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Catalog: | HY-19736 |
Brand: | MCE |
CAS: | 934369-14-9 |
MDL | MFCD28396419 |
---|---|
Molecular Weight | 364.27 |
Molecular Formula | C18H19Cl2N3O |
SMILES | ClC1=CC=C(/N=C(NNC2=CC=C(Cl)C=C2)/C(C(C)(C)C)=O)C=C1 |
TY-52156 is a potent and selective S1P 3 receptor antagonist with a K i value of 110 nM [1] .
Ki: 110 nM (S1P 3 ) [1]
TY-52156 inhibits the S1P
3
receptor-dependent increase in [Ca
2+
]
i
[1]
.
TY-52156 shows submicromolar potency and a high degree of selectivity for S1P
3
receptor
[1]
.
TY-52156 (10 μM; 10 min) inhibits S1P-induced p44/p42 MAPK phosphorylation
[1]
.
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Western Blot Analysis [1]
Cell Line: | Chinese hamster ovary K1 cells |
Concentration: | 10 μM |
Incubation Time: | 10 min |
Result: | Inhibited S1P-induced p44/p42 MAPK phosphorylation. |
TY-52156 (10 mg/kg, 30 mg/kg; p.o.) suppresses S1P
3
receptor-induced bradycardia after oral administration in vivo
[1]
.
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Model: | Male SD rats (290–340 g) [1] |
Dosage: | 10 mg/kg, 30 mg/kg |
Administration: | Oral administration |
Result: | Inhibited S1P 3 receptor-induced bradycardia after oral administration in vivo. |
Solid
Room temperature in continental US; may vary elsewhere.
Powder | -20°C | 3 years |
---|---|---|
4°C | 2 years | |
In solvent | -80°C | 6 months |
-20°C | 1 month |
DMSO : ≥ 100 mg/mL ( 274.52 mM )
* "≥" means soluble, but saturation unknown.
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 2.7452 mL | 13.7261 mL | 27.4522 mL |
5 mM | 0.5490 mL | 2.7452 mL | 5.4904 mL |
10 mM | 0.2745 mL | 1.3726 mL | 2.7452 mL |
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