产品
编 号：F118415
分子式：C16H13ClN6O5
分子量：404.76
分子式：C16H13ClN6O5
分子量：404.76
产品类型
规格
价格
是否有货
10mM*1mL in DMSO
询价
询价
5mg
询价
询价
10mg
询价
询价
25mg
询价
询价
50mg
询价
询价
结构图
CAS No: 1315380-70-1
产品详情
生物活性：
VU591 hydrochloride is a potent, selective renal outer medullary potassium channel (ROMK or Kir1.1) inhibitor, with an IC50 of 0.24 μM. VU591 hydrochloride can be used for neurological research with HY-108585A (the equivalent of VU591 hydrochloride).
体内研究：
VU591 hydrochloride (i.c.v.; 1.842 μg) significantly decreases the immobile time in TST.Animal Model:Male ICR mice
Dosage:1.842 μg
Administration:i.c.v.; 1.842 μg
Result:Showed antidepressive effect in the tail suspension test (TST).
体外研究：
VU591 hydrochloride is a selective ROMK inhibitor and a ROMK channel pore blocker. VU591 can bind serum protein and has high metabolic stability.
VU591 hydrochloride is a potent, selective renal outer medullary potassium channel (ROMK or Kir1.1) inhibitor, with an IC50 of 0.24 μM. VU591 hydrochloride can be used for neurological research with HY-108585A (the equivalent of VU591 hydrochloride).
体内研究：
VU591 hydrochloride (i.c.v.; 1.842 μg) significantly decreases the immobile time in TST.Animal Model:Male ICR mice
Dosage:1.842 μg
Administration:i.c.v.; 1.842 μg
Result:Showed antidepressive effect in the tail suspension test (TST).
体外研究：
VU591 hydrochloride is a selective ROMK inhibitor and a ROMK channel pore blocker. VU591 can bind serum protein and has high metabolic stability.
产品资料
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