ChemicalBook--->CAS DataBase List--->711019-86-2

711019-86-2

711019-86-2 Structure

711019-86-2 Structure
IdentificationBack Directory
[Name]

MRS 2578
[CAS]

711019-86-2
[Synonyms]

CS-1109
MRS 2578
MRS-2578; MRS2578
MRS 2578 USP/EP/BP
MRS 2578 >=95% (HPLC)
MRS 2578;MRS-2578; MRS2578
1,4-DI[3-(3-ISOTHIOCYANATOPHENYL)THIOUREIDO]BUTANE
N,N''-1,4-BUTANEDIYLBIS[N'-(3-ISOTHIOCYANATOPHENYL)THIOUREA]
1,1'-(Butane-1,4-diyl)bis(3-(3-isothiocyanatophenyl)thiourea)
Thiourea, N,N''-1,4-butanediylbis[N'-(3-isothiocyanatophenyl)-
N',N'''-butane-1,4-diylbis[1-(3-isothiocyanatophenyl)(thiourea)]
Thiourea, N,N''-1,4-butanediylbis[N'-(3-isothiocyanatophenyl)- (9CI)
[EINECS(EC#)]

200-258-5
[Molecular Formula]

C20H20N6S4
[MDL Number]

MFCD07370141
[MOL File]

711019-86-2.mol
[Molecular Weight]

472.67
Chemical PropertiesBack Directory
[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
[form ]

solid
[pka]

11.80±0.70(Predicted)
[color ]

white
[InChIKey]

QOHNRGHTJPFMSL-UHFFFAOYSA-N
Safety DataBack Directory
[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
Hazard InformationBack Directory
[Description]

MRS2578 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.
[Uses]

MRS 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

[Uses]

MRS 2578 is a selective P2Y66?receptor antagonist.
[Biological Activity]

Selective 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 Actions]

MRS 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]

Store at 2-8°C
[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.
Spectrum DetailBack Directory
[Spectrum Detail]

MRS 2578(711019-86-2)1HNMR
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