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    72263-05-9

    中文名稱 CONGLOBATIN
    英文名稱 CONGLOBATIN
    CAS 72263-05-9
    分子式 C28H38N2O6
    分子量 498.61
    MOL 文件 72263-05-9.mol
    72263-05-9 結(jié)構(gòu)式 72263-05-9 結(jié)構(gòu)式

    基本信息

    中文別名
    成球菌素
    英文別名
    FW-04-806
    CONGLOBATIN
    Conglobatin, >=99%
    (3E,5R,7S,8S,11E,13R,15S,16S)-3,5,7,11,13,15-Hexamethyl-8,16-bis(5-oxazolylmethyl)-1,9-dioxacyclohexadeca-3,11-diene-2,10-dione
    1,9-Dioxacyclohexadeca-3,11-diene-2,10-dione, 3,5,7,11,13,15-hexamethyl-8,16-bis(5-oxazolylmethyl)-, (3E,5R,7S,8S,11E,13R,15S,16S)-

    物理化學(xué)性質(zhì)

    密度1.060±0.06 g/cm3 (20 ºC 760 Torr)
    儲(chǔ)存條件-20°C
    溶解度DMF: soluble; DMSO: soluble; Ethanol: soluble; Methanol: soluble
    形態(tài)白色至類白色固體

    安全數(shù)據(jù)

    WGK Germany3
    海關(guān)編碼29419000

    常見問(wèn)題列表

    生物活性
    Conglobatin (FW-04-806) 是一種從 Streptomyces conglobatus 培養(yǎng)物中分離得到的大環(huán)內(nèi)酯雙內(nèi)酯。Conglobatin 是一種具有口服活性的 Hsp90 抑制劑,可以與 Hsp90 的 N 末端域結(jié)合,并破壞 Hsp90-Cdc37 復(fù)合物的形成。Conglobatin 可誘導(dǎo)人乳腺癌細(xì)胞和食道鱗狀細(xì)胞癌細(xì)胞凋亡,并在體內(nèi)表現(xiàn)出抗腫瘤活性。
    靶點(diǎn)

    HSP90

    體外研究

    Conglobatin (6.25-100 μM; 48 h) markedly inhibits the proliferation of SKBR3 and MCF-7 cells, with IC 50 s of 12.11 and 39.44 μM, respectively.
    Conglobatin inhibits cell proliferation in EC109, KYSE70, KYSE450, KYSE150, KYSE180, and KYSE510 cells, with IC 50 s of 16.43, 15.89, 10.94, 10.50, 10.28, and 9.31 μM, respectively.
    Conglobatin (10-40 μM; 24 h) displays obvious arrest of SKBR3 and MCF-7 cells in the G2/M phase. Conglobatin induces apoptosis through caspase-dependent pathways in SKBR3 and MCF-7 cells.
    Conglobatin (10-40 μM; 3-24 h) reduces Hsp90 client protein levels and induces proteasome-dependent degradation.
    Conglobatin binds to the N-terminal of Hsp90, does not affect ATP-binding capability of Hsp90, but inhibits Hsp90/Cdc37 chaperone/co-chaperone interactions.

    Cell Proliferation Assay

    Cell Line: SKBR3 and MCF-7 cells
    Concentration: 6.25, 12.5, 25, 50, 100 μM
    Incubation Time: 48 hours
    Result: Inhibited the proliferation of SKBR3 and MCF-7 cells in a dose-dependent manner.

    Cell Cycle Analysis

    Cell Line: SKBR3 and MCF-7 cells
    Concentration: 10, 20, 40 μM
    Incubation Time: 24 hours
    Result: Increased the G2/M cell population and decreased the population in the S and G0/G1 phases.

    Western Blot Analysis

    Cell Line: SKBR3 and MCF-7 cells
    Concentration: 10, 20, 40 μM
    Incubation Time: 3, 6, 12, 24 hours
    Result: Decreased the levels of the client proteins HER2, p-HER2, Raf-1, Akt, and p-Akt in a dose and time-dependent manner in SKBR3 cells.
    Reduced the the levels of the client proteins Raf-1, Akt, and p-Akt in a dose and time-dependent manner in MCF-7 cells.
    體內(nèi)研究

    Conglobatin (50-200 mg/kg; i.g. q3d for 24 d) inhibits the tumor growth of SKBR3 and MCF-7 human breast cancer xenograft models in a dose-dependent manner.
    Conglobatin (4-8 mg/kg; i.p. daily for 21 days) inhibits tumor growth in EC109 and KYSE510 tumor xenograft models with low toxicity

    Animal Model: BALB/c (nu/nu) athymic mice with SKBR3 and MCF-7 tumor xenograft
    Dosage: 50, 100, 200 mg/kg
    Administration: Oral gavage every 3 days for 24 days
    Result: Showed inhibition of tumor growth at a rate of 39.1%, 52.7%, and 67.5% in the SKBR3 cell line groups and 27.3%, 39.8%, 54.3% in the MCF-7 cell line groups at the three increasing doses, respectively.
    Was well tolerated.
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