keep away from direct sunlight
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
VU590 is a potent and moderately selective inhibitor of extrarenal medullary potassium ROMK (Kir1.1).VU590 inhibits Kir7.1 and modulates uterine myometrial contractility and melanocortin signalling.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
2 mg | In stock | $ 53.00 | |
5 mg | In stock | $ 84.00 | |
10 mg | In stock | $ 122.00 | |
25 mg | In stock | $ 196.00 | |
50 mg | In stock | $ 296.00 | |
100 mg | In stock | $ 439.00 | |
500 mg | In stock | $ 987.00 |
Description | VU590 is a potent and moderately selective inhibitor of extrarenal medullary potassium ROMK (Kir1.1).VU590 inhibits Kir7.1 and modulates uterine myometrial contractility and melanocortin signalling. |
Targets&IC50 | Kir7.1:8 μM, Kir1.1:290 nM |
Molecular Weight | 488.53 |
Formula | C24H32N4O7 |
CAS No. | 313505-85-0 |
keep away from direct sunlight
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: < 20 mg/mL, Sonication is recommended.
H2O: 1 mg/mL (2.05 mM), Sonication is recommended.
You can also refer to dose conversion for different animals. More
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc.
VU590 313505-85-0 Membrane transporter/Ion channel Potassium Channel VU-590 (hydrochloride) VU-590 VU590 (hydrochloride) VU 590 inhibitor inhibit