Cat. No.: HY-N0594

Deacetylasperulosidic Acid

Customer Review

Based on 1 Customer Validation

Deacetylasperulosidic Acid is an orally active antioxidant. Deacetylasperulosidic Acid exerts a definite in vivo antioxidant effect and alleviates oxidative stress injury by enhancing SOD activity. In atopic dermatitis models, Deacetylasperulosidic Acid corrects Th2-skewed immune imbalance and reduces allergy-related factors; in immunosuppression models, it activates cellular immunity, enhances NK cell activity and IL-2 production. Deacetylasperulosidic Acid can be used in the research of atopic dermatitis.

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

Purity: 99.44%
CAS No.: 14259-55-3
Formula: C₁₆H₂₂O₁₁
Molecular Weight:390.34

Storage:

-20°C, protect from light

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

Deacetylasperulosidic Acid Chemical Structure

CAS No.: 14259-55-3

Size

Price

Stock

Quantity

Amount: USD 0.00

* Please select Quantity before adding items.

Top Publications Citing

Use of MCE Products

Fluorescent Dye

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

Biological Activity
- Description
- IC₅₀ & Target
- In Vitro
- In Vivo
Chemical Information
Solvent & Solubility
- In Vitro
- In Vivo
Purity & Documentation
References
Help & FAQs
Classifications
Bioz

Biological Activity

Description

IC₅₀ & Target

IL-2

All Interleukin Related Isoforms :

All TNF Receptor Isoforms :

In Vitro

Deacetylasperulosidic Acid reduced 4-nitroquinoline 1-oxide-induced genotoxicity by 98.96%^[1].
Deacetylasperulosidic Acid inhibited low-density lipoprotein oxidation^[1].
Deacetylasperulosidic Acid inhibited release of tumor necrosis factor-alpha^[1].
Deacetylasperulosidic Acid suppressed the induction of chromosome aberrations^[1].
Deacetylasperulosidic Acid demonstrates anti-atopic activity in human HaCaT keratinocytes, HMC-1 mast cells, and EOL-1 eosinophils by supporting immune balance and skin barrier function^[3].

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

In Vivo

Deacetylasperulosidic Acid (15-60 mg/kg; p.o.; daily; 7 days) exerts dose-dependent in vivo antioxidant activity in Wistar rats, with significant reductions in serum MDA (19.7-22.6%) and increases in serum SOD activity (11.3-13.0%) at doses of 30 and 60 mg/kg body weight administered daily for 7 days^[1].
Deacetylasperulosidic Acid (30-100 mg/kg; p.o.; daily; 14 days) at 100 mg/kg inhibits EC₅₀-induced reduction of IL-2 production, while 30 mg/kg and 100 mg/kg increase NK cell cytotoxicity to 12% and 21%, respectively, with no impact on splenic lymphocyte subpopulations^[2].
Deacetylasperulosidic acid (3-12 mg/kg; p.o.; daily; 4 weeks) alleviates atopic dermatitis in DNCB-induced NC/Nga mice in a dose-dependent manner by reducing pruritus, restoring immune balance, and repairing skin barrier function, with the 12 mg/kg dose achieving near-normal levels for most measured parameters^[3].

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

Animal Model:

Wistar rats (male and female, 180-200 g)^[1]
Dosage:

15 mg/kg; 30 mg/kg; 60 mg/kg
Administration:

p.o.; daily; 7 days
Result:

Caused non-significant reduction in mean serum malondialdehyde (MDA) and 10% increase in mean serum superoxide dismutase (SOD) activity at 15 mg/kg.
Induced significant 19.7% reduction in mean serum MDA and significant 11.3% increase in mean serum SOD activity at 30 mg/kg.
Induced significant 22.6% reduction in mean serum MDA and significant 13.0% increase in mean serum SOD activity at 60 mg/kg.
Did not significantly alter serum glutathione peroxidase (GPx) activity at any tested dose.

Animal Model:

ICR (female, 6 weeks old)^[2]
Dosage:

30 mg/kg; 100 mg/kg
Administration:

p.o.; daily; 7-14 days
Result:

Inhibited the reduction of ear swelling by 55%.
Inhibited the reduction of ear swelling by 52%.
Inhibited the reduction of IL-2 production in EC-sup-treated mice.
Increased NK cell cytotoxicity to 12%.
Increased NK cell cytotoxicity to 21%.
Had no effect on splenic lymphocyte subpopulations (CD3+, CD4+, CD8+, B220+, CD49b+ cell percentages).

Animal Model:

BALB/c (female, 6 weeks old)^[2]
Dosage:

30 mg/kg; 100 mg/kg
Administration:

p.o.; daily; 14 days
Result:

Resulted in a non-statistically significant increasing trend in IL-2 production and non-statistically significant decreasing trends in IL-4 and IL-10 production.
Had no effect on splenic lymphocyte subpopulations (CD3+, CD4+, CD8+, B220+, CD49b+ cell percentages).

Animal Model:

NC/Nga (male, 4 weeks old, DNCB-induced atopic dermatitis)^[3]
Dosage:

3 mg/kg; 6 mg/kg; 12 mg/kg
Administration:

p.o.; daily; 4 weeks
Result:

Reduced dermatitis scores, scratching behavior, and ear thickness in a dose-dependent manner, with 12 mg/kg showing greater efficacy than prednisolone for ear thickness by week 14.
Reduced epidermal thickness and the number of infiltrated mast cells and eosinophils in dorsal skin in a dose-dependent manner; 12 mg/kg achieved epidermal thickness (14.7 μm) and inflammatory cell counts similar to normal mice.
Reduced serum IgE and histamine levels in a dose-dependent manner, with all doses showing greater inhibition than prednisolone.
Reduced serum IgG1 levels and increased serum IgG2a levels in a dose-dependent manner, normalizing the IgG1/IgG2a ratio; 12 mg/kg restored the ratio to near-normal levels.
Reduced serum levels of Th2 (IL-4, IL-10, TSLP), pro-inflammatory (IL-1β, IL-6, TNF-α), and chemokine (TARC, MDC, RANTES) factors, and restored serum levels of Th1 (IL-12, IFN-γ) factors in a dose-dependent manner; 12 mg/kg restored IL-12 and IFN-γ to normal levels.
Reduced splenocyte secretion of Th2 (IL-4, IL-5, IL-10, IL-13, IL-31, IL-33, TSLP), pro-inflammatory (IL-1β, IL-6, TNF-α), Th9/Th17/Th22 (IL-9, IL-17, IL-22), and chemokine (TARC, MDC, RANTES) factors, and restored splenocyte secretion of Th1 (IL-12, IFN-γ) factors in a dose-dependent manner; 12 mg/kg restored IL-12 and IFN-γ to normal levels.
Reduced dorsal skin gene expression of Th2 activation-related factors (CCR4, IL-25, IL-33, TSLP, TARC, MDC, RANTES), Th2 (IL-4, IL-5, IL-10, IL-13, IL-31), pro-inflammatory (IL-1β, IL-6, TNF-α), and Th9/Th17/Th22 (IL-9, IL-17, IL-22) factors, and restored dorsal skin gene expression of Th1 (IL-12, IFN-γ) factors in a dose-dependent manner; 12 mg/kg restored IL-12 and IFN-γ to normal levels.
Increased dorsal skin pro-filaggrin gene expression and skin barrier-related protein (filaggrin, involucrin, loricrin) levels in a dose-dependent manner; 12 mg/kg restored these to levels similar to normal mice, with greater efficacy than prednisolone.

Chemical Information

CAS No. 14259-55-3
Appearance Solid
Molecular Weight 390.34
Formula C₁₆H₂₂O₁₁
Color White to off-white
SMILES

O[C@H]([C@@H](O)[C@@H]1O)[C@](O[C@@H]1CO)([H])O[C@H]2[C@@](C(CO)=C[C@@H]3O)([H])[C@@]3([H])C(C(O)=O)=CO2
Structure Classification
- Terpenoids
- Iridoids
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

-20°C, protect from light

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

Solvent & Solubility

In Vitro:

DMSO : 100 mg/mL (256.19 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

H₂O : 50 mg/mL (128.09 mM; Need ultrasonic)

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

2.5619 mL

12.8093 mL

25.6187 mL

5 mM

0.5124 mL

2.5619 mL

5.1237 mL

10 mM

0.2562 mL

1.2809 mL

2.5619 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.

* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

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 (6.40 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 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 (6.40 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 (6.40 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.

Working solution concentration: 0.22 mg/mL

This product has good water solubility, please refer to the measured solubility data in water/PBS/Saline for details.

The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only.If necessary, please contact

MedChemExpress (MCE) .

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (289 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]. Ma DL, et al. In vivo antioxidant activity of deacetylasperulosidic Acid in noni. J Anal Methods Chem. 2013;2013:804504. [Content Brief]

[2]. Murata K, et al. Activation of cell-mediated immunity by Morinda citrifolia fruit extract and its constituents. Nat Prod Commun. 2014;9(4):445-450. [Content Brief]

[3]. Oh JS, et al. Deacetylasperulosidic Acid Ameliorates Pruritus, Immune Imbalance, and Skin Barrier Dysfunction in 2,4-Dinitrochlorobenzene-Induced Atopic Dermatitis NC/Nga Mice. Int J Mol Sci. 2021;23(1):226. Published 2021 Dec 25. [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
H₂O / DMSO	1 mM	2.5619 mL	12.8093 mL	25.6187 mL	64.0467 mL
	5 mM	0.5124 mL	2.5619 mL	5.1237 mL	12.8093 mL
	10 mM	0.2562 mL	1.2809 mL	2.5619 mL	6.4047 mL
	15 mM	0.1708 mL	0.8540 mL	1.7079 mL	4.2698 mL
	20 mM	0.1281 mL	0.6405 mL	1.2809 mL	3.2023 mL
	25 mM	0.1025 mL	0.5124 mL	1.0247 mL	2.5619 mL
	30 mM	0.0854 mL	0.4270 mL	0.8540 mL	2.1349 mL
	40 mM	0.0640 mL	0.3202 mL	0.6405 mL	1.6012 mL
	50 mM	0.0512 mL	0.2562 mL	0.5124 mL	1.2809 mL
	60 mM	0.0427 mL	0.2135 mL	0.4270 mL	1.0674 mL
	80 mM	0.0320 mL	0.1601 mL	0.3202 mL	0.8006 mL
	100 mM	0.0256 mL	0.1281 mL	0.2562 mL	0.6405 mL

* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

Keywords

Product Name:
Cat. No.:
Quantity:
MCE Japan Authorized Agent:

Product Name:
CAS No.:
Species:
Purity:
Quantity:

Deacetylasperulosidic Acid

Apoptosis Compound Library

Immunology/Inflammation Compound Library

Natural Product Library

Anti-Aging Compound Library

Antioxidant Compound Library

Differentiation Inducing Compound Library

Glycoside Compound Library

Oxygen Sensing Compound Library

Medicine Food Homology Compound Library

Terpenoids Library

Traditional Chinese Medicine Active Compound Library

Anti-Parkinson's Disease Compound Library

Neurodegenerative Disease-related Compound Library

Angiogenesis-Related Compound Library

Antidepressant Compound Library

Anti-inflammatory Traditional Chinese Medicine Active Compound Library

Plant-Sourced Natural Product Library

Anti-Prostate Cancer Compound Library

Anti-Pulmonary Fibrosis Compound Library

Mitochondrial Protection Compound Library

Membrane Protein-targeted Compound Library

Membrane Receptor-targeted Compound Library

Autoimmune Disease Compound Library

Cytokine Inhibitors Library

Multi-Target Compound Library

Radioprotector Library

Bioactive Compound Library Max

MCE Bioactive Compound Library

Natural Product Library Plus

Natural Product and Natural Product-Like Compound Library

Bioactive Compound Library

Anti-Fibrosis Compound Library

Miao Ethnicity Medicine Compound Library

Heat-Clearing and Detoxification Traditional Chinese Medicine Compound Library

Non-Alcoholic Fatty Liver Disease (NAFLD) Compound Library

High-Throughput Bioactive Compound Library

High-Throughput Natural Product Library

Ancient Chinese Classical Formulas Traditional Chinese Medicine Active Compound Library

Anti-Rheumatic Arthritis Compound Library

Antitussive and Antiasthmatic Traditional Chinese Medicine Active Compound Library

Diarrhea-Related Traditional Chinese Medicine Active Compound Library

Mongolian Medicine Compound Library

Tonifying Traditional Chinese Medicine Monomer Compound Library

Mass Spectrometry Natural Product Library

All Interleukin Related Isoforms

All TNF Receptor Isoforms

Biological Activity

Chemical Information

Solvent & Solubility

Purity & Documentation

References

Help & FAQs

Complete Stock Solution Preparation Table

Deacetylasperulosidic Acid Related Classifications

HY-N0594 Related Classifications