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SUBEROSIN

Basic information Safety Supplier Related

SUBEROSIN Basic information

Product Name:
SUBEROSIN
Synonyms:
  • 6-Isopentenyl-7-methoxy-2H-1-benzopyran-2-one
  • 7-Methoxy-6-(3-methyl-2-butenyl)-2H-1-benzopyran-2-one
  • Cork zanthoxylin
  • 2H-1-Benzopyran-2-one, 7-methoxy-6-(3-methyl-2-buten-1-yl)-
  • 7-methoxy-6-(3-methylbut-2-enyl)chromen-2-one
  • Nuclear factor-κB,Inhibitor,Nuclear factor-kappaB,NF-κB,Suberosin,inhibit
  • Suberosin, 10 mM in DMSO
CAS:
581-31-7
MF:
C15H16O3
MW:
244.29
EINECS:
200-258-5
Product Categories:
  • Coumarins
Mol File:
581-31-7.mol
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SUBEROSIN Chemical Properties

Melting point:
87.5 °C(Solv: methanol (67-56-1))
Boiling point:
158-172 °C(Press: 0.05 Torr)
Density 
1.126±0.06 g/cm3(Predicted)
storage temp. 
4°C, protect from light
solubility 
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form 
Cryst.
color 
White to off-white
LogP
3.870 (est)
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SUBEROSIN Usage And Synthesis

Chemical Properties

Soluble in methanol, ethanol, DMSO and other organic solvents, from white solanaceous, white pair of cotyledons (for the leaves of the Cornusaceae plant (Mulai) wood).

Uses

Suberosin, isolated from Plumbago zeylanica, exhibits anti-inflammatory and anticoagulant activity. Suberosin suppresses PHA-induced PBMC proliferation and arrested cell cycle progression from the G1 transition to the S phase through the modulation of the transcription factors NF-AT and NF-κB[1][2].

Definition

ChEBI: A natural product found in Citropsis articulata.

References

[1] Y-C Chen, et al. Suberosin inhibits proliferation of human peripheral blood mononuclear cells through the modulation of the transcription factors NF-AT and NF-jB. British Journal of Pharmacology (2007) 150, 298-312.
[2] Golfakhrabadi F, et al. Anticoagulant activity of isolated coumarins (suberosin and suberenol) and toxicity evaluation of Ferulago carduchorum in rats. Pharm Biol. 2014 Oct;52(10):1335-40. DOI:10.3109/13880209.2014.892140

SUBEROSINSupplier

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