Ginsenoside Rg5

Base Information

Chemical Name:Ginsenoside Rg5
CAS No.:186763-78-0
Molecular Formula:C₄₂H₇₀O₁₂
Molecular Weight:767.011
Hs Code.:
ChEMBL ID:CHEMBL400244
DSSTox Substance ID:DTXSID501317132
Nikkaji Number:J2.505.148C
Wikidata:Q27136475
Mol file:186763-78-0.mol

Synonyms:ginsenoside Rg5

Suppliers and Price of Ginsenoside Rg5

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 Rg5
5mg
$ 921.00

Usbiological
Ginsenoside Rg5
1mg
$ 418.00

TRC
Ginsenoside Rg5
1mg
$ 380.00

Sigma-Aldrich
Ginsenoside Rg5 phyproof? Reference Substance
10MG
$ 481.00

Sigma-Aldrich
Ginsenoside Rg5 analytical standard
5mg
$ 553.00

Medical Isotopes, Inc.
Ginsenoside Rg5 98%
10 mg
$ 867.00

ChemScene
Ginsenoside Rg5 99.86%
10mg
$ 540.00

ChemScene
Ginsenoside Rg5 99.86%
5mg
$ 336.00

Chemenu
Ginsenoside Rg5 98%
10mg
$ 295.00

Cayman Chemical
Ginsenoside Rg5 ≥95%
10mg
$ 448.00

Total 51 raw suppliers

Chemical Property of Ginsenoside Rg5

Chemical Property:

Vapor Pressure:1.93E-34mmHg at 25°C
Boiling Point:859.7°C at 760 mmHg
PKA:12.85±0.70(Predicted)
Flash Point:473.7°C
PSA：198.76000
Density:1.28±0.1 g/cm3 (20 ºC 760 Torr)
LogP:2.81010
Storage Temp.:2-8°C
XLogP3:5.4
Hydrogen Bond Donor Count:8
Hydrogen Bond Acceptor Count:12
Rotatable Bond Count:9
Exact Mass:766.48672766
Heavy Atom Count:54
Complexity:1380

Purity/Quality:

95%-98% ^*data from raw suppliers

Ginsenoside Rg5 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=CCC=C(C)C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)O)C)C
Isomeric SMILES:CC(=CC/C=C(\C)/[C@H]1CC[C@@]2([C@@H]1[C@@H](C[C@H]3[C@]2(CC[C@@H]4[C@@]3(CC[C@@H](C4(C)C)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O)C)C)O)C)C
Uses Ginsenoside Rg5 is an aromatase inhibitor from Panax ginseng leaves. Also, it ameliorates cisplatin-induced nephrotoxicity in mice through inhibition of inflammation, oxidative stress, and apoptosis.

Technology Process of Ginsenoside Rg5

There total 4 articles about Ginsenoside Rg5 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:

: ginsenoside Rb₁

: 592550-52-2
[12β,20(S),25-trihydroxydammar-3-O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranoside]

: [12β,20(R),25-trihydroxydammar-3-O-β-D-glucopyranosyl-β-(1→2)-β-D-glucopyranoside]

: 38243-03-7
20(R)-ginsenoside Rg₃

: 14197-60-5,38243-03-7,126252-51-5
ginsenoside Rg₃

: 186763-78-0,74964-14-0
3β,12β-dihydroxydammar-20(22),24-diene-3-O-β-D-glucopyranosyl(1->2)-β-D-glucopyranoside

: 494753-69-4
3β-O-[β-D-glucopyranosyl-(1→2)-β-D-glucopyranosyl]-5R,9R,13R-dammarane-20(21),24(25)-diene-12β-ol

Guidance literature:: With iron(III) chloride; water; In ethanol; at 40 ℃; for 12h;
DOI:10.1248/cpb.c18-00426

Reference yield:

: 41753-43-9,132929-86-3
Ginsenoside Rb₁

: 38243-03-7
20(R)-ginsenoside Rg₃

: 14197-60-5,38243-03-7,126252-51-5
ginsenoside Rg₃

: 186763-78-0,74964-14-0
ginsenoside Rg₅

: 494753-69-4
3β-O-[β-D-glucopyranosyl-(1→2)-β-D-glucopyranosyl]-5R,9R,13R-dammarane-20(21),24(25)-diene-12β-ol

Guidance literature:: With glycine; at 120 ℃;
DOI:10.1016/j.bmcl.2008.07.056

Reference yield:

: 38243-03-7
20(R)-ginsenoside Rg₃

: 186763-78-0,74964-14-0
ginsenoside Rg₅

Guidance literature:: 20(R)-ginsenoside Rg₃; With pyridine; dmap; acetic anhydride; at 20 ℃; for 10h; Cooling with ice;

With triethylsilane; boron trifluoride diethyl etherate; In dichloromethane; at 20 ℃; Cooling with ice;

With potassium hydroxide; In 1,4-dioxane; methanol; for 10h; Reflux;