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  • 迷迭香酚

    Rosmanol

    迷迭香酚
    产品编号 CFN93024
    CAS编号 80225-53-2
    分子式 = 分子量 C20H26O5 = 344.45
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Diterpenoids
    植物来源 The herbs of Salvia officinalis
    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
    迷迭香酚 CFN93024 80225-53-2 1mg QQ客服:215959384
    迷迭香酚 CFN93024 80225-53-2 5mg QQ客服:215959384
    迷迭香酚 CFN93024 80225-53-2 10mg QQ客服:215959384
    迷迭香酚 CFN93024 80225-53-2 20mg QQ客服:215959384
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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
  • Centralised Purchases Unit (CPU), B.I.T.S (India)
  • National Cancer Center Research Institute (Japan)
  • Institute of Tropical Disease Universitas Airlangga (Indonesia)
  • Texas A&M University (USA)
  • FORTH-IMBB (Greece)
  • Northeast Normal University Changchun (China)
  • Leibniz Institute of Plant Biochemistry (Germany)
  • Technical University of Denmark (Denmark)
  • Monash University Malaysia (Malaysia)
  • Celltrion Chemical Research Institute (Korea)
  • Regional Crop Research Institute (Korea)
  • Korea Intitute of Science and Technology (KIST) (Korea)
  • University of Ioannina (Greece)
  • Uniwersytet Gdański (Poland)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • J of the Korean Society of Food Science and Nutrition2019, 32(2):148-154
  • Molecules.2022, 27(13):4227.
  • Drug Chem Toxicol.2020, 1-14.
  • FASEB J.2022, 36(7):e22387.
  • South African J of Botany2020, 135:50-57
  • Res Rep Urol.2022, 14:313-326.
  • Phytother Res.2019, 33(5):1490-1500
  • Toxicol Appl Pharmacol.2022, 434:115815.
  • Agronomy2022, 12(10), 2426.
  • Processes2020, 8(12),1540.
  • J Pharm Pharmacol.2022, rgac033.
  • BMC Complement Altern Med.2017, 17(1):393
  • Food Chem Toxicol.2023, 176:113802.
  • Front Immunol.2018, 9:2655
  • Curr Eye Res.2018, 43(1):27-34
  • Journal of Molecular Liquids2022, 364:120062.
  • Reprod Sci.2022,10.1007/s43032-022-01117-4.
  • Saf Health Work.2019, 10(2):196-204
  • Antioxidants (Basel).2021, 10(10):1620.
  • Front Pharmacol.2021, 12:762829.
  • Phytomedicine.2019, 58:152893
  • Life (Basel).2022, 12(10):1630.
  • J Adv Res.2021, 35:245-257.
  • ...
  • 生物活性
    Description: Rosmanol has antioxidant activity, it can activate the antioxidant response element, it also has biphasic modulation of GABAA receptors, demonstrates CNS activity in mouse models of antinociception, antidepressant and anxiolysis. Rosmanol exhibits significant cytotoxicity towards the neuroblastoma cells, it potently induces apoptosis through both the mitochondrial apoptotic pathway and death receptor pathway in human colon adenocarcinoma COLO 205 cells.Rosmanol has anti-inflammatory activity, it potently inhibits lipopolysaccharide-induced iNOS and COX-2 expression through downregulating MAPK, NF-kappaB, STAT3 and C/EBP signaling pathways.
    Targets: GABA Receptor | Nrf2 | PARP | Bcl-2/Bax | Caspase | NOS | COX | PGE | STAT | ERK | p38MAPK | PI3K | Akt | NF-kB
    In vitro:
    Acta Societatis Botanicorum Poloniae, 1997, 66(3-4):347-349.
    Rosmanol controls explants browning of Hypericum Canariensis L. During the In Vitro establishment of shoots[Reference: WebLink]
    An efficient method for eradication of browning exudate was developed for Hypericum canariensis.
    METHODS AND RESULTS:
    For this purpose the effect of natural products on browning exudates were investigated in four types of culture media: Murashige and Skoog (MS, 1962); Gamborg's (B5, 1979); Woody Plant Medium (WPM, Lloyd and McCown 1981) and modified Quoirin and Lepoivre (QL.4) (Mederos 1991, Mederos et al. 1995) basal macroelements; these basal macroelements were supplemented with the microelement formula described by Murashige and Skoog (MS, 1962). During the establishment of shoots organogenesis potential was achieved in the Murashige and Skoog (MS, 1962) and modified Quoirin and Lepoivre (QL. 4) (Mederos 1991, Mederos et al. 1995) media after browning exudates was eliminated by Rosmanol treatments.
    CONCLUSIONS:
    Rosmanol is a powerful diterpenic antioxidanl isolated from Salvia canariensis L., a medicinal species endemic to the Canary Islands.
    J Pharm Pharm Sci. 2015;18(4):448-59.
    Antidepressant, Anxiolytic and Antinociceptive Activities of Constituents from Rosmarinus Officinalis.[Pubmed: 26626245]
    Recently, rosemary extracts standardized to diterpenes (e.g. carnosic acid and carnosol) have been approved by the European Union (EU) and given a GRAS (Generally Recognized as Safe) status in the United States by the Food and Drug Administration (FDA).
    METHODS AND RESULTS:
    Incorporation of rosemary into our food system and through dietary selection (e.g. Mediterranean Diet) has increased the likelihood of exposure to diterpenes in rosemary. In consideration of this, a more thorough understanding of rosemary diterpenes is needed to understand its potential for a positive impact on human health. Three agents in particular have received the most attention that includes carnosic acid, carnosol, and Rosmanol with promising results of anti-cancer activity. These studies have provided evidence of diterpenes to modulate deregulated signaling pathways in different solid and blood cancers. Rosemary extracts and the phytochemicals therein appear to be well tolerated in different animal models as evidenced by the extensive studies performed for approval by the EU and the FDA as an antioxidant food preservative.
    CONCLUSIONS:
    This mini-review reports on the pre-clinical studies performed with carnosic acid, carnosol, and Rosmanol describing their mechanism of action in different cancers.
    Cancer Lett. 2015 Oct 28;367(2):93-102.
    Diterpenes from rosemary (Rosmarinus officinalis): Defining their potential for anti-cancer activity.[Pubmed: 26170168]
    Recently, rosemary extracts standardized to diterpenes (e.g. carnosic acid and carnosol) have been approved by the European Union (EU) and given a GRAS (Generally Recognized as Safe) status in the United States by the Food and Drug Administration (FDA).
    METHODS AND RESULTS:
    Incorporation of rosemary into our food system and through dietary selection (e.g. Mediterranean Diet) has increased the likelihood of exposure to diterpenes in rosemary. In consideration of this, a more thorough understanding of rosemary diterpenes is needed to understand its potential for a positive impact on human health. Three agents in particular have received the most attention that includes carnosic acid, carnosol, and Rosmanol with promising results of anti-cancer activity. These studies have provided evidence of diterpenes to modulate deregulated signaling pathways in different solid and blood cancers. Rosemary extracts and the phytochemicals therein appear to be well tolerated in different animal models as evidenced by the extensive studies performed for approval by the EU and the FDA as an antioxidant food preservative.
    CONCLUSIONS:
    This mini-review reports on the pre-clinical studies performed with carnosic acid, carnosol, and Rosmanol describing their mechanism of action in different cancers.
    Nat Prod Lett. 2002 Aug;16(4):277-81.
    Antioxidant capacity of abietanes from Sphacele salviae.[Pubmed: 12168765 ]

    METHODS AND RESULTS:
    Carnosol 1, Rosmanol 2, carnosic acid 3 and 20-deoxocarnosol 4, the main phenolic abietanes present in aerial parts of the Chilean medicinal plant Sphacele salviae were tested for antioxidant activity of measuring the decay of the radical cation diphenyl-picrylhydrazyl (DPPH).
    CONCLUSIONS:
    All compounds displayed higher antioxidant levels than BHT under the same conditions and carnosic acid was more efficient than vitamin E.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.9032 mL 14.5159 mL 29.0318 mL 58.0636 mL 72.5795 mL
    5 mM 0.5806 mL 2.9032 mL 5.8064 mL 11.6127 mL 14.5159 mL
    10 mM 0.2903 mL 1.4516 mL 2.9032 mL 5.8064 mL 7.2579 mL
    50 mM 0.0581 mL 0.2903 mL 0.5806 mL 1.1613 mL 1.4516 mL
    100 mM 0.029 mL 0.1452 mL 0.2903 mL 0.5806 mL 0.7258 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
    7beta-甲氧基迷迭香酚 ; 7beta-Methoxyrosmanol CFN92990 24703-38-6 C21H28O5 = 360.44 5mg QQ客服:2159513211
    7-乙氧基迷迭香酚; 7-Ethoxyrosmanol CFN91119 111200-01-2 C22H30O5 = 374.5 10mg QQ客服:2159513211
    鼠尾草酸; Carnosic acid CFN99102 3650-09-7 C20H28O4 = 332.43 20mg QQ客服:2056216494
    12-O-甲基鼠尾草酸; 12-O-Methylcarnosic acid CFN89377 62201-71-2 C21H30O4 = 346.46 5mg QQ客服:2159513211
    11-Hydroxy-12-methoxyabietatriene; 11-Hydroxy-12-methoxyabietatriene CFN92286 16755-54-7 C21H32O2 = 316.5 5mg QQ客服:215959384
    11-羟基柳杉酚; 11-Hydroxy-sugiol CFN90366 88664-08-8 C20H28O3 = 316.43 5mg QQ客服:1457312923
    丹参酚酮; Salvinolone CFN92243 120278-22-0 C20H26O3 = 314.4 5mg QQ客服:2056216494
    6-羟基丹参酚酮; 14-Deoxycoleon U CFN97924 88664-09-9 C20H26O4 = 330.4 5mg QQ客服:3257982914
    20-去氧鼠尾草酚; 20-Deoxocarnosol CFN92175 94529-97-2 C20H28O3 = 316.4 5mg QQ客服:1413575084
    2,11,12-Trihydroxy-7,20-epoxy-8,11,13-abietatriene; 2,11,12-Trihydroxy-7,20-epoxy-8,11,13-abietatriene CFN95428 1608462-12-9 C20H28O4 = 332.4 10mg QQ客服:1457312923

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