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Roxatidine

Basic information Safety Supplier Related

Roxatidine Basic information

Product Name:
Roxatidine
Synonyms:
  • ROXATIDINE
  • n-{3-[3-(1-piperidinylmethyl)phenoxy]propyl}hydroxyacetamide
  • 2-Hydroxy-N-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]acetamide
  • 2-Hydroxy-N-[3-[m-(piperidinomethyl)phenoxy]propyl]acetamide
  • ROXATIDINE ENTERPRISE STANDARD
  • RoxatidineAcetateHclBase
  • ROXATIDINE(SUBJECTTOPATENTFREE)
  • desacetyl-TZU-0460
CAS:
78273-80-0
MF:
C17H26N2O3
MW:
306.4
Product Categories:
  • APIs
Mol File:
78273-80-0.mol
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Roxatidine Chemical Properties

Melting point:
59-60 °C
Boiling point:
524.3±45.0 °C(Predicted)
Density 
1.137±0.06 g/cm3(Predicted)
storage temp. 
-20°
solubility 
Soluble in DMSO (up to 25 mg/ml).
pka
13.34±0.10(Predicted)
form 
oil
color 
Colorless to pale yellow
Stability:
Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 3 months.
CAS DataBase Reference
78273-80-0(CAS DataBase Reference)
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Roxatidine Usage And Synthesis

Description

Roxatidine (78273-80-0) is a novel histamine H2 receptor antagonist.1?Suppresses inflammatory responses via inhibition of NFκB and p38 MAPK activation in LPS-induced RAW 264.7 macrophages.2?Clinically useful agent for prevention and healing of gastric and duodenal ulcers and bleeding.3?Attenuates degradation of extracellular matrix in osteoarthritis models by inactivating the NFkB pathway.4

Uses

Anti-ulcerative.

References

1) Mills and Wood (1989),?The pharmacology of histamine H2-receptor antagonists; Methods Find. Exp. Clin. Pharmacol., 11 Suppl. 1?87 2) Cho?et al. (2011), Roxatidine suppresses inflammatory responses via inhibition of NF-κB and p38 MAPK activation in LPS-induced RAW 264.7 macrophages; J. Cell. Biochem.,?112?3648 3) Imaeda?et al.?(2011),?Effect of lansoprazole versus roxatidine on prevention of bleeding and promotion of ulcer healing after endoscopic submucosal dissection for superficial gastric neoplasia; J. Gastroenterol.,?46?1267 4) Ze?et al. (2017),?Roxatidine Attenuates Degradation of Extracellular Matrix;?Biomed. Pharmacother.,?95?1156

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