39432-56-9

Basic information

• Product Name: Eleutheroside E
• Synonyms: Eleutheroside;b-D-Glucopyranoside,[(1R,3aR,4S,6aS)-tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diyl]bis(2,6-diMethoxy-4,1-phenylene)bis-;[(1R,3aR,4S,6aS)-Tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diyl]bis(2,6-dimethoxy-4,1-phenylene) bis-β-D-glucopyranoside;(-)-SYRINGARESINOL DIGLUCOSIDE;ELEUTHEROSIDE E;(2R,3S,4R,5R,6S)-2-[4-[4-[3,5-Dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[4,3-c]furan-1-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol;Related CAS No: 19046-36-7 96038-87-8 66791-77-3;Manyprickle Acathopanax Root
• CAS NO: 39432-56-9
• Molecular Formula: C₃₄H₄₆O₁₈
• Molecular Weight: 742.72
• EINECS: 1592732-453-0
• Product Categories: pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Coumarins;chemical reagent
• Mol File: 39432-56-9.mol
• Article Data: 1

Chemical Properties

• Melting Point: 269～270℃
• Boiling Point: 935.7 °C at 760 mmHg
• Flash Point: 519.7 °C
• Appearance: /
• Density: 1.474 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.615
• Storage Temp.: 2-8°C
• Solubility: DMSO (Slightly), Ethyl Acetate (Slightly), Pyridine (Slightly, Sonicated)
• PKA: 12.45±0.70(Predicted)
• Stability: Hygroscopic
• CAS DataBase Reference: Eleutheroside E(CAS DataBase Reference)
• NIST Chemistry Reference: Eleutheroside E(39432-56-9)
• EPA Substance Registry System: Eleutheroside E(39432-56-9)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• Safety Statements: 24/25
• WGK Germany: 3
• Hazardous Substances Data: 39432-56-9(Hazardous Substances Data)

Usage

Uses

Eleutheroside E is used in the treatment of collagen-induced arthritis. Used in the suppression of inflammatory cytokine release. Successful in the treatment of rheumatoid arthritis. Also used in the regulation of adipogenesis

InChI:InChI=1/C34H46O18/c1-43-17-5-13(6-18(44-2)31(17)51-33-27(41)25(39)23(37)21(9-35)49-33)29-15-11-48-30(16(15)12-47-29)14-7-19(45-3)32(20(8-14)46-4)52-34-28(42)26(40)24(38)22(10-36)50-34/h5-8,15-16,21-30,33-42H,9-12H2,1-4H3/t15?,16?,21-,22+,23-,24+,25+,26-,27-,28+,29?,30?,33+,34-

Upstream product

• 487-35-4 (+/-)-syringaresinol 
• 20675-96-1 trans-sinapyl alcohol 
• 6746-69-6 C₅₀H₆₂O₂₆ 

Downstream Products

• 487-35-4 (-)-Syringaresinol 
• 487-35-4 (+)-dia-syringaresinol 
• 6746-69-6 C₅₀H₆₂O₂₆ 

Relevant articles and documents

SYNTHESIS OF BIOLOGICALLY ACTIVE TETRAHYDROFUROFURANLIGNAN-(SYRINGIN, PINORESINOL)- MONO- AND BIS-GLYCOSIDES

The naturally occuring tetrahydrofurofuran-lignan-(syringaresinol, pinoresinol)-mono- and bis-glucosides were synthesized and their structures thereby confirmed.Key Word Index - Ligan-glucosides; synthesis; syringaresinol and pinoresinol glucosides.