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About This Item
Empirical Formula (Hill Notation):
C8H10O3
CAS Number:
Molecular Weight:
154.16
PubChem Substance ID:
UNSPSC Code:
12352200
Beilstein/REAXYS Number:
2208118
MDL number:
SMILES string
OCCc1ccc(O)c(O)c1
InChI
1S/C8H10O3/c9-4-3-6-1-2-7(10)8(11)5-6/h1-2,5,9-11H,3-4H2
InChI key
JUUBCHWRXWPFFH-UHFFFAOYSA-N
Biochem/physiol Actions
Metabolite of oleuropein. Antioxidant. Inhibits the rate of cancer cell proliferation and induces cancer cell apoptosis.
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signalword
Warning
hcodes
pcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
10 - Combustible liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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Anna Sgarbossa et al.
Chemico-biological interactions, 199(2), 87-95 (2012-06-28)
Phenylpropanoids have several highly significant biological properties in both plants and animals. Four phenylpropanoid glycosides (PPGs), verbascoside (VB), forsythoside B (FB), echinacoside (EC) and campneoside I (CP), were purified and tested for their capability to activate NRF2 and induce phase
Mendel Friedman et al.
Journal of food science, 76(8), M558-M563 (2012-03-16)
The foodborne pathogen Staphylococcus aureus produces the virulent staphylococcal enterotoxin A (SEA), a single chain protein which consists of 233 amino acid residues with a molecular weight of 27078 Da. SEA is a superantigen that is reported to contribute to
J J Reyes et al.
European journal of nutrition, 52(2), 591-599 (2012-05-16)
To investigate the in vitro antiplatelet and anti-inflammatory effects of five alkyl hydroxytyrosol (HT) ether derivatives in human whole blood and compare these effects with those of HT. Blood samples from healthy volunteers were incubated with HT and HT alkyl
