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Astramembrannin I

Base Information Edit
  • Chemical Name:Astramembrannin I
  • CAS No.:83207-58-3
  • Molecular Formula:C41H68O14
  • Molecular Weight:784.983
  • Hs Code.:29389090
  • UNII:3A592W8XKE
  • DSSTox Substance ID:DTXSID301347884
  • Metabolomics Workbench ID:63896
  • Nikkaji Number:J427.610H
  • Wikidata:Q27256953
  • Mol file:83207-58-3.mol
Astramembrannin I

Synonyms:3beta,6alpha,16beta,20R,24S; astragaloside IV of astragaloside A;astragaloside A;astragaloside IV;astragaloside-A;astramembrannin I;cyclosiversioside F

Suppliers and Price of Astramembrannin I
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • AstragalosideA
  • 5mg
  • $ 185.00
  • TRC
  • AstragalosideA
  • 1mg
  • $ 45.00
  • DC Chemicals
  • AstragalosideA >98%
  • 250 mg
  • $ 500.00
  • DC Chemicals
  • AstragalosideA >98%
  • 100 mg
  • $ 250.00
  • Crysdot
  • AstragalosideA 98+%
  • 50mg
  • $ 236.00
  • Cayman Chemical
  • Astragaloside A ≥98%
  • 50mg
  • $ 900.00
  • Cayman Chemical
  • Astragaloside A ≥98%
  • 1mg
  • $ 45.00
  • Cayman Chemical
  • Astragaloside A ≥98%
  • 5mg
  • $ 191.00
  • Cayman Chemical
  • Astragaloside A ≥98%
  • 10mg
  • $ 338.00
  • Ambeed
  • (2R,3R,4S,5S,6R)-2-(((2aR,3R,4S,5aS,5bS,7S,7aR,9S,11aR,12aS)-4-Hydroxy-3-((2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyltetrahydrofuran-2-yl)-2a,5a,8,8-tetramethyl-9-(((2S,3R,4S,5R)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)oxy)hexadecahydrocyclopenta[a]cyclopropa[e]phenanthren-7-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol 98+%
  • 1g
  • $ 323.00
Total 73 raw suppliers
Chemical Property of Astramembrannin I Edit
Chemical Property:
  • Appearance/Colour:white powder 
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:284-286oC 
  • Refractive Index:1.62 
  • Boiling Point:895.666 °C at 760 mmHg 
  • PKA:12.91±0.70(Predicted) 
  • Flash Point:495.481 °C 
  • PSA:228.22000 
  • Density:1.395 g/cm3 
  • LogP:0.72410 
  • Storage Temp.:under inert gas (nitrogen or Argon) at 2-8°C 
  • XLogP3:1.3
  • Hydrogen Bond Donor Count:9
  • Hydrogen Bond Acceptor Count:14
  • Rotatable Bond Count:7
  • Exact Mass:784.46090684
  • Heavy Atom Count:55
  • Complexity:1460
Purity/Quality:

98%min *data from raw suppliers

AstragalosideA *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)O)C)O)C)C)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(CO8)O)O)O)C
  • Isomeric SMILES:C[C@]12CC[C@@]34C[C@@]35CC[C@@H](C([C@@H]5[C@H](C[C@H]4[C@@]1(C[C@@H]([C@@H]2[C@@]6(CC[C@@H](O6)C(C)(C)O)C)O)C)O[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO)O)O)O)(C)C)O[C@H]8[C@@H]([C@H]([C@@H](CO8)O)O)O
  • Uses Astragalosides are bioactive saponins isolated from dried roots of plants of the genus Astragalus, which is used in traditional Chinese medicine. Astragaloside A, also known as astragaloside IV, is known to have diverse protective effects for the cardiovascular, immune, digestive, and nervous systems. More specifically, it protects cardiomyocytes from apoptosis resulting from ischemia/reperfusion and inhibits inflammation signaled through TNF-α. Furthermore, astragaloside A stimulates angiogenesis, promotes the differentiation of neural stem cells, and increases neuroregeneration.
Technology Process of Astramembrannin I

There total 13 articles about Astramembrannin I which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
hesperidinase; In water; acetone; at 35 ℃; for 36h;
DOI:10.1248/cpb.31.709
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