;1,4-DI[3-(3-ISOTHIOCYANATOPHENYL)THIOUREIDO]BUTANE;N',N'''-butane-1,4-diylbis[1-(3-isothiocyanatophenyl)(thiourea)];Thiourea, N,N''-1,4-butanediylbis[N'-(3-isothiocyanatophenyl)-;MRS 2578;MRS-2578; MRS2578;MRS-2578; MRS2578;CS-1109
CAS:711019-86-2
MF:C20H20N6S4
MW:472.67
EINECS:200-258-5
Product Categories:Inhibitors
Mol File:711019-86-2.mol
MRS 2578 Structure
MRS 2578 Chemical Properties
Melting point 170 - 173°C
Boiling point 652.7±65.0 °C(Predicted)
density 1.31
storage temp. 2-8°C
solubility DMSO: ~17 mg/mL
pka11.80±0.70(Predicted)
form solid
color white
InChIKeyQOHNRGHTJPFMSL-UHFFFAOYSA-N
Safety Information
Hazard Codes Xn
Risk Statements 20/21/22-36/37/38-42
Safety Statements 22-26-36/37/39-45
RIDADR UN 2811 6.1/PG 3
WGK Germany 3
MSDS Information
ProviderLanguage
SigmaAldrich English
MRS 2578 Usage And Synthesis
DescriptionMRS2578 is an antagonist of the purinergic P2Y6 receptor (IC50s = 37 and 98 nM for human and rat receptors, respectively). It is without effect at other purinergic receptors. MRS2578 is used to study the cellular and physiological roles of P2Y6.
UsesMRS 2578 has been used an antagonist of purinoceptor P2Y6:
  • to study the role of purinergic receptor in Up4A-induced relaxation in coronary small arteries from swine
  • in P. aeruginosa infected mice to test its effect on the inflammatory responses
  • to test its inhibition on neutrophil extracellular traps and monosodium urate (MSU) crystals formation in polymorphonuclear leukocytes

UsesMRS 2578 is a selective P2Y66?receptor antagonist.
Biological ActivitySelective antagonist of P2Y 6 nucleotide receptors; IC 50 values are 37 and 98 nM at human and rat P2Y 6 receptors respectively. Displays no activity at P2Y 1 , P2Y 2 , P2Y 4 and P2Y 11 receptors (IC 50 > 10 μ M). Inhibits agonist-induced cardiomyocyte contraction and UDP-induced phagocytosis.
Biochem/physiol ActionsMRS 2578 elicits cytoprotective functionality in neuroblastoma cells and prevents dopaminergic neuron death under in vitro and in vivo conditions. It also protects microglia by delaying lipopolysaccharide-induced death.
storage-20°C (desiccate)
references[1] mamedova l k, joshi b v, gao z g, et al. diisothiocyanate derivatives as potent, insurmountable antagonists of p2y6 nucleotide receptors[j]. biochemical pharmacology, 2004, 67(9): 1763-1770.
MRS 2578 Preparation Products And Raw materials
Veliparib N-cyclohexyl-2-(N-(3-fluorophenyl)-2-(2-Methyl-1H-iMidazol-1-yl)acetaMido)-2-(o-tolyl)acetaMide 2-METHOXYESTRADIOL SB 431542 Saracatinib CCT 137690 MRS 2578 Benzenamine, 3-isothiocyanato- (9CI)

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