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Astragaloside VI

Product Name
Astragaloside VI
CAS No.
84687-45-6
Chemical Name
Astragaloside VI
Synonyms
Astragaloside VI;β-D-Glucopyranoside, (3β,6α,16β,20R,24S)-20,24-epoxy-3-[(2-O-β-D-glucopyranosyl-β-D-xylopyranosyl)oxy]-16,25-dihydroxy-9,19-cyclolanostan-6-yl;(3beta,6alpha,16beta,20R,24S)-20,24-Epoxy-3-[(2-O-beta-D-glucopyranosyl-beta-D-xylopyranosyl)oxy]-16,25-dihydroxy-9,19-cyclolanostan-6-yl beta-D-glucopyranoside
CBNumber
CB51469395
Molecular Formula
C47H78O19
Formula Weight
947.11
MOL File
84687-45-6.mol
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Astragaloside VI Property

Density 
1.46±0.1 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
Soluble in DMSO
pka
12.89±0.70(Predicted)
form 
Solid
color 
White to yellow
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

ChemScene
Product number
CS-0034273
Product name
AstragalosideVI
Purity
≥98.0%
Packaging
5mg
Price
$490
Updated
2021/12/16
Biorbyt Ltd
Product number
orb572863
Product name
Astragaloside VI
Packaging
100mg
Price
$1431.4
Updated
2021/12/16
Biorbyt Ltd
Product number
orb572863
Product name
Astragaloside VI
Packaging
250mg
Price
$2839
Updated
2021/12/16
Biorbyt Ltd
Product number
orb572863
Product name
Astragaloside VI
Packaging
1g
Price
$5654.2
Updated
2021/12/16
DC Chemicals
Product number
DC12126
Product name
AstragalosideVI
Purity
>98%
Packaging
1g
Price
$3800
Updated
2021/12/16
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Astragaloside VI Chemical Properties,Usage,Production

Biological Activity

Astragaloside VI accelerates wound healing by activating the epidermal growth factor receptor/extracellular signal-regulated kinase (EGFR/ERK) signaling pathway.

in vitro

Pretreatment with Astragaloside VI (AS-VI) at 1 μM increases EGFR activation in HaCaT cells. Astragaloside VI, a major intestinal metabolite of astragalosides, exerts the strongest EGFR activation. In HaCaT cells, the positive control, EGF expectedly results in 1.5±0.03-fold increase in cell proliferation, compared to the control. Astragaloside VI at the indicated concentrations also significantly promots cell proliferation in both HaCaT and HDF cells. Astragaloside VI promotes neural stem cell proliferation and enhances neurological function recovery in transient cerebral ischemic injury via activating EGFR/MAPK signaling cascades.

in vivo

Astragaloside VI improves wound healing, compared to the control. In the simple noninfected wound model, wound healing in mice is accelerated by Astragaloside VI, where in the time required for wound closure is shortened by approximately 2-4 days , compared to that in the control group. Topical treatment with Astragaloside VI reduces the volume of pus produced, compared to the control group. Astragaloside VI treated wounds show an accelerated rate of healing, compared to the control and vaseline groups. By day 22, the Astragaloside VI -treated wounds fully close, whereas the blank and vaseline-treated wounds do not fully close until day 26. Angiogenesis is a crucial step in the formation of granulation tissue and wound healing. Astragaloside VI increases blood vessel formation in both the non -infected and infected wound models. Astragaloside VI could effectively activate EGFR/MAPK signaling cascades, promote NSCs proliferation and neurogenesis in transient cerebral ischemic br ains, and improve the repair of neurological functions in post-ischemic stroke rats.

target

EGFR

Astragaloside VI Preparation Products And Raw materials

Raw materials

Preparation Products

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Astragaloside VI Suppliers

TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32161
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
52924
Advantage
58
MedChemExpress
Tel
--
Fax
--
Email
sales@medchemexpress.com
Country
United States
ProdList
6398
Advantage
58

84687-45-6, Astragaloside VIRelated Search:


  • Astragaloside VI
  • (3beta,6alpha,16beta,20R,24S)-20,24-Epoxy-3-[(2-O-beta-D-glucopyranosyl-beta-D-xylopyranosyl)oxy]-16,25-dihydroxy-9,19-cyclolanostan-6-yl beta-D-glucopyranoside
  • β-D-Glucopyranoside, (3β,6α,16β,20R,24S)-20,24-epoxy-3-[(2-O-β-D-glucopyranosyl-β-D-xylopyranosyl)oxy]-16,25-dihydroxy-9,19-cyclolanostan-6-yl
  • 84687-45-6
  • saponins