Solasonin

Base Information Edit

Chemical Name:Solasonin
CAS No.:19121-58-5
Molecular Formula:C₄₅H₇₃NO₁₆
Molecular Weight:884.072
Hs Code.:
European Community (EC) Number:242-826-6
NSC Number:82149
Wikipedia:Solasonine
ChEMBL ID:CHEMBL1967295
Mol file:19121-58-5.mol

Synonyms:alpha-solamargine;alpha-solamarine;alpha-solamarine, (3beta,22alpha,25R)-isomer;alpha-solasonine;solasonine

Suppliers and Price of Solasonin

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

Usbiological
Solasonine
10mg
$ 390.00

TRC
α-Solasonine
1mg
$ 115.00

Medical Isotopes, Inc.
Solasonine 98%
1000 mg
$ 1567.00

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

Biosynth Carbosynth
Solasonine
2 mg
$ 75.00

Biosynth Carbosynth
Solasonine
1 mg
$ 50.00

Biosynth Carbosynth
Solasonine
5 mg
$ 125.00

Biosynth Carbosynth
Solasonine
10 mg
$ 200.00

Biosynth Carbosynth
Solasonine
25 mg
$ 375.00

Biorbyt Ltd
Solasonine
100 mg
$ 799.00

Total 90 raw suppliers

Chemical Property of Solasonin Edit

Chemical Property:

Melting Point:301-303℃
Refractive Index:1.627
PKA:12.78±0.70(Predicted)
PSA：258.71000
Density:1.42 g/cm³
LogP:0.11590
XLogP3:1.1
Hydrogen Bond Donor Count:10
Hydrogen Bond Acceptor Count:17
Rotatable Bond Count:8
Exact Mass:883.49293524
Heavy Atom Count:62
Complexity:1630

Purity/Quality:

HPLC≥98% ^*data from raw suppliers

Solasonine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1
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=C6[C@@]5(CC[C@@H](C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1
Description This gly<:oalkaloid occurs in several species of Solanum including S. aviculare, S. sodomeum, S. verbascifolium and S. xanthocarpum. The alkaloid crystallizes from 80 per cent EtOH with 4.5 H20, m.p. 245-250°C (dec.), the anhydrous form being obtained from absolute MeOH. It has [α]25D - 68° (EtOH) and yields the following salts: hydrochloride, m.p. 265°C; picrate, m.p. 199-201 °C; picrolonate, m.p. 230-loC and the acetyl derivative, m.p. l35-8°C. On alkaline hydrolysis, the alkaloid gives solasodine and one mole each of galactose, glucose and rhamnose. The solution in concentrated H2S04 eventually gives a crimson colour with a brown fluorescence.
Uses α-Solasonine is a natural glycoalkaloid compound which has been shown to inhibit Gli-mediated transcritional activity.

Technology Process of Solasonin

There total 2 articles about Solasonin 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: 45.0%