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IC1310 香荆芥酚 抑制剂/拮抗剂/激动剂 索莱宝

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  • ¥220 - 736
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  • 北京
  • IC1310
  • 2025年12月18日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 保存条件

      Store at 2-8℃,2 years

    • 保质期

      Store at 2-8℃,2 years

    • 英文名

      Carvacrol

    • 库存

      现询

    • 供应商

      北京索莱宝科技有限公司

    • CAS号

      499-75-2

    • 规格

      200mg/100mg/20mg

    规格:200mg产品价格:¥736.0
    规格:100mg产品价格:¥490.0
    规格:20mg产品价格:¥220.0

    Carvacrol 是唇形科植物中的单萜酚类,具有抗氧化、抗炎、抗癌活性。Carvacrol 可导致 G0/G1 细胞周期停滞,下调 Notch-1 和 Jagged-1,诱导凋亡。

    基本信息
    CASNo.499-75-2
    中文名称香荆芥酚
    英文名称Carvacrol
    别名cymophenol;O-Thymol;Karvakrol;香芹酚
    分子式C10H14O
    分子量150.22
    溶解性Soluble in DMSO
    纯度HPLC≥98%
    外观(性状)Colorless to light yellow Liquid
    储存条件Store at 2-8℃,2 years
    密度0.976g/mL
    ECEINECS 207-889-6
    MDLMFCD00002236
    SMILESCC(C)C1=CC(O)=C(C)C=C1
    InChIKeyRECUKUPTGUEGMW-UHFFFAOYSA-N
    InChIInChI=1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4-7,11H,1-3H3
    PubChem CID10364
    靶点Others
    通路Others
    背景说明Carvacrol 是唇形科植物中的单萜酚类,具有抗氧化、抗炎、抗癌活性。Carvacrol 可导致 G0/G1 细胞周期停滞,下调 Notch-1 和 Jagged-1,诱导凋亡。
    生物活性Carvacrol (Cymophenol), monoterpenic phenol isomeric with thymol, has diverse activities such as antimicrobial, antitumor, an-timutagenic, antigenotoxic, analgesic, antispasmodic, anti-inflammatory, angiogenic, antiparasitic, antiplatelet, AChE inhibitory, antielastase, insecticidal, antihepatotoxic and hepatoprotective activities.[1-2]
    In VitroCarvacrol(CVC)possesses weak antioxidant and cytotoxic activity in cultured primary rat neurons. In addition,Carvacrol has weak antioxidant properties and little anticancer potentials in rat N2a neuroblastoma cell line[1]. Carvacrol is a novel inhibitor of transient receptor potential(TRP)channels in drosophila and mammalian. In human hepatoma HepG2 cells,Carvacrol induces cell apoptosis by selectively decreasing phosphorylation of extracellular signal-regulated kinase 1/2(ERK1/2)and P38; In human macrophage-like U937 cells,in response to lipopolysaccharide treatment,Carvacrol activates peroxisome proliferator-activated receptors(PPAR alpha and gamma)and suppresses cyclooxygenase-2(COX-2)mRNA and protein expression[2].
    细胞实验Carvacrol has the ability to protect liver against ischemia/reperfusion injury in rats. In the central nervous system,Carvacrol is regarded as a potential drug for Alzheimer's disease due to its inhibitory effect on acetylcholinesterase(AChE)activity by using phenolic hydroxyl group of carvacrol to bind to AChE and leading to a loss of function of AChE. In addition,Carvacrol is found to have an antidepressant-like effect in mice by affecting the dopaminergic system. Dietary carvacrol supplementation prevents high fat diet-induced obesity by modulating gene expressions that lead to adipogenesis and inflammation. Carvacrol crosses the blood-brain barrier easily and rapidly[2].
    细胞实验The cells are seeded in 48-well plates. Cells are incubated at 37 °C in a humidified 5 % CO2/95 % air mixture and treated with carvacrol at different concentrations(10,25,50,100,200 and 400 mg/L)for 24 h. MTT substrate solution is used. Briefly,MTT is added to the cell cultures for 3 h. Formed formazan crystals are dissolved in dimethyl sulfoxide(DMSO),MTT is added to the cell cultures for 3 h. Formed formazan crystals are dissolved in dimethyl sulfoxide(DMSO).[1]
    动物实验Animal Models: Male ICR mice; Dosages: 50 mg/kg; Administration: i.c.v.[2]
    数据来源文献[1] Elanur Ayd n, et al. Cytotechnology. 2014, 66(1): 149–157.
    [2] Yu H, et al. PLoS One. 2012, 7(3):e33584.
    单位

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