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Natrium-1-methyl-5-(4-methylbenzoyl)-1H-pyrrol-2-acetat

Tolmetin sodium Struktur
35711-34-3
CAS-Nr.
35711-34-3
Bezeichnung:
Natrium-1-methyl-5-(4-methylbenzoyl)-1H-pyrrol-2-acetat
Englisch Name:
Tolmetin sodium
Synonyma:
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
Summenformel:
C15H14NNaO3
Molgewicht:
279.27
MOL-Datei:
35711-34-3.mol

Natrium-1-methyl-5-(4-methylbenzoyl)-1H-pyrrol-2-acetat Eigenschaften

Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitssch?dlich bei Verschlucken. Akute Toxizit?t oral Kategorie 4 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P270, P301+P312, P330, P501
Sicherheit
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P270 Bei Gebrauch nicht essen, trinken oder rauchen.
P301+P312 BEI VERSCHLUCKEN: Bei Unwohlsein GIFTINFORMATIONSZENTRUM/Arzt/... (geeignete Stelle für medizinische Notfallversorgung vom Hersteller/Lieferanten anzugeben) anrufen.
P330 Mund ausspülen.
P501 Inhalt/Beh?lter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.

Natrium-1-methyl-5-(4-methylbenzoyl)-1H-pyrrol-2-acetat Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

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

Pharmakokinetik

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.

Nebenwirkungen

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.

Stoffwechsel

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.

Natrium-1-methyl-5-(4-methylbenzoyl)-1H-pyrrol-2-acetat Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Natrium-1-methyl-5-(4-methylbenzoyl)-1H-pyrrol-2-acetat Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 48)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
CONIER CHEM AND PHARMA LIMITED
+8618523575427
sales@conier.com China 49374 58
Career Henan Chemica Co
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1026@dideu.com China 22784 58
GIHI CHEMICALS CO.,LIMITED
+8618058761490
info@gihichemicals.com China 49978 58
TargetMol Chemicals Inc.
+8613564774135
zijue.cai@tsbiochem.com United States 19885 58
Hangzhou Yuhao Chemical Technology Co., Ltd 0571-82693216
info@yuhaochemical.com China 9387 52
Beijing HuaMeiHuLiBiological Chemical 010-56205725
waley188@sohu.com China 12335 58
Shanghai Hekang Biotechnology Co., Ltd. 18939837085
youchemicals@gmail.com China 1830 55
Beijing Solarbio Science & Tecnology Co., Ltd. 010-50973186 4009686088
3193328036@qq.com China 18338 68

35711-34-3(Natrium-1-methyl-5-(4-methylbenzoyl)-1H-pyrrol-2-acetat)Verwandte Suche:


  • 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
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