Cat. No.: HY-N0809

Sesamolin

2 Cited Publications

Customer Review

Based on 2 publication(s) in Google Scholar

Sesamolin, isolated from Sesamum indicum, has antioxidative activity, Sesamolin inhibits lipid peroxidation and shows neuroprotection effect. Sesamolinl potently inhibits MAPK cascades by preventing phosphorylation of JNK, p38 MAPKs, and caspase-3 but not ERK-MAPK expression. Sesamolin is orally active.

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

Purity: 98.51%
CAS No.: 526-07-8
Formula: C₂₀H₁₈O₇
Molecular Weight:370.35

Storage:

4°C, protect from light

* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

Sesamolin Chemical Structure

CAS No.: 526-07-8

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Top Publications Citing

Use of MCE Products

Fluorescent Dye

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

Biological Activity
- Description
- In Vitro
- In Vivo
Chemical Information
Publications (2)
Solvent & Solubility
- In Vitro
- In Vivo
Purity & Documentation
References
Help & FAQs
Classifications
Bioz

Biological Activity

Description

All p38 MAPK Isoforms :

All JNK Isoforms :

All Caspase Isoforms :

All NF-κB Isoforms :

In Vitro

Sesamolin (0.5-50 μM, 1-2 h) reduces the release of LDH and ROS generation in H₂O₂ or hypoxia-stimulated PC12 cell, increases the cell viability, and exhibits antioxidant activity.
Sesamolin (0-10 μM, 5 days) inhibits RANKL-induced formation and differentiation of osteoclast in bone marrow macrophages, inhibits the bone resorption of osteoclasts through inhibition of NF-κB/MAPK signaling pathway, and suppression of c-Fos and NFATc1 expressions^[5].

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

Cell Viability Assay

Cell Line:

PC12
Concentration:

0.5-50 μM
Incubation Time:

1-2 h
Result:

Increased H₂O₂ or hypoxia-inhibited cell viability.

Western Blot Analysis

Cell Line:

bone marrow macrophages
Concentration:

10 μM
Incubation Time:

5 days
Result:

Inhibited levels of c-Fos and NFATc1.

In Vivo

Sesamolin (5 mg/kg, ip, every two days for 42 days) reduces the bone loss in mouse OVX-induced osteoporosis models^[5].
Sesamolin (60 mg/kg, po, twice a day for 3 weeks) improves metabolic disorders, attenuates hepatic steatosis, alleviates endotoxemia and systemic inflammation, alters the composition of gut microbiota, changes serum metabolites and metabolomics pathways, thereby ameliorating high-fat and high-fructose diet -induced non-alcoholic fatty liver disease in mouse models^[6].

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

Animal Model:

Mouse OVX-induced osteoporosis models^[5]
Dosage:

5 mg/kg
Administration:

ip, every two days for 42 days
Result:

Reduced the bone loss and increased trabecular parameters.

Animal Model:

High-fat and high-fructose diet -induced non-alcoholic fatty liver disease (NAFLD) in mouse models^[6]
Dosage:

60 mg/kg
Administration:

po, twice a day for 3 weeks (from 9th week to 12th week)
Result:

Inhibited weight gain, reduced the liver weight.
Reduced serum levels of glucose, insulin, HOMA-IR, total cholesterol, HDL-C, LDL-C, endotoxin, LBP, IL-6, TNF-α, AST and ALT.
Altered the composition of the gut flora, increased the relative abundance of beneficial bacteria and decreased the relative abundance of harmful bacteria.

Chemical Information

CAS No. 526-07-8
Appearance Solid
Molecular Weight 370.35
Formula C₂₀H₁₈O₇
Color White to off-white
SMILES

[H][C@@]12[C@@](CO[C@@H]2C3=CC(OCO4)=C4C=C3)([H])[C@H](OC1)OC5=CC(OCO6)=C6C=C5
Structure Classification
- Phenylpropanoids
- Other Phenylpropanoids
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

4°C, protect from light

* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

Publications (2)

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Journal Impact Factor

Int Immunopharmacol

Hepatocyte-derived exosomes deliver H2AFJ to hepatic stellate cells and promote liver fibrosis via the MAPK/STMN1 axis activation. [Abstract]

2023 Feb:115:109605. PMID: 36608439

Sesamolin purchased from MedChemExpress. Usage Cited in: Int Immunopharmacol. 2023 Feb:115:109605. [Abstract]

Sesamolin inhibits exosomal H2AFJ-induced migration and invasion of HSCs, while simultaneous overexpression of STMN1 promotes HSC migration and invasion again.

Sesamolin purchased from MedChemExpress. Usage Cited in: Int Immunopharmacol. 2023 Feb:115:109605. [Abstract]

Both treatment with Sesamolin (5 μM; 24 h) and oe-STMN1 increases STMN1 expression in HSCs co-cultured with exosomes overexpressing H2AFJ in HSCs.
Heliyon

The topoisomerase inhibitor CPT-11 prevents the growth and metastasis of lung cancer cells in nude mice by inhibiting EGFR/MAPK signaling pathway. [Abstract]

2023 Apr 27;9(5):e15805. PMID: 37251857

Solvent & Solubility

In Vitro:

DMSO : 100 mg/mL (270.01 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

View the Complete Stock Solution Preparation Table

Preparing Stock Solutions

View the Complete Stock Solution Preparation Table

Concentration Solvent Mass

1 mg

5 mg

10 mg

Concentration

Solvent

Mass

1 mM

2.7001 mL

13.5007 mL

27.0015 mL

5 mM

0.5400 mL

2.7001 mL

5.4003 mL

10 mM

0.2700 mL

1.3501 mL

2.7001 mL

Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.

Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Molarity Calculator

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Concentration Concentration

Volume Volume

Molecular Weight Molecular Weight

Dilution Calculator

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

Concentration _(start) Concentration _(start)

Volume _(start) Volume _(start)

Concentration _(final) Concentration _(final)

Volume _(final) Volume _(final)

In Vivo:

Select the appropriate dissolution method based on your experimental animal and administration route.

Stock Solution Working Solution

For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

Protocol 1

Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline

Solubility: 2.5 mg/mL (6.75 mM); Suspended solution; Need ultrasonic

This protocol yields a suspended solution of 2.5 mg/mL. Suspended solution can be used for oral and intraperitoneal injection.

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

Protocol 2

Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)

Solubility: ≥ 2.5 mg/mL (6.75 mM); Clear solution

This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.

Protocol 3

Add each solvent one by one: 10% DMSO 90% Corn Oil

Solubility: ≥ 2.5 mg/mL (6.75 mM); Clear solution

This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown). If the continuous dosing period exceeds half a month, please choose this protocol carefully.

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL Corn oil, and mix evenly.

In Vivo Dissolution Calculator

Please enter the basic information of animal experiments:

Dosage Dosage
mg/kg
Animal Weight (Per Animal) Animal Weight (Per Animal)
g
Dosing Volume (Per Animal) Dosing Volume (Per Animal)
μL
Number of Animals Number of Animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Please enter your animal formula composition:

%
DMSO +

Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
%
+
+
%
Tween-80 + +
%
Saline +

The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).

Working solution concentration: 0.22 mg/mL

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (279 KB)
SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 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]. Dorothea Bedigian, et al. Sesamin, sesamolin and the origin of sesame. Biochemical Systematics and Ecology. Volume 13, Issue 2, 23 May 1985, Pages 133-139.

[2]. Myung-Hwa Kang, et al. Sesamolin Inhibits Lipid Peroxidation in Rat Liver and Kidney. The Journal of Nutrition, Volume 128, Issue 6, June 1998, Pages 1018–1022.

[3]. Rolis Chien‐Wei Hou, et al. Protective effects of sesamin and sesamolin on hypoxic neuronal and PC12 cells. [Content Brief]

[4]. Lim JS, et al. Comparative analysis of sesame lignans (sesamin and sesamolin) in affecting hepatic fatty acid metabolism in rats. Br J Nutr. 2007 Jan;97(1):85-95. [Content Brief]

[5]. Yang X, et al., Sesamolin Protects Mice From Ovariectomized Bone Loss by Inhibiting Osteoclastogenesis and RANKL-Mediated NF-κB and MAPK Signaling Pathways. Front Pharmacol. 2021 Jun 14;12:664697. [Content Brief]

[6]. Yu J, et al., Sesamolin Alleviates Nonalcoholic Fatty Liver Disease through Modulating Gut Microbiota and Metabolites in High-Fat and High-Fructose Diet-Fed Mice. Int J Mol Sci. 2022 Nov 10;23(22):13853. [Content Brief]

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Complete Stock Solution Preparation Table

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg
DMSO	1 mM	2.7001 mL	13.5007 mL	27.0015 mL	67.5037 mL
	5 mM	0.5400 mL	2.7001 mL	5.4003 mL	13.5007 mL
	10 mM	0.2700 mL	1.3501 mL	2.7001 mL	6.7504 mL
	15 mM	0.1800 mL	0.9000 mL	1.8001 mL	4.5002 mL
	20 mM	0.1350 mL	0.6750 mL	1.3501 mL	3.3752 mL
	25 mM	0.1080 mL	0.5400 mL	1.0801 mL	2.7001 mL
	30 mM	0.0900 mL	0.4500 mL	0.9000 mL	2.2501 mL
	40 mM	0.0675 mL	0.3375 mL	0.6750 mL	1.6876 mL
	50 mM	0.0540 mL	0.2700 mL	0.5400 mL	1.3501 mL
	60 mM	0.0450 mL	0.2250 mL	0.4500 mL	1.1251 mL
	80 mM	0.0338 mL	0.1688 mL	0.3375 mL	0.8438 mL
	100 mM	0.0270 mL	0.1350 mL	0.2700 mL	0.6750 mL

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Sesamolin

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Publications Citing Use of MedChemExpress (MCE) Sesamolin

All p38 MAPK Isoforms

All JNK Isoforms

All Caspase Isoforms

All NF-κB Isoforms

Biological Activity

Chemical Information

Publications (2)