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Hypothemycin |产品详情|进口橙子视频旧款采购网




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    上海橙子视频app安卓下载生物科技公司
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    Hypothemycin
    品牌:AG Scientific
    货号:
    规格:250 ug
    货期:

    CAS:76958-67-3Formula:C19H22O8MW:378.375Appearance:SolidPurity:98%(HPLC)

    商品详情 参考文献 相关资料

    The resorcyclic acid lactone Hypothemycin isolated from Phoma sp. has antifuangal and anticancer activity.

    Hypothemycin normalized the morphology and inhibited anchorage-independent growth of Ki-ras transformed normal rat kidney(NRK) cells with selectivity and potency comparable to or greater than that of the MEK inhibitor U0126. It is also potent and selective threonine/tyrosine-specific kinase.

    Hypothemycin inhibits proliferation of mouse and human T-cells and modulates production of cytokines during T-cell activation. It facilitates the ubiquitinylation process of cyclin D1.

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    Product References

    • The Resorcylic Acid Lactone Hypothemycin Selectively Inhibits the Mitogen-Activated Protein Kinase Kinase-Extracellular Signal-Regulated Kinase Pathway in Cells, Biol. Pharm, Hidesuke Fukazawa, 33(2) (2010)?

    • Gene for the Biosesynthesis of the Fungal Polyketides Hypothemycin from Hypomyces subiculosus and Radicicol from Pochonia chlamydosporia, Microbiol, Christopher D. Reeves, et al., vol. 74, no. 16 (2008)

    • Semiynthesis and Cytotoxicity of Hypothemycin Analogues, ChemMedChem, Brian R.Hearn Dr., et al., vol. 2 (2007)

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    Additional Information

    Product #H-2403
    CAS #76958-67-3
    FormulaC19 H22 O8
    MW378.375
    AppearanceSolid
    Purity98% (HPLC)
    SolubilitySoluble in DMSO or acetone; insoluble in methanol or water
    Storage Temp-20°C
    Therapeutic AreaOncological Disorders
    UseHypothemycin exhibits antifungal and cytotoxic activity against some tumor cell lines partly attributed to inhibition of Ras-inducible genes

    Additional Information

    ChemACXX1867744-0
    InChIInChI=1S/C19H22O8/c1-9-4-3-5-12(20)17(23)14(22)8-15-18(27-15)11-6-10(25-2)7-13(21)16(11)19(24)26-9/h3,5-7,9,14-15,17-18,21-23H,4,8H2,1-2H3/b5-3-/t9-,14-,15+,17+,18+/m0/s1
    SMILESC[C@H]1C/C=CC(=O)[C@H]([C@H](C[C@@H]2[C@H](O2)C3=C(C(=CC(=C3)OC)O)C(=O)O1)O)O
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