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Cat. No.: HY-N21753

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Dehydrodicatechin A

Dehydrodicatechin A is a biflavan catechin dimer and antioxidant. Dehydrodicatechin A is isolated from the roots of Hagenia abyssinica, the stem bark of Choerospondias axillaries, the stems of Entada phaseoloides, and Calligonum comosum. Dehydrodicatechin A exhibits ABTS⁺ radical cation, DPPH, ABTS, and superoxide anion radical scavenging activities, as well as ferric reducing/antioxidant power. Dehydrodicatechin A inhibits Lipase. Dehydrodicatechin A is used in studies on polycystic ovary syndrome, Ehrlich ascites, and Doxorubicin (HY-15142)-induced cardiotoxicity.

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CAS No.: 36048-23-4
Formule: C₃₀H₂₄O₁₂
Masse moléculaire:576.50

Stockage:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (298 KB)

Dehydrodicatechin A Chemical Structure

CAS No.: 36048-23-4

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Quantité

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Use of MCE Products

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

Activité biologique
- Description
- In Vitro
Chemical Information
Pureté et documentation
Références
Calculators
Help & FAQs
Classifications
Bioz

Activité biologique

Description

In Vitro

Oxidative StressAnti-cancerOthers

Oxidative Stress

Dehydrodicatechin A (6 min) exhibits strong antioxidant activity in the ABTS⁺ radical cation scavenging assay, with an IC₅₀ of 9.041 μg/mL^[1].
Dehydrodicatechin A (15 min) exhibits moderate antioxidant activity in DPPH, ABTS, and β-carotene-linoleate assays, but shows weak ferric reducing ability and negligible superoxide radical scavenging activity^[8].

Anti-cancer

Dehydrodicatechin A (100 µg/mL; 24 h) does not exhibit significant inhibitory effects on K562 cell proliferation^[3].

Others

Dehydrodicatechin A (50.0 µg/mL; 24 h) shows significant protective effects against hypoxia-induced injury in cultured PC12 cells^[3].
Dehydrodicatechin A exhibits high pancreatic lipase inhibitory activity^[5].

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

Cell Viability Assay^[3]

Cell Line:

K562 human chronic myelogenous leukemia cells
Concentration:

100 µg/mL
Incubation Time:

24 h
Result:

Showed an inhibition rate of -16.2% on K562 cells.
Showed no distinction in cell morphology from the control group.

Cell Viability Assay^[3]

Cell Line:

PC12 cells
Concentration:

50.0 µg/mL
Incubation Time:

24 h
Result:

Showed a cell viability of 122.7% in PC12 cells, compared to a control group viability of 90.0%.

Chemical Information

CAS No. 36048-23-4
Masse moléculaire 576.50
Formule C₃₀H₂₄O₁₂
SMILES

O[C@@]12C[C@]3([C@]4([H])[C@@](CC5=C(O)C=C(O)C=C5O4)([H])O2)C(C6=C(O[C@H](C7=CC(O)=C(C=C7)O)[C@H](C8)O)C8=C(O)C=C6O3)=CC1=O
Structure Classification
- Phenols
- Polyphenols
Initial Source
Livraison

Room temperature in continental US; may vary elsewhere.
Stockage

Please store the product under the recommended conditions in the Certificate of Analysis.

Pureté et documentation

Select Batch:

Pureté: 99.98%

Assay: 99.98%

ee.: 99.98%

Fiche technique (298 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)
Instruction de manipulation (2659 KB)

Références

[1]. Fan M, et al. Antioxidant and anti-proliferative properties of Hagenia abyssinica roots and their potentially active components. Antioxidants. 2020 Feb 6;9(2):143.

[2]. Bannour M, et al. Phenolic profiling and antioxidant capacity of Calligonum azel Maire, a Tunisian desert plant. Food research international (Ottawa, Ont.). 2017 Nov;101:148-154.

[3]. Li CW, et al. One new and nine known flavonoids from Choerospondias axillaries and their in vitro antitumor, anti-hypoxia and antibacterial activities. Molecules (Basel, Switzerland). 2014 Dec 19;19(12):21363-77.

[4]. Tahmasebi F, et al. Antioxidant effects of calligonum extract on ovarian tissue of PCO model: An experimental study. International journal of reproductive biomedicine. 2018 Oct;16(10):641-648.

[5]. Jeon S Y, Imm J Y. Lipase inhibition and cholesterol-lowering activities of laccase-catalyzed catechin polymers[J]. Food Science and Biotechnology, 2014, 23(5): 1703-1707.

[6]. Shalabi M, et al. Anticancer activity of Aloe vera and Calligonum comosum extracts separetely on hepatocellular carcinoma cells. Asian Pacific Journal of Tropical Biomedicine. 2015 May 1;5(5):375-81.

[7]. Ashour OM, et al. Evaluation of the potential cardioprotective activity of some Saudi plants against doxorubicin toxicity. Zeitschrift fur Naturforschung. C, Journal of biosciences. 2012;67(5-6):297-307.

[8]. Dong Y, et al. Antioxidant phenolic compounds from the stems of Entada phaseoloides. Chemistry & biodiversity. 2012 Jan;9(1):68-79.

Calculators

Calculateur de molarité

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

Mass Mass

Concentration Concentration

Volume Volume

Molecular Weight Molecular Weight

Calculateur de dilution

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

Concentration _(start) Concentration _(start)

Volume _(start) Volume _(start)

Concentration _(final) Concentration _(final)

Volume _(final) Volume _(final)

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.

Bioz

Keywords

MOQ

Minimum order quantity

100 mg

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