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抑制剂&激动剂
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  • 抑制剂&激动剂
    9
    TargetMol | Inhibitors_Agonists
  • 抗体抑制剂
    1
    TargetMol | Inhibitory_Antibodies
  • F-050
    T70106186835-06-3
    F-050 is a biochemical that has been shown to inhibit platelet aggregation induced by CaCl2, arachidonic acid, collagen, adenosine diphosphate (ADP) and thrombin in guinea pigs, rabbits and rats in vitro. F-050 may be useful in the treatment of thrombotic diseases.
    • ¥ 10600
    6-8周
    规格
    数量
  • Chlorpromazine Sulfone Hydrochloride
    T7010518683-73-3
    Chlorpromazine Sulfone Hydrochloride is a metabolite of Chlorpromazine -- an anti-emetic and anti-psychotic agent. It may also be used as a potential N-methyltransferase inhibitor.
    • ¥ 10600
    6-8周
    规格
    数量
  • PF 05089771 tosylate
    T75021430806-04-4
    PF 05089771 tosylate 是口服有效的、选择性的Nav1.7丙烯酰胺抑制剂。PF 05089771 tosylate 具有用于疼痛和糖尿病神经性疾病的研究。
    • ¥ 560
    In stock
    规格
    数量
  • PF 05089771
    PF-05089771, PF05089771
    T7502L1235403-62-9
    PF 05089771是具有口服有效的、选择性的 Nav1.7丙烯酰胺抑制剂。PF-05089771在疼痛和糖尿病神经性疾病的研究中具有价值。
    • ¥ 647
    In stock
    规格
    数量
  • PF-05085727
    T164821415637-72-7
    PF-05085727 inhibits PDE2A >4,000-fold selectivity over PDE1 and PDE3-11. PF-05085727 is an effective, selective and brain penetrant inhibitor of cGMP-dependent PDE2A (IC50=2 nM) .
    • ¥ 484
    5日内发货
    规格
    数量
  • PKF050-638
    T16548528893-52-9
    PKF050-638 inhibits the CRM1-mediated Rev nuclear export by disrupting CRM1-NES interaction. PKF050-638 is an effective and selective inhibitor of HIV-1 Rev (IC50=0.04 μM).
    • ¥ 10600
    6-8周
    规格
    数量
  • Azamitosene
    T70894135513-52-9
    Azamitosene is a DNA cleaving agent exhibiting G and A base specificity. Azamitosene may exhibit a growth inhibitory effect on human gastric cancer cells.
    • ¥ 10600
    6-8周
    规格
    数量
  • PF05020182
    T708961354712-92-7
    PF05020182 is novel potent and selective Kv7.2 4 potassium channel opener. PF-05020182 (2) significantly inhibits convulsions in the MES assay at doses tested, consistent with in vitro activity measure. The physiochemical properties, in vitro and in vivo activities of PF-05020182 support further development as an adjunctive treatment of refractory epilepsy. Facilitating activation, or delaying inactivation, of the native Kv7 channel reduces neuronal excitability, which may be beneficial in controlling spontaneous electrical activity during epileptic seizures.
    • ¥ 10600
    6-8周
    规格
    数量
  • Utomilumab
    乌托鲁单抗, PF-2566, PF 05082566
    T767051417318-27-4
    Utomilumab (PF 05082566) 是一种人源化靶向T 细胞共刺激受体4-1BB CD137的 IgG2 抗体,也是一种 4-1BB CD137 激动剂。Utomilumab 具有抗肿瘤活性,可用于研究晚期恶性肿瘤患者。
    • ¥ 2480
    In stock
    规格
    数量
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