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CAS RN: 124750-99-8 | Product Number: L0232

Losartan Potassium


Purity: >98.0%(T)(HPLC)
Synonyms:
  • 2-Butyl-4-chloro-1-[[2'-(1H-tetrazol-5-yl)-1,1'-biphenyl-4-yl]methyl]imidazole-5-methanol Potassium Salt
Product Documents:
5G
$179.00
9   7   3  
25G
$538.00
2   1   ≥40 

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Product Number L0232
Purity / Analysis Method >98.0%(T)(HPLC)
Molecular Formula / Molecular Weight C__2__2H__2__2ClKN__6O = 461.01 
Physical State (20 deg.C) Solid
Storage Temperature Room Temperature (Recommended in a cool and dark place, <15°C)
CAS RN 124750-99-8
Reaxys Registry Number 5900704
PubChem Substance ID 125307522
SDBS (AIST Spectral DB) 52825
Merck Index (14) 5583
MDL Number

MFCD02092704

Specifications
Appearance White to Almost white powder to crystal
Purity(HPLC) min. 98.0 area%
Purity(Nonaqueous Titration) min. 98.0 %
Properties (reference)
GHS
Related Laws:
RTECS# NI6755100
Transport Information:
HS Number 2933.99.9701
Application
Losartan Potassium: A Water-Soluble, Reversible and Non-Competitive Antagonist of the AT1 Receptor

Angiotensin II is formed from angiotensin I in a reaction catalyzed by angiotensin converting enzyme (ACE). Angiotensin II is a potent vasoconstrictor, and an important component in the pathophysiology of hypertension. Angiotensin II can activate two different receptors, AT1 and AT2. The most important vasoconstrictor action of angiotensin II are mediate trough AT1 receptors. Losartan [L0378] is a prodrug, and its active metabolite (EXP3174) works as a reversible, non-competitive antagonist of the AT1 receptor.1,2) In addition, neither losartan nor its active metabolite inhibits ACE nor do they bind to or block other hormone receptors or ion channels known to be important in cardiovascular regulation. In clinical, its water-soluble potassium salt (DUP 753) is used for the treatment of hypertension. Recently, AT1 receptor antagonists (blockers), such as losartan, are expected as therapeutics for reducing the aggressiveness and mortality from SARS-CoV-2 virus infections.3) (The product is for research purpose only.)

References


PubMed Literature


TCIMAIL
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