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O-Desmethyl-N-deschlorobenzoyl Indomethacin

O-Desmethyl-N-deschlorobenzoyl Indomethacin Struktur
50995-53-4
CAS-Nr.
50995-53-4
Englisch Name:
O-Desmethyl-N-deschlorobenzoyl Indomethacin
Synonyma:
Indomethacin Impurity 6;Indomethacin Impurity 6-d3;5-Hydroxy-2-Methyl-1H-indole-3-acetic Acid;O-Desmethyl-N-deschlorobenzoyl Indomethacin;1H-Indole-3-acetic acid, 5-hydroxy-2-methyl-
CBNumber:
CB92508923
Summenformel:
C11H11NO3
Molgewicht:
205.21
MOL-Datei:
50995-53-4.mol

O-Desmethyl-N-deschlorobenzoyl Indomethacin Eigenschaften

Schmelzpunkt:
181-184°C
storage temp. 
Hygroscopic, -20°C Freezer, Under Inert Atmosphere
L?slichkeit
DMSO (Slightly), Methanol (Slightly)
Aggregatzustand
Solid
Farbe
Light Brown

Sicherheit

O-Desmethyl-N-deschlorobenzoyl Indomethacin Chemische Eigenschaften,Einsatz,Produktion Methoden

Chemische Eigenschaften

Light Brown Solid

Verwenden

O-Desmethyl-N-deschlorobenzoyl indomethacin is a metabolite of the non-steroidal anti-inflammatory drug (NSAID) and COX inhibitor indomethacin. It is formed from indomethacin in isolated rabbit hepatocytes. O-Desmethyl-N-deschlorobenzoyl indomethacin (600 μM) decreases the viability of HL-60 leukemia cells when cultured with glucose oxidase. It has also been used in the synthesis of prostaglandin D2 (PGD2) receptor antagonists.

Einzelnachweise

[1] KAZUHIKO TORISU . Development of a prostaglandin D2 receptor antagonist: discovery of a new chemical lead[J]. European Journal of Medicinal Chemistry, 2005, 40 5: Pages 505-519. DOI:10.1016/j.ejmech.2004.11.011.
[2] M A EVANS. Indomethacin Metabolism in Isolated Neonatal and Fetal Rabbit Hepatocytes[J]. Pediatric Research, 1981, 15 11: 1406-1410. DOI:10.1203/00006450-198111000-00003.
[3] ANDREW G.M. MORGAN . An evaluation of myeloperoxidase-mediated bio-activation of NSAIDs in promyelocytic leukemia (HL-60) cells for potential cytotoxic selectivity[J]. Toxicology letters, 2017, 280: Pages 48-56. DOI:10.1016/j.toxlet.2017.07.894.
[4] KAZUHIKO TORISU . Discovery of new chemical leads for prostaglandin D2 receptor antagonists[J]. Bioorganic & Medicinal Chemistry Letters, 2004, 14 17: Pages 4557-4562. DOI:10.1016/j.bmcl.2004.06.006.

O-Desmethyl-N-deschlorobenzoyl Indomethacin Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


O-Desmethyl-N-deschlorobenzoyl Indomethacin Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 25)Lieferanten
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TargetMol Chemicals Inc.
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J & K SCIENTIFIC LTD. 18210857532; 18210857532
jkinfo@jkchemical.com China 96815 76
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shchemsky@sina.com China 32321 50
Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627
info@efebio.com China 9804 58
Shanghai Anmike Chemical Co. Ltd. 微信 17321281695 18019252918
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Shenzhen Polymeri Biochemical Technology Co., Ltd. +86-400-002-6226 +86-13028896684;
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Jinan blalong chemical co. LTD 2710913286@.com
1513643261@qq.com China 14246 58
Energy Chemical 021-58432009 400-005-6266
marketing@energy-chemical.com China 44918 58
TargetMol Chemicals Inc. 4008200310 15002144251
marketing@tsbiochem.com China 24957 58
Shanghai Zerui Biotechnology Co., Ltd. 021-54580889 18321124657
1054713992@qq.com China 10608 58

50995-53-4()Verwandte Suche:


  • O-Desmethyl-N-deschlorobenzoyl Indomethacin
  • 5-Hydroxy-2-Methyl-1H-indole-3-acetic Acid
  • Indomethacin Impurity 6
  • Indomethacin Impurity 6-d3
  • 1H-Indole-3-acetic acid, 5-hydroxy-2-methyl-
  • 50995-53-4
  • Heterocycles
  • Indole Derivatives
  • Intermediates & Fine Chemicals
  • Metabolites & Impurities
  • Pharmaceuticals
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