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  • 百秋李醇

    Patchouli alcohol

    百秋李醇
    产品编号 CFN98118
    CAS编号 5986-55-0
    分子式 = 分子量 C15H26O = 222.36
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Sesquiterpenoids
    植物来源 The herbs of Pogostemon cablin (Blanco) Benth.
    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
    百秋李醇 CFN98118 5986-55-0 10mg QQ客服:215959384
    百秋李醇 CFN98118 5986-55-0 20mg QQ客服:215959384
    百秋李醇 CFN98118 5986-55-0 50mg QQ客服:215959384
    百秋李醇 CFN98118 5986-55-0 100mg 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
  • University of Hawaii Cancer Center (USA)
  • University of South Australia (Australia)
  • Martin Luther University of Halle-Wittenberg (Germany)
  • University of Lodz (Poland)
  • Gyeongsang National University (Korea)
  • University of Indonesia (Indonesia)
  • Johannes Gutenberg University Mainz (JGU) (Germany)
  • Aarhus University (Denmark)
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  • University of Maryland (USA)
  • University of Madras (India)
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  • Research Unit Molecular Epigenetics (MEG) (Germany)
  • Anna University (India)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Front Chem.2022, 10:1048467.
  • Toxicological Research2020, doi: 10.1007.
  • Biosci Rep.2020, 40(8):BSR20201219.
  • J Vet Sci.2020, 21(3):e39.
  • Anticancer Res.2014, 34(7):3505-9
  • Allergol Immunopathol (Madr).2022, 1;50(4):23-30.
  • Sci Rep.2019, 9(1):4342
  • Industrial Crops and Products2022, 188:115638
  • Kor. J. Herbol.2019, 34(2):59-66
  • Biol Pharm Bull.2018, 41(11):1685-1693
  • Biol Pharm Bull.2018, 41(1):65-72
  • Applied Biological Chemistry2023, 66:42.
  • J Agric Food Chem.2021, 69(46):14037-14047.
  • Viruses.2021, 13(11):2118.
  • Plant Methods.2017, 13:108
  • PLoS One.2022, 17(4):e0267007.
  • The Korea Journal of Herbology2020, 35(3):33-45.
  • World J Mens Health.2019, 10.5534
  • Planta Med.2022, a-1876-3009.
  • Ind. J. Pharm. Edu. Res.2023; 57(3):1132-1139.
  • Oncotarget.2017, 8(64):108006-108019
  • FEMS Microbiol Lett.2017, 364(11)
  • Plos One.2019, 15(2):e0220084
  • ...
  • 生物活性
    Description: Patchouli alcohol has anti-inflammatory, neuroprotective, anti-cancer, anti-oxidant, gastroprotective, immunomodulatory, and antibacterial effects, which may be mediated, at least in part, by down-regulation of the mRNA expression of a panel of inflammatory mediators, such as TNF-α, IL-1β, IL-6, iNOS and COX-2. Patchouli alcohol significantly accelerates the recovery of the UV-induced skin lesions, evidently through anti-oxidant and anti-inflammatory action, as well as down-regulation of the MMP-1 and MMP-3 expression.
    Targets: TNF-α | PGE | COX | IL Receptor | SOD | MMP(e.g.TIMP) | CDK | p65 | NF-kB | HDAC | c-Myc | NO | NOS | Antifection
    In vitro:
    Int Immunopharmacol. 2013 Jun;16(2):184-90.
    Patchouli alcohol, an essential oil of Pogostemon cablin, exhibits anti-tumorigenic activity in human colorectal cancer cells.[Pubmed: 23602914]
    Patchouli alcohol (PA) is one of the important compounds isolated from the essential oil of Pogostemon cablin (patchouli). PA has neuroprotective, anti-influenza and anti-inflammatory activities. However, anti-cancer activity of PA has not been studied so far. We performed in vitro study to investigate whether PA affects proliferation and apoptosis of human colorectal cancer cells, and to define potential molecular mechanisms.
    METHODS AND RESULTS:
    PA suppressed cell growth and induced apoptosis in a dose-dependent manner in human colorectal cancer cells (HCT116, SW480). In addition, PA decreased cell growth in MCF7, BxPC3, PC3, and HUVEC cells. Exposure of PA to HCT116 and SW480 cells activated p21 expression and suppressed the expressions of cyclin D1 and cyclin-dependent kinase 4 (CDK4) in a dose-dependent manner. In addition, PA attenuated the expressions of HDAC2 (histone deacetylase 2) and c-myc, and HDAC enzyme activity. We also observed that PA induced the transcriptional activity of NF-κB through an increase of nuclear translocation of p65.
    CONCLUSIONS:
    These findings suggest that PA exerts an anti-cancer activity by decreasing cell growth and increasing apoptosis in human colorectal cancer cells. The proposed mechanisms include the inhibition of HDAC2 expression and HDAC enzyme activity, and subsequent downregulation of c-myc and activation of NF-κB pathway.
    J Agric Food Chem. 2003 Jul 30;51(16):4585-8.
    Toxicity and repellency of patchouli oil and patchouli alcohol against Formosan subterranean termites Coptotermes formosanus Shiraki (Isoptera: Rhinotermitidae).[Pubmed: 14705881 ]
    Patchouli oil obtained from Pogostemon cablin (Blanco) Benth and its main constituent, patchouli alcohol, were tested for their repellency and toxicity against Formosan subterranean termites (Coptotermes formosanus Shiraki). Both were found to be toxic and repellent. Unusual tissue destruction was noted inside the exoskeleton of the termite after patchouli alcohol was topically applied to the dorsum.
    In vivo:
    Chem Biol Interact. 2014 Oct 5;222:27-36.
    Gastroprotective effect and mechanism of patchouli alcohol against ethanol, indomethacin and stress-induced ulcer in rats.[Pubmed: 25168850 ]
    Pogostemonis Herba is an important Chinese medicine widely used in the treatment of gastrointestinal dysfunction. Patchouli alcohol (PA), a tricyclic sesquiterpene, is the major active constituent of Pogostemonis Herba. This study aimed to investigate the possible anti-ulcerogenic potential of PA and the underlying mechanism against ethanol, indomethacin and water immersion restraint-induced gastric ulcers in rats.
    METHODS AND RESULTS:
    Gross and histological gastric lesions, biochemical and immunological parameters were taken into consideration. The gastric mucus content and the antisecretory activity were analyzed through pylorus ligature model in rats. Results indicated that oral administration with PA significantly reduced the ulcer areas induced by ethanol, indomethacin and water immersion restraint. PA pretreatment significantly promoted gastric prostaglandin E2 (PGE2) and non-protein sulfhydryl group (NP-SH) levels, upregulated the cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) mRNA expression, and considerably boosted the gastric blood flow (GBF) and gastric mucus production in comparison with vehicle. In addition, PA modulated the levels of interleukin-6 (IL-6), interleukin-10 (IL-10) and tumor necrosis factor-α (TNF-α). The levels of glutathione (GSH), catalase (CAT) and malonaldehyde (MDA) were also restored by PA. However, the gastric secretion parameters (pH, volume of gastric juice and pepsin) did not show any significant alteration.
    CONCLUSIONS:
    These findings suggest that PA exhibited significant gastroprotective effects against gastric ulceration. The underlying mechanisms might involve the stimulation of COX-mediated PGE2, improvement of antioxidant and anti-inflammatory status, preservation of GBF and NP-SH, as well as boost of gastric mucus production.
    Trop. J.Pharm. Res., 2013, 12(4):559-65.
    Immunomodulatory Potential of Patchouli Alcohol Isolated from Pogostemon cablin (Blanco) Benth (Lamiaceae) in Mice[Reference: WebLink]
    To isolate and purify patchouli alcohol (PA), a tricyclic sesquiterpene constituent of Pogostemon cablin, and investigate its immunomodulatory potential in Kunming mice.
    METHODS AND RESULTS:
    PA was prepared from an ethanol aqueous extract of P. cablin by silica gel column chromatography, and further purified by crystallization using n-hexane. Purity was assessed by analytical gas chromatography (GC) and confirmation of chemical structure performed by Fourier transform infrared (FTIR), nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry (MS). The effect of PA from Pogostemon cablin on immunological function was studied by macrophage phagocytosis, immune organ index, serum immunoglobulin level and delayed type hypersensitivity (DTH) in mice that were administered orally doses of 20, 40 and 80 mg/kg. The purity of PA was 99.3%. The oral administration of PA (40, or 80 mg/kg body weight) significantly increased the phagocytic index (p < 0.05), compared with prednisone acetate (PR) group. Administration of PA (80 mg/kg) boosted the production of circulating serum IgM (0.081 ± 0.010) and IgG (1.296 ± 0.120), while IgM and IgG in PR group was 0.069 ± 0.011 (p < 0.01) and 1.180 ± 0.070 (p < 0.01) respectively. However, PA (20 mg/kg) treatment elicited significant decrease in DTH induced by 2, 4-dinitro-chlorobenzene (DNCB) in mice (1.03 ± 0.40, p < 0.05), in comparison to DNCB-induced group (1.67 ± 0.84 mg).
    CONCLUSIONS:
    These results suggest that PA has significant immunomodulatory properties which probably act by activating mononuclear phagocytic system, augmenting humoral immune response while suppressing cellular immune response.
    Front Pharmacol . 2018 Nov 22;9:1347.
    Unraveling the Novel Protective Effect of Patchouli Alcohol Against Helicobacter pylori-Induced Gastritis: Insights Into the Molecular Mechanism in vitro and in vivo[Pubmed: 30524287]
    Abstract Patchouli alcohol (PA), a natural tricyclic sesquiterpene extracted from Pogostemon cablin (Blanco) Benth. (Labiatae), has been found to exhibit anti-Helicobacter pylori and anti-inflammatory properties. In this study, we investigated the protective effect of PA against H. pylori-induced gastritis in vitro and in vivo, and determined the underlying mechanism. In the in vivo experiment, a C57BL/6 mouse model of gastritis was established using H. pylori SS1, and treatments with standard triple therapy or 5, 10, and 20 mg/kg PA were performed for 2 weeks. Results indicated that PA effectively attenuated oxidative stress by decreasing contents of intracellular reactive oxygen species (ROS) and malonyldialdehyde (MDA), and increasing levels of non-protein sulfhydryl (NP-SH), catalase and glutathione (GSH)/glutathione disulphide (GSSG). Additionally, treatment with PA significantly attenuated the secretions of interleukin 1 beta (IL-1β), keratinocyte chemoattractant and interleukin 6 (IL-6). PA (20 mg/kg) significantly protected the gastric mucosa from H. pylori-induced damage. In the in vitro experiment, GES-1 cells were cocultured with H. pylori NCTC11637 at MOI = 100:1 and treated with different doses of PA (5, 10, and 20 μg/ml). Results indicated that PA not only significantly increased the cell viability and decreased cellular lactate dehydrogenase (LDH) leakage, but also markedly elevated the mitochondrial membrane potential and remarkably attenuated GES-1 cellular apoptosis, thereby protecting gastric epithelial cells against injuries caused by H. pylori. PA also inhibited the secretions of pro-inflammatory factors, such as monocyte chemotactic protein 1 (MCP-1), tumor necrosis factor-α (TNF-α) and IL-6. Furthermore, after PA treatment, the combination of NACHT, LRR, and PYD domains-containing protein 3 (NLRP3) and cysteine-aspartic proteases 1 (CASPASE-1), the expression levels of NLRP3 inflammasome-related proteins, such as thioredoxin-interacting protein (TXNIP), pro-CASPASE-1, cle-CASPASE-1, and NLRP3 and genes (NLRP3 and CASPASE1) were significantly decreased as compared to the model group. In conclusion, treatment with PA for 2 weeks exhibited highly efficient protective effect against H. pylori-induced gastritis and related damages. The underlying mechanism might involve antioxidant activity, inhibition of pro-inflammatory factor and regulation of NLRP3 inflammasome function. PA exerted anti-H. pylori and anti-gastritis effects and thus had the potential to be a promising candidate for treatment of H. pylori-related diseases. Keywords: Helicobacter pylori; gastric epithelial cell; gastritis; inflammasome; oxidative injury; patchouli alcohol.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 4.4972 mL 22.4861 mL 44.9721 mL 89.9442 mL 112.4303 mL
    5 mM 0.8994 mL 4.4972 mL 8.9944 mL 17.9888 mL 22.4861 mL
    10 mM 0.4497 mL 2.2486 mL 4.4972 mL 8.9944 mL 11.243 mL
    50 mM 0.0899 mL 0.4497 mL 0.8994 mL 1.7989 mL 2.2486 mL
    100 mM 0.045 mL 0.2249 mL 0.4497 mL 0.8994 mL 1.1243 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
    3,6-Caryolanediol; 3,6-Caryolanediol CFN99658 155485-76-0 C15H26O2 = 238.4 5mg QQ客服:2056216494
    1,9-Caryolanediol 9-acetate; 1,9-Caryolanediol 9-acetate CFN99659 155488-34-9 C17H28O3 = 280.4 5mg QQ客服:215959384
    丁香三环烷二醇; Clovanediol CFN98308 2649-64-1 C15H26O2 = 238.4 5mg QQ客服:3257982914
    二乙酸丁香三环烷二醇酯; Clovanediol diacetate CFN98309 2649-68-5 C19H30O4 = 322.4 5mg QQ客服:2056216494
    1,7-二表-8,15-柏木烷二醇; 1,7-Diepi-8,15-cedranediol CFN98639 40768-81-8 C15H26O2 = 238.4 5mg QQ客服:2159513211
    百秋李醇; Patchouli alcohol CFN98118 5986-55-0 C15H26O = 222.36 20mg QQ客服:1457312923

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