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    TargetMol | Inhibitors_Agonists
  • Pitavastatin methyl ester
    T68566849811-78-5
    Pitavastatin methyl ester is the methyl ester derivative of Pitavastatin -- a competitive inhibitor of HMG-CoA reductase and an anti-lipemic agent.
    • ¥ 10600
    6-8周
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  • Indolmycin
    吲哚霉素, TAK-083, TAK083, PA-155A, PA155A
    T2188721200-24-8
    Indolmycin(吲哚霉素)是一种对多种细菌有效的抗生素, 能够抑制色氨酸- trna合成酶(TrpRS),一种细菌中蛋白质合成所必需的酶,竞争性地直接结合TrpR的活性位点并导致细菌死亡。
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  • Fadolmidine HCl
    T70077189353-32-0
    Fadolmidine, also known as MPV-2426, is a novel and potent alpha2 -adrenoceptor (alpha2) -AR) agonist developed for spinal analgesia. Fadolmidine displayed high affinity and full agonist efficacy at all three human alpha2-adrenoceptor subtypes (A, B and C) in transfected CHO cells with EC50 values (nM) of 0.4, 4.9 and 0.5, respectively. Fadolmidine inhibited also electrically evoked contractions in rat vas deferens demonstrating the activation of rodent presynaptic alpha2D-adrenoceptors with an EC50 value of 6.4 nM. Moreover, fadolmidine was a full agonist at human alpha1A-adrenoreceptor (EC50 value 22 nM) and alpha1B-adrenoreceptor (EC50 value 3.4 nM) in human LNCaP cells and transfected HEK cells, respectively. Agonism at the alpha1-adrenoceptor was also observed in rat vas deferens preparations although at lower potency (EC50 value 5.6 microM). Fadolmidine demonstrated potent alpha2-adrenoceptor agonist activity also in vivo by inhibiting electrically induced tachycardia i......
    • ¥ 10600
    6-8周
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    数量
  • Fadolmidine
    T70078189353-31-9
    Fadolmidine is a novel and potent alpha2 -adrenoceptor (alpha2) -AR) agonist developed for spinal analgesia.
    • ¥ 10600
    6-8周
    规格
    数量