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  • Ginsenoside Rc

    Catalog No. CFN99973
    CAS No. 11021-14-0
    Molecular Weight: 1079.27
    Molecular Formula C53H90O22
    DBs [PubChem]:53789932
    [ChEMBL]:77154
    [PCIDB]:30397

    Standard 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

    Biological Activity

    Ginsenoside Rc (Rc), a protopanaxadiol type ginsenoside, is the active component mainly responsible for the therapeutic and pharmacologic properties of ginseng, which are derived from its suppression of superoxide-induced free radicals, Rc  can modulate Forkhead box O (FoxO1)phosphorylation through activation of PI3K/Akt and inhibition of AMPK and FoxO1 acetylation through interaction with CBP and SIRT1, and that this leads to upregulation of catalase under conditions of oxidative stress.[1]
    Ginsenoside Rc from Korean Red Ginseng (Panax ginseng C.A. Meyer) exhibits anticancer and anti-inflammatory activities, can attenuate inflammatory symptoms of gastritis, hepatitis and arthritis.[2]
    Ginsenoside Rc and Re induce c-fos in MCF-7 human breast carcinoma cells at both the mRNA and protein levels,  they act via other transcription factors and not via estrogen receptor in c-Fos expression.[3]
    Ginsenoside Rc significantly enhances glucose uptake by inducing ROS generation, which leads to AMPK and p38 MAPK activation.,consequently, it can be used as a potent natural anti-diabetic agent.[4]
    Ginsenoside Rc can promote anti-adipogenic activity on 3T3-L1 adipocytes by down-regulating C/EBPα and PPARγ.[5]

    Product

    Official website: Ginsenoside Rc
    Japanese website: Ginsenoside Rc
    Chinese website: Ginsenoside Rc

    References

    [1] Kim D H, Chan H P, Park D, et al. Arch Pharm Res, 2014, 37(6):813-20.
    [2] Tao Y, Man H R, Lee J, et al. Am J Chinese Med, 2016:1-21.
    [3] Lee Y J, Jin Y R, Lim W C, et al. Arch Pharm Res, 2003, 26(1):53-7.
    [4] Lee M S, Hwang J T, Kim S H, et al. J Ethnopharmacol, 2010, 127(3):771-6.
    [5] Yang J W, Kim S S. Molecules, 2015, 20(1):1293-303.
    [6] Gao Y, Zang P, Hao J, et al. J Med Plants Res. 2012,6(15):3030-6.

    Product Use Citation