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  • 青榆烯C

    Lacinilene C

    青榆烯C
    产品编号 CFN98653
    CAS编号 41653-72-9
    分子式 = 分子量 C15H18O3 = 246.3
    产品纯度 >=98%
    物理属性 Yellow powder
    化合物类型 Sesquiterpenoids
    植物来源 The barks of Ulmus parvifolia Jacq.
    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
    青榆烯C CFN98653 41653-72-9 1mg QQ客服:3257982914
    青榆烯C CFN98653 41653-72-9 5mg QQ客服:3257982914
    青榆烯C CFN98653 41653-72-9 10mg QQ客服:3257982914
    青榆烯C CFN98653 41653-72-9 20mg 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
  • Indian Institute of Science (India)
  • Martin Luther University of Halle-Wittenberg (Germany)
  • Universidad Miguel Hernández (Spain)
  • Srinakharinwirot University (Thailand)
  • Fraunhofer-Institut für Molekularbiologie und Angewandte ?kologie IME (Germany)
  • National Cancer Institute (USA)
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  • 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 Cosmetics and Cosmetology2019, 225-231
  • ACS Nano.2018, 12(4):3385-3396
  • Front Endocrinol (Lausanne).2020, 11:568436.
  • J Integr Plant Biol.2023, 13564.
  • J.Food Processing & Preservation2022, jfpp.16666
  • Int Immunopharmacol.2021, 100:108073.
  • Phytomedicine.2018, 38:45-56
  • Biomedicines.2022, 10(5):1170
  • J Ethnopharmacol.2022, 282:114574.
  • Front Pharmacol.2020, 11:566490.
  • J of Applied Biological Chem.2020, 63(2):147-152
  • GxABT2022, 2268.2:15515.
  • Inflammation2015, 38(1):445-55
  • Korean J Environ Agric.2018, 37(4):260-267
  • J Agric Food Chem.2020, 68(43):12164-12172.
  • Food Research2022, 6(6): 30-38.
  • Korean J. Medicinal Crop Sci.2021, 29(1):45-50.
  • Int J Mol Sci.2021, 22(21):11836.
  • Food Research2021, 5(1):65-71
  • J. Korean Wood Sci. Technol.2022, 50(5):338-352.
  • J Ethnopharmacol.2017, 206:327-336
  • Nat Commun.2021, 12(1):681.
  • Oncol Rep.2016, 35(3):1356-64
  • ...
  • 生物活性
    Description: Lacinilene C, lacinilene C 7-methyl ether, scopoletin, 2-hydroxy-7-methoxycadalene and 2,7-dihydroxycadalene are 5 induced phytoalexins in cotton leaves. Lacinilene C methyl ether elicits contraction of TSM by enhancing the movement of calcium through potential-dependent channels of smooth muscle cell membranes.
    Targets: P450 (e.g. CYP17) | 5-HT Receptor | Histamine Receptor
    In vitro:
    Phytochemistry. 2015 Jul;115:59-69.
    RNAi construct of a cytochrome P450 gene CYP82D109 blocks an early step in the biosynthesis of hemigossypolone and gossypol in transgenic cotton plants.[Pubmed: 25794893 ]
    Naturally occurring terpenoid aldehydes from cotton, such as hemigossypol, gossypol, hemigossypolone, and the heliocides, are important components of disease and herbivory resistance in cotton.
    METHODS AND RESULTS:
    These terpenoids are predominantly found in the glands. Differential screening identified a cytochrome P450 cDNA clone (CYP82D109) from a Gossypium hirsutum cultivar that hybridized to mRNA from glanded cotton but not glandless cotton. Both the D genome cotton Gossypium raimondii and A genome cotton Gossypium arboreum possessed three additional paralogs of the gene. G. hirsutum was transformed with a RNAi construct specific to this gene family and eight transgenic plants were generated stemming from at least five independent transformation events. HPLC analysis showed that RNAi plants, when compared to wild-type Coker 312 (WT) plants, had a 90% reduction in hemigossypolone and heliocides levels, and a 70% reduction in gossypol levels in the terminal leaves, respectively. Analysis of volatile terpenes by GC-MS established presence of an additional terpene (MW: 218) from the RNAi leaf extracts. The (1)H and (13)C NMR spectroscopic analyses showed this compound was δ-cadinen-2-one.
    CONCLUSIONS:
    Double bond rearrangement of this compound gives 7-hydroxycalamenene, a lacinilene C pathway intermediate. δ-Cadinen-2-one could be derived from δ-cadinene via a yet to be identified intermediate, δ-cadinen-2-ol. The RNAi construct of CYP82D109 blocks the synthesis of desoxyhemigossypol and increases the induction of lacinilene C pathway, showing that these pathways are interconnected. Lacinilene C precursors are not constitutively expressed in cotton leaves, and blocking the gossypol pathway by the RNAi construct resulted in a greater induction of the lacinilene C pathway compounds when challenged by pathogens.
    Environ Res. 1988 Feb;45(1):118-26.
    Lacinilene C methyl ether (LCME) constricts tracheal smooth muscle.[Pubmed: 3338430]
    Lacinilene C methyl ether (LCME) is a constituent of the cotton plant and has been implicated as a causative agent of byssinosis.
    METHODS AND RESULTS:
    The effect of synthetic Lacinilene C methyl ether on the behavior of isolated strips of canine tracheal smooth muscle (TSM) was examined in tissue bath experiments. Lacinilene C methyl ether (0.64-6.6 x 10(-4) M) caused slowly developing but strong and sustained contractions of TSM strips. Blockade of acetycholine, 5-hydroxytryptamine (5-HT), and histamine H1 receptors with atropine, methysergide, and pyrilamine, respectively, had no effect on constrictions induced by Lacinilene C methyl ether. In contrast, the calcium channel antagonist, verapamil, significantly reduced the response to Lacinilene C methyl ether. Moreover, addition of the beta receptor agonist, isoproterenol, at the peak of Lacinilene C methyl ether-induced contractions relaxed tissues in a concentration-dependent manner.
    CONCLUSIONS:
    We conclude that Lacinilene C methyl ether elicits contraction of TSM by enhancing the movement of calcium through potential-dependent channels of smooth muscle cell membranes. This mechanism of action does not require activation of specific membrane receptors for acetylcholine, 5-HT, and histamine.
    Phytochemistry, 1990 ,29 (6):1789-91.
    Stress effects on cotton leaf phytoalexins elicited by cell free-mycelia extracts of Aspergillus flavus.[Reference: WebLink]

    METHODS AND RESULTS:
    The concentrations of five induced phytoalexins, Lacinilene C, Lacinilene C 7-methyl ether, scopoletin, 2-hydroxy-7-methoxycadalene, and 2,7-dihydroxycadalene, were determined in cotton leaves treated with cell-free mycelial extracts of Aspergillus flavus under a light regime of 14 hr light/10 hr dark and temperature cycles of25/20°, 30/25°, 35/30° and 40/35°. Maximum concentrations were present in plants maintained at a post-inoculation temperature regime of 30/25°.
    CONCLUSIONS:
    In a separate experiment, the concentrations of the same elicited phytoalexins were measured in cotton leaves treated with the fungal elicitor and maintained at different levels of plant moisture stress. Leaf moisture stress values less than -11.7 bars resulted in decreased production of the five cotton leaf phytoalexins determined two days after the fungal elicitor was applied.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 4.0601 mL 20.3004 mL 40.6009 mL 81.2018 mL 101.5022 mL
    5 mM 0.812 mL 4.0601 mL 8.1202 mL 16.2404 mL 20.3004 mL
    10 mM 0.406 mL 2.03 mL 4.0601 mL 8.1202 mL 10.1502 mL
    50 mM 0.0812 mL 0.406 mL 0.812 mL 1.624 mL 2.03 mL
    100 mM 0.0406 mL 0.203 mL 0.406 mL 0.812 mL 1.015 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
    5-异丙基-3,8-二甲基-2-萘酚; 7-Hydroxycadalene CFN89214 2102-75-2 C15H18O = 214.30 5mg QQ客服:1457312923
    3-乙酰氧基-4,7(11)-杜松萜二烯-8-酮; 3-Acetoxy-4,7(11)-cadinadien-8-one CFN99070 104975-02-2 C17H24O3 = 276.4 5mg QQ客服:215959384
    9-酮-10,11-脱氢泽兰素; 9-Oxo-10,11-dehydroageraphorone CFN97272 79491-71-7 C15H20O2 = 232.3 5mg QQ客服:215959384
    3,8-二氧代-7alpha-羟基-4,11(12)-四去氢杜松烷; 7alpha-Hydroxy-4,11-cadinadiene-3,8-dione CFN96752 1423809-64-6 C15H20O3 = 248.32 5mg QQ客服:215959384
    10alpha-羟基日本刺参萜-4-酮/刺参酮; Oplopanone CFN99884 1911-78-0 C15H26O2 = 238.4 5mg QQ客服:3257982914
    款冬酮; Tussilagone CFN90629 104012-37-5 C23H34O5 = 390.51 20mg QQ客服:2056216494
    Reneilmol; Reneilmol CFN98296 260968-11-4 C15H28O3 = 256.4 5mg QQ客服:1457312923
    Longiferone B; Longiferone B CFN89084 1639810-67-5 C15H22O = 218.34 5mg QQ客服:1457312923
    [2R-(2alpha,4alpha,4abeta,5alpha,7beta,7abeta)]-六氢-4-甲氧基-7a-甲基-8-亚甲基-2,5-甲桥环戊二烯并-1,3-二恶英-7-醇; 1-O-Methyljatamanin D CFN96381 54656-47-2 C11H16O4 = 212.3 5mg QQ客服:215959384
    Ylangenyl acetate; Ylangenyl acetate CFN96414 90039-63-7 C17H26O2 = 262.39 5mg QQ客服:215959384

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