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SOLASODINE

CAS No.
126-17-0
Chemical Name:
SOLASODINE
Synonyms
Solasodin;Salasdine;Nsc178260;SOLASODINE;Salasodine;Sosasodine;NSC 179187;Solanidine-S;PURAPURIDINE;Solancarpine
CBNumber:
CB5132193
Molecular Formula:
C27H43NO2
Molecular Weight:
413.64
MDL Number:
MFCD00037844
MOL File:
126-17-0.mol
MSDS File:
SDS
Last updated:2024-01-05 11:48:35

SOLASODINE Properties

Melting point 200-202°
alpha D25 -98° (c = 0.14 in methanol); D -113° (CHCl3)
Boiling point 532.75°C (rough estimate)
Density 1.0159 (rough estimate)
refractive index 1.6400 (estimate)
storage temp. 2-8°C
solubility DMSO: soluble0.5mg/mL, clear (warmed)
pka pKb 6.30(at 25℃)
form powder
color white to beige
optical activity [α]/D -88 to -98°, c = 0.2 in methanol
InChIKey KOZCINYDCJVLDW-GCGBSLFCSA-N
CAS DataBase Reference 126-17-0(CAS DataBase Reference)
FDA UNII L40Y453Y96
NIST Chemistry Reference Solasodine(126-17-0)

SAFETY

Risk and Safety Statements

Safety Statements  22-24/25
RTECS  WF1300000

SOLASODINE price More Price(37)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SML1141 Solasodine ≥95% (HPLC) 126-17-0 5mg $76.7 2024-03-01 Buy
Sigma-Aldrich SML1141 Solasodine ≥95% (HPLC) 126-17-0 25mg $297 2024-03-01 Buy
Usbiological 466370 Solasodine 126-17-0 5mg $305 2021-12-16 Buy
TRC S676553 Solasodine 126-17-0 50mg $385 2021-12-16 Buy
Usbiological 300992 Solasodine 126-17-0 10mg $393 2021-12-16 Buy
Product number Packaging Price Buy
SML1141 5mg $76.7 Buy
SML1141 25mg $297 Buy
466370 5mg $305 Buy
S676553 50mg $385 Buy
300992 10mg $393 Buy

SOLASODINE Chemical Properties,Uses,Production

Description

There is still some doubt as to whether this base occurs as such in Solanum aviculare and S. xanthocarpum or whether it is an artifact formed from Sola_x0002_sonine (q.v.) during the extraction process. The base is laevorotatory having [α]20D - 92.4° (C6H6) and the following salts and derivatives have been prepared: hydrochloride, m.p. 314°C; hydriodide, m.p. 293°C; oxalate, m.p. 248°C; tartrate, m.p. 222°C; picrate, m.p. 1.4l-2°C; picrolonate, m.p. 234°C; acetyl derivative, m.p. 195°C; benzoyl compound, m.p. 2l6-7°C and the 3:5-dinitrobenzoyl derivative, m.p. 191.5-193°C. The alkaloid forms a sparingly soluble digitonide and yields Diels's hydrocarbon on selenium dehydrogenation.

Uses

A potentially useful precursor.

Uses

antineoplastic, antiinflammatory

Uses

Solasodine is a potentially useful precursor for steroidal compounds and hormones, this is usually found in plants from the solanaceae family. It also has potent cytotoxic and anti-inflammatory effects.

Uses

Starting material for steroidal drugs.

Definition

ChEBI: Solasodine is an oxaspiro compound and steroid alkaloid sapogenin with formula C27H43NO2 found in the Solanum (nightshade) family. It is used as a precursor in the synthesis of complex steroidal compounds such as contraceptive pills. It has a role as a plant metabolite, a teratogenic agent, a diuretic, an antifungal agent, a cardiotonic drug, an immunomodulator, an antipyretic, an apoptosis inducer, an antioxidant, an antiinfective agent, an anticonvulsant, a central nervous system depressant and an antispermatogenic agent. It is an azaspiro compound, an oxaspiro compound, an alkaloid antibiotic, a hemiaminal ether, a sapogenin and a steroid alkaloid. It is a conjugate base of a solasodine(1+).

General Description

This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate. Produced by PhytoLab GmbH & Co. KG

Biochem/physiol Actions

Solasodine is a neuroprotective antioxidant glycoalkaloid of Solanum species. Solasodine increases superoxide dismutase (SOD), catalase (CAT),and glutathione (GSH) levels, while reducing lipid peroxidation (LPO) and nitric oxide (NO) levels in the brains of ischemia/reperfusion (I/R)-injury model in rats. Also, Solasonine displayed multiple activities including, anti-cancer and leishmanicidal activities.

Safety Profile

Poison by intraperitoneal route. Moderately toxic by ingestion. Experimental teratogenic and reproductive effects. When heated to decomposition it emits toxic fumes of NOx.

Purification Methods

Solasodine crystallises (as monohydrate) from MeOH as lustrous plates (on heating, the plates change to needles as they melt and resolidify in needles), or aqueous 80% EtOH, and sublimes at high vacuum. After recrystallisation from H2O, m 198-199o, then from Me2CO/H2O, m 199-201o, it has [] D 22 -109.3o (c 0.581, CHCl3). On TLC with silica gel G (*C6H6/absolute EtOH, 8:2) it has RF 0.45. IR (KBr): max at 10.3, 10.4, 11.2, 11.5 (azaoxaspirane bands). [Schreiber & Rnsch Tetrahedron 20 1939 1964, Uhle J Org Chem 27 656 1962, Kessar et al. Tetrahedron 27 2153 1971, Beilstein 27 III/IV 2000.]

References

Rochelmeyer, Chen., Arch. Pharm., 277,329 (1939)
Briggs., J. Chem. Soc., 3, (1942)
Briggs et al., ibid, 3013 (1950)
Absolute configuration: Boll, Phillipsborn., Acta Chem. Scand., 19, 1365 (1965)
Synthesis: Schreiber, Walther, Ronsch., Tetrahedron, 20, 1939 (1964)
Adam, Schreiber., Experientia, 21,471 (1965)
Adam, Schreiber., Tetrahedron, 22,3591 (1966)

514-32-9
126-17-0
Synthesis of SOLASODINE from Furosta-5,20(22)-dien-3-ol, 26-amino-, (3β,25R)-
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View Lastest Price from SOLASODINE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
SOLASODINE pictures 2024-04-07 SOLASODINE
126-17-0
US $0.00-0.00 / kg 0.10000000149011612kg ≥98%HPLC 20tons Chongqing Zhihe Biopharmaceutical Co., Ltd.
Solasodine pictures 2023-02-24 Solasodine
126-17-0
US $0.00 / mg 5mg ≥98%(HPLC) 10 g Shanghai Standard Technology Co., Ltd.
SOLASODINE pictures 2019-07-06 SOLASODINE
126-17-0
US $2.00 / kg 1kg 99% 100kg Career Henan Chemical Co
  • SOLASODINE pictures
  • SOLASODINE
    126-17-0
  • US $0.00-0.00 / kg
  • ≥98%HPLC
  • Chongqing Zhihe Biopharmaceutical Co., Ltd.
  • Solasodine pictures
  • Solasodine
    126-17-0
  • US $0.00 / mg
  • ≥98%(HPLC)
  • Shanghai Standard Technology Co., Ltd.
  • SOLASODINE pictures
  • SOLASODINE
    126-17-0
  • US $2.00 / kg
  • 99%
  • Career Henan Chemical Co

SOLASODINE Spectrum

(3beta,22alpha,25r)-spirosol-5-en-3-o SOLANCARPIDINE SOLASOD-5-EN-3BETA-OL SOLASODINE PURAPURIDINE delta5-20betaf,22alphaf,25alphaf,27-azaspirosten-3beta-ol Salasdine Salasodine Solanidine-S Solasodin Solasodine hydrochloride base Sosasodine Spiro[8H-naphth[2',1':4,5]indeno[2,1-b]furan-8,2'-piperidine], spirosol-5-en-3-ol deriv. Spirosol-5-en-3-ol Spirosol-5-en-3-ol, (3beta,22alpha,25R)- 5-SOLASODEN-3BETA-OL Solasod-5-en-3β-ol Salasod-5-en-3β-ol Nsc178260 Solancarpine (3β,22α,25R)-Spirosol-5-en-3-ol NSC 179187 Solasod-5-en-3β-ol (7CI,8CI) Solanum nigrum L. Spirosol-5-en-3-ol, (3β,22α,25R)- (4S,5'R,6aR,6bS,8aS,8bR,9S,10R,11aS,12aS,12bS)-5',6a,8a,9-Tetramethyl-1,3,4,5,6,6a,6b,7,8,8a,8b,9,11a,12,12a,12b-hexadecahydrospiro[naphtho[2',1':4,5]indeno[2,1-b]furan-10,2'-piperidin]-4-ol (2'R,4S,5'R,6aR,6bS,8aS,8bR,9S,11aS,12aS,12bS)-5',6a,8a,9-tetramethyl-1,3,4,5,6,6a,6b,7,8,8a,8b,9,11a,12,12a,12b-hexadecahydrospiro[naphtho[2',1':4,5]indeno[2,1-b]furan-10,2'-piperidin]-4-ol Solasodine extrapure, 98% SOLANI NIGERI HERBA (-)-Solasodine Fluoroestradiol Impurity 36 126-17-0 C27H43NO2 chemical reagent pharmaceutical intermediate phytochemical reference standards from Chinese medicinal herbs (TCM). standardized herbal extract Alkaloids