Gitogenin

Base Information

Chemical Name:Gitogenin
CAS No.:511-96-6
Molecular Formula:C27H44 O4
Molecular Weight:432.644
Hs Code.:
European Community (EC) Number:866-822-4
UNII:60ZMY8IH51
DSSTox Substance ID:DTXSID101023656
Nikkaji Number:J6.270G
Wikidata:Q5880476
Metabolomics Workbench ID:35104
ChEMBL ID:CHEMBL1770687
Mol file:511-96-6.mol

Synonyms:gitogenin

Suppliers and Price of Gitogenin

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
Gitogenin
20mg
$ 632.00

TRC
Gitogenin
1mg
$ 65.00

JR MediChem
Gitogenin 98%
20mg
$ 1500.00

DC Chemicals
Gitogenin >98%,StandardReferencesGrade
20 mg
$ 280.00

Crysdot
Gitogenin 95+%
100mg
$ 550.00

ChemScene
Gitogenin
10mg
$ 403.00

ChemScene
Gitogenin
5mg
$ 237.00

ChemScene
Gitogenin
20mg
$ 686.00

Biorbyt Ltd
Gitogenin
100 mg
$ 1254.60

Biorbyt Ltd
Gitogenin
20 mg
$ 596.70

Total 38 raw suppliers

Chemical Property of Gitogenin

Chemical Property:

Vapor Pressure:1.22E-13mmHg at 25°C
Melting Point:272-273oC
Refractive Index:1.4840 (estimate)
Boiling Point:534.2oC at 760 mmHg
PKA:14.62±0.70(Predicted)
Flash Point:276.9oC
PSA：58.92000
Density:1.16g/cm3
LogP:4.76460
XLogP3:5.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:432.32395988
Heavy Atom Count:31
Complexity:726

Purity/Quality:

99%, ^*data from raw suppliers

Gitogenin ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)O)C)C)C)OC1
Isomeric SMILES:C[C@@H]1CC[C@@]2([C@H]([C@H]3[C@@H](O2)C[C@@H]4[C@@]3(CC[C@H]5[C@H]4CC[C@@H]6[C@@]5(C[C@H]([C@@H](C6)O)O)C)C)C)OC1
Uses Gitogenin is isolated from a methanolic extract of the whole plant of Tribulus longipetalus which exhibits inhibitory activities against α-glucosidase, lipoxygenase, acetylcholinesterase and butyrylcholinesterase.

Technology Process of Gitogenin

There total 14 articles about Gitogenin 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:

: 1499187-77-7
(25R)-2α-hydroxy-5α-spirostan-3β-yl O-β-D-galactopyranosyl-(1 → 2)-O-[β-D-glucopyranosyl-(1 → 3)]-O-β-D-glucopyranosyl-(1 → 4)-β-D-galactopyranoside

: 50-99-7
D-glucose

: 59-23-4
D-Galactose

: 511-96-6
gitogenin

Guidance literature:: With naringinase; potassium acetate; acetic acid; In aq. buffer; at 20 ℃; for 49h; pH=4.3; Enzymatic reaction;
DOI:10.1016/j.phytochem.2013.09.023

Reference yield:

: 1499190-07-6
(25R)-26-[(β-D-glucopyranosyl)oxy]-2α,22α-dihydroxy-5α-furostan-3β-yl O-β-D-galactopyranosyl-(1 → 2)-O-[β-D-glucopyranosyl-(1 → 3)]-O-β-D-glucopyranosyl-(1 → 4)-β-D-galactopyranoside

: 50-99-7
D-glucose

: 59-23-4
D-Galactose

: 511-96-6
gitogenin

Guidance literature:: With naringinase; potassium acetate; acetic acid; In aq. buffer; at 20 ℃; for 49h; pH=4.3; Enzymatic reaction;
DOI:10.1016/j.phytochem.2013.09.023

Reference yield:

: (25R)-26-[(β-D-glucopyranosyl)oxy]-2α-hydroxy-5α-furost-20(22)-en-3β-yl O-β-D-galactopyranosyl-(1 → 2)-O-[β-D-xylopyranosyl-(1 → 3)]-O-β-D-glucopyranosyl-(1 → 4)-β-D-galactopyranoside

: 58-86-6
D-xylose

: 50-99-7
D-glucose

: 59-23-4
D-Galactose

: 511-96-6
gitogenin

Guidance literature:: With naringinase; potassium acetate; acetic acid; In aq. buffer; at 20 ℃; for 49h; pH=4.3; Enzymatic reaction;
DOI:10.1016/j.phytochem.2013.09.023