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ID4120 3,6-二羟基黄酮 抑制剂/拮抗剂/激动剂 索

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  • 北京
  • ID4120
  • 2025年10月10日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 保存条件

      Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year

    • 保质期

      Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year

    • 英文名

      3,6-Dihydroxyflavone

    • 库存

      现询

    • 供应商

      北京索莱宝科技有限公司

    • CAS号

      108238-41-1

    • 规格

      100mg/50mg/25mg/10mg/5mg

    规格:100mg产品价格:¥2590.0
    规格:50mg产品价格:¥1840.0
    规格:25mg产品价格:¥1290.0
    规格:10mg产品价格:¥790.0
    规格:5mg产品价格:¥490.0

    基本信息
    CASNo.108238-41-1
    中文名称3,6-二羟基黄酮
    英文名称3,6-Dihydroxyflavone
    别名;6-Hydroxyflavonol;3,6-dihydroxy-flavone;Uracil,5-chloro
    分子式C15H10O4
    分子量254.24
    溶解性Soluble in DMSO ≥5mg/mL(Need ultrasonic)
    纯度≥98%
    外观(性状)Light yellow to light brown Solid
    储存条件Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
    MDLMFCD00143082
    SMILESC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=CC(=C3)O)O
    InChIKeyXHLOLFKZCUCROE-UHFFFAOYSA-N
    InChIInChI=1S/C15H10O4/c16-10-6-7-12-11(8-10)13(17)14(18)15(19-12)9-4-2-1-3-5-9/h1-8,16,18H
    PubChem CID688659
    靶点Others
    通路Others
    背景说明是一种化合物,具有抗癌活性。
    生物活性3,6-Dihydroxyflavone is an anti-cancer agent. 3,6-Dihydroxyflavone dose- and time-dependently decreases cell viability and induces apoptosis by activating caspase cascade, cleaving poly (ADP-ribose) polymerase (PARP). 3,6-Dihydroxyflavone increases intracellular oxidative stress and lipid peroxidation[1].
    In Vitro3,6-dihydroxyflavone dose- and time-dependently decreases cell viability and induces Apoptosis by activating Caspase cascade, cleaving poly (ADP-ribose) polymerase (PARP). The anti-cancer effects of 3,6-dihydroxyflavone are associated with the generation of Reactive Oxygen Species, the altered glutathione-redox balance as significantly decreased glutathione (GSH) and its ratio to gluthatione disulfide (GSSG), and the accumulation of lipid peroxidation indicator malondialdehyde. Addition of antioxidant N-acetylcysteine (NAC) prevents the elevation of Reactive Oxygen Species induced by 3,6-dihydroxyflavone and partially suppresses the cytotoxic effects. Furthermore, 3,6-dihydroxyflavone reduces cell membrane fluidity and induces the loss of mitochondrial membrane potential. 3,6-Dihydroxyflavone was also found to modulate the activities of mitogen-activated protein kinase (MAPK) family members, which includes increased protein kinase of 38 kDa (p38), c-Jun N-terminal kinase (JNK), and decreased extracellular signal-regulated kinase (ERK) activation. The effect of 3,6-dihydroxyflavone on MAPKs pathway could be abrogated by co-treatment with NAC.3,6-dihydroxyflavone increases intracellular oxidative stress and lipid peroxidation, thereby affecting the physical and functional properties of plasma membrane, as well as MAPKs signal pathway, which are likely to play a role in the 3,6-dihydroxyflavone-induced HL-60 cell cytotoxicities.[1]
    数据来源文献[1]. Chang H, et al. 3,6-Dihydroxyflavone induces apoptosis in leukemia HL-60 cell via reactive oxygen species-mediated p38 MAPK/JNK pathway. Eur J Pharmacol. 2010;648(1-3):31-38.
    单位

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    图标文献和实验
    相关实验
    • 【求助】关于gsk3-beta功能的疑问

      , we may find much more references regarding this issue. http://books.google.com/books?id=3mgPzNFjcWAC&pg=PA51&lpg=PA51&dq=gsk+tyrosine+phosphorylation+and+activity&source=bl&ots=x5ueTldpez&sig=CqRFJleXtEBn9OfelhODPAc28xs&hl=en&ei=KerNSu-XGcem8Abm-qmABA&sa=X&oi=book_result&ct

    •  微量元素

      )及磷脂过氧化氢谷胱甘肽氧化酶(PHGSH�x)的组成成分。GSH�x中每克分子酶四聚体含有4克原子硒,硒半胱氨酸的硒醇是酶的催化中心。该酶在人体内起抗氧化作用,能催化GSH与胞液中的过氧化物反应,防止过氧化物对机体的损伤。GSH�x活力下降,线粒体不可逆地失去容积控制和收缩能力并最后破裂。缺硒所致肝坏死可能是过氧化物代谢受损的结果。PHGSH�x与GSH�x不同,它存在于肝和心肌细胞线粒体内膜间隙中,作用是抗氧化、维持线粒体的完整,避免脂质过氧化物伤害。此外,I型碘甲腺原氨酸5′-脱碘酶(5′�ID

    • Use of Chromophoric Ligands to Visually Screen Co‐Crystals of Putative Protein‐Nucleic Acid Complexes

      of complex and protein alone with the naked eye or a light microscope, crystals of covalently Cy5?labeled DNA can be directly used for X?ray diffraction data collection. Curr. Protoc. Nucleic Acid Chem. 46:7.15.1?7.15.8. © 2011 by John Wiley & Sons

    图标技术资料

    暂无技术资料 索取技术资料

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