Ginsenoside Rc

CAS : 11021-14-0

Ref. TR-G410210

Informations sur le produit

• Nom: Ginsenoside Rc
• Synonymes: ß-D-Glucopyranoside, (3ß,12ß)-20-[(6-O-a-L-arabinofuranosyl-ß-D-glucopyranosyl)oxy]-12-hydroxydammar-24-en-3-yl 2-O-ß-D-glucopyranosyl-, Dammarane, ß-D-glucopyranoside deriv., (3ß,12ß)-20-[(6-O-a-L-Arabinofuranosyl-ß-D-glucopyranosyl)oxy]-12-hydroxydammar-24-en-3-yl 2-O-ß-D-glucopyranosyl-ß-D-glucopyranoside, NSC 310104, Panaxoside Rc, (3β,12β)-20-[(6-O-α-<span class="text-smallcaps">L</smallcap>-Arabinofuranosyl-β-<smallcap>D</smallcap>-glucopyranosyl)oxy]-12-hydroxydammar-24-en-3-yl 2-O-β-<smallcap>D</smallcap>-glucopyranosyl-β-<smallcap>D</span>-glucopyranoside, 12-hydroxy-20-[(6-O-pentofuranosylhexopyranosyl)oxy]dammar-24-en-3-yl 2-O-hexopyranosylhexopyranoside, Dammarane, β-<span class="text-smallcaps">D</span>-glucopyranoside deriv., Ginsenoside Rc, Ginsenoside Rb2, β-<span class="text-smallcaps">D</smallcap>-Glucopyranoside, (3β,12β)-20-[(6-O-α-<smallcap>L</smallcap>-arabinofuranosyl-β-<smallcap>D</smallcap>-glucopyranosyl)oxy]-12-hydroxydammar-24-en-3-yl 2-O-β-<smallcap>D</span>-glucopyranosyl-
• CAS: 11021-14-0

Description

Stability Hygroscopic
Applications Ginsenoside Rc displays anti-proliferative effects in human breast cancer cell lines.
References Lee, Y. et al.: Arch. Pharm. Res., 26, 53 (2003);

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 1079.27
• Formule: C₅₃H₉₀O₂₂
• Couleur/Forme: Neat
• InChI: InChI=1S/C53H90O22/c1-23(2)10-9-14-53(8,75-47-43(67)39(63)37(61)29(72-47)22-68-45-41(65)36(60)28(21-56)69-45)24-11-16-52(7)33(24)25(57)18-31-50(5)15-13-32(49(3,4)30(50)12-17-51(31,52)6)73-48-44(40(64)35(59)27(20-55)71-48)74-46-42(66)38(62)34(58)26(19-54)70-46/h10,24-48,54-67H,9,11-22H2,1-8H3/t24-,25+,26+,27+,28-,29+,30-,31+,32-,33-,34+,35+,36-,37+,38-,39-,40-,41+,42+,43+,44+,45+,46-,47-,48-,50-,51+,52+,53-/m0/s1
• Code InChI: InChIKey=JDCPEKQWFDWQLI-LUQKBWBOSA-N
• SMILES: CC(C)=CCC[C@](C)(O[C@@H]1O[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O)[C@@H](O)[C@H](O)[C@H]1O)[C@H]1CC[C@]2(C)[C@@H]1[C@H](O)C[C@@H]1[C@@]3(C)CC[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(C)(C)[C@@H]3CC[C@]12C