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  • 茄尼醇; 茄呢醇; 九聚异戌二烯醇

    Solanesol

    茄尼醇; 茄呢醇; 九聚异戌二烯醇
    产品编号 CFN90454
    CAS编号 13190-97-1
    分子式 = 分子量 C45H74O = 631.07
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Miscellaneous
    植物来源 The herbs of Nicotiana tabacum 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
    提供自定义包装
    产品名称 产品编号 CAS编号 包装 QQ客服
    茄尼醇; 茄呢醇; 九聚异戌二烯醇 CFN90454 13190-97-1 10mg QQ客服:3257982914
    茄尼醇; 茄呢醇; 九聚异戌二烯醇 CFN90454 13190-97-1 20mg QQ客服:3257982914
    茄尼醇; 茄呢醇; 九聚异戌二烯醇 CFN90454 13190-97-1 50mg QQ客服:3257982914
    茄尼醇; 茄呢醇; 九聚异戌二烯醇 CFN90454 13190-97-1 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 British Columbia (Canada)
  • University of Helsinki (Finland)
  • Anna University (India)
  • Centralised Purchases Unit (CPU), B.I.T.S (India)
  • Leibniz-Institut für Pflanzenbiochemie (IPB) (Germany)
  • China Medical University (Taiwan)
  • Instituto Politécnico de Bragan?a (Portugal)
  • University of Cincinnati (USA)
  • Max-Planck-Insitut (Germany)
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  • Universiti Sains Malaysia (Malaysia)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Inflammation2015, 38(1):445-55
  • J Ethnopharmacol.2017, 206:73-77
  • Theranostics.2023, 13(9):3103-3116.
  • Molecules.2017, 22(2)
  • Indian J Pharm Sci.2022, 84(3):144-151
  • Cell Metab.2020, S1550-4131(20)30002-4
  • Molecules 2022, 27(3),960.
  • Allergol Immunopathol (Madr).2022, 1;50(4):23-30.
  • J Ginseng Res.2022, 46(1):104-114.
  • Horticulturae2020, 6(4),76.
  • J Agric Food Chem.2016, 64(35):6783-90
  • Pharmaceutics.2022, 14(5):945.
  • Molecules.2022, 27(5):1675
  • Naunyn Schmiedebergs Arch Pharmacol.2017, 390(10):1073-1083
  • iScience.2023, 26(9):107602.
  • Nutrients.2023, 15(3):753.
  • Journal of Apicultural Research2021, 60(1).
  • Biomol Ther (Seoul).2023, 31(1):40-47.
  • Anal Bioanal Chem.2018, 410(5):1561-1569
  • Oxid Med Cell Longev.2022, 2022:5888636.
  • Plant Archives2020, 2(1),2929-2934
  • J Nat Prod.2023, 86(2):264-275.
  • Journal of Apicultural Research2021, 60(1)
  • ...
  • 生物活性
    Description: Solanesol can effectively scavenge lipid radicals to block lipid peroxidation, and inhibit effects on tyrosinase; it also can protect ethanol-induced L02 cell damage, which might be attributed to the activation of HO-1 and Hsp70.
    Targets: HSP (e.g. HSP90) | HO-1 | Caspase | PARP
    In vitro:
    Toxicol In Vitro. 2015 Apr;29(3):600-8.
    Solanesol protects human hepatic L02 cells from ethanol-induced oxidative injury via upregulation of HO-1 and Hsp70.[Pubmed: 25645596]

    METHODS AND RESULTS:
    In present study, we showed that the mRNA and protein levels of HO-1 and Hsp70 in solanesol-treated L02 cells were significantly increased. The induction of the HO-1 by solanesol is majorly achieved via enhancing the nuclear translocation and transactivity of Nrf2 through enhancement of Hsp90-Keap1 interaction, while solanesol-elevated Hsp70 is related with promoting the nuclear translocation of HSF1 through the involvement of chaperones interaction. Furthermore, the induction of HO-1 and Hsp70 by solanesol could protect against ethanol-induced liver injury, including significantly suppressing the elevation of the activities of LDH and AST, attenuating ethanol-induced increase of the MDA, ROS level and decrease of the GSH level. Moreover, solanesol also suppressed ethanol-induced apoptosis of L02 cells by inhibition of nuclear morphological damage, procaspase 3 and cleavage of caspase 3 and PARP, suggesting solanesol may be beneficial against ALD. Solanesol also promoted tBHQ-mediated protective effects. However, treatment cells with SnPP or PES markedly abrogated the protective effects of solanesol on ethanol-induced cell injury.
    CONCLUSIONS:
    These results strongly suggested that solanesol could protect ethanol-induced L02 cell damage, which might be attributed to the activation of HO-1 and Hsp70.
    Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 2014 Aug;31(4):833-6, 841.
    Antioxidant function of solanesol and its inhibitory effect on tyrosinase[Pubmed: 25464797]
    The present paper intends to discuss the antioxidant and tyrosinase inhibition effect of solanesol from three aspects of ultraviolet radiation and free radical scavenging.
    METHODS AND RESULTS:
    The paper makes a survey on diurnal variation rule of the minimum ultraviolet transmittance and ultraviolet transmittance of solanesol, hydroxyl (OH) free radical scavenging method of Smirnoff reaction system model, superoxide anion O2- free radical scavenging method of pyrogallol autoxidation, and the inhibitory effect of solanesol on tyrosinase activity by enzyme kinetic method. The experiment results showed that solanesol could effectively scavenge lipid radicals to block lipid peroxidation, and inhibit effects on tyrosinase.
    METHODS AND RESULTS:
    Solanesol is a natural extract which could be used to prevent senile atrophy of human skin and senile plaque.
    Biomolecules . 2019 Aug 2;9(8):334.
    Bioactivities and Medicinal Value of Solanesol and Its Accumulation, Extraction Technology, and Determination Methods[Pubmed: 31382471]
    Abstract Solanesol, an aliphatic terpene alcohol composed of nine isoprene units, is mainly found in solanaceous plants. Particularly, tobacco (Nicotiana tabacum), belonging to the Solanaceae family, is the richest plant source of solanesol, and its leaves have been regarded as the ideal material for solanesol extraction. Since the discovery of solanesol in tobacco, significant progress has been achieved in research on solanesol's bioactivities, medicinal value, accumulation, extraction technology, and determination methods. Solanesol possesses strong free radical absorption ability and antioxidant activity owing to the presence of several non-conjugated double bonds. Notably, solanesol's anti-inflammatory, neuroprotective, and antimicrobial activities have been previously demonstrated. Solanesol is a key intermediate in the synthesis of coenzyme Q10, vitamin K2, and the anticancer agent synergiser N-solanesyl-N,N'-bis(3,4-dimethoxybenzyl) ethylenediamine. Other applications of solanesol include solanesol derivative micelles for hydrophobic drug delivery, solanesol-derived scaffolds for bioactive peptide multimerization, and solanesol-anchored DNA for mediating vesicle fusion. Solanesol accumulation in plants is influenced by genetic and environmental factors, including biotic stresses caused by pathogen infections, temperature, illumination, and agronomic measures. Seven extraction technologies and seven determination methods of solanesol are also systematically summarized in the present review. This review can serve as a reference for solanesol's comprehensive application. Keywords: accumulation; bioactivity; determination methods; extraction technology; medicinal value; solanesol.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.5846 mL 7.9231 mL 15.8461 mL 31.6922 mL 39.6153 mL
    5 mM 0.3169 mL 1.5846 mL 3.1692 mL 6.3384 mL 7.9231 mL
    10 mM 0.1585 mL 0.7923 mL 1.5846 mL 3.1692 mL 3.9615 mL
    50 mM 0.0317 mL 0.1585 mL 0.3169 mL 0.6338 mL 0.7923 mL
    100 mM 0.0158 mL 0.0792 mL 0.1585 mL 0.3169 mL 0.3962 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
    甘油三油酸酯; Glycerine trioleate CFN90141 122-32-7 C57H104O6 = 885.44 20mg QQ客服:215959384
    花生四烯酸; Arachidonic acid CFN90058 506-32-1 C20H32O2 = 304.47 20mg QQ客服:3257982914
    月桂酸; Lauric acid CFN90493 143-07-7 C12H24O2 = 200.31 20mg QQ客服:215959384
    棕榈酸; 十六酸; 软脂酸; Palmitic acid CFN99716 57-10-3 C16H32O2 = 256.42 20mg QQ客服:215959384
    二十三碳酸; Tricosanoic acid CFN98571 2433-96-7 C23H46O2 = 354.61 20mg QQ客服:2056216494
    二十八烷酸; Octacosanoic Acid CFN98572 506-48-9 C28H56O2 = 424.74 20mg QQ客服:3257982914
    硬脂酸,十八碳酸,十八酸,十八(烷)酸; Stearic Acid CFN93165 57-11-4 C18H36O2 = 284.5 20mg QQ客服:3257982914
    亚油酸; Linoleic acid CFN93168 60-33-3 C18H32O2 = 280.5 20mg QQ客服:3257982914
    油酸; Oleic acid CFN94800 112-80-1 C18H34O2 = 282.5 20mg QQ客服:1457312923
    9,16-二氧代-10,12,14-十八碳三烯酸; 9,16-Dioxo-10,12,14-octadecatrienoic acid CFN98082 217810-46-3 C18H26O4 = 306.4 5mg QQ客服:1413575084

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