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CAS:2123483-49-6|WNK-IN-11-d3

  • 产品货号:DT2025061197
  • 发布时间:2025-06-04
  • 产品CAS :2123483-49-6
  • 产品规格:mg(更多包装需求请咨询客服)
  • 产品纯度:≥98%
  • 产品货期:现货下单后48小时内发货,定制产品4-8周。
  • 运输条件:顺丰常规运输
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货号:DT2025061197
CAS:2123483-49-6
规格:mg(更多包装需求请咨询客服)
纯度:≥98%
生产商:试剂家

生物活性:WNK-IN-11-d3 is an orally active, selective and potent With-No-Lysine (WNK) kinase inhibitor. WNK-IN-11-d3 is effective at regulating cardiovascular homeostasis[1].
IC50 & Target:WNK[1]
体内研究(In Vivo)
WNK-IN-11 D3 (1.5 mg/kg; p.o.) shows an improved rat PK profile, including lower clearance, improvement in absolute oral exposure, and a 2-fold improvement in oral bioavailability[1].
WNK-IN-11 D3 (30 mg/kg; p.o.) shows significant reductions in systolic blood pressure (SBP) vs untreated mice[1].
WNK-IN-11 D3 (0~100 mg/kg; p.o.) induces dose dependent diuresis, natriuresis, and kaliuresis, from 10 to 100 mg/kg[1].
WNK-IN-11 D3 shows trends toward reduction of blood pressure, stroke volume, and total peripheral resistance, while increasing heart rate. WNK-IN-11 D3 shows efficacy in rodent models of hypertension and volume overload[1].
试剂家 has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Model:
Sprague−Dawley rats[1]
Dosage:
1.5 mg/kg
Administration:
P.o.
Result:
Showed an improved rat PK profile, including lower clearance, improvement in absolute oral exposure, and a 2-fold improvement in oral bioavailability.
Animal Model:
FVB mice[1]
Dosage:
30 mg/kg
Administration:
P.o.
Result:
Showed significant reductions in systolic blood pressure (SBP) vs untreated mice.
Animal Model:
FVB mice[1]
Dosage:
0~100 mg/kg
Administration:
P.o.
Result:
Induced dose dependent diuresis, natriuresis, and kaliuresis, from 10 to 100 mg/kg.
分子量:465.41
Formula:C21H18D3Cl2N5OS
CAS 号:2123483-49-6
非标记 CAS:2123489-30-3
性状:固体
颜色:Off-white to light yellow
运输条件:Room temperature in continental US; may vary elsewhere.
储存方式:Powder:-20°C:3 years,4°C:2 years
In solvent:-80°C:6 months,-20°C:1 month

常见基团 common groups
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