JavaScript is disabled in your browser. Please enable JavaScript to view this website.
AB142646

Ginsenoside Rb1, Natural triterpenoid saponin

Be the first to review this product! Submit a review

|

(3 Publications)

MW 1109.3 Da, Purity >98%. Natural triterpenoid saponin with variety of biological activities. Shown to promote adipogenesis. Active in vitro and in vivo.

View Alternative Names

1300015D22Rik, 5' AMP activated protein kinase gamma 1 subunit, 5' AMP activated protein kinase subunit gamma 1, 5''-AMP-activated protein kinase subunit beta-1, 5''-AMP-activated protein kinase subunit gamma-1, 5'-AMP-activated protein kinase beta-1 subunit, 5'-AMP-activated protein kinase catalytic subunit alpha-2, AAKB1_HUMAN, AAKG1_HUMAN, AAPK2_HUMAN, ACACA kinase, AMP activated protein kinase noncatalytic gamma 1 subunit, AMP-ACTIVATED PROTEIN KINASE, NONCATALYTIC, BETA-1, AMP-activated protein kinase beta subunit, AMP-activated, noncatalytic, beta-1, AMPK, AMPK alpha 2 chain, AMPK beta 1 chain, AMPK gamma 1 chain, AMPK gamma1, AMPK subunit alpha-2, AMPK subunit beta-1, AMPK subunit gamma-1, AMPK-BETA-1, AMPK2, AMPKa2, AMPKalpha2, AMPKb, AMPKg, AU021155, Acetyl-CoA carboxylase kinase, E430008F22, HAMPKb, HMGCR kinase, Hydroxymethylglutaryl-CoA reductase kinase, MGC17785, MGC8666, PRKAA, PRKAA2, PRKAB1, PRKAG 1, Protein kinase AMP activated alpha 2 catalytic subunit, Protein kinase AMP activated catalytic subunit alpha 2, Protein kinase AMP activated gamma 1 non catalytic subunit, Protein kinase AMP activated non catalytic subunit beta 1, protein kinase, AMP-activated, beta 1 non-catalytic subunit, protein kinase, AMP-activated, noncatalytic gamma-1, protein kinase, AMP-activated, noncatalytic, beta-1

1 Images
Chemical Structure - Ginsenoside Rb1, Natural triterpenoid saponin (AB142646)
  • Chemical Structure

Lab

Chemical Structure - Ginsenoside Rb1, Natural triterpenoid saponin (AB142646)

2D chemical structure image of ab142646, Ginsenoside Rb1, Natural triterpenoid saponin

Key facts

CAS number

41753-43-9

Purity

>98%

Form

Solid

form

Source

Panax quinquefolius

Molecular weight

1109.3 Da

Molecular formula

C<sub>5</sub><sub>4</sub>H<sub>9</sub><sub>2</sub>O<sub>2</sub><sub>3</sub>

PubChem

9898279

Nature

Native

Solubility

Soluble in water

Soluble in ethanol

Biochemical name

Ginsenoside rb1

Biological description

Natural triterpenoid saponin with variety of biological activities. Shown to promote adipogenesis. Active in vitro and in vivo.

Canonical smiles

CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)O)C)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O)C

Isomeric smiles

CC(=CCC[C@@](C)([C@H]1CC[C@@]2([C@@H]1[C@@H](C[C@H]3[C@]2(CC[C@@H]4[C@@]3(CC[C@@H](C4(C)C)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O)C)C)O)C)O[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO[C@H]8[C@@H]([C@H]([C@@H]([C@H](O8)CO)O)O)O)O)O)O)C

InChi

InChI=1S/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

InChiKey

GZYPWOGIYAIIPV-JBDTYSNRSA-N

IUPAC Name

(2R,3R,4S,5S,6R)-2-[[(2R,3S,4S,5R,6S)-6-[(2S)-2-[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-12-hydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylhept-5-en-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

Properties and storage information

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate long-term storage conditions
+4°C
Storage information
The product can be stored for up to 12 months

Product protocols

Publications (3)

Recent publications for all applications. Explore the full list and refine your search

Frontiers in pharmacology 10:1154 PubMed31680950

2019

Ginsenoside Rb1 Induces Beta 3 Adrenergic Receptor-Dependent Lipolysis and Thermogenesis in 3T3-L1 Adipocytes and Mice.

Applications

Unspecified application

Species

Unspecified reactive species

Seona Lim,Jinbong Park,Jae-Young Um

Nature cell biology 21:203-213 PubMed30664786

2019

An IRAK1-PIN1 signalling axis drives intrinsic tumour resistance to radiation therapy.

Applications

Unspecified application

Species

Unspecified reactive species

Peter H Liu,Richa B Shah,Yuanyuan Li,Arshi Arora,Peter Man-Un Ung,Renuka Raman,Andrej Gorbatenko,Shingo Kozono,Xiao Zhen Zhou,Vincent Brechin,John M Barbaro,Ruth Thompson,Richard M White,Julio A Aguirre-Ghiso,John V Heymach,Kun Ping Lu,Jose M Silva,Katherine S Panageas,Avner Schlessinger,Robert G Maki,Heath D Skinner,Elisa de Stanchina,Samuel Sidi

CNS neuroscience & therapeutics 24:930-939 PubMed29524300

2018

Estrogen receptor-β of microglia underlies sexual differentiation of neuronal protection via ginsenosides in mice brain.

Applications

Unspecified application

Species

Unspecified reactive species

Seungyeop Lee,Si-On Lee,Gyu-Lee Kim,Dong-Kwon Rhee
View all publications

Product promise

We are committed to supporting your work with high-quality reagents, and we're here for you every step of the way. In the unlikely event that one of our products does not perform as expected, you're protected by our Product Promise.
For full details, please see our Terms & Conditions

Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.

For licensing inquiries, please contact partnerships@abcam.com