Basic information Safety Supplier Related

3,5-DIHYDROXY-4'-BROMOSTILBENE

Basic information Safety Supplier Related

3,5-DIHYDROXY-4'-BROMOSTILBENE Basic information

Product Name:
3,5-DIHYDROXY-4'-BROMOSTILBENE
Synonyms:
  • 3,5-DIHYDROXY-4'-BROMOSTILBENE
  • 5-[(E)-2-(4-Bromophenyl)vinyl]benzene-1,3-diol
  • 4-Bromo-Resveratrol
  • 5-[(1E)-2-(4-Bromophenyl)ethenyl]-1,3-benzenediol
  • 5-[(E)-2-(4-bromophenyl)ethenyl]benzene-1,3-diol
  • 5-[(E)-2-(4-bromophenyl)vinyl]resorcinol
  • 1,3-Benzenediol, 5-[(1E)-2-(4-bromophenyl)ethenyl]-
  • Resveratrol 4-Bromo Impurity
CAS:
1224713-90-9
MF:
C14H11BrO2
MW:
291.14
EINECS:
808-419-8
Mol File:
Mol File
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3,5-DIHYDROXY-4'-BROMOSTILBENE Chemical Properties

storage temp. 
2-8°C
solubility 
DMSO: soluble20mg/mL, clear
form 
powder
color 
white to yellow to brown
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26
WGK Germany 
3
HazardClass 
IRRITANT
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3,5-DIHYDROXY-4'-BROMOSTILBENE Usage And Synthesis

Biological Activity

4'-bromo-resveratrol is a sirt1 and sirt3 inhibitor.sirtuins are protein deacetylases regulating aging processes and many physiological functions. resveratrol activates human sirt1 and inhibits sirt3, and can mimic calorie restriction effects including lifespan extension in lower organisms.

in vitro

sirtuin modulation was studied by using 4’-bromo-resveratrol in a previous study. 4’-bromo-resveratrol inhibited sirt3 with much higher potency than resveratrol, and it also inhibited rather than activated sirt1. crystal structures of human sirt3/peptide complexes of 4’ -bromo-resveratrol identified two binding sites. an internal site caused the potent inhibitory effect. 4’-bromo-resveratrol interfered with nad+ and substrate peptide binding, and it extended its bromo-phenyl group in a unrecognized site pocket. the second binding site for 4’-bromo-resveratrol was found to be located on the surface of sirt3 and connected via two helices to peptide-binding active site loops. in sirt1, this site appeared to comprise a residue that was essential for its activation by small molecules and 4’-bromo-resveratrol therefore constituted a candidate for the long-sought allosteric sirt1 activator binding site [1].

References

[1] nguyen gt, gertz m, steegborn c. crystal structures of sirt3 complexes with 4'-bromo-resveratrol reveal binding sites and inhibition mechanism. chem biol. 2013 nov 21;20(11):1375-85.

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