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Art. -Nr.: HY-N8448

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3,4-Di-O-caffeoyl quinic acid methyl ester

(Synonyms: Macroantoin F)

3,4-Di-O-caffeoyl quinic acid methyl ester (Macroantoin F) is a dicaffeoyl derivative isolated from the rhizome of Elephantopus scaber Linn. 3,4-Di-O-caffeoyl quinic acid methyl ester exhibited in vitro antiviral activity against respiratory syncytial virus (RSV) with an IC₅₀ value of 0.78 μg/mL.

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Reinheit: 98.77%

CAS. Nr.: 114637-83-1

Formel: C₂₆H₂₆O₁₂

Molecular Weight:530.48

Speicherung:

-20°C, protect from light

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

Data Sheet (281 KB)

SDS

COA

3,4-Di-O-caffeoyl quinic acid methyl ester Chemical Structure

CAS. Nr.: 114637-83-1

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Data Sheet (281 KB)

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Biologische Aktivität

Beschreibung

3,4-Di-O-caffeoyl quinic acid methyl ester (Macroantoin F) is a dicaffeoyl derivative isolated from the rhizome of Elephantopus scaber Linn. 3,4-Di-O-caffeoyl quinic acid methyl ester exhibited in vitro antiviral activity against respiratory syncytial virus (RSV) with an IC₅₀ value of 0.78 μg/mL^[1].

Cellular Effect

Cell Line

Type Value Description References

BV-2 IC₅₀
24.58 μM
Compound: 9

Anti-neuroinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-induced nitric oxide production after 10 mins by Griess assay relative to control

Anti-neuroinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-induced nitric oxide production after 10 mins by Griess assay relative to control
[PMID: 23462643]

Jurkat IC₅₀
>35 mM
Compound: 4

Cytotoxicity against human Jurkat T cells

Cytotoxicity against human Jurkat T cells
[PMID: 15921434]

Jurkat IC₅₀
>35 μM/mL
Compound: 4

Cytotoxicity against human Jurkat T cells

Cytotoxicity against human Jurkat T cells
[PMID: 15921434]

Chemical Information

CAS. Nr. 114637-83-1

Appearance Solid

Molecular Weight 530.48

Formel C₂₆H₂₆O₁₂

Color White to off-white

SMILES

O=C(O[C@H]1[C@H](OC(/C=C/C2=CC(O)=C(O)C=C2)=O)[C@H](O)C[C@](C(OC)=O)(O)C1)/C=C/C3=CC(O)=C(O)C=C3

Synonyms

Macroantoin F

Structure Classification

Phenols

Polyphenols

Initial Source

Plants

Leguminosae

Amorpha fruticosaL.

Plants

Compositae

Versand

Room temperature in continental US; may vary elsewhere.

Speicherung

-20°C, protect from light

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

Reinheit & Dokumentation

Select Batch:

Reinheit: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (281 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)

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)

Verweise

[1]. Hua-Wei Geng, et al. Antiviral dicaffeoyl derivatives from Elephantopus scaber. Journal of Asian Natural Products Research.Volume 13, 2011 - Issue 7.

Calculators

Molaritätsrechner

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

Mass

=
Konzentration

×
Volumen

×
Molecular Weight

Verdünnungsrechner

Konzentration _{(Stammlösung)} × Volumen _{(Stammlösung)} = Konzentration _{(Ziellösung)} × Volumen _{(Ziellösung)}

Konzentration _{(Stammlösung)}

×

Volumen _{(Stammlösung)}

=

Konzentration _{(Ziellösung)}

×

Volumen _{(Ziellösung)}

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.

3,4-Di-O-caffeoyl quinic acid methyl ester Related Classifications

Art. -Nr.: HY-N8448

Anti-infection

RSV

Disease Areas

Infection

Natürliche Produkte

Plants Phenols

Leguminosae Compositae Polyphenols

Amorpha fruticosaL.

Reference Standards

Natural Product Standards

Phenols

Infection

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Keywords

3,4-Di-O-caffeoyl quinic acid methyl ester
114637-83-1
Macroantoin F
RSV
dicaffeoyl derivative
antiviral
Inhibitor
inhibitor
inhibit

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Cell Line	Type	Value	Description	References
BV-2	IC₅₀	24.58 μM Compound: 9	Anti-neuroinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-induced nitric oxide production after 10 mins by Griess assay relative to control Anti-neuroinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-induced nitric oxide production after 10 mins by Griess assay relative to control	[PMID: 23462643]
Jurkat	IC₅₀	>35 mM Compound: 4	Cytotoxicity against human Jurkat T cells Cytotoxicity against human Jurkat T cells	[PMID: 15921434]
Jurkat	IC₅₀	>35 μM/mL Compound: 4	Cytotoxicity against human Jurkat T cells Cytotoxicity against human Jurkat T cells	[PMID: 15921434]

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