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  • DNA Ligase from T4-infected Escherichia coli
    TS1002

    Astragaloside A(黄芪甲苷) is the primary pure saponin isolated from Astragalus membranaceus, which has been widely used for the treatment of cardiovascular diseases.

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  • DNA Ligase from T4-infected Escherichia coli
    TS1012

    Gambogic Acid(藤黄酸) activates caspases with EC50 of 0.78-1.64 &muM and competitively inhibits Bcl-XL, Bcl-2, Bcl-W, Bcl-B, Bfl-1 and Mcl-1 with IC50 of 1.47, 1.21, 2.02, 0.66, 1.06 and 0.79 &muM, respectively.

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  • DNA Ligase from T4-infected Escherichia coli
    TS1319

    Betulinic acid(白桦脂酸), a pentacyclic triterpenoid from Syzigium claviflorum, is a inhibitor of HIV-1 with EC50 of 1.4 muM.

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  • DNA Ligase from T4-infected Escherichia coli
    TS1322

    Demethylzeylasteral(去甲泽拉木醛), the active component isolated from Tripterygium wilfordii Hook F., inhibits UDP-glucuronosyltransferase (UGT) isoforms UGT1A6 and UGT2B7 with immunosuppressive effects.  

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  • DNA Ligase from T4-infected Escherichia coli
    TS1323

    Berbamine (BBM) 2HCl( 小檗胺二盐酸盐) is a natural bisbenzylisoquinoline product isolated from traditional Chinese herbal medicine Berberis amurensis. It is a novel inhibitor of bcr/abl fusion gene with potent anti-leukemia activity and also an inhibitor of NF-κB.  

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  • DNA Ligase from T4-infected Escherichia coli
    TS1324

    Cordycepin(虫草素) is an adenosine analogue, which is readily phosphorylated to its mono-, di-, and triphosphate intracellularly. It has a very potent anti-cancer, anti-oxidant and anti-inflammatory activities.  

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  • DNA Ligase from T4-infected Escherichia coli
    TS1325

    (+)-Fangchinoline(防己诺林碱) is a phytochemical that has been shown to elicit anti-cancer effects in prostate and breast cancer cell lines via inducing G1 cell cycle arrest. It has also been shown to possess neuroprotective activity.  

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  • DNA Ligase from T4-infected Escherichia coli
    TS1326

    Rosmarinic acid (RA)(迷迭香酸) is a naturally occurring hydroxylated compound. It has the ability to block complement fixation, inhibit lipoxygenase and cyclooxygenase activity and inhibit the  of CCL11 and CCR3 by suppressing the IKK-β activity in NF-κB activation signaling.  

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