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Catalog: | HY-19715 |
Brand: | MCE |
CAS: | 1687736-54-4 |
MDL | MFCD28411624 |
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Molecular Weight | 298.34 |
Molecular Formula | C16H18N4O2 |
SMILES | O=C(NCC(N1CCCC1)=O)NC2=CC=C3C=NC=CC3=C2 |
SGC707 is a potent, selective, and non-competitive PRMT3 ( protein arginine methyltransferase 3 ) inhibitor ( IC 50 =31 nM, K d =53 nM).
PRMT3 31 nM (IC 50 ) |
SGC707 (0-10 μM; 6 h) binds to PRMT3 in both HEK293 and A549 cells [1] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Cell Viability Assay [1]
Cell Line: | HEK293 and A549 cells |
Concentration: | 0-10 μM |
Incubation Time: | 6 hours |
Result: | Stabilized PRMT3 in both HEK293 and A549 cells with EC 50 values of 1.3 μM and 1.6 μM, respectively. |
SGC707 (intraperitoneal injection; 10 mg/kg; 3 times per week; 3 w) treatment reduces hepatic steatosis and plasma triglyceride levels and induces pruritus in Western-type diet-fed LDL receptor knockout mice [2] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Model: | Western-type diet-fed LDL (lipoprotein) receptor knockout mice [2] |
Dosage: | 10 mg/kg |
Administration: | Intraperitoneal injection; 10 mg/kg; 3 times per week; 3 weeks |
Result: | Exhibited 50% lower liver triglyceride stores as well as 32% lower plasma triglyceride levels. |
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 ( 335.19 mM )
* "≥" means soluble, but saturation unknown.
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 3.3519 mL | 16.7594 mL | 33.5188 mL |
5 mM | 0.6704 mL | 3.3519 mL | 6.7038 mL |
10 mM | 0.3352 mL | 1.6759 mL | 3.3519 mL |
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