Cat. No.: HY-N8630

Oleacein

Name: Oleacein
Brand: MedChemExpress
SKU: HY-N8630
Price: 220.00 USD
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Oleacein is an orally active Oleuropein derivative found in J. grandiflorum, possessing NLRP3/ACE inhibitory, anti-inflammatory, antioxidant, and free radical scavenging activities. Oleacein reduces oxidative stress, pro-inflammatory factor release, leukocyte infiltration, and blood-brain barrier disruption by inhibiting the inflammasome, NF-κB, and AKT/ERK pathways, while upregulating Nrf-2/HO-1 and IL-10, and induces endothelial cell apoptosis. Oleacein can bind TrkB to activate BDNF/TrkB signaling to alleviate neuroinflammation, and modulates metabolic pathways such as PPARγ, adiponectin, SREBP-1, and Glut-4, affecting lipid accumulation and adipocyte function. Oleacein can be used in research related to autoimmune diseases, metabolic diseases, cancer, and depression.

For research use only. We do not sell to patients.

Purity : 90.0%
CAS No.: 149183-75-5
Formula: C₁₇H₂₀O₆
Molecular Weight:320.34

Storage:

Pure form -20°C, 3 years ; In solvent -80°C, 6 months , -20°C, 1 month

Oleacein Chemical Structure

CAS No.: 149183-75-5

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Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity
- Description
- In Vitro
- In Vivo
Chemical Information
Purity & Documentation
References
Calculators
Help & FAQs
Classifications
Bioz

Biological Activity

Description

All NOD-like Receptor (NLR) Isoforms :

All NF-κB Isoforms :

All Interleukin Related Isoforms :

All ERK Isoforms :

All Akt Isoforms :

In Vitro

Adaptive ImmunityImmune Tolerance & ImmunosuppressionAnti-cancerLipid MetabolismCell Cycle RegulationApoptosisInnate ImmunityCytokines & ChemokinesInflammasomeLipid Inflammatory MediatorsOxidative StressLocal Vascular RegulationOthers

Adaptive Immunity

Immune Tolerance & Immunosuppression

Oleacein (10-20 µM; 72 h) inhibits antigen-specific proliferation in splenocytes from MOG35-55-immunized EAE mice in a dose-dependent manner^[1].

Anti-cancer

Oleacein (72 h) reduces BAEC viability with an IC₅₀ of 189 µM, whereas HGF-1 and HeLa cells show lower sensitivity^[5].
Oleacein (1-50 µM; 24 hours) increases BDNF mRNA expression in SH-SY5Y cells in a dose-dependent manner; co-application with ANA-12 (HY-12497), LY294002 (HY-10108), or PD98059 (HY-12028) blocks this increase^[6].

Anti-cancer

Lipid Metabolism

Cell Cycle Regulation

Oleacein (10 µM; 24 hours) upregulates cell cycle-related and BDNF-co-expressed neurogenesis genes in SH-SY5Y cells while downregulating inflammatory response genes^[6].

Apoptosis

Oleacein (10-20 µM; 24 h) prevents t-BOOH-induced apoptosis in RGC-5 cells^[1].
Oleacein (overnight) induces early apoptosis in BAEC^[5].
Oleacein (30 min) activates caspase 3/7 in BAEC^[5].
Oleacein (100-200 µM; overnight) induces PARP-1 cleavage in BAEC^[5].

Cell Cycle Regulation

Apoptosis

Oleacein (overnight) induces subG1 DNA fragmentation and reduces the G0/G1 phase BAEC population, indicating that apoptosis occurs^[5].

Innate Immunity

Oleacein (1-25 µM; 24 h) does not affect the viability of BV2 microglia^[1].
Oleacein (20 µM; 24 h) does not alter the phagocytic activity of LPS-stimulated BV2 microglia^[1].

Innate Immunity

Adaptive Immunity

Anti-cancer

Lipid Metabolism

Oleacein (10 µM; 24 h) reverses LPS-induced inflammatory transcriptomic changes in SH-SY5Y cells, including the upregulation of PI3K/Akt/MAPK-related genes and the downregulation of the NF-κB/TNF/IL17 pathway^[6].

Innate Immunity

Cytokines & Chemokines

Inflammasome

Oleacein (1-20 µM; 24 h) reduces LPS-induced TNFα and IL-1β secretion in BV2 microglial cells^[1].

Innate Immunity

Inflammasome

Lipid Inflammatory Mediators

Oxidative Stress

Oleacein (1-20 µM; preincubation for 30 min) inhibits LPS (HY-D1056)-induced phosphorylation of p65-NFκB and expression of NLRP3, iNOS, and COX-2 in BV2 microglial cells^[1].

Innate Immunity

Oxidative Stress

Oleacein (1-20 µM; 24 h) inhibits LPS-induced intracellular ROS accumulation in BV2 microglial cells^[1].
Oleacein (1-50 μM; 40 min) inhibits f-MLP (HY-P0224) and PMA (HY-18739)-induced ROS production in human PMNs, with IC₅₀ values of 1.8 μM and 1.5 μM, respectively^[2].
Oleacein (1-50 μM; 15 min preincubation) inhibits MPO release from human PMNs with an IC₅₀ of 8.8 μM^[2].

Lipid Metabolism

Oleacein (10-100 µM; 8 days) inhibits lipid droplet accumulation in 3T3-L1 adipocytes, downregulates FAS and PPARγ, and simultaneously upregulates Adiponectin^[3].

Local Vascular Regulation

Oleacein (100-200 µM; 7 hours) inhibits wound healing migration of BAEC^[5].
Oleacein (100 µM) reduces the invasion of BAECs through Matrigel^[5].
Oleacein (100-200 µM) reduces MMP-2 release/activity in BAEC conditioned medium^[5].
Oleacein (100 µM; 5 hours) completely prevents tube formation by BAECs on Matrigel^[5].
Oleacein (100 µM) does not disrupt preformed BAEC tubular networks^[5].
Oleacein (25-100 µM; 2 hours) impairs FBS-induced phosphorylation of AKT and ERK1/2 in BAEC^[5].

Oxidative Stress

Oleacein (20 µM; 24 h) reduces H₂O₂- and t-BOOH-induced superoxide anion production in RGC-5 cells^[1].
Oleacein (1-50 μM; 45 min) scavenges superoxide anions in the cell-free xanthine/xanthine oxidase assay, with an IC₅₀ of 17.1 μM^[2].
Oleacein (1-50 μM; 40 min) has an IC₅₀ of 50.6 μM in the cell-free HRPO/luminol assay^[2].
Oleacein (1-50 μM; 5 min) scavenges HOCl in a cell-free TNB assay with an IC₅₀ of 1.5 μM^[2].
Oleacein (5-50 μM; 60 min) scavenges nitric oxide in the cell-free DAF-2 assay with an IC₅₀ of 3.3 μM^[2].
Oleacein (1-50 μM; 20 min) inhibits ONOO^--activated luminol chemiluminescence in a cell-free assay, with an IC₅₀ of 3.7 μM^[2].

Others

Oleacein binds immobilized human TrkB ECD with 411.8 RU and a K_d of 0.26, exhibiting a higher and more stable binding affinity than 7,8-DHF^[6].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay^[1]

Cell Line:

BV2 microglia
Concentration:

0.5, 1, 10 and 25 µM
Incubation Time:

24 h
Result:

No cytotoxic effect on BV2 cells was observed after 24 h at 1-24 µM.

Western Blot Analysis^[1]

Cell Line:

BV2 microglia
Concentration:

1, 10, 20 µM
Incubation Time:

Pre-incubation for 30 min; 4 h; 24 h (LPS stimulation)
Result:

LPS-induced phosphorylation of p65-NFκB and overexpression of NLRP3 were up-regulated after 4 h, and Oleacein reduced this upregulation.
Cell preincubation with Oleacein also led to a dose-dependent inhibition of LPS-induced iNOS and COX-2 production, whereas Oleacein did not affect their basal expression per se.

ELISA Assay^[1]

Cell Line:

BV2 microglia
Concentration:

1, 10, 20 µM
Incubation Time:

24 h
Result:

The presence of Oleacein also reduced the ability of LPS to induce TNFα and mature IL-1β secretion in a dose-dependent manner.

Apoptosis Analysis^[1]

Cell Line:

RGC-5 retinal ganglion cells
Concentration:

10, 20 µM
Incubation Time:

24 h
Result:

Apoptotic cells increased to 48.4% from 2.7% without stimulus at 24 h.
After coincubation with Oleacein, t-BOOH-induced apoptotic cells decreased to 11.5% at 10 µM and 5.2% at 20 µM.

Cell Migration Assay ^[5]

Cell Line:

BAEC
Concentration:

100, 200 µM
Incubation Time:

7 h
Result:

The results showed that OLCN inhibited EC migration significantly after 7 h of incubation at both 100 and 200 µM, and this effect was observed in a dose-response manner.
No sign of cell damage was observed at higher doses of the compounds during the assay.

Western Blot Analysis^[5]

Cell Line:

BAEC
Concentration:

25, 50, 100 µM
Incubation Time:

2 h
Result:

However, in presence of OLCN and OLCT, the phosphorylation of these signaling proteins was strongly decreased in BAEC at 25, 50, and 100 µM, pointing to an impairment of the activation of the studied signaling pathways by the compounds.

Real Time qPCR^[6]

Cell Line:

Human neuroblastoma SH-SY5Y cells
Concentration:

1, 5, 10, 20, 30, 40 and 50 µM
Incubation Time:

24 h (OC incubation); 24 h (inhibitor co-incubation)
Result:

A dose-dependent increase in BDNF expression in SH-SY5Y cells resulted from OC, starting from 10 µM.
Co-administration of OC with ANA-12, LY294002, or PD98059 inhibited the OC-induced upregulation of BDNF expression.

In Vivo

Adaptive ImmunityCytokines & ChemokinesImmune Tolerance & ImmunosuppressionOxidative StressLocal Vascular RegulationInnate ImmunityInflammasomeLipid Inflammatory MediatorsLipid MetabolismCarbohydrate MetabolismOthers

Adaptive Immunity

Cytokines & Chemokines

Immune Tolerance & Immunosuppression

Oxidative Stress

Local Vascular Regulation

Oleacein (10 mg/kg; intraperitoneal injection; daily; from the day of immunization to the end of the experiment (approximately 22-24 days after immunization)) attenuates the severity of EAE and CNS inflammation, demyelination, BBB disruption, and oxidative damage in MOG_35-55-immunized female C57BL/J6 mice^[1].

Innate Immunity

Adaptive Immunity

Cytokines & Chemokines

Oleacein (10 mg/kg; oral; daily; for 10 consecutive days) attenuates LPS (HY-D1056)-induced depressive-like behaviors and hippocampal neuroinflammation in ICR mice^[6].

Innate Immunity

Adaptive Immunity

Inflammasome

Oxidative Stress

Oleacein (0.01% w/w, equivalent to 100 mg/kg; oral administration via fresh feed; daily; 24 weeks) ameliorates pristane (HY-N7819)-induced lupus nephritis in BALB/c mice by reducing renal histopathological injury and immune complex deposition and by modulating inflammatory, oxidative, and epigenetic pathways^[8].

Innate Immunity

Cytokines & Chemokines

Lipid Inflammatory Mediators

Oxidative Stress

Immune Tolerance & Immunosuppression

Oleacein (0.025% w/w; oral; ad libitum; from 6 weeks before collagen-induced arthritis induction until the end of the experiment) prevents collagen-induced arthritis in DBA-1/J mice, reducing arthritis severity, joint histopathology, and inflammatory and oxidative biomarkers^[7].

Lipid Metabolism

Carbohydrate Metabolism

Innate Immunity

Oleacein (20 mg/kg; oral (gavage); once daily; for 5 weeks) prevents high-fat diet-induced adipocyte enlargement and adipose tissue inflammatory infiltration, while modulating markers of adipogenesis and insulin sensitivity^[3].
Oleacein (20 mg/kg; oral (gavage); once daily; 8 weeks) reduces adipocyte size and inflammatory infiltration, decreases PPARγ and SREBP-1, increases Adiponectin, and restores muscle Glut-4^[3] in already obese HFD-fed mice.

Lipid Metabolism

Oxidative Stress

Carbohydrate Metabolism

Local Vascular Regulation

Oleacein (50 mg/kg; oral; five days per week; 10 weeks) prevents diet-induced dyslipidemia and hepatic steatosis in ApoE-KO mice, reduces serum cholesterol, LDL, and TAGs, decreases hepatic TAG accumulation, and modulates lipid metabolism and antioxidant pathways^[4].

Others

Oleacein (10 mg/kg; oral; single dose) increases BDNF expression in the brain of Bdnf-IRES-AkaLuc mice^[6].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model:

C57BL/J6 (female, 8-10 weeks old)^[1]
Dosage:

10 mg/kg
Administration:

i.p.; daily; from immunization day until the end of the experiment (~22-24 days postimmunization)
Result:

Delayed EAE onset and reduced severity.
Untreated EAE mice began showing symptoms around day 10; first neurological symptoms (score 1) were observed at day 9 with mean day of onset 11.6.
OLE-treated EAE mice showed no disease signs at that time and only minimal pathological abnormalities.
On day 24, untreated EAE mice had an average disease score of 2.5, whereas in OLE-treated EAE mice 9/11 showed inability to curl the distal end of the tail (score 0.5) and 2/11 showed tail atony (score 1).
Reduced serum MOG35-55-specific IgG1 by 64% in EAE mice.
Histological evaluation showed reduced leukocyte infiltration in optic nerve, spinal cord, and cerebellum, and decreased demyelination in optic nerve of OLE-treated EAE mice.
Prevented EAE-induced BBB disruption, shown by reduced brain IgG extravasation, and did not modify BBB integrity in control animals.
In spinal cord, OLE prevented EAE-induced increases in TNFα, MCP-1, GM-CSF, IL-13, and IL-33, and increased IL-10.
In serum, OLE prevented EAE-induced increases in TNFα and GM-CSF; the serum active IL-1β increase was lower (~80%) in OLE-treated EAE mice.
Inhibited EAE-induced superoxide anion production in cerebellum, spinal cord, and optic nerve; prevented increases in MDA and AOPP in serum and spinal cord; ameliorated the EAE-induced drop in serum FRAP, although it did not normalize it; and increased serum Sestrin-3 levels in EAE mice.

Animal Model:

C57BL/6JOlaHsd (male; 5-week-old at start)^[3]
Dosage:

20 mg/kg
Administration:

p.o. (oral gavage); once daily; for 5 weeks
Result:

After 5 weeks, oleacein prevented the increase in adipocyte size in HFD-fed mice compared with HFD-only mice and reduced inflammatory infiltration of macrophages and lymphocytes, as assessed by CD68 and CD45 immunohistochemistry.
FSP1 mRNA expression was about 50% lower in mice given HFD plus this compound than in HFD mice.
In abdominal adipose tissue, FAS and SREBP-1 protein levels were reduced and Adiponectin levels were increased in mice given HFD plus this compound compared with HFD mice; PPARγ was unchanged.
Glut-4 immunostaining was higher in abdominal fat and muscle tissues of mice given HFD plus this compound than in HFD mice.

Animal Model:

C57BL/6JOlaHsd (male; from initial HFD group after first 5-week period)^[3]
Dosage:

20 mg/kg
Administration:

p.o. (oral gavage); once daily; for an additional 8 weeks
Result:

After the additional 8 weeks, this compound reduced PPARγ and SREBP-1 protein expression and increased Adiponectin production compared with HFD-only mice; FAS expression was unchanged.
Adipocyte cell size and inflammatory infiltrate results were similar to the first set, with lower adipocyte size and reduced inflammatory infiltration in mice given HFD plus this compound.
Glut-4 immunoreactivity was increased in fat and muscle; the increase in muscle paralleled enhanced Glut-4 protein expression in muscle plasma membranes by Western blot.

Animal Model:

ApoE-knockout (ApoE-KO; C57BL/6J background; male; 11 weeks old at study start)^[4]
Dosage:

50 mg/kg
Administration:

oral; five days per week; 10 weeks
Result:

In ApoE-KO + ATD + OLEA mice, food intake was 20.39 g/week, beverage intake was 43.88 mL/week, and total energy intake was 91.74 kcal/week.
Did not reduce body weight in ApoE-KO + ATD mice.
Reduced serum total cholesterol and c-LDL, did not affect c-HDL, reduced serum TAGs toward WT + STD levels, and reduced the TAGs/HDL ratio to levels comparable to WT + STD.
Liver TAG content was reduced by more than 50% compared with both WT + ATD and ApoE-KO + ATD groups, although it remained approximately double the WT + STD level.
Liver weight was 1379.8 mg; serum ALT was 36.13 U/L; serum AST was 62.17 U/L; ALT and AST trended lower than in ApoE-KO + ATD, with no signs of hepatic toxicity.
Liver histology showed less intense Oil Red-O staining and fewer, smaller fat vacuoles; aorta histology showed less endothelium denudation and reduced intima/media disorganization and thickening.
Hepatic SOD1 and SOD2 mRNA expression were normalized to WT + STD levels, and serum SOD activity was increased.
Hepatic SCD1, FABP1, and CPT1 were downregulated; ACADL was modestly increased; MMP9 expression showed a trend toward reduction; most other lipid-metabolism genes did not differ.
GTT and ITT showed no differences in glucose handling, though the OLEA-supplemented group showed a trend toward improved glycaemic control at week 10.

Animal Model:

Bdnf-IRES-AkaLuc (C57BL/6J background)^[6]
Dosage:

10 mg/kg body weight
Administration:

p.o.; single dose
Result:

A single oral dose of this compound (10 mg/kg) significantly augmented BDNF protein expression in the mouse brain compared with the saline baseline (Fig. 1C, D); n = 4 per group.

Animal Model:

ICR (male, 8 weeks old)^[6]
Dosage:

10 mg/kg body weight
Administration:

p.o.; daily; 10 consecutive days
Result:

Tail suspension test: immobility time 60.21 s in the this compound group.
Hippocampal mRNA expression: Tnf 0.74, Il6 0.81, Il1β 2.06, Bdnf 0.89.
Hippocampal protein: proBDNF 0.32 pg/µg protein; mBDNF 0.13 pg/µg protein.
DNA microarray (OC+LPS vs LPS): 219 genes differentially expressed, with 113 upregulated and 106 downregulated; 11 genes upregulated by LPS were downregulated by this compound.
Interleukin and TNF signal intensities were decreased in the this compound condition.
MCODE analysis of the functional network showed that antigen presentation and natural killer cell-mediated cytotoxicity were upregulated in the LPS condition but downregulated in the this compound condition.
Functional enrichment implicated PI3K/Akt and MAPK pathways.

Animal Model:

DBA-1/J (male, 3 weeks old at housing, 4 weeks old at randomization, 10 weeks old at CIA induction)^[7]
Dosage:

0.025% w/w, equivalent to 250 mg/kg
Administration:

p.o.; ad libitum; starting 6 weeks before CIA induction and continuing until the end of the experiment (day 43 after the first immunization); fresh diet provided daily
Result:

In CIA mice fed the this compound diet, arthritis onset was delayed and footpad thickness and inflammation of forelegs and hind legs were reduced compared with SD-CIA mice from days 35 to 42.
Histopathological scores in the this compound group were: soft tissue inflammation mild (+); synovial infiltration negative (−); inflammatory pannus negative (−); cartilage loss and bone resorption negative (−).
Inflammatory and arthritic signs were almost not detected; synovium appearance was similar to controls; only some samples showed moderate inflammation and mild proliferation of synovial cells.
MMP-9 immunostaining in the this compound group was similar to controls.
Showed only some cells of synovial villi immunopositive, while chondrocytes and surface cells remained negative.
Paw homogenate levels of IL-1β, TNF-α, IL-6, and IL-17 were reduced in this compound-fed mice compared with CIA controls.
Serum MMP-3 levels were reduced in this compound-enriched diet-fed mice compared with CIA controls.
COX-2 and mPGES-1 protein expression levels in paw homogenates were reduced in this compound-fed mice compared with CIA controls, and PGE2 levels were reduced.
iNOS protein expression in paws was downregulated in this compound-fed mice compared with CIA controls.
Induced Nrf2 and HO-1 overexpression in paw homogenates compared with CIA controls.
pJAK-3 and pSTAT-3 protein expression in hind paw homogenates was suppressed in this compound-fed mice compared with CIA controls.
JNK and p38 phosphorylation in hind paw homogenates was ameliorated in this compound-fed mice compared with CIA controls.
IκB-α degradation was prevented and p65 phosphorylation was reduced in this compound-fed mice compared with CIA controls.

Animal Model:

BALB/c (female, 25 g, 12 weeks old at supply, randomized at 16 weeks of age)^[8]
Dosage:

0.01% (w/w) OLA, corresponding to 100 mg/kg in supplemented chow
Administration:

p.o. via fresh diet; daily; 24 weeks starting at 16 weeks of age
Result:

Otherwise, dietary OLA significantly ameliorated these manifestations in lymphoid organs, decreasing splenomegaly.
The changes observed in the thymus weight were not statistically significant.
In OLA-supplemented mice, renal histopathological alterations were: hemorrhage 5%, inflammatory cells 30%, glomeruli alterations 25%, and interstitial fibrosis 5%.
However, after dietary supplementation with OLA, only a few mesangial deposits were identified in the renal glomeruli by IHC; no extraglomerular deposits were detected.
In IF, immunocomplexes were found in mesangial cells, with some subendothelial deposits having a granular appearance.
Nevertheless, no extraglomerular deposits were observed.
However, dietary supplementation with OLA significantly downregulated the expression of the proinflammatory enzymes COX-2, iNOS, and mPGES-1 to levels similar to those of the naïve control animals.
However, an OLA-enriched diet significantly downregulated the phosphorylation of JAK3 and STAT3.
On the other hand, we detected a significant increase in Nrf-2 protein expression in the OLA-supplemented group.
This increase was also found in HO-1 protein expression, but it was not statistically significant.
Interestingly, the OLA-enriched diet reduced p65 and p50 translocation to the nucleus compared to the SD-pristane group.
Nevertheless, an OLA-supplemented diet significantly decreased the phosphorylation of ERK and JNK MAPKs.
Nonetheless, OLA dietary supplementation significantly modulated the activation of the canonical inflammasome via the inhibition of NLRP3 and caspase-1 protein expression.
However, no statistically significant changes in ASC expression were observed after OLA dietary supplementation.
Moreover, the OLA-enriched diet also significantly regulated the non-canonical inflammasome, down-regulating pro-caspase 11 protein expression.
Collectively, the levels of IL-18 were also reduced by an OLA-enriched diet.
However, a diet supplemented with OLA could not counteract the endothelial response after ACh exposure.
In contrast, OLA-enriched diets normalized NOX-1 protein expression.
The OLA diet was not able to significantly reduce the phosphorylation of Thr495 peNOS.
Nevertheless, after 6 months, the OLA-supplemented diet was able to counteract the miRNA overexpression and modulate the expression of miRNA-24-3p, miRNA-146a, miRNA-23b, and miRNA-126 in comparison to the SD-pristane group.
Furthermore, an OLA-supplemented diet was able to restore DNMT-1 expression in renal tissue from pristane-induced mice.

Related Protocols :

Chemical Information

CAS No. 149183-75-5
Appearance Oil
Molecular Weight 320.34
Formula C₁₇H₂₀O₆
Color Light yellow to brown
SMILES

C/C=C(C=O)\[C@@H](CC=O)CC(OCCC1=CC=C(O)C(O)=C1)=O
Structure Classification
- Phenols
- Polyphenols
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Pure form	-20°C	3 years
In solvent	-80°C	6 months
	-20°C	1 month

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (313 KB)
SDS (252 KB)
- English - EN (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

References

[1]. Gutiérrez-Miranda B, et al. Oleacein Attenuates the Pathogenesis of Experimental Autoimmune Encephalomyelitis through Both Antioxidant and Anti-Inflammatory Effects. Antioxidants (Basel, Switzerland). 2020 Nov 21;9(11):1161.

[2]. Czerwińska M, et al. A comparison of antioxidant activities of oleuropein and its dialdehydic derivative from olive oil, oleacein. Food Chemistry. 2012 Apr 1;131(3):940-7.

[3]. Lepore SM, et al. Oleacein Prevents High Fat Diet-Induced Adiposity and Ameliorates Some Biochemical Parameters of Insulin Sensitivity in Mice. Nutrients. 2019 Aug 07;11(8):1829.

[4]. Ormonde B, et al. Oleacein prevents metabolic dysfunction-associated hepatic steatosis and dyslipidaemia in ApoE-KO mice. Food & function. 2026 Jun 08;17(11):4850-4864.

[5]. Marrero AD, et al. Anti-angiogenic effects of oleacein and oleocanthal: New bioactivities of compounds from Extra Virgin Olive Oil. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2023 Sep;165:115234.

[6]. Wakasugi D, et al. A rare olive compound oleacein functions as a TrkB agonist and mitigates neuroinflammation both in vitro and in vivo. Cell communication and signaling : CCS. 2024 Jun 04;22(1):309.

[7]. Rosillo MÁ, et al. Dietary oleacein, a secoiridoid from extra virgin olive oil, prevents collagen-induced arthritis in mice. Food & function. 2024 Jan 22;15(2):838-852.

[8]. Muñoz-García R, et al. Effects of Dietary Oleacein Treatment on Endothelial Dysfunction and Lupus Nephritis in Balb/C Pristane-Induced Mice. Antioxidants (Basel, Switzerland). 2023 Jun 19;12(6):1303.

[9]. Somanadhan B, et al. Angiotensin converting enzyme (ACE) inhibitors from Jasminum azoricum and Jasminum grandiflorum. Planta Med. 1998 Apr;64(3):246-50. [Content Brief]

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Oleacein

All NOD-like Receptor (NLR) Isoforms

All NF-κB Isoforms

All Interleukin Related Isoforms

All ERK Isoforms

All Akt Isoforms