Solasonine | CAS:19121-58-5 | Manufacturer ChemFaces

Solasonine

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According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.

Size /Price /Stock	10 mM * 1 mL in DMSO / $60.5 / In-stock
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Description:

Solasonine displays leishmanicidal activity against promastigote forms of L. amazonensis.

Targets:

Antifection

In vitro:

Phytochemistry. 1994 Nov;37(4):1007-11.

Interactions between the glycoalkaloids solasonine and solamargine in relation to inhibition of fungal growth.[Pubmed: 7765652]

Inhibition of mycelium development in Phoma medicaginis and Rhizoctonia solani by solamargine and Solasonine generally increased with increasing pH. P. medicaginis was the more susceptible species and solamargine the more potent compound.
METHODS AND RESULTS:
Solasonine was inactive against R. solani over the tested pH range (5-8). Dose-response curves confirmed these differential effects. Solamargine caused 50% growth inhibition in P. medicaginis at 60 microM (at pH 7) whereas no other treatment achieved this effect at 100 microM. Combinations of 50 microM of each glycoalkaloid produced synergistic effects against both fungi, especially R. solani which was essentially unaffected by either compound, by significantly inhibited by a 1:1 mixture of the two. The magnitude of the synergism was not affected by a pH change between 6 and 7. Spore germination in Alternaria brassicicola was markedly inhibited by 100 microM solamargine but unaffected by 100 microM Solasonine or either compound at 50 microM. In P. medicaginis, neither glycoalkaloid was inhibitory up to 150 microM.
CONCLUSIONS:
In combination, the two compounds caused synergistic effects in both species, but to a much greater extent in A. brassicicola.

Food Chem . 2013 Nov 15;141(2):1181-6.

Purification, antitumor activity in vitro of steroidal glycoalkaloids from black nightshade (Solanum nigrum L.)[Pubmed: 23790901]

Abstract Six steroidal glycoalkaloids (1-6) were isolated and purified from Solanum nigrum L. (SNL) by acid extraction and alkaline precipitation, various chromatographic techniques, and their structures were elucidated by spectroscopic data. Antitumor activity, structure-activity and its molecular mechanism were investigated by methyl thiazolyl tetrazolium (MTT) method, flow cytometry, colorimetric assay and an immunocytochemical method. Experimental results showed that compounds 1 (Solasonine), 2 (β1-Solasonine), 3 (solamargine) and 6 (solanigroside P) have cytotoxicity to MGC-803 cells. Compounds with three sugar units and a-l-rhamnopyranose at C-2 or a hydroxyl group on the steroidal backbone may be potential candidates for the treatment of gastric cancer. The mechanism of action may be related to the decrease of mutation p53, the increase of the ratio of Bax to Bcl-2 and the activation of caspase-3 to induce apoptosis.

Solasonine Description

Source:	The herbs of Solanum nigrum L.
Solvent:	DMSO, Pyridine, Methanol, Ethanol, etc.
Storage:	Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C). Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
After receiving:	The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.

Cell Research:

Chem Biodivers. 2013 Apr;10(4):642-8.

In vitro leishmanicidal and cytotoxic activities of the glycoalkaloids from Solanum lycocarpum (Solanaceae) fruits.[Pubmed: 23576350]

Leishmaniasis is an infection caused by a protozoan parasite of the genus Leishmania and is the second most prevalent parasitic protozoal disease after malaria in the world.
METHODS AND RESULTS:
We report the in vitro leishmanicidal activity on promastigote forms of Leishmania amazonensis and cytotoxicity, using LLCMK2 cells, of the glycoalkaloids from the fruits of Solanum lycocarpum, determined by colorimetric methods. The alkaloidic extract was obtained by acid-base extraction; solamargine and Solasonine were isolated by silica-gel chromatography, followed by reversed-phase HPLC final purification. The alkaloidic extract, solamargine, Solasonine, as well as the equimolar mixture of the glycoalkaloids solamargine and Solasonine displayed leishmanicidal activity against promastigote forms of L. amazonensis, whereas the aglycone solasodine was inactive. After 24 and 72 h of incubation, most of the samples showed lower cytotoxicities (IC50 6.5 to 124 μM) as compared to leishmanicidal activity (IC50 1.1 to 23.6 μM). The equimolar mixture solamargine/Solasonine was the most active with an IC50 value of 1.1 μM, after 72 h. Likewise, solamargine was the most active after 24 h with an IC50 value of 14.4 μM, both in comparison with the positive control amphotericin B.

Product Name	Solasonine
Price:	$168 / 20mg
CAS No.:	19121-58-5
Catalog No.:	CFN90156
Molecular Formula:	C₄₅H₇₃NO₁₆
Molecular Weight:	884.06 g/mol
Purity:	>=98%
Type of Compound:	Alkaloids
Physical Desc.:	Powder
Source:	The herbs of Solanum nigrum L.
Solvent:	DMSO, Pyridine, Methanol, Ethanol, etc.
Download:	COA MSDS SDF Manual
Similar structural:	Comparison (Web) (SDF)
Guestbook:

Size /Price /Stock	10 mM * 100 uL in DMSO / Inquiry / In-stock 10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries	Anti-proliferation Compound Library Quality control indexes Compound Library Anti-trypanosoma Compound Library Anti-multidrug resistance Compound Library Alkaloids Compound Library Antifection Inhibitor Library

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	1.1311 mL	5.6557 mL	11.3114 mL	22.6229 mL	28.2786 mL
5 mM	0.2262 mL	1.1311 mL	2.2623 mL	4.5246 mL	5.6557 mL
10 mM	0.1131 mL	0.5656 mL	1.1311 mL	2.2623 mL	2.8279 mL
50 mM	0.0226 mL	0.1131 mL	0.2262 mL	0.4525 mL	0.5656 mL
100 mM	0.0113 mL	0.0566 mL	0.1131 mL	0.2262 mL	0.2828 mL

CFN93102	Solamarine	20318-30-3	884.1	C₄₅H₇₃NO₁₆
CFN90930	Tomatine	17406-45-0	1034.2	C₅₀H₈₃NO₂₁
CFN70371	Demissidine	474-08-8	399.7	C₂₇H₄₅NO
CFN70454	Solanidine	80-78-4	397.6	C₂₇H₄₃NO
CFN00450	alpha-Chaconine	20562-03-2	852.06	C₄₅H₇₃NO₁₄
CFN90560	alpha-Solanine	20562-02-1	868.06	C₄₅H₇₃NO₁₅
CFN90928	Cyclopamine	4449-51-8	411.6	C₂₇H₄₁NO₂
CFN90955	Jervine	469-59-0	425.6	C₂₇H₃₉NO₃
CFN98144	Peimisine	19773-24-1	427.62	C₂₇H₄₁NO₃
CFN95990	5-Epikarelinine	2102716-91-4	459.6	C₂₇H₄₁NO₅