Epimedin C

CAS: 110642-44-9

Ref. TR-E588875

Produktinformation

• Name: Epimedin C
• Synonyme: 4H-1-Benzopyran-4-one, 3-[[6-deoxy-2-O-(6-deoxy-a-L-mannopyranosyl)-a-L-mannopyranosyl]oxy]-7-(ß-D-glucopyranosyloxy)-5-hydroxy-2-(4-methoxyphenyl)-8-(3-methyl-2-buten-1-yl)-, 4H-1-Benzopyran-4-one, 3-[[6-deoxy-2-O-(6-deoxy-a-L-mannopyranosyl)-a-L-mannopyranosyl]oxy]-7-(ß-D-glucopyranosyloxy)-5-hydroxy-2-(4-methoxyphenyl)-8-(3-methyl-2-butenyl)- (9CI), 3-[[6-Deoxy-2-O-(6-deoxy-a-L-mannopyranosyl)-a-L-mannopyranosyl]oxy]-7-(ß-D-glucopyranosyloxy)-5-hydroxy-2-(4-methoxyphenyl)-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one, Baohuoside VI, Epimedin C(Primary Standard), 3-((6-Deoxy-2-O-(6-deoxy-alpha-L-mannopyranosyl)-alpha-L-mannopyranosyl)oxy)-7-(beta-D-glucopyranosyloxy)-5-hydroxy-2-(4-methoxyphenyl)-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one, (4-Methoxyphenyl)-8-(3-Methyl-2-Buten-1-Yl)-, 4H-1-Benzopyran-4-one,3-[[6-deoxy-2-O-(6-deoxy-α-L-mannopyranosyl)- α-L-mannopyranosyl]oxy]-, 7-(β-D-glucopyranosyloxy)-5-hydroxy-2-, 3-{[6-deoxy-2-O-(6-deoxy-alpha-L-mannopyranosyl)-alpha-L-mannopyranosyl]oxy}-5-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-en-1-yl)-4-oxo-4H-chromen-7-yl beta-D-glucopyranoside
• CAS: 110642-44-9

Beschreibung

Applications Epimedin C has a potential to treat cardiovascular diseases and bone loss. A natural flavonoid extract from Epimedium sagittatum it is used as a health-promoting agent in Chinese traditional medicine.
References Zeng, S. et al.: Plant Cell, Tissue. Organ Cult., 115, 355 (2013);

• Marke: TRC

Chemische Eigenschaften

• Molekulargewicht: 822.80
• Formel: C₃₉H₅₀O₁₉
• Farbe/Form: Neat
• InChl: InChI=1S/C39H50O19/c1-14(2)6-11-19-21(54-38-32(50)29(47)26(44)22(13-40)55-38)12-20(41)23-27(45)35(33(56-34(19)23)17-7-9-18(51-5)10-8-17)57-39-36(30(48)25(43)16(4)53-39)58-37-31(49)28(46)24(42)15(3)52-37/h6-10,12,15-16,22,24-26,28-32,36-44,46-50H,11,13H2,1-5H3/t15-,16-,22+,24-,25-,26+,28+,29-,30+,31+,32+,36+,37-,38+,39-/m0/s1
• InChI Key: InChIKey=AMVODTGMYSRMNP-BPFDTTLHSA-N
• SMILES: CC1(O)CC[C@@H]2[C@@H]3CCC4=CC(=O)C(C=O)=C[C@]4(C)[C@@H]3[C@@H](O)C[C@@]21C