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Oleuropein - analytical standard,≥98%(HPLC), high purity , CAS No.32619-42-4, Agonist of TAS2R8

  • analytical standard
  • Moligand™
  • ≥98%(HPLC)
Item Number
O101532
Grouped product items
SKUSizeAvailabilityPrice Qty
O101532-20mg
20mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$275.90
View related series
TAS2R8 Agonist

Basic Description

SynonymsOleuropein|32619-42-4|Oleoeuropein|oleoeuropeine|2-(3,4-Dihydroxyphenyl)ethyl (2S-(2alpha,3E,4beta))-3-ethylidene-2-(beta-D-glucopyranosyloxy)-3,4-dihydro-5-(methoxycarbonyl)-2H-pyran-4-acetate|2O4553545L|methyl (4S,5E,6S)-4-[2-[2-(3,4-dihydroxyphenyl)eth
Specifications & PurityMoligand™, analytical standard, ≥98%(HPLC)
Biochemical and Physiological MechanismsOleuropein, found in olive leaves and oil, exerts antioxidant, anti-inflammatory and anti-atherogenic effects through direct inhibition of PPARγ transcriptional activity. Oleuropein induces apoptosis in breast cancer cells via the p53-dependent pathway an
Storage TempStore at 2-8°C,Argon charged
Shipped InWet ice
Gradeanalytical standard, Moligand™
Action TypeAGONIST
Mechanism of actionAgonist of TAS2R8

Associated Targets

HDAC6 Tclin Histone deacetylase 6 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TAS2R8 Tchem Taste receptor type 2 member 8 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ALOX5 Tclin Arachidonate 5-lipoxygenase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name methyl (4S,5E,6S)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate
INCHI InChI=1S/C25H32O13/c1-3-13-14(9-19(29)35-7-6-12-4-5-16(27)17(28)8-12)15(23(33)34-2)11-36-24(13)38-25-22(32)21(31)20(30)18(10-26)37-25/h3-5,8,11,14,18,20-22,24-28,30-32H,6-7,9-10H2,1-2H3/b13-3+/t14-,18+,20+,21-,22+,24-,25-/m0/s1
InChi Key RFWGABANNQMHMZ-ZCHJGGQASA-N
Canonical SMILES CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O
Isomeric SMILES C/C=C/1\[C@@H](C(=CO[C@H]1O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O
WGK Germany 3
PubChem CID 5281544
Molecular Weight 540.51

Certificates

Certificate of Analysis(COA)

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3 results found

Lot NumberCertificate TypeDateItem
J2213946Certificate of AnalysisJul 04, 2024 O101532
G23151137Certificate of AnalysisMay 08, 2023 O101532
E2305083Certificate of AnalysisJul 14, 2022 O101532

Chemical and Physical Properties

SolubilitySoluble in water, acetone, ethanol, pyridine, glacial acetic acid , 5% aq NaOH, dioxane, butano, ethyl acetate, butyl acetate, DMF (50 mg/ml), and methanol. Insoluble in ether, chloroform, petr ether, benzene, and carbon tetrachloride.
SensitivityHygroscopic
Specific Rotation[α]-165° (C=0.5,EtOH)
Melt Point(°C)89 °C

Safety and Hazards(GHS)

WGK Germany 3
Merck Index 6830

Related Documents

Alternative Products

References

1. Bisignano G, Tomaino A, Lo Cascio R, Crisafi G, Uccella N, Saija A.  (1999)  On the in-vitro antimicrobial activity of oleuropein and hydroxytyrosol..  J Pharm Pharmacol,  51  (8): (971-4).  [PMID:10504039]
2. Omar SH.  (2010)  Oleuropein in olive and its pharmacological effects..  Sci Pharm,  78  (2): (133-54).  [PMID:21179340]

Solution Calculators