Basic information Safety Supplier Related

RU 28362

Basic information Safety Supplier Related

RU 28362 Basic information

Product Name:
RU 28362
Synonyms:
  • 11,17-dihydroxy-6-methyl-17-(1-propynyl)androsta-1,4,6-triene-3-one
  • (11β,17β)-11,17-Dihydroxy-6-methyl-17-(1-propynyl)-androsta-1,4,6-trien-3-one
  • 11β,17β-Dihydroxy-6-methyl-17-(1-propynyl)androsta-1,4,6-trien-3-one
  • Androsta-1,4,6-trien-3-one, 11,17-dihydroxy-6-methyl-17-(1-propynyl)-, (11β,17β)-
CAS:
74915-64-3
MF:
C23H28O3
MW:
352.47
Mol File:
74915-64-3.mol
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RU 28362 Chemical Properties

Boiling point:
533.2±50.0 °C(Predicted)
Density 
1.21±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
DMSO: 33 mg/mL, soluble
form 
solid
pka
12.82±0.70(Predicted)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
1
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RU 28362 Usage And Synthesis

Uses

RU28362 is a potent and selective glucocorticoid agonist. RU28362 increases the Bnip3 mRNA levels in neurons. RU28362 inhibits adrenocorticotrophic hormone (ACTH) and corticosterone secretion[1][2]. RU28362 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

in vivo

RU28362 (150 μg/kg; i.p.) inhibits adrenocorticotrophic hormone (ACTH) and corticosterone secretion and selectively suppressed the stress-induced increase in POMC hnRNA in the anterior pituitary gland[2].

Animal Model:250-350 g, adult male Sprague-Dawley rats[2]
Dosage:150 μg/kg
Administration:I.p.; 60 min before exposure to a 15-min period of restraint stress
Result:Inhibited adrenocorticotrophic hormone (ACTH) and corticosterone secretion and selectively suppressed the stress-induced increase in POMC hnRNA in the anterior pituitary gland.

References

[1] Sandau US, et al. Glucocorticoids exacerbate hypoxia-induced expression of the pro-apoptotic gene Bnip3 in the developing cortex. Neuroscience. 2007 Jan 19;144(2):482-94. DOI:10.1016/j.neuroscience.2006.10.003
[2] Ginsberg AB, et al. Specific and time-dependent effects of glucocorticoid receptor agonist RU28362 on stress-induced pro-opiomelanocortin hnRNA, c-fos mRNA and zif268 mRNA in the pituitary. J Neuroendocrinol. 2006 Feb;18(2):129-38. DOI:10.1111/j.1365-2826.2005.01396.x

RU 28362Supplier

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TargetMol Chemicals Inc.
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