17 Results for "

furosemide

" in MedChemExpress (MCE) Product Catalog:
Products (17)

17 Results for "furosemide" in MCE Product Catalog:

10
10 Publications Verification
Cat. No.: HY-B0135
CAS No.: 54-31-9
Target:  

GABA Receptor

Furosemide is an orally active GABAA receptor antagonist. Furosemide inhibits carbonic anhydrase, the sodium-chloride cotransporter, sodium reabsorption, tubuloglomerular feedback, and GABA-induced chloride flux. Furosemide can be used as a diuretic reagent. Furosemide is applied in the research of hepatic necrosis, sepsis-associated acute kidney injury, hypoalbuminemia-related fluid retention, and congestive heart failure .
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10
10 Publications Verification
Cat. No.: HY-B0135A
CAS No.: 41733-55-5
Target:  

GABA Receptor

Furosemide sodium is an orally active GABAA receptor antagonist. Furosemide sodium inhibits carbonic anhydrase, the sodium-chloride cotransporter, sodium reabsorption, tubuloglomerular feedback, and GABA-induced chloride flux. Furosemide sodium can be used as a diuretic reagent. Furosemide sodium is applied in the research of hepatic necrosis, sepsis-associated acute kidney injury, hypoalbuminemia-related fluid retention, and congestive heart failure .
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Cat. No.: HY-B0135S
CAS No.: 1189482-35-6
Furosemide-d5 is the deuterated-labeled Furosemide (HY-B0135). Furosemide is an orally active GABAA receptor antagonist. Furosemide inhibits carbonic anhydrase, the sodium-chloride cotransporter, sodium reabsorption, tubuloglomerular feedback, and GABA-induced chloride flux. Furosemide can be used as a diuretic reagent. Furosemide is applied in the research of hepatic necrosis, sepsis-associated acute kidney injury, hypoalbuminemia-related fluid retention, and congestive heart failure .
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Cat. No.: HY-B0135R
CAS No.: 54-31-9
Furosemide (Standard) is the analytical standard of Furosemide (HY-B0135). This product is intended for research and analytical applications. Furosemide is an orally active GABAA receptor antagonist. Furosemide inhibits carbonic anhydrase, the sodium-chloride cotransporter, sodium reabsorption, tubuloglomerular feedback, and GABA-induced chloride flux. Furosemide can be used as a diuretic reagent. Furosemide is applied in the research of hepatic necrosis, sepsis-associated acute kidney injury, hypoalbuminemia-related fluid retention, and congestive heart failure .
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Cat. No.: HY-W278566
CAS No.: 3086-91-7
Target:  

Drug Metabolite

Saluamine is an important N-dealkylated metabolite of Furosemide (HY-B0135) that is produced by microbial transformation and bile metabolism. Saluamine is a contaminant .
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Cat. No.: HY-B0135AR
CAS No.: 41733-55-5
Furosemide (sodium) (Standard) is the analytical standard of Furosemide (sodium). This product is intended for research and analytical applications. Furosemide sodium is a potent and orally active inhibitor of Na+/K+/2Cl- (NKCC) cotransporter, NKCC1 and NKCC2 [1]. Furosemide sodium is also a GABAA receptors antagonist and displays 100-fold selectivity for α6-containing receptors than α1-containing receptors. Furosemide sodium acts as a loop diuretic and used for the study of congestive heart failure, hypertension and edema .
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Cat. No.: HY-167082
CAS No.: 124788-46-1
AY 31906 is an orally active pyrimidine sulfonamide diuretic. AY 31906 exhibits potent diuretic and natriuretic activities in rats and dogs, along with relatively potassium-sparing properties. AY 31906 exhibits superior activity to Furosemide (HY-B0135). AY-31906 also has antihypertensive effects and can be used in the research of cardiovascular diseases .
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Cat. No.: HY-W344337
CAS No.: 72967-59-0
Synonyms: furosemide acyl-β-D-glucuronide
Target:  

Drug Metabolite

Research Areas:  

Cardiovascular Disease Cancer

Furosemide AG (Furosemide acyl-β-D-glucuronide) is an acyl-β-D-glucuronide metabolite of Furosemide (HY-B0135). Furosemide AG can be used in the research of neutropenia and thrombocytopenia .
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Cat. No.: HY-W278566R
CAS No.: 3086-91-7
Saluamine (Standard) is the analytical standard of Saluamine (HY-W278566). This product is intended for research and analytical applications. Saluamine is an important N-dealkylated metabolite of Furosemide (HY-B0135) that is produced by microbial transformation and bile metabolism .
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Cat. No.: HY-B0135B
CAS No.: 42461-27-8
Target:  

GABA Receptor

Furosemide hydrochloride is an orally active GABAA receptor antagonist. Furosemide hydrochloride inhibits carbonic anhydrase, the sodium-chloride cotransporter, sodium reabsorption, tubuloglomerular feedback, and GABA-induced chloride flux. Furosemide hydrochloride can be used as a diuretic reagent. Furosemide hydrochloride is applied in the research of hepatic necrosis, sepsis-associated acute kidney injury, hypoalbuminemia-related fluid retention, and congestive heart failure .
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Cat. No.: HY-W012510
CAS No.: 50-84-0
Target:  

Drug Intermediate

Research Areas:  

Others

Furosemide impurity 6 is an impurity of Furosemide.
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Cat. No.: HY-W140611
CAS No.: 4793-38-8
Target:  

Drug Intermediate

Research Areas:  

Others

Furosemide impurity 7 is an impurity of Furosemide.
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Cat. No.: HY-Z8151
CAS No.: 5046-19-5
Target:  

Drug Intermediate

Research Areas:  

Others

Furosemide impurity 3 is an impurity of Furosemide.
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Cat. No.: HY-W208353
CAS No.: 4818-59-1
Synonyms: Isofurosemide
Target:  

Drug Intermediate

Research Areas:  

Others

Furosemide impurity 1 (Isofurosemide) is an impurity of Furosemide.
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Cat. No.: HY-118233
CAS No.: 114417-20-8
Synonyms: M 17055
Target:  

Chloride Channel

Research Areas:  

Neurological Disease

Alilusem potassium is a diuretic. In anesthetized dogs undergoing water diuresis, Alilusem potassium effectively decreased free water clearance and increased Na+ and Cl- levels in excreted urine. When combined with Furosemide (HY-B0135) or Hydrochlorothiazid, Alilusem potassium further inhibited free water clearance. Alilusem potassium inhibited the lumen-positive transepithelial voltage and lumen-to-cistern Cl- flux in isolated rabbit cortical thick ascending limbs of Henle .
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Cat. No.: HY-187790
CAS No.: 82924-03-6
Synonyms: CGS 13945
Pentopril (CGS 13945) is an orally active angiotensin-converting enzyme (ACE) inhibitor. Pentopril is hydrolyzed by esterases in vivo to form an active ACE inhibitor metabolite. Pentopril can be used in the research of hypertension and congestive heart failure .
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Cat. No.: HY-P87092
Synonyms: Electroneutral potassium chloride cotransporter 2 antibody; Electroneutral potassium-chloride cotransporter 2 antibody; Erythroid K Cl cotransporter 2 antibody; furosemide sensitive K Cl cotransporter antibody; hKCC2 antibody; K-Cl cotransporter 2 antibody; KCC 2 antibody; KCC2 antibody; KIAA1176 antibody; Neuronal K Cl cotransporter antibody; Electroneutral potassium chloride cotransporter 2 antibody; Electroneutral potassium-chloride cotransporter 2 antibody; Erythroid K Cl cotransporter 2 antibody; furosemide sensitive K Cl cotransporter antibody; hKCC2 antibody; K-Cl cotransporter 2 antibody; KCC 2 antibody; KCC2 antibody; KIAA1176 antibody; Neuronal K Cl cotransporter antibody; Neuronal K-Cl cotransporter antibody; Potassium Chloride Cotransporter antibody; Potassium chloride transporter 5 antibody; rKCC2 antibody; S12A5 antibody; S12A5_HUMAN antibody; SLC12A5 antibody; Solute carrier family 12 (potassium chloride transporter) member 5 antibody; Solute carrier family 12 member 5 antibody;

Host:  

Mouse

Application:  

IHC-F, WB

Reactivity:  

Mouse, Rat

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