Sodium 4-Aminosalicylate

Sodium 4-Aminosalicylate is an antibiotic used to treat tuberculosis via NF-κB inhibition and free radical scavenging.

Sodium 4-Aminosalicylate Chemical Structure

Sodium 4-Aminosalicylate Chemical Structure

CAS No. 6018-19-5

Purity & Quality Control

Batch: S407301 DMSO]42 mg/mL]false]Water]42 mg/mL]false]Ethanol]Insoluble]false Purity: 99.74%
99.74

Sodium 4-Aminosalicylate Related Products

Signaling Pathway

Biological Activity

Description Sodium 4-Aminosalicylate is an antibiotic used to treat tuberculosis via NF-κB inhibition and free radical scavenging.
Features 4-Aminosalicylate is considered to be the active moiety of sulfasalazine.
Targets
NF-κB [6]
In vitro
In vitro 4-Aminosalicylate reacts promptly with DPPH, suggesting a potent radical scavenger activity. 4-Aminosalicylate exhibits peroxyl radical scavenging activity generated by the water-soluble 2,2'-azobis-(2-amidinopropane hydrochloride) azoinitiator of peroxyl radicals, as evidenced by the inhibition of cis-parinaric acid fluorescence decay or oxygen consumption. 4-Aminosalicylate rapidly scavenges peroxyl radicals in the aqueous phase, producing a concentration-dependent inhibition period similar to Trolox or cysteine, suggesting an antioxidant activity of chain-breaking type. [1] [14C]4-Aminosalicylate transforms to a number of metabolites, among which we have characterized salicylate and gentisate, in activated mononuclear cells and activated granulocytes. 4-Aminosalicylate (0.65 mM) diminishes the lethal effect on cultured Chinese hamster ovary cells of adding either superoxide radical or hydrogen peroxide. [2] Aminosalicylate (25 mM) stimulates phospholipase D in a time- and concentration-dependent manner via a pathway involving inositol 1,4,5-trisphosphate generation, calcium fluxes, and Gi/Go in cultured mouse peritoneal macrophages. 4-aminosalicylate (20 mM) increases the levels of inositol 1,4,5-trisphosphate by 260% after treatment of macrophages. 4-aminosalicylate (5 mM) potentiates the activation of PLD by protein kinase C in cultured mouse peritoneal macrophages. [3] 4-aminosalicylate (0.1 mM) decreases the LTB4 synthesis in a dose-related fashion in isolated colonic mucosal cells, thus diminishes the LTB4/PGE2 ratio. [4] 4-aminosalicylate (0.1 mg/mL) is preferentially transported in the basolateral (BL) to apical (AP) direction, and the N-acetyl metabolite appeared only in the AP compartment. [5]
In Vivo
In vivo 4-aminosalicylate (7.5 mg/mL, regional perfusions) results in the appearance of N-acetyl-5-aminosalicylic acid in the intestinal lumen in the anesthetized rat. [5]

Chemical Information & Solubility

Molecular Weight 211.15 Formula

C7H7NO3.2H2O.Na

CAS No. 6018-19-5 SDF Download Sodium 4-Aminosalicylate SDF
Smiles C1=CC(=C(C=C1N)O)C(=O)[O-].O.O.[Na+]
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 42 mg/mL ( (198.91 mM) Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : 42 mg/mL

Ethanol : Insoluble


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In vivo
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