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Catalog: | HY-123983 |
Brand: | MCE |
CAS: | 922050-57-5 |
MDL | - |
---|---|
Molecular Weight | 317.75 |
Molecular Formula | C13H8ClN5OS |
SMILES | N#CCSC1=NC(N(C2=CC=CC(Cl)=C2)N=C3)=C3C(N1)=O |
HS56 is an ATP-competitive dual Pim/DAPK3 inhibitor with K i values of 0.26, 0.208, 2.94, and >100 μM for DAPK3, Pim-3, Pim-1, and Pim-2, respectively. HS56 inhibits LC20 phosphorylation and smooth muscle contraction. HS56 decreases blood pressure in spontaneously hypertensive mice. HS56 can be used in research of hypertension [1] .
PIM3 0.208 μM (Ki) |
PIM1 2.94 μM (Ki) |
PIM2 >100 μM (Ki) |
HS56 (50 μM; 16 h) delays force onset, decreases contractile force, and reduces LC20 phosphorylation in excised rat caudal arterial VSM tissues [1] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Western Blot Analysis [1]
Cell Line: | VSM tissues |
Concentration: | 50 μM |
Incubation Time: | 16 hours |
Result: | Modulated LC20 phosphorylation in VSM tissues. |
HS56 (10 and 20 mg/kg; i.v.; single injection) decreases blood pressure (BP) in spontaneously hypertensive mice [1] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Model: | Spontaneously hypertensive renin transgene and wild-type (WT) mice [1] |
Dosage: | 10 and 20 mg/kg |
Administration: | Intravenous injection, single injection |
Result: | Induced dose-dependent decreases in systolic blood pressure. |
Room temperature in continental US; may vary elsewhere.
Please store the product under the recommended conditions in the Certificate of Analysis.
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