Eudesmin

Modify Date: 2025-08-24 17:01:09

Eudesmin Structure
Eudesmin structure
Common Name Eudesmin
CAS Number 526-06-7 Molecular Weight 386.438
Density 1.2±0.1 g/cm3 Boiling Point 517.3±50.0 °C at 760 mmHg
Molecular Formula C22H26O6 Melting Point 108.5-109.5℃
MSDS N/A Flash Point 209.8±30.0 °C

 Use of Eudesmin


Eudesmin ((-)-Eudesmin) impairs adipogenic differentiation via inhibition of S6K1 signaling pathway. Eudesmin possesses diverse therapeutic effects, including anti-tumor, anti-inflammatory, and anti-bacterial activities[1].

 Names

Name 1H,3H-Furo[3,4-c]furan, 1,4-bis(3,4-dimethoxyphenyl)tetrahydro-, (1.α.,3a.α.,4.α.,6a.α.)-(-)
Synonym More Synonyms

 Eudesmin Biological Activity

Description Eudesmin ((-)-Eudesmin) impairs adipogenic differentiation via inhibition of S6K1 signaling pathway. Eudesmin possesses diverse therapeutic effects, including anti-tumor, anti-inflammatory, and anti-bacterial activities[1].
Related Catalog
Target

S6K1[1]

In Vitro Treatment of mesenchymal stem cells (MSCs) with Eudesmin (20, 40, and 80μM) disturbs adipogenesis via suppression of S6K1 signaling pathway. Eudesmin treatment inhibits activation and nuclear translocation of S6K1. S6K1-mediated phosphorylation of H2B at serine 36 (H2BS36p) is reduced upon Eudesmin treatment[1].
References

[1]. Ki Hong Nam, et al. Eudesmin Impairs Adipogenic Differentiation via Inhibition of S6K1 Signaling Pathway. Biochem Biophys Res Commun. 2018 Nov 10;505(4):1148-1153.

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 517.3±50.0 °C at 760 mmHg
Melting Point 108.5-109.5℃
Molecular Formula C22H26O6
Molecular Weight 386.438
Flash Point 209.8±30.0 °C
Exact Mass 386.172943
PSA 55.38000
LogP 3.08
Vapour Pressure 0.0±1.3 mmHg at 25°C
Index of Refraction 1.547
InChIKey PEUUVVGQIVMSAW-UHFFFAOYSA-N
SMILES COc1ccc(C2OCC3C(c4ccc(OC)c(OC)c4)OCC23)cc1OC
Storage condition 2-8°C

 Safety Information

Hazard Codes Xn
Risk Phrases 22
Safety Phrases 36

 EudesminBioassay

View more

Name: Antifungal activity against Phomopsis obscurans assessed as growth inhibition at 50 u...
Source: ChEMBL
Target: Phomopsis obscurans
External Id: CHEMBL3052906
Name: Antifungal activity against Colletotrichum acutatum assessed as growth inhibition at ...
Source: ChEMBL
Target: Colletotrichum acutatum
External Id: CHEMBL3052908
Name: Antifungal activity against Colletotrichum gloeosporioides assessed as growth inhibit...
Source: ChEMBL
Target: Colletotrichum gloeosporioides
External Id: CHEMBL3052909
Name: Antifungal activity against Diaporthe ampelina assessed as growth inhibition at 50 to...
Source: ChEMBL
Target: Diaporthe ampelina
External Id: CHEMBL3052910
Name: Antifungal activity against Colletotrichum fragariae assessed as growth inhibition at...
Source: ChEMBL
Target: Colletotrichum fragariae
External Id: CHEMBL3052911
Name: Antifungal activity against Phomopsis obscurans assessed as growth inhibition at 50 t...
Source: ChEMBL
Target: Phomopsis obscurans
External Id: CHEMBL3052912
Name: Antifungal activity against Fusarium oxysporum assessed as growth inhibition at 50 to...
Source: ChEMBL
Target: Fusarium oxysporum
External Id: CHEMBL3052913
Name: Antialgal activity against Planktothrix agardhii assessed as inhibition measured for ...
Source: ChEMBL
Target: Planktothrix agardhii
External Id: CHEMBL3052942
Name: Small-molecule inhibitors of ST2 (IL1RL1)
Source: 20881
Target: interleukin-1 receptor-like 1 isoform [homo sapiens]
External Id: ST2_IL33_Inhibitors_Primary_Screening_77700
Name: Inhibition of LPS-induced nitric oxide production in mouse RAW264.7 cells after 24 hr...
Source: ChEMBL
Target: RAW264.7
External Id: CHEMBL3611158
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 Synonyms

Pinoresinol dimethyl ether
Eudesamin,Eudesmin
(1S,3aR,4S,6aR)-1,4-Bis(3,4-dimethoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan
(7S,7’S,8R,8’R)-eudesmin
(1S,3aR,4S,6aR)-1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan
eudesmin
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