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Rutaecarpine

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Rutaecarpine Basic information

Product Name:
Rutaecarpine
Synonyms:
  • 3-[6-(dimethylcarbamoylamino)hexyl]-1,1-dimethyl-urea
  • 1,1'-Hexamethylenebis[3,3-dimethylurea]
  • N,N''-1,6-Hexanediylbis[N',N'-dimethylurea]
  • Rutaecarpine
  • Ai3-51108
  • Brn 2116874
  • Nsc 255317
  • Urea, 1,1'-hexamethylenebis(3,3-dimethyl-
CAS:
20575-76-2
MF:
C12H26N4O2
MW:
258.36
Mol File:
20575-76-2.mol
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Rutaecarpine Chemical Properties

Boiling point:
512.3±33.0 °C(Predicted)
Density 
1.021±0.06 g/cm3(Predicted)
pka
13.98±0.46(Predicted)
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Rutaecarpine Usage And Synthesis

Biological Functions

Rutaecarpine also inhibits accumulation of macrophages and cholesterol in atherosclerotic lesions and increases cholesterol excretion in other animal models. Additionally, rutaecarpine inhibits hypoxia-induced production of ROS and lactate dehydrogenase and suppresses apoptosis in myocardiocytes. In other cellular models, rutaecarpine decreases corticosterone production, potentially through inhibition of cAMP, 3β-hydroxysteroid dehydrogenase, and 11β-hydroxylase activity.

Biological Activity

Rutaecarpine is an indoloquinazoline alkaloid originally found in Evodia; it exhibits anti-inflammatory, anti-atherosclerotic, cardioprotective, anorexigenic, and anti-obesity activities. Rutaecarpine inhibits COX-2 and also decreases food intake, weight gain, and serum glucose, leptin, and insulin levels in vivo by inhibiting expression of neuropeptide Y and AgRP.

Mechanism of action

Rutaecarpine also inhibits production of ROS, NO, and iNOS, potentially through inhibition of NADPH oxidase. In macrophages, rutaecarpine inhibits arachidonic acid release and decreases production of prostaglandin E2 (PGE2); in other in vitro models, it inhibits collagen-stimulated formation of thromboxane B2 and inosine monophosphate.

RutaecarpineSupplier

Zhengzhou Guancheng Laboratory equipment Sales
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Dideu Industries Group Limited
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