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sodium 3-(aminosulphonyl)-5-(butylamino)-4-phenoxybenzoate

CAS No.
28434-74-4
Chemical Name:
sodium 3-(aminosulphonyl)-5-(butylamino)-4-phenoxybenzoate
Synonyms
Bumetanide sodium;BuMetanide (sodiuM salt);PKNSNFSHDGKUOA-UHFFFAOYSA-N;Sodium 3-(aminosulfonyl)-5-(butylamino)-4-phenoxybenzoate;sodium 3-(aminosulphonyl)-5-(butylamino)-4-phenoxybenzoate;3-Aminosulfonyl-5-butylamino-4-phenoxybenzoic acid sodium salt
CBNumber:
CB5886861
Molecular Formula:
C17H19N2NaO5S
Molecular Weight:
386.39793
MDL Number:
MOL File:
28434-74-4.mol
Last updated:2026-05-11 16:31:51

sodium 3-(aminosulphonyl)-5-(butylamino)-4-phenoxybenzoate Properties

FDA UNII 1QC8KM52D1

sodium 3-(aminosulphonyl)-5-(butylamino)-4-phenoxybenzoate Chemical Properties, Uses, Production

Uses

Bumetanide sodium, a highly potent loop diuretic, is a Na+-K+-Cl+ cotransporter (NKCC) blocker. Bumetanide sodium is a selective NKCC1 inhibitor, and also inhibits NKCC2, with IC50s of 0.68 and 4.0 μM for hNKCC1A and hNKCC2A, respectively[1][2].

in vivo

Bumetanide sodium (7.6-30.4 mg/kg; i.v.) attenuates the decrease in apparent diffusion coefficients (ADC) ratios for both cortex and striatum (by 40-67%), indicating reduced edema formation[3].
Bumetanide sodium also reduces infarct size[3].
Bumetanide sodium shows different half-lives of 21.4 min, 53.8 min and 137 min following 2 mg/kg, 8 mg/kg and 20 mg/kg intravenous injection, respectively, in rats[4].

References

[1] Lykke K, et al. The search for NKCC1-selective drugs for the treatment of epilepsy: Structure-function relationship of bumetanide and various bumetanide derivatives in inhibiting the human cation-chloride cotransporter NKCC1A. Epilepsy Behav. 2016 Jun;59: DOI:10.1016/j.yebeh.2016.03.021
[2] Ciaran Richardson, et al. Regulation of the NKCC2 ion cotransporter by SPAK-OSR1-dependent and -independent pathways. J Cell Sci. 2011 Mar 1;124(Pt 5):789-800. DOI:10.1242/jcs.077230
[3] Martha E O'Donnell, et al. Bumetanide inhibition of the blood-brain barrier Na-K-Cl cotransporter reduces edema formation in the rat middle cerebral artery occlusion model of stroke. J Cereb Blood Flow Metab. 2004 Sep;24(9):1046-56. DOI:10.1097/01.WCB.0000130867.32663.90
[4] S H Lee, et al. Pharmacokinetics and pharmacodynamics of bumetanide after intravenous and oral administration to rats: absorption from various GI segments. J Pharmacokinet Biopharm. 1994 Feb;22(1):1-17.6 DOI:10.1007/BF02353407

28395-03-1
28434-74-4
Synthesis of sodium 3-(aminosulphonyl)-5-(butylamino)-4-phenoxybenzoate from Bumetanide

sodium 3-(aminosulphonyl)-5-(butylamino)-4-phenoxybenzoate Preparation Products And Raw materials

Raw materials

Preparation Products

sodium 3-(aminosulphonyl)-5-(butylamino)-4-phenoxybenzoate Suppliers

Global Suppliers ( 2)
Supplier Tel Email Country ProdList Advantage
DAYANG CHEM (HANGZHOU) CO.,LTD +86-88938639 +86-17705817739 info@dycnchem.com China 53589 58
TargetMol Chemicals Inc. 13564774135 marketing@targetmol.com United States 19950 58

View Latest Price from sodium 3-(aminosulphonyl)-5-(butylamino)-4-phenoxybenzoate manufacturers

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Bumetanide sodium pictures 2026-05-11 Bumetanide sodium
28434-74-4
10g TargetMol Chemicals Inc.

28434-74-4 (sodium 3-(aminosulphonyl)-5-(butylamino)-4-phenoxybenzoate ) Related Search:

sodium 3-(aminosulphonyl)-5-(butylamino)-4-phenoxybenzoate 3-Aminosulfonyl-5-butylamino-4-phenoxybenzoic acid sodium salt BuMetanide (sodiuM salt) Sodium 3-(aminosulfonyl)-5-(butylamino)-4-phenoxybenzoate PKNSNFSHDGKUOA-UHFFFAOYSA-N Bumetanide sodium 28434-74-4 C17H20N2O5SNa