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TargetMol产品目录中 "2-pyrrolidinone"的结果
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  • 抑制剂&激动剂
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    TargetMol | Inhibitors_Agonists
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    TargetMol | Inhibitors_Agonists
  • 2-Pyrrolidinone
    2-吡咯烷酮
    T5296616-45-5
    2-Pyrrolidinone 是一种存在于甘蓝中的特性化合物,并显示抗癌特性。它是 γ-氨基丁酸 (GABA) 的内酰胺环化产物。
    5日内发货
    询价
    TargetMol | Inhibitor Sale
  • 5-Hydroxy-2-pyrrolidinone
    TN311762312-55-4
    5-Hydroxy-2-pyrrolidinone是一种天然产物,属于马钱科醉鱼草属,其产品编号为 TN3117,CAS号为 62312-55-4。5-Hydroxy-2-pyrrolidinone可用作对照参考。
    • ¥ 2380
    待询
    规格
    数量
  • N-Methylpyrrolidone
    N-甲基吡咯烷酮, 1-Methyl-2-pyrrolidinone
    T5851872-50-4
    N-Methylpyrrolidone (1-Methyl-2-pyrrolidinone) 是一种有机极性溶剂,是一种五元环酰胺,普遍用于粘合剂,油漆,燃料和药品的生产。
    • ¥ 183
    In stock
    规格
    数量
  • Felipyrine
    PYPEPYRONE, 2-PYRROLIDINONE, 1-PHENYL-3-(1-PIPERIDINYL)-
    T2019921980-49-0
    Felipyrine为一种1-芳基-2-吡咯烷酮衍生物,具有抗炎作用。
    • 待询
    10-14周
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  • KMN-80
    T374411628759-75-0
    The prostaglandin E receptor 4 (EP4) is one of four G protein-coupled receptors that mediate the actions of prostaglandin E2 . Binding of PGE2 to the EP4 receptor causes an increase in intracellular cyclic AMP, which plays important roles in bone formation and resorption, cancer, and atherosclerosis. KMN-80 is a substituted γ-lactam (pyrrolidinone) derivative of PGE1 that acts as a selective and potent agonist of EP4 with an IC50 value of 3 nM (IC50 = 1.4 μM for EP3 and > 10 μM for all other prostanoid receptors). In functional assays it has been shown to stimulate secreted alkaline phosphatase gene reporter activity in EP4-transfected HEK293 cells with an EC50 value of 0.19 nM, demonstrating >5,000 and 50,000-fold selectivity against EP2 and TP, respectively. KMN-80 can induce the differentiation of bone marrow stem cells from both young and aged rats into osteoblasts in vitro (EC50s = 20 and 153 nM, respectively) and exhibits favorable tolerability up to at least 10 μM, whereas the EP4 agonist L-902,688 is highly cytotoxic at similar concentrations in these cells. KMN-80 has been used to repair calvarial defects in an in vivo rat craniomaxillofacial reconstruction model (rate of reduction in defect size equivalent to BMP-2 treated rats) and to promote bone formation in a rat incisor tooth socket model.
    • 待估
    35日内发货
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  • (R)-(+)-Blebbistatin O-Benzoate
    T712071217635-67-0
    (R)-(+)-Blebbistatin O-Benzoate is a derivative of Blebbistatin. (R)-(+)-Blebbistatin is a 1-phenyl-2-pyrrolidinone derivative and a selective inhibitor of non-muscle myosin II. It blocks cell blebbing rapidly and reversibly and also disrupts directed cell migration and cytokinesis in vertebrate cell. (R)-(+)-Blebbistatin can also inhibit contraction of the cleavage furrow without disrupting mitosis or contractile ring assembly. (R)-(+)-Blebbistatin is suitable as a negative control for (S)-(-)-Blebblastatin.
    • ¥ 10600
    6-8周
    规格
    数量