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TAXIFOLIN 3-O-RHAMNOSIDE

Product Name
TAXIFOLIN 3-O-RHAMNOSIDE
CAS No.
29838-67-3
Chemical Name
TAXIFOLIN 3-O-RHAMNOSIDE
Synonyms
Astilbin;(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-3,4-dihydro-2H-chroMen-3-yl 6-deoxy-alpha-L-Mannopyranoside;Loastilin;Astilbin-RM;Taxifolin 3-rhaMnoside;Taxifolin 3-o-rhamnoside;Astilbin (6CI, 7CI, 8CI);Dihydroquercetin 3-rhamnoside;Astilbin Taxifolin 3-O-rhaMnoside;Astilbin, 98%, from Smilax glabra Roxb.
CBNumber
CB7507018
Molecular Formula
C21H22O11
Formula Weight
450.4
MOL File
29838-67-3.mol
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TAXIFOLIN 3-O-RHAMNOSIDE Property

Melting point:
180 °C (decomp)
Boiling point:
801.1±65.0 °C(Predicted)
Density 
1.74
storage temp. 
Sealed in dry,2-8°C
solubility 
H2O: soluble1mg/mL, clear, colorless
pka
7.34±0.60(Predicted)
form 
A crystalline solid
color 
White to off-white
Water Solubility 
H2O: 1mg/mL, clear, colorless
InChIKey
ZROGCCBNZBKLEL-MQGABXIONA-N
SMILES
O([C@]1([H])O[C@@H](C)[C@H](O)[C@@H](O)[C@H]1O)[C@H]1C(C2=C(C=C(O)C=C2O[C@@H]1C1C=CC(O)=C(O)C=1)O)=O |&1:1,4,6,8,10,12,22,r|
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Safety

Hazard Codes 
N
Risk Statements 
50
Safety Statements 
61
RIDADR 
UN 3077 9 / PGIII
WGK Germany 
3
HS Code 
29389090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H400Very toxic to aquatic life

Precautionary statements

P273Avoid release to the environment.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
A2862
Product name
Astilbin from Engelhardtia roxburghiana
Purity
≥98%
Packaging
10mg
Price
$205
Updated
2025/07/31
Cayman Chemical
Product number
28267
Product name
Astilbin
Packaging
10mg
Price
$109
Updated
2024/03/01
Cayman Chemical
Product number
28267
Product name
Astilbin
Packaging
100mg
Price
$537
Updated
2024/03/01
Cayman Chemical
Product number
28267
Product name
Astilbin
Packaging
5mg
Price
$62
Updated
2024/03/01
Cayman Chemical
Product number
28267
Product name
Astilbin
Packaging
25mg
Price
$239
Updated
2024/03/01
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TAXIFOLIN 3-O-RHAMNOSIDE Chemical Properties,Usage,Production

Description

Astilbin is a flavonoid that has been found in S. glabra and has diverse biological activities. It inhibits cisplatin-induced increases in apoptosis and accumulation of reactive oxygen species (ROS) in HEK293 cells when used at a concentration of 200 μM. Astilbin (50 mg/kg) increases renal glutathione (GSH) levels and superoxide dismutase (SOD) and catalase activity and reduces serum creatinine and blood urea nitrogen (BUN) levels, renal IL-1β, IL-6, and TNF-α levels, apoptosis in kidney tissue, and kidney injury in a mouse model of cisplatin-induced nephrotoxicity. It reduces loss of dopaminergic neurons in the substantia nigra and increases striatal GSH levels and SOD activity in a mouse model of MPTP-induced Parkinson''s disease when administered at a dose of 50 mg/kg per day. Astilbin also reduces descent time in a pole test and increases traction test score in a mouse model of Parkinson''s disease, indicating reduced motor deficits. It reduces cell viability of MDA-MB-231 and MCF-7 cells (IC50s = 167.9 and 191.6 μM, respectively), as well as inhibits migration and increases apoptosis when used at concentrations of 50 and 200 μM. Astilbin (20 mg/kg every other day for 14 days) reduces tumor growth in an MCF-7 mouse xenograft model.

Chemical Properties

White crystalline powder, soluble in boiling water, almost insoluble in ether, from Poria cocos, Sarsaparilla, yellow wolfberry Engelhardtia roxburghiana Wall. red velvet goat's foot.

Uses

Astilbin displays anti-depressant activity involving monoaminergic neurotransmitters an the BDNF signal pathway. Anti-oxidant.

Definition

ChEBI: A flavanone glycoside that is (+)-taxifolin substituted by a alpha-L-rhamnosyl moiety at position 3 via a glycosidic linkage.

in vivo

To explore whether Astilbin improves CDDP-induced nephrotoxicity in vivo, an acute cisplatin nephrotoxic mouse model is established. Single injection of CDDP with 8 mg/kg dose results in notable weight loss compared with control group. However, the phenomenon is significantly alleviated by Astilbin at dose of 50 mg/kg. The mice fed Astilbin alone do not show any obvious alteration in body weight. Similarly, serum creatinine (SCr) and blood urea nitrogen (BUN) are higher in CDDP-treated mice than in control group. Treatment with Astilbin also decreases SCr and BUN levels. To examine the protective effect of Astilbin on CDDP-induced renal histopathological damage, the mouse kidney sections are stained with H&E. The mice in control group and Astilbin treated group have normal kidney morphology, while kidneys in CDDP group show severe damage with tubular degeneration, necrosis and cystic dilatation of the tubules with focal hemorrhages. Administration of Astilbin mitigated kidney injury, resulting in lower histopathological score compared to CDDP group. The apoptosis of renal cells is also detected using TUNEL staining to determine whether Astilbin treatment decreased renal cell apoptosis in CDDP-induced acute nephrotoxic mice[1].

IC 50

NRF2; NF-κB

References

[1] SI-WEI WANG . Astilbin ameliorates cisplatin-induced nephrotoxicity through reducing oxidative stress and inflammation[J]. Food and Chemical Toxicology, 2018, 114: Pages 227-236. DOI: 10.1016/j.fct.2018.02.041
[2] YING-LI ZHU . Neuroprotective effects of Astilbin on MPTP-induced Parkinson’s disease mice: Glial reaction, α-synuclein expression and oxidative stress[J]. International immunopharmacology, 2019, 66: Pages 19-27. DOI: 10.1016/j.intimp.2018.11.004
[3] XIAOQI SUN. Caspase-dependent mitochondrial apoptotic pathway is involved in astilbin-mediated cytotoxicity in breast carcinoma cells.[J]. Oncology reports, 2018, 40 4: 2278-2286. DOI: 10.3892/or.2018.6602

TAXIFOLIN 3-O-RHAMNOSIDE Preparation Products And Raw materials

Raw materials

Preparation Products

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TAXIFOLIN 3-O-RHAMNOSIDE Suppliers

Sichuan Hongen Plant Technology Co., Ltd.
Tel
+86-17340288373
Fax
86-838-2803556
Email
2370026295@qq.com
Country
China
ProdList
37
Advantage
58
Chembest Research Laboratories Limited
Tel
+86-21-20908456
Fax
021-58180499
Email
sales@BioChemBest.com
Country
China
ProdList
6003
Advantage
61
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Fax
021-64823266
Email
chenyj@titansci.com
Country
China
ProdList
14101
Advantage
59
Shandong Xiya Chemical Co., Ltd
Tel
4009903999 13355009207
Fax
0539-6365991
Email
3007715519@qq.com
Country
China
ProdList
18729
Advantage
57
Sichuan Kulinan Technology Co., Ltd
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11705
Advantage
57
Sinopharm Chemical Reagent Co,Ltd.
Tel
86-21-63210123
Fax
86-21-63290778 86-21-63218885
Email
sj_scrc@sinopharm.com
Country
China
ProdList
9815
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79
Aktin Chemicals, Inc.
Tel
86-28-85159085
Fax
86-28-85152372
Email
info@aktinchem.com
Country
China
ProdList
297
Advantage
62
Shenzhen Sungening Bio-Tech Co., Ltd
Tel
+86-0755-89668383
Fax
+86-0755-89594066/4038
Email
sales@sungening.com
Country
China
ProdList
1319
Advantage
65
Hangzhou Yuhao Chemical Technology Co., Ltd
Tel
0571-82693216
Fax
+86-571-82880190
Email
info@yuhaochemical.com
Country
China
ProdList
6387
Advantage
52
Dalian Meilun Biotech Co., Ltd.
Tel
0411-62910999 13889544652
Email
sales@meilune.com
Country
China
ProdList
4747
Advantage
58
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View Lastest Price from TAXIFOLIN 3-O-RHAMNOSIDE manufacturers

Shaanxi Dideu New Materials Co. Ltd
Product
sucrose palmitate 29838-67-3
Price
US $0.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
1000kgs
Release date
2025-11-21
Shaanxi Dideu New Materials Co. Ltd
Product
Astilbin Taxifolin 3-O-rhaMnoside 29838-67-3
Price
US $0.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
1000kgs
Release date
2025-11-21
Hovane Phytochemicals Co., Ltd
Product
Astilbin 29838-67-3
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
80%HPLC
Supply Ability
1 ton
Release date
2024-11-11

29838-67-3, TAXIFOLIN 3-O-RHAMNOSIDERelated Search:


  • Taxifolin 3-o-rhamnoside
  • Astilbin
  • Astilbin Taxifolin 3-O-rhaMnoside
  • (2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-3,4-dihydro-2H-chroMen-3-yl 6-deoxy-alpha-L-Mannopyranoside
  • Taxifolin 3-rhaMnoside
  • Astilbin froM Engelhardtia roxburghiana
  • Dihydroquercetin 3-rhamnoside
  • Astilbin, 98%, from Smilax glabra Roxb.
  • (2R,3R)-3-[(6-Deoxy-alpha-L-mannopyranosyloxy)]-2-(3,4-dihydroxy-phenyl)-2,3-dihydro-5,7-dihydroxy-4H-chromen-4-one
  • (2S,3S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-methyl-oxan-2-yl]oxy-chroman-4-one
  • (2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-methyl-oxan-2-yl]oxy-chroman-4-one
  • 4H-1-Benzopyran-4-one, 3-[(6-deoxy-α-L-mannopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-, (2R,3R)-
  • (2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3-dihydrochromen-4-one
  • (2R,3R)-2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)chroman-4-one
  • (2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-3,4-dihy...
  • Astilbin (6CI, 7CI, 8CI)
  • Loastilin
  • Astilbin-RM
  • (2R,3R)-3-[(6-Deoxy-α-L-mannopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-4H-1-benzopyran-4-one
  • 29838-67-3
  • Inhibitors
  • chemical reagent
  • pharmaceutical intermediate
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
  • standardized herbal extract