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Cat. No.: HY-N1652

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2,3,8-Tri-O-methylellagic acid

(Synonyms: 3,3′,4-Tri-O-methylellagic acid)

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2,3,8-Tri-O-methylellagic acid is a terpenoids that can be isolated from the stem bark of Neoboutonia macrocalyx. 2,3,8-Tri-O-methylellagic acid is found to be 50 times more active than the parent ellagic acid.

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

Purity: 97.0%
CAS No.: 1617-49-8
Formula: C₁₇H₁₂O₈
Molecular Weight:344.27

Storage:

-20°C, protect from light

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

2,3,8-Tri-O-methylellagic acid Chemical Structure

CAS No.: 1617-49-8

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Use of MCE Products

Fluorescent Dye

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

Biological Activity
- Description
- Cellular Effect
Chemical Information
Purity & Documentation
References
Calculators
Help & FAQs
Classifications
Bioz

Biological Activity

Description

Cellular Effect

Cell Line	Type	Value	Description	References
Col2	ED₅₀	>5 μg/mL Compound: 10	Cytotoxicity against human Col2 cells after 72 hrs by sulforhodamine B assay Cytotoxicity against human Col2 cells after 72 hrs by sulforhodamine B assay	[PMID: 18271551]
HT-29	IC₅₀	>10 μM Compound: S3	Cytotoxicity against human HT-29 cells assessed as reduction in cell viability after 72 hrs by CellTiter 96 aqueous one solution assay Cytotoxicity against human HT-29 cells assessed as reduction in cell viability after 72 hrs by CellTiter 96 aqueous one solution assay	[PMID: 30057155]
HT-29	IC₅₀	>10 μM Compound: S3	Inhibition of mitochondrial membrane potential in human HT-29 cells after 3 hrs by JC-1 staining based fluorescence assay Inhibition of mitochondrial membrane potential in human HT-29 cells after 3 hrs by JC-1 staining based fluorescence assay	[PMID: 30057155]
KB	ED₅₀	>5 μg/mL Compound: 10	Cytotoxicity against human KB cells after 72 hrs by sulforhodamine B assay Cytotoxicity against human KB cells after 72 hrs by sulforhodamine B assay	[PMID: 18271551]
Lu1	ED₅₀	>5 μg/mL Compound: 10	Cytotoxicity against human Lu1 cells after 72 hrs by sulforhodamine B assay Cytotoxicity against human Lu1 cells after 72 hrs by sulforhodamine B assay	[PMID: 18271551]
MCF7	ED₅₀	>5 μg/mL Compound: 10	Cytotoxicity against human MCF7 cells after 72 hrs by sulforhodamine B assay Cytotoxicity against human MCF7 cells after 72 hrs by sulforhodamine B assay	[PMID: 18271551]
MDA-MB-435	IC₅₀	>10 μM Compound: S3	Cytotoxicity against human MDA-MB-435 cells assessed as reduction in cell viability after 72 hrs by CellTiter 96 aqueous one solution assay Cytotoxicity against human MDA-MB-435 cells assessed as reduction in cell viability after 72 hrs by CellTiter 96 aqueous one solution assay	[PMID: 30057155]
OVCAR-3	IC₅₀	>10 μM Compound: S3	Cytotoxicity against human OVCAR3 cells assessed as reduction in cell viability after 72 hrs by CellTiter 96 aqueous one solution assay Cytotoxicity against human OVCAR3 cells assessed as reduction in cell viability after 72 hrs by CellTiter 96 aqueous one solution assay	[PMID: 30057155]
P388	ED₅₀	>5 μg/mL Compound: 10	Cytotoxicity against mouse P388 cells after 72 hrs by sulforhodamine B assay Cytotoxicity against mouse P388 cells after 72 hrs by sulforhodamine B assay	[PMID: 18271551]

Chemical Information

CAS No. 1617-49-8
Appearance Solid
Molecular Weight 344.27
Formula C₁₇H₁₂O₈
Color White to off-white
SMILES

O=C1C2=CC(OC)=C(OC)C(O3)=C2C4=C(C3=O)C=C(O)C(OC)=C4O1
Synonyms

3,3′,4-Tri-O-methylellagic acid
Structure Classification
- Phenols
- Monophenols
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)

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (271 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]. Maffo, Timoleon, Uzor, et al. Terpenoids from the stem bark of Neoboutonia macrocalyx (Euphorbiaceae). Phytochemistry Letters, 2015.

[2]. Ashraful Alam, et al. Total synthesis of 3,3′,4-tri-O-methylellagic acid from gallic acid. Tetrahedron, 2007, 63(42):10454-10465.

Calculators

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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.

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100 mg

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