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Tolmetin sodium

Tolmetin sodium Structure
CAS No.
35711-34-3
Chemical Name:
Tolmetin sodium
Synonyms
TOLECTIN;Sodium tolmetin;TOLMETIN SODIUM;Tolmetin Sodium Salt;Tolmetin sodium USP/EP/BP;sodium 1-methyl-5-(4-methylbenzoyl)-1H-pyrrole-2-acetate;sodium:2-[1-methyl-5-(4-methylbenzoyl)pyrrol-2-yl]acetate;1-Methyl-5-p-toluoyl-1H-pyrrole-2-acetic acid sodium salt;1-Methyl-5-(p-toluoyl)-1H-pyrrole-2-acetic acid sodium salt;SodiuM 2-(1-Methyl-5-(4-Methylbenzoyl)-1H-pyrrol-2-yl)acetate
CBNumber:
CB6397353
Molecular Formula:
C15H14NNaO3
Molecular Weight:
279.27
MOL File:
35711-34-3.mol
Modify Date:
2023/5/4 17:34:38

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P330-P501

Tolmetin sodium Chemical Properties,Uses,Production

Uses

Tolmetin Sodium is a non-steroidal anti-inflammatory drug.

Pharmacokinetics

Tolmetin sodium is rapidly and almost completely absorbed on oral administration, with peak plasma levels being attained within the first hour of administration. It has a relatively short plasma half-life of approximately 1 hour because of extensive first-pass metabolism, involving hydroxylation of the p-methyl group to the primary alcohol, which is subsequently oxidized to the dicarboxylic acid.

Clinical Use

Tolmetin is synthesized straightforwardly from 1-methylpyrrole. It was introduced in the United States in 1976 and like other NSAIDs, inhibits prostaglandin biosynthesis. Tolmetin, however, also inhibits polymorph migration and decreases capillary permeability. Its anti-inflammatory activity, as measured in the carrageenan-induced rat paw edema and cotton pellet granuloma assays, is intermediate between those of phenylbutazone and indomethacin.

Side effects

The most frequently adverse reactions are those involving the GI tract (e.g., abdominal pain, discomfort, and nausea) but appear to be less than those observed with aspirin. The CNS effects (e.g., dizziness and drowsiness) also are observed. Few cases of overdosage have been reported, but in such cases, recommended treatment includes elimination of the drug from the GI tract by emesis or gastric lavage and elimination of the acidic drug from the circulatory system by enhancing alkalinization of the urine with sodium bicarbonate.

Metabolism

This metabolite is inactive in standard in vivo anti-inflammatory assays. The free acid (pKa = 3.5) is highly bound to plasma proteins (99%), and excretion of tolmetin and its metabolites occurs primarily in the urine.Approximately 15 to 20% of an administered dose is excreted unchanged and 10% as the glucuronide conjugate of the parent drug. Conjugates of the dicarboxylic acid metabolite account for the majority of the remaining administered drug.

Tolmetin sodium Preparation Products And Raw materials

Tolmetin sodium Suppliers

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CONIER CHEM AND PHARMA LIMITED +8618523575427 China 49391 58 Inquiry
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Wuhan Xinyang Ruihe Chemical Technology Co., Ltd. 13720181483 13720181483 China 4545 58 Inquiry
Hubei widely chemical technology Co., Ltd. 027-83989310 18627915365 China 1295 58 Inquiry
TOLMETIN SODIUM sodium 1-methyl-5-(4-methylbenzoyl)-1H-pyrrole-2-acetate TOLECTIN 1-Methyl-5-(p-toluoyl)-1H-pyrrole-2-acetic acid sodium salt 1-Methyl-5-p-toluoyl-1H-pyrrole-2-acetic acid sodium salt Sodium tolmetin SodiuM 2-(1-Methyl-5-(4-Methylbenzoyl)-1H-pyrrol-2-yl)acetate tolmetin sodium:sodium 1-methyl-5-(4-methylbenzoyl)-1h-pyrrole-2-acetate sodium:2-[1-methyl-5-(4-methylbenzoyl)pyrrol-2-yl]acetate Tolmetin Sodium Salt Tolmetin sodium USP/EP/BP 35711-34-3