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  • DNA Ligase from T4-infected Escherichia coli
    TS2343

    Bevantolol hydrochloride(盐酸贝凡洛尔) is a cardioselective, beta adrenoceptor antagonist, devoid of intrinsic β sympathomimetic activity and with weak membrane-stabilizing and local anesthetic properties.

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  • DNA Ligase from T4-infected Escherichia coli
    TS2350

    Thiocolchicoside(硫秋水仙苷) is a natural occuring glycoside originated from the flower seeds of superba gloriosa with anti-inflammatory and analgesic properties as well as pronounced convulsant activity. It is also an antagonist of GABAA receptor.

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  • DNA Ligase from T4-infected Escherichia coli
    TS2361

    Pramipexole dihydrochloride(盐酸普拉克索) is a dopamine agonist of the non-ergoline class indicated for treating Parkinson's disease (PD) and restless legs syndrome (RLS) with Ki values of 3.9 nM, 2.2 nM, 0.5 nM and 5.1 nM for D2S receptor, D2L receptor, D3 receptor and D4 receptor.

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  • DNA Ligase from T4-infected Escherichia coli
    TS2364

    Duloxetine(LY-248686)(度洛西丁) is a potent inhibitor of serotonin (5-hydroxytryptamine, 5-HT) and noradrenaline (NE) uptake in vitro and in vivo and is 3- to 5-times more effective at inhibiting 5-HT uptake.

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  • DNA Ligase from T4-infected Escherichia coli
    TS2366

    Donepezil(多奈哌齐) is a piperidine based, potent, specific, non-competitive and reversible inhibitor of acetylcholinesterase (AChE) used for the treatment of mild to moderate dementia of the Alzheimer's type.

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  • DNA Ligase from T4-infected Escherichia coli
    TS2368

    Acotiamide(阿考替胺) is a novel acetylcholinesterase inhibitor with fundus-relaxing and gastroprokinetic properties.

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  • DNA Ligase from T4-infected Escherichia coli
    TS2378

    Labetalone hydrochloride(盐酸拉贝洛尔酮) is hydrochloride form of labetalone, a blocker of both alpha- and beta-adrenergic receptors that is used as an antihypertensive.

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  • DNA Ligase from T4-infected Escherichia coli
    TS2409

    Homotaurine(3-氨基-1-丙磺酸) is a synthetic organic compound that has GABAergic activity by mimicking GABA. It is a GABAA partial agonist as well as a GABAB receptor partial agonist with low efficacy.

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