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  • 澳洲茄边碱

    Solamargine

    澳洲茄边碱
    产品编号 CFN90159
    CAS编号 20311-51-7
    分子式 = 分子量 C45H73NO15 = 868.06
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Alkaloids
    植物来源 The herbs of Solanum nigrum L.
    ChemFaces的产品在影响因子大于5的优秀和顶级科学期刊中被引用
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    产品名称 产品编号 CAS编号 包装 QQ客服
    澳洲茄边碱 CFN90159 20311-51-7 10mg QQ客服:3257982914
    澳洲茄边碱 CFN90159 20311-51-7 20mg QQ客服:3257982914
    澳洲茄边碱 CFN90159 20311-51-7 50mg QQ客服:3257982914
    澳洲茄边碱 CFN90159 20311-51-7 100mg QQ客服:3257982914
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    ChemFaces的产品在许多优秀和顶级科学期刊中被引用

    Cell. 2018 Jan 11;172(1-2):249-261.e12.
    doi: 10.1016/j.cell.2017.12.019.
    IF=36.216(2019)

    PMID: 29328914

    Cell Metab. 2020 Mar 3;31(3):534-548.e5.
    doi: 10.1016/j.cmet.2020.01.002.
    IF=22.415(2019)

    PMID: 32004475

    Mol Cell. 2017 Nov 16;68(4):673-685.e6.
    doi: 10.1016/j.molcel.2017.10.022.
    IF=14.548(2019)

    PMID: 29149595

    ACS Nano. 2018 Apr 24;12(4): 3385-3396.
    doi: 10.1021/acsnano.7b08969.
    IF=13.903(2019)

    PMID: 29553709

    Nature Plants. 2016 Dec 22;3: 16206.
    doi: 10.1038/nplants.2016.205.
    IF=13.297(2019)

    PMID: 28005066

    Sci Adv. 2018 Oct 24;4(10): eaat6994.
    doi: 10.1126/sciadv.aat6994.
    IF=12.804(2019)

    PMID: 30417089
    我们的产品现已经出口到下面的研究机构与大学,并且还在增涨
  • University of Hawaii Cancer Center (USA)
  • University of Medicine and Pharmacy (Romania)
  • University of Ioannina (Greece)
  • Research Unit Molecular Epigenetics (MEG) (Germany)
  • Chang Gung University (Taiwan)
  • Florida International University (USA)
  • Universiti Kebangsaan Malaysia (Malaysia)
  • Kitasato University (Japan)
  • University of Liège (Belgium)
  • University of Maryland (USA)
  • Universite Libre de Bruxelles (Belgium)
  • Universidad de Antioquia (Colombia)
  • Aarhus University (Denmark)
  • Griffith University (Australia)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Eur Rev Med Pharmacol Sci.2020, 24(9):5127-5139.
  • Int J Mol Sci.2022, 23(11):6172.
  • Korean J Environ Agric.2018, 37(4):260-267
  • Institut Pasteur Korea2020, doi: 10.21203.
  • Environ Toxicol.2021, 36(9):1848-1856.
  • Molecules.2021, 26(23):7390.
  • Pharmaceuticals (Basel).2021, 14(8):742.
  • Appl. Sci.2020, 10(5),1713.
  • Pharmaceutics.2021, 13(11):1839.
  • J Korean Med Obes Res.2023, 23:10-7
  • Horticulturae2020, 6(4),76.
  • Biomolecules.2019, 9(11):E696
  • Int Immunopharmacol.2023, 7:127:111322.
  • Antiviral Res.2013, 98(3):386-93
  • Phytomedicine.2021, 2(82):153452
  • Vietnam J. Chemistry2022, 60(2):211-222
  • J of Applied Biological Chem.2020, 63(2):147-152
  • EXCLI J.2023, 22:482-498.
  • Int. J. Mol. Sci.2022, 23(8), 4130.
  • J Ethnopharmacol.2021, 267:113615.
  • J Chromatogr B Analyt Technol Biomed Life Sci.2021, 1187:123012.
  • Chem Res Toxicol. 2022, acs.chemrestox.2c00049.
  • Food Chem.2023, 404(Pt A):134517.
  • ...
  • 生物活性
    Description: Solamargine has potential anti-trypanosomal, and anti-cancer activities; interactions between the glycoalkaloids solasonine and solamargine have inhibition of fungal growth. Solamargine significantly inhibits migration and invasion of HepG2 cells by down-regulating MMP-2 and MMP-9 expression and activity.
    Targets: MMP(e.g.TIMP) | p53 | Bcl-2/Bax | Caspase | Antifection
    In vitro:
    Toxicol In Vitro. 2015 Aug;29(5):893-900.
    Solamargine inhibits migration and invasion of human hepatocellular carcinoma cells through down-regulation of matrix metalloproteinases 2 and 9 expression and activity.[Pubmed: 25819016]
    Solamargine is a steroidal alkaloid glycoside isolated from Solanum nigrum. The aim of this study was to investigate the effects of solamargine on tumor migration and invasion in aggressive human hepatocellular carcinoma cells.
    METHODS AND RESULTS:
    The MTT assay was used to assess the effects of solamargine on the viability of HepG2 cells. Migration and invasion ability of HepG2 cells under solamargine treatment were examined by a wound healing migration assay and Boyden chamber assay, respectively. Western blotting assays were used to detect the expression of MMP-2 and MMP-9 proteins and MMP-2 and MMP-9 activity were analyzed by gelatin zymography assay. Solamargine reduced HepG2 cell viability in a concentration-dependent manner. At 7.5μM solamargine decreased cell viability by less than 20% in HepG2 cells. A wound healing migration assay and Boyden chamber invasion assay showed that solamargine significantly inhibited in vitro migration and invasion of HepG2 cells. At the highest dose, solamargine decreased cell migration and invasion by more than 70% and 72% in HepG2 cells, respectively. Western blotting and gelatin zymography results showed that solamargine reduced expression and function of MMP-2 and MMP-9 proteins.
    CONCLUSIONS:
    In conclusion, the results showed that solamargine significantly inhibits migration and invasion of HepG2 cells by down-regulating MMP-2 and MMP-9 expression and activity.
    An Acad Bras Cienc. 2013 Sep;85(3):903-7.
    In vitro trypanocidal activity of solamargine and extracts from Solanum palinacanthum and Solanum lycocarpum of Brazilian cerrado.[Pubmed: 24068082]

    METHODS AND RESULTS:
    The present investigation was to evaluate the potential trypanocidal activity of crude ethanolic extract of the fruits of Solanum palinacanthum, Solanum lycocarpum and the glycoalcaloid, solamargine. S. palinacanthum and S. lycocarpum fruit powders were submitted to exhaustively extraction with 96% ethanol and solamargine were isolated from the extract of S. palinacanthum. Both extracts and solamargine were analysed for trypanocidal activity by using MTT colorimetric assay. Extracts of S. palinacanthum showed to be more active (IC50 = 175.9 μg.ml-1) than S. lycocarpum (IC50 = 194.7 μg.ml-1). Solamargine presented a strong activity (IC50 = 15.3 μg.ml-1), which can explain the better activity of the both extracts. Benznidazol (IC50 = 9.0 μg.ml-1) is the only drug used to treat Chagas' disease.
    CONCLUSIONS:
    These findings demonstrate for the first time that ethanol extracts obtained from both fruits of S. palinacanthum and S. lycocarpum and also solamargine have a potential anti-trypanosomal activity.
    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. Solasonine was inactive against R. solani over the tested pH range (5-8). Dose-response curves confirmed these differential effects.
    METHODS AND RESULTS:
    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.
    In vivo:
    Int J Oncol . 2019 May;54(5):1545-1554.
    Solamargine inhibits gastric cancer progression by regulating the expression of lncNEAT1_2 via the MAPK signaling pathway[Pubmed: 30864686]
    Abstract Solamargine, a derivative from the steroidal solasodine in Solanum species, has exhibited anticancer activities in numerous types of cancer; however, its role in gastric cancer (GC) remains unknown. In the present study, it was demonstrated that Solamargine suppressed the viability of five gastric cancer cell lines in a dose‑dependent manner and induced notable alterations in morphology. Treatment with Solamargine promoted cell apoptosis (P<0.01). Solamargine increased the expression of long noncoding RNA (lnc) p53 induced transcript and lnc nuclear paraspeckle assembly transcript 1 (NEAT1)_2 (P<0.01) in GC by reducing the phosphorylation of extracellular signal‑regulated kinase (Erk)1/2 mitogen‑activated protein kinase (MAPK). To gain insight into the potential mechanism, an Erk1/2 inhibitor (U0126) was applied. The results revealed that lncNEAT1_2 expression levels increased, which was consistent with the effects of Solamargine. Downregulation of lncNEAT1_2 in GC cells revealed no effect on the expression levels of total Erk1/2 and, and counteracted the effect of Solamargine. Solamargine was observed to increase the expression of lncNEAT1_2 via the Erk1/2 MAPK signaling pathway. Of note, the knockdown of lncNEAT1_2 reduced the inhibitory effect of Solamargine (P<0.05). Additionally, experiments in vivo and in primary GC cells from patients demonstrated that Solamargine significantly suppressed tumor growth (P<0.05). In vivo analysis of a xenograft mouse model further supported that Solamargine could induce the apoptosis of cancer cells in tumor tissue as observed by a terminal deoxynucleotidyl transferase‑mediated dUTP‑biotin nick end labeling and H&E staining (P<0.05). Experiments in primary GC cells from patients verified the anti‑tumor effect of Solamargine. In summary, the findings of the present study indicated that Solamargine inhibited the progression of GC by regulating lncNeat1_2 via the MAPK pathway.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.152 mL 5.76 mL 11.5199 mL 23.0399 mL 28.7999 mL
    5 mM 0.2304 mL 1.152 mL 2.304 mL 4.608 mL 5.76 mL
    10 mM 0.1152 mL 0.576 mL 1.152 mL 2.304 mL 2.88 mL
    50 mM 0.023 mL 0.1152 mL 0.2304 mL 0.4608 mL 0.576 mL
    100 mM 0.0115 mL 0.0576 mL 0.1152 mL 0.2304 mL 0.288 mL
    * Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
    部分图片展示
    产品名称 产品编号 CAS编号 分子式 = 分子量 位单 联系QQ
    澳洲茄碱; Solasonine CFN90156 19121-58-5 C45H73NO16 = 884.06 20mg QQ客服:215959384
    澳洲茄边碱; Solamargine CFN90159 20311-51-7 C45H73NO15 = 868.06 20mg QQ客服:1457312923
    beta-澳洲茄边碱; Khasianine CFN90387 32449-98-2 C39H63NO11 = 721.93 20mg QQ客服:3257982914
    Beta-茄边碱; Beta-Solamarine CFN90552 3671-38-3 C45H73NO15 = 868.07 5mg QQ客服:2056216494
    澳茄新碱; Solasurine CFN90553 27028-76-8 C39H63NO11 = 721.92 5mg QQ客服:1457312923
    澳洲边茄碱; Solamarine CFN93102 20318-30-3 C45H73NO16 = 884.1 5mg QQ客服:1413575084
    番茄碱苷; Tomatine CFN90930 17406-45-0 C50H83NO21 = 1034.2 20mg QQ客服:3257982914
    垂茄啶; Demissidine CFN70371 474-08-8 C27H45NO = 399.7 5mg QQ客服:3257982914
    茄啶; Solanidine CFN70454 80-78-4 C27H43NO = 397.6 5mg QQ客服:1413575084
    卡茄碱; alpha-Chaconine CFN00450 20562-03-2 C45H73NO14 = 852.06 5mg QQ客服:215959384

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