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  • DNA Ligase from T4-infected Escherichia coli
    TL0001

    Pravastatin sodium(普伐他汀钠) is a competitive, water-soluble HMG-CoA reductase inhibitor.Inhibits cholesterol synthesis in vivo (Ki ~1 nM).

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  • DNA Ligase from T4-infected Escherichia coli
    TL0007

    Lovastatin(洛伐他汀) is a cholesterol lowering drug and competitive inhibitor of HMG-CoA reductase, a rate limiting enzyme in cholesterol synthesis.

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  • DNA Ligase from T4-infected Escherichia coli
    TL0019

    Ketoconazole(酮康唑) is a synthetic derivative of phenylpiperazine with broad antifungal properties and potential antineoplastic activity. Ketoconazole inhibits sterol 14-a-dimethylase, a microsomal cytochrome P450-dependent enzyme, thereby disrupting synthesis of ergosterol, an important component of the fungal cell wall.

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  • DNA Ligase from T4-infected Escherichia coli
    TL0035

    Fluvastatin Sodium(氟伐他汀钠) is the sodium salt of a synthetic lipid-lowering agent with potential antineoplastic activity.

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  • DNA Ligase from T4-infected Escherichia coli
    TL0036

    Simvastatin(辛伐他汀) is a HMG-CoA Reductase Inhibitor. The mechanism of action of simvastatin is as a Hydroxymethylglutaryl-CoA Reductase Inhibitor.

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  • DNA Ligase from T4-infected Escherichia coli
    TL0041

    Adapalene(阿达帕林) is a topical retinoid-like compound, chemically similar to vitamin A. Although the exact mechanism of action is unknown, adapalene binds to specific retinoic acid receptors in the nucleus, leading to specific gene .

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  • DNA Ligase from T4-infected Escherichia coli
    TL0045

    Sildenafil citrate(枸橼酸西地那非) functions as a selective and competitive inhibitor of type 5 phosphodiesterases (PDE5) on smooth muscle cells in the penis and pulmonary vasculature.

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  • DNA Ligase from T4-infected Escherichia coli
    TL0047

    Atorvastatin Calcium(阿托伐他汀钙) is the calcium salt of atorvastatin, a synthetic lipid-lowering agent. Atorvastatin is a HMG-CoA Reductase Inhibitor. The mechanism of action of atorvastatin is as a Hydroxymethylglutaryl-CoA Reductase Inhibitor.

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