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41753-43-9

  • Product Name:Ginsenoside Rb1
  • Molecular Formula:C54H92O23
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Product Details

Purity:99%

Ginsenoside Rb1 Cas No.41753-43-9 In Bulk Supply

41753-43-9 Name

Name

Ginsenoside Rb1

Synonym

GINSENOSIDE GINSENOSIDE-RB1;GINSENOSIDE RB1;GINSENOSIDE RBL;(3beta,12beta)-20-[(6-o-beta-d-glucopyranosyl-beta-d-glucopyranosyl)oxy]-12-hydroxydammar-24-en-3-yl2-o-beta-d-glucopyranosyl-beta-d-glucopyranoside;2-O-beta-glucopyranosyl-(3beta,12beta)-20-[(6-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy]-12-hydroxydammar-24-en-3-yl-beta-D-glucopyranoside;Ginsenoside Rb1 std.;ginsenoside-rb1from panax quinquefolium (american ginseng)root;Ginsenoside Rb1 (CAS# 41753-43-9)

 

41753-43-9 Biological Activity

Related Catalog

Signaling Pathways >> Autophagy >> Autophagy

Signaling Pathways >> Immunology/Inflammation >> IRAK

Signaling Pathways >> Protein Tyrosine Kinase/RTK >> IRAK

Signaling Pathways >> Autophagy >> Mitophagy

Signaling Pathways >> Membrane Transporter/Ion Channel >> Na+/K+ ATPase

Research Areas >> Inflammation/Immunology

Natural Products >> Terpenoids and Glycosides

Target

Na+, K+-ATPase:6.3 μM (IC50)

IRAK-1

p65

Autophagy

Mitophagy

Plant Extract Ginsenoside Rb1 Cas No.41753-43-9 Usage

Ginsenoside Rb1, the effective constituent of ginseng, has been demonstrated to play favorable roles in improving the immunity system. Ginsenoside Rb1 (or Ginsenoside Rb1 or GRb1 or GRb1) is a chemical compound belonging to the ginsenoside family. It is one of the primary constituents of traditional Chinese medicine, Ginseng. Reference standard in the analysis of herbal medicinal products. A major bioactive component of panax ginseng that promotes neurotransmitter release by modulating phosphorylation of synapsins through a cAMP-dependent protein kinase pathway. It has been reported to display immunostimulatory and anticancer effects.

 

InChI:InChI=1/C54H92O23/c1-23(2)10-9-14-54(8,77-48-44(69)40(65)37(62)29(74-48)22-70-46-42(67)38(63)34(59)26(19-55)71-46)24-11-16-53(7)33(24)25(58)18-31-51(5)15-13-32(50(3,4)30(51)12-17-52(31,53)6)75-49-45(41(66)36(61)28(21-57)73-49)76-47-43(68)39(64)35(60)27(20-56)72-47/h10,24-49,55-69H,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-,49-,51-,52+,53+,54?/m0/s1

41753-43-9 Relevant articles

Acylated protopanaxadiol-type ginsenosides from the root of Panax ginseng

Zhu, Guo-Yuan,Li, Ying-Wei,Kwok-Po Hau, Desmond,Jiang, Zhi-Hong,Yu, Zhi-Ling,Fong, Wang-Fun

experimental part, p. 1853 - 1863 (2012/01/13)

Six new protopanaxadiol-type ginsenosides, named ginsenosides Ra 4-Ra9 (1-6, resp.), along with 14 known dammarane-type triterpene saponins, were isolated from the root of Panax ginseng, one of the most important Chinese medicinal herbs. 

Ginsenoside Rb1 ameliorates the abnormal hepatic glucose metabolism by activating STAT3 in T2DM mice

Weixuan Wang , Wenjing Zhan , Mingjie Liang , Yuanfeng Huang, Yuan Liu, Lexun Wang, Weijian Bei, Jiao Guo

Journal of Functional Foods Volume 104, May 2023, 105534

Ginsenoside Rb1, a major bioactive component of Panax ginseng C. A. Mey., exerts beneficial effects on type 2 diabetes mellitus (T2DM), but its underlying mechanism is unclear. In summary, our study showed that Rb1 improved T2DM by regulating hepatic glucose metabolism. More importantly, our experiments first demonstrated that STAT3 is an important regulator in Rb1-ameliorated glucose disorder in the liver of T2DM mice.

41753-43-9 Process route

(20S)-3-O-{β-D-6-O-[(E)-but-2-enoyl]glucopyranosyl-(1->2)-β-D-glucopyranosyl}-20-O-[β-D-glucopyranosyl-(1->6)-β-D-glucopyranosyl]protopanaxadiol
1346522-89-1

(20S)-3-O-{β-D-6-O-[(E)-but-2-enoyl]glucopyranosyl-(1->2)-β-D-glucopyranosyl}-20-O-[β-D-glucopyranosyl-(1->6)-β-D-glucopyranosyl]protopanaxadiol

Ginsenoside Rb<sub>1</sub>
41753-43-9,132929-86-3

Ginsenoside Rb1

Conditions
Conditions Yield
With sodium methylate; In methanol; at 20 ℃; for 12h;
 
malonyl-ginsenoside Rb<sub>1</sub>
88140-34-5

malonyl-ginsenoside Rb1

malonic acid
141-82-2

malonic acid

ginsenoside Rb<sub>1</sub>
41753-43-9,132929-86-3

ginsenoside Rb1

Conditions
Conditions Yield
With potassium hydroxide; In methanol; at 22 ℃; for 0.5h; Product distribution; malonic acid determined as its methyl ester by GLC;
 

41753-43-9 Upstream products

  • 1346522-89-1
    1346522-89-1

    (20S)-3-O-{β-D-6-O-[(E)-but-2-enoyl]glucopyranosyl-(1->2)-β-D-glucopyranosyl}-20-O-[β-D-glucopyranosyl-(1->6)-β-D-glucopyranosyl]protopanaxadiol

  • 88140-34-5
    88140-34-5

    malonyl-ginsenoside Rb1

41753-43-9 Downstream products

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    38243-03-7

    20(R)-ginsenoside Rg3

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    ginsenoside Rg3

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    ginsenoside Rg5