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        AC-73_775294-71-8_產品詳情
        775294-71-8
        • names:

          AC-73

        • CAS號:

          775294-71-8

          MDL Number:
        • MF(分子式): C21H21NO2 MW(分子量): 319.4
        • EINECS: Reaxys Number:
        • Pubchem ID:2989791 Brand:BIOFOUNT
        AC-73
        AC-73(775294-71-8)是 Cluster of Differentiation 147 (CD147) 的第一種特定的口服生物利用的抑制劑,可特異性破壞 CD147 的二聚化 (結合位點在 CD147 的 N 端 IgC2 域中包括 Glu64 和 Glu73),從而抑制 CD147/ERK1/2/STAT3/MMP-2 途徑,并抑制肝癌細胞的運動和侵襲。AC-73 還是一種抗增殖藥,也是白血病細胞自噬的誘導劑。
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        中文別名 AC-73(775294-71-8)
        英文別名 AC-73,775294-71-8
        CAS號 775294-71-8
        Inchi InChI=1S/C21H21NO2/c23-20-8-4-7-19(13-20)21(24)15-22-14-16-9-11-18(12-10-16)17-5-2-1-3-6-17/h1-13,21-24H,14-15H2
        InchiKey UECKKYNEEBRMIL-UHFFFAOYSA-N
        分子式 Formula C21H21NO2
        分子量 Molecular Weight 319.4
        溶解度Solubility
        性狀 白色至灰白色固體粉末
        儲藏條件 Storage conditions storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
        AC-73(CAS:775294-71-8)實驗注意事項:
        1.實驗前需戴好防護眼鏡,穿戴防護服和口罩,佩戴手套,避免與皮膚接觸。
        2.實驗過程中如遇到有毒或者刺激性物質及有害物質產生,必要時實驗操作需要手套箱內完成以免對實驗人員造成傷害
        3.實驗后產生的廢棄物需分類存儲,并交于專業生物廢氣物處理公司處理,以免造成環境污染Experimental considerations:
        1. Wear protective glasses, protective clothing and masks, gloves, and avoid contact with the skin during the experiment.
        2. The waste generated after the experiment needs to be stored separately, and handed over to a professional biological waste gas treatment company to avoid environmental pollution.
        產品說明 AC-73(cas:775294-71-8) 是Cluster of Differentiation 147 (CD147)的第一種特定的口服生物利用的抑制劑
        IntroductionAC3 is a first specific, orally active inhibitor of cluster of differentiation 147 (CD147), which specifically disruptsCD147dimerization, thereby mainly suppressing theCD147/ERK1/2/STAT3/MMP pathways.
        Application1AC3 is also an antiroliferative drug and an inducer of autophagyin leukemic cells.
        Application2AC3 inhibits the motility and invasion of hepatocellular carcinoma cells.
        Application3
        IC50 & Target CD147 
          In Vitro ※ AC-73 (5-10 μM; 24 hours; SMMC-7721 and Huh-7 cells) treatment significantly decreases the migration ability of SMMC-7721 and Huh-7 cells in a dose-dependent manner and decreases the invasion of two HCC cells in a dose-dependent manner at 24 hours. AC-73 treatment reduces HCC metastases. There are no obvious effects on cell viability when two HCC cells are treated with AC-73 at a maximum concentration of 20 μM. The possible binding sites of AC-73 on CD147 included Glu64 and Glu73 in the N-terminal IgC2 domain, which two residues are located in the dimer interface of CD147.
        ※ AC-73 (5-10 μM; 24 hours; SMMC-7721 cells) treatment could significantly inhibit both MMP-2 and MMP-9 mRNA expression at the concentration of 10 μM, especially MMP-2, but no obvious effect on MMP-1, MMP-3, MMP-7, MMP-11 nor MMP-13. AC-73 could dose dependently reduce the expression of MMP-2 mRNA level and secretion of the protein level using RT-qPCR analysis and gelatin zymography experiments.
        ※ AC-73 (5-20 μM; 6 hours; SMMC-7721 cells) treatment dose-dependently suppresses the phosphorylation of ERK1/2 and STAT3.
        Cell Line: SMMC-7721 cells
        Concentration: 5 μM or 10 μM
        Incubation Time: 24 hours
        Result: Significantly inhibited both MMP-2 and MMP-9 mRNA expression at the concentration of 10 μM. Dose dependently reduced the expression of MMP-2 mRNA level and secretion of the protein level using RT-qPCR analysis and gelatin zymography experiments.
          In Vivo AC-73 (25-50 mg/kg; for 4 weeks; Male BALB/c nu/nu mice) treatment significantly decreases the incidence of metastatic foci in nude mice. AC-73 inhibits the phosphorylation of ERK1/2 and STAT3 in a dose-dependent manner. MMP-2 is also reduced by AC-73. AC-73 could not inhibit tumor cell proliferation in vivo.
        Animal Model: Male BALB/c nu/nu mice (4-6 weeks) with SMMC-7721 cells
        Dosage: 25 mg/kg, 50 mg/kg
        Administration: Injected; daily; for 3 weeks
        Result: Significantly decreased the incidence of metastatic foci in nude mice. Inhibited the phosphorylation of ERK1/2 and STAT3 in a dose-dependent manner. MMP-2 was also reduced.
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