Ginsenoside Re

Base Information

Chemical Name:Ginsenoside Re
CAS No.:52286-59-6
Molecular Formula:C48H82O18
Molecular Weight:947.168
Hs Code.:29389090
European Community (EC) Number:257-814-6
UNII:46F3R0BL3I
DSSTox Substance ID:DTXSID801317298
Nikkaji Number:J38.851C
Wikidata:Q27105064
Metabolomics Workbench ID:155112
ChEMBL ID:CHEMBL510095

Synonyms:ginsenoside Re;ginsenoside-Re

Suppliers and Price of Ginsenoside Re

Supply Marketing:

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

Usbiological
Ginsenoside Re
20mg
$ 263.00

Usbiological
Ginsenoside Re
100mg
$ 355.00

TRC
Ginsenoside Re
250mg
$ 275.00

TCI Chemical
Ginsenoside Re
250MG
$ 652.00

TCI Chemical
Ginsenoside Re
50MG
$ 211.00

Sigma-Aldrich
Ginsenoside Re phyproof? Reference Substance
10 mg
$ 192.00

Sigma-Aldrich
Ginsenoside Re analytical standard
10mg
$ 301.00

Sigma-Aldrich
Ginsenoside Re primary pharmaceutical reference standard
10mg
$ 524.00

Medical Isotopes, Inc.
Ginsenoside Re
10 mg
$ 610.00

Labseeker
Ginsenoside Re 95
1g
$ 400.00

Total 89 raw suppliers

Chemical Property of Ginsenoside Re

Chemical Property:

Appearance/Colour:White powder
Vapor Pressure:0mmHg at 25°C
Melting Point:201～203℃
Refractive Index:1.61
Boiling Point:1011.8 °C at 760 mmHg
PKA:12.85±0.70(Predicted)
Flash Point:565.7 °C
PSA：298.14000
Density:1.38 g/cm³
LogP:-0.02840
Storage Temp.:2-8°C
Solubility.:DMSO (Slightly), Methanol (Slightly), Pyridine (Slightly)
XLogP3:1.6
Hydrogen Bond Donor Count:12
Hydrogen Bond Acceptor Count:18
Rotatable Bond Count:12
Exact Mass:946.55011576
Heavy Atom Count:66
Complexity:1700

Purity/Quality:

99%, ^*data from raw suppliers

Ginsenoside Re ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xn
Hazard Codes:Xn
Statements: 20/21/22
Safety Statements: 26-36

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CC4(C(CC(C5C4(CCC5C(C)(CCC=C(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)O)C7(C3C(C(CC7)O)(C)C)C)C)CO)O)O)O)O)O
Isomeric SMILES:C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@H]2[C@H]([C@@H]([C@H](O[C@H]2O[C@H]3C[C@@]4([C@H](C[C@H]([C@H]5[C@]4(CC[C@@H]5[C@](C)(CCC=C(C)C)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O)C)O)[C@@]7([C@@H]3C([C@H](CC7)O)(C)C)C)C)CO)O)O)O)O)O
Recent ClinicalTrials:A Clinical Trial of Ginseng in Diabetes
Uses Ginsenoside Re is an extract from ginger, responsible for some of the pharmacological functions. It displays cardiac contractility, anti-ischemic and anti-arrythmic activities.

Technology Process of Ginsenoside Re

There total 1 articles about Ginsenoside Re 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:

Reference yield: