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  • Heparin EY2200

    Heparin, a highly sulfated glycosaminoglycan, is widely used as an injectable anticoagulant, and has the highest negative charge density of any known biological molecule.

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  • C34 EY2201

    TLR4 inhibitor; attenuates TLR4 signaling in enterocytes and macrophages in vitro, and reduces systemic inflammation in mouse models of endotoxemia and necrotizing enterocolitis (NEC). Also suppresses LPS signaling in human ileum displaying NEC ex-vivo. Displays no significant effects on signaling via TLR2 or TLR9.

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  • Norfluoxetine Hydrochloride EY2202

    Norfluoxetine Hydrochloride is a fluoxetine metabolite; more potent inhibitor of serotonin uptake than fluoxetine with a half-life in vivo of 5-7 days.

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  • Halofuginone EY2203

    Halofuginone is the competitively inhibitor of prolyl-tRNA synthetase with Ki of 18.3 nM.It could also down-regulate Smad3 and blocked TGF-β signaling at 10 ng/ml in mammal.

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  • ISO 1 EY2040

    ISO 1 is an inhibitor of MIF d-dopachrome tautomerase activity with an IC50 of about 7 uM.

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  • Heparin EY2200

    Heparin, a highly sulfated glycosaminoglycan, is widely used as an injectable anticoagulant, and has the highest negative charge density of any known biological molecule.

    More
  • C34 EY2201

    TLR4 inhibitor; attenuates TLR4 signaling in enterocytes and macrophages in vitro, and reduces systemic inflammation in mouse models of endotoxemia and necrotizing enterocolitis (NEC). Also suppresses LPS signaling in human ileum displaying NEC ex-vivo. Displays no significant effects on signaling via TLR2 or TLR9.

    More
  • Norfluoxetine Hydrochloride EY2202

    Norfluoxetine Hydrochloride is a fluoxetine metabolite; more potent inhibitor of serotonin uptake than fluoxetine with a half-life in vivo of 5-7 days.

    More
  • Halofuginone EY2203

    Halofuginone is the competitively inhibitor of prolyl-tRNA synthetase with Ki of 18.3 nM.It could also down-regulate Smad3 and blocked TGF-β signaling at 10 ng/ml in mammal.

    More
  • ISO 1 EY2040

    ISO 1 is an inhibitor of MIF d-dopachrome tautomerase activity with an IC50 of about 7 uM.

    More
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