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APIGENIN-6-GLUCOSIDE-8-ARABINOSIDE

Product Name
APIGENIN-6-GLUCOSIDE-8-ARABINOSIDE
CAS No.
51938-32-0
Chemical Name
APIGENIN-6-GLUCOSIDE-8-ARABINOSIDE
Synonyms
Schaftos;Shaftoside;Schaftoside-RM;Trifarotene Impurity 7;Schaftoside, 10 mM in DMSO;Apigenin 8-C-α-L-arabinoside 6-C-β-D-glucoside;6-C-beta-D-Glucosyl-8-C-alpha-L-arabinosylapigenin;Schaftoside, 98%, from Desmodium styracifolium (Osbeck) Merr.;5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3R,4R,5S,6R)-3,4,5-...;4',5,7-Trihydroxy-6-(β-D-glucopyranosyl)-8-(α-L-arabinopyranosyl)flavone
CBNumber
CB31484635
Molecular Formula
C26H28O14
Formula Weight
564.5
MOL File
51938-32-0.mol
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APIGENIN-6-GLUCOSIDE-8-ARABINOSIDE Property

Melting point:
228℃
Boiling point:
935.0±65.0 °C(Predicted)
Density 
1.766
storage temp. 
2-8°C
solubility 
DMSO : 250 mg/mL (442.88 mM; Need ultrasonic)
form 
Solid
pka
5.70±0.40(Predicted)
color 
Yellow
InChIKey
NIABBGMPPWXWOJ-JQSBCWDXSA-N
SMILES
OC1=C([C@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)C(O)=C2C(C=C(C3C=CC(O)=CC=3)OC2=C1[C@@H]1OC[C@H](O)[C@H](O)[C@H]1O)=O |&1:3,4,5,7,9,30,33,35,37,r|
LogP
0.040 (est)
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Safety

Safety Statements 
24/25
WGK Germany 
3
RTECS 
DJ2977250
HS Code 
29389090
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
PHL83325
Product name
Schaftoside
Purity
phyproof? Reference Substance
Packaging
10mg
Price
$392
Updated
2025/07/31
Cayman Chemical
Product number
27950
Product name
Schaftoside
Packaging
1mg
Price
$46
Updated
2024/03/01
Cayman Chemical
Product number
27950
Product name
Schaftoside
Packaging
25mg
Price
$861
Updated
2024/03/01
Cayman Chemical
Product number
27950
Product name
Schaftoside
Packaging
5mg
Price
$219
Updated
2024/03/01
Cayman Chemical
Product number
27950
Product name
Schaftoside
Packaging
10mg
Price
$414
Updated
2024/03/01
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APIGENIN-6-GLUCOSIDE-8-ARABINOSIDE Chemical Properties,Usage,Production

Chemical Properties

White crystalline powder, soluble in methanol, derived from Desmodium styracifolium.

Uses

Schaftoside is an inhibitor of cholestorol gallstone formation. Prevents hepatic fatty degeneration in mice.

Definition

ChEBI: A C-glycosyl compound that is apigenin substituted by beta-D-glucopyranosyl and an alpha-L-arabinopyranosyl moieties at positions 6 and 8 via C-glycos dic linkages.

IC 50

TLR4

APIGENIN-6-GLUCOSIDE-8-ARABINOSIDE Preparation Products And Raw materials

Raw materials

Preparation Products

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APIGENIN-6-GLUCOSIDE-8-ARABINOSIDE Suppliers

China 198 United Kingdom 2 United States 9 USA 1 Global 210
EMMX Biotechnology LLC
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888-539-0666
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info@emmx.com
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View Lastest Price from APIGENIN-6-GLUCOSIDE-8-ARABINOSIDE manufacturers

Shaanxi Didu New Materials Co. Ltd
Product
APIGENIN-6-GLUCOSIDE-8-ARABINOSIDE 51938-32-0
Price
US $1.50/g
Min. Order
1g
Purity
99.0% Min
Supply Ability
100 Tons
Release date
2025-06-06
Shanghai Standard Technology Co., Ltd.
Product
Schaftoside 51938-32-0
Price
US $0.00/mg
Min. Order
5mg
Purity
≥98%(HPLC)
Supply Ability
10 g
Release date
2019-12-12
Career Henan Chemical Co
Product
APIGENIN-6-GLUCOSIDE-8-ARABINOSIDE 51938-32-0
Price
US $1.00/KG
Min. Order
1g
Purity
99%
Supply Ability
100KG
Release date
2018-12-24

51938-32-0, APIGENIN-6-GLUCOSIDE-8-ARABINOSIDERelated Search:

2β,27-Dihydroxy-3β-(β-D-glucopyranosyloxy)oleana-12-ene-23,28-dioic acid Neosperidin dihydrochalcone neo-gambogic acid (+)-Camptothecin Berberine DARUTIGENOL Valtrate Synephrine Parthenolide Baicalin Asiaticoside BAVACHININ A FORSYTHIN ORIENTIN Schisandrin A AURANTIO-OBTUSIN ARTEMISININ Hydroxysafflor yellow A

  • 8-(α-L-Arabinopyranosyl)-6-(β-D-glucopyranosyl)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
  • Shaftoside
  • Apigenin 8-C-α-L-arabinoside 6-C-β-D-glucoside
  • 6-C-beta-D-Glucosyl-8-C-alpha-L-arabinosylapigenin
  • 4',5,7-Trihydroxy-6-(β-D-glucopyranosyl)-8-(α-L-arabinopyranosyl)flavone
  • Schaftoside, 98%, from Desmodium styracifolium (Osbeck) Merr.
  • 5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]-8-[(2S,3R,4S,5S)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl]-4H-chromen-4-one (non-preferred name)
  • 5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2ytetrahydH-chromen-4-one (non-preferred name)
  • Schaftos
  • 5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3R,4R,5S,6R)-3,4,5-...
  • Mitochondrial Metabolism,Inhibitor,Dynamin,Schaftoside,Toll-like Receptor (TLR),Autophagy,inhibit,MyD88
  • 4H-1-Benzopyran-4-one, 8-α-L-arabinopyranosyl-6-β-D-glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-
  • Trifarotene Impurity 7
  • 5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-8-((2S,3R,4S,5S)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)-4H-chromen-4-one
  • Schaftoside-RM
  • Schaftoside, 10 mM in DMSO
  • 51938-32-0
  • chemical reagent
  • pharmaceutical intermediate
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
  • standardized herbal extract
  • plant extract
  • Tri-substituted Flavones