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LCZ696 936623-90-4

简要描述:LCZ696 936623-90-4
LCZ696, consisting of valsartan and sacubitril in 1:1 molar ratio, is an orally bioavailable, dual-acting angiotensin receptor-neprilysin inhibitor (ARNi) for hypertension and heart

  • 产品型号:abs47027992
  • 厂商性质:生产厂家
  • 更新时间:2026-01-12
  • 访  问  量:595

详细介绍

品牌absinCAS936623-90-4
分子式C24H29N5O3.C24H29NO5.5/2H2O.3Na纯度≥98%
分子量915.98货号abs47027992
规格5mg供货周期现货
主要用途is an orally bioavailable应用领域化工,生物产业,农林牧渔,制药/生物制药,综合

LCZ696 936623-90-4

产品描述
描述

LCZ696, consisting of valsartan and sacubitril in 1:1 molar ratio, is an orally bioavailable, dual-acting angiotensin receptor-neprilysin inhibitor (ARNi) for hypertension and heart failure. Phase 3.

纯度
≥98%
储存/保存方法
Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
基本信息
别名
奥帕曲拉;缬sha坦;Sacubitril;valsartan
外观
white powder
可溶性/溶解性
DMSO : 28 mg/mL (30.6 mM)
Ethanol : 9 mg/mL (9.82 mM), warmed
Water : 92 mg/mL (100.4 mM)
生物活性
靶点
RAAS
In vitro(体外研究)
LCZ696 is a single molecule that is comprised of molecular moieties of valsartan, an ARB, and AHU377, a neprilysin inhibitor (1:1 ratio).
In vivo(体内研究)
LCZ696 exerts a blood pressure lowering effect. Blood pressure reduction by LCZ696 is associated with a significant increase in urinary sodium excretion and sympathetic activity suppression. LCZ696 significantly ameliorates cardiac hypertrophy and inflammation, coronary arterial remodeling, and vascular endothelial dysfunction in high-salt loaded SHRcp compared with valsartan. The neprilysin inhibitor component of LCZ696, LBQ657, inhibits hypertrophy but not fibrosis. The angiotensin receptor blocker component of LCZ696, valsartan inhibits both hypertrophy and fibrosis. Dual valsartan+LBQ augment the inhibitory effects of valsartan and the highest doses completely abrogate angiotensin II-mediated effects. Pre-treatment with LCZ696 reduces the ischemic area. The decrease in cerebral blood flow in the peripheral region of the ischemic area is significantly attenuated by pre-treatment with LCZ696. LCZ696 pre-treatment significantly decreases the increase of superoxide anion production in the cortex on the ischemic side.
研究领域
研究领域
Cardiovascular
CancerCancer Metabolism
CancerTumor biomarkers
NeuroscienceEndocrine system
Drug DiscoverySmall Molecule DrugLead Compound Discovery
LCZ696 936623-90-4温馨提示:本产品仅作科研实验使用,不支持临床等研究

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