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抑制剂&激动剂
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  • 抑制剂&激动剂
    7
    TargetMol | Inhibitors_Agonists
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    TargetMol | Natural_Products
  • Calcimycin
    离子载体(钙镁盐混合物), Antibiotic A-23187, A-23187
    T10662L52665-69-7
    Calcimycin (A-23187) 是抗生素和二价阳离子离子载体。它抑制革兰氏阳性细菌和一些真菌生长,也抑制 ATP 酶的活性并解耦哺乳动物细胞的氧化磷酸化。它通过增加细胞内钙浓度诱导 Ca2+依赖性细胞死亡。
    • ¥ 950
    In stock
    规格
    数量
  • 4-Bromo A23187
    4-​Bromo A23187
    T1013776455-48-6
    4-Bromo A23187 is a halogenated analog of the calcium ionophore A-23187. 4-Bromo A23187 is a calcium modulator and induces apoptosis in different cells.
    • ¥ 1980
    35日内发货
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    数量
  • Calcimycin hemicalcium salt
    Antibiotic A-23187 hemicalcium salt,A-23187 hemicalcium salt
    T1066259450-89-4
    Calcimycin (A-23187) hemicalcium salt is an antibiotic and a unique divalent cation ionophore (like calcium and magnesium). It induces Ca2+-dependent cell death by increasing intracellular calcium concentration.
    • ¥ 10600
    待询
    规格
    数量
  • Diffractaic Acid
    NSC 5901, 地弗地衣酸, NSC 685595
    T4114436-32-8
    Diffractaic Acid (NSC 685595) 是松萝的主要成分,具有止痛和解热效果,在各种疾病研究中可作为有效的促凋亡剂。
    • ¥ 993
    In stock
    规格
    数量
  • Calcimycin hemimagnesium
    T7565672124-77-7
    Calcimycin (A-23187) hemimagnesium,一种具有抗生素功能的独特二价阳离子离子载体(例如钙离子和镁离子),通过提高细胞内钙浓度而诱导Ca2+依赖性细胞死亡。该化合物还能抑制革兰氏阳性细菌和部分真菌生长,同时抑制ATP酶活性并解耦哺乳动物细胞的氧化磷酸化(OXPHOS),触发细胞凋亡(apoptosis)。
    • 待询
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  • U-51605
    T8457564192-56-9
    U-51605, a stable analog of the endoperoxide prostaglandin H2 (PGH2), functions as an inhibitor with greater selectivity towards prostacyclin (PGI) synthase over thromboxane (TX) synthase. It also acts as a partial agonist at TP receptors. Studies show that at a concentration of 2.8 µM, U-51605 effectively inhibits PGI synthase in human foreskin fibroblasts, while a concentration of 5.6 µM is required to inhibit human platelet TX synthase. Furthermore, U-51605, at up to 1 µM, decreases the release of prostacyclin in SHR aorta triggered by the calcium ionophore A-23187 without impacting TXA2 production, and notably enhances the release of PGE2 and PGF2α.
    • 待询
    8-10周
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  • Morolic acid
    TN4584559-68-2
    Morolic acid and moronic acid have shown sustained antidiabetic and antihyperglycemic action possibly mediated by an insulin sensitization with consequent changes of glucose, cholesterol and triglycerides, in part mediated by inhibition of 11β-HSD 1. Moro
    • ¥ 3230
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