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.
パッケージサイズ | 在庫状況 | 単価(税別) | |||
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2 mg | 在庫あり | ¥ 12,500 | |||
5 mg | 在庫あり | ¥ 19,500 | |||
10 mg | 在庫あり | ¥ 28,000 | |||
25 mg | 在庫あり | ¥ 45,000 | |||
50 mg | 在庫あり | ¥ 68,000 | |||
100 mg | 在庫あり | ¥ 101,000 | |||
500 mg | 在庫あり | ¥ 226,500 |
説明 | 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. |
ターゲット&IC50 | Kir7.1:8 μM, Kir1.1:290 nM |
分子量 | 488.53 |
分子式 | 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. 詳細
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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 inhibitor inhibit