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phox-i2

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    17
    TargetMol | Activity
  • Peptide Products
    2
    TargetMol | inventory
Phox-I2
T25952353495-22-4
Phox-I2 is an NOX2-specific inhibitor. Phox-I2 reverts ROS-accumulation and leads to refusion of mitochondrial networks.
  • $77
In Stock
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QTY
[Leu15]-Gastrin I human acetate(39024-57-2 Free base)
T8761L
[Leu15]-Gastrin I human acetate(39024-57-2 Free base) is a useful organic compound for research related to life sciences and the catalog number is T8761L.
  • $195
In Stock
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Methanesulfonato(2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)(2'-methylamino-1,1'-biphenyl-2-yl)palladium(II)
T672401599466-81-5
Methanesulfonato(2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)(2'-methylamino-1,1'-biphenyl-2-yl)palladium(II) is a useful organic compound for research related to life sciences. The catalog number is T67240 and the CAS number is 1599466-81-5.
    7-10 days
    Inquiry
    Topoisomerase I/II inhibitor 2
    T61045
    Topoisomerase I II inhibitor 2 (compound 1a) is a DNA topoisomerase I II dual inhibitor that significantly reduces xenograft tumor growth in a mouse model, indicating its potential use in treating liver cancer. It is a potent topoisomerase inhibitor with IC50 values of 6.83 μM and 9.82 μM for LM9 cells and Huh7 cells [1].
    • $1,520
    10-14 weeks
    Size
    QTY
    Topoisomerase I inhibitor 2
    T606172588211-44-1
    Topoisomerase I inhibitor 2 (ZML-8) is a highly selective DNA topoisomerase I (Top1) inhibitor that impedes Top1 activity, causing DNA damage. It arrests the cell cycle at the G2 M phase and induces apoptosis, exhibiting anti-tumor effects [1].
    • $1,520
    6-8 weeks
    Size
    QTY
    Topo I/COX-2-IN-2
    T62241
    Topo I COX-2-IN-2 (Compound W10) is a potent dual inhibitor of Topo I (IC50: 0.90 μM) and COX-2 (IC50: 2.31 μM), inducing apoptosis in cancer cells via the mitochondrial pathway.
    • $1,520
    10-14 weeks
    Size
    QTY
    hCA I-IN-2
    T639722417232-12-1
    hCA I-IN-2 (Compound 6d) is a selective inhibitor of human carbonic anhydrase I (hCA I) with inhibition constants (Ki) as follows: 18.8 nM for hCA I, 375.1 nM for hCA II, 1721 nM for hCAIX, and 283.9 nM for hCAXII.
    • $1,520
    6-8 weeks
    Size
    QTY
    MMP-2/MMP-9 Inhibitor I
    T21512193807-58-8
    MMP-2 MMP-9-IN-1 is a potent, highly selective, and orally bioavailable inhibitor of type IV collagenases [MMP-9 and MMP-2], exhibiting IC50 values of 0.24 μM for MMP-9 and 0.31 μM for MMP-2, which can be used to study cancer.
    • $54
    In Stock
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    QTY
    Methanesulfonato(2-dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl)(2'-amino-1,1'-biphenyl-2-yl)palladium(II)
    T646281445085-77-7
    Methanesulfonato(2-dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl)(2'-amino-1,1'-biphenyl-2-yl)palladium(II) is a useful organic compound for research related to life sciences. The catalog number is T64628 and the CAS number is 1445085-77-7.
      7-10 days
      Inquiry
      2-(Dicyclohexylphosphino)-2',4',6'-tri-i-propyl-1,1'-biphenyl
      T65998564483-18-7
      2-(Dicyclohexylphosphino)-2',4',6'-tri-i-propyl-1,1'-biphenyl is a useful organic compound for research related to life sciences. The catalog number is T65998 and the CAS number is 564483-18-7.
        7-10 days
        Inquiry
        Topo I/COX-2-IN-1
        T61939
        Topo I COX-2-IN-1 (1H-30) is a potent Topo I COX-2 inhibitor with IC50 values of 0.24 μM for COX-2 and 4.42 μM for Topo I. It induces apoptosis and inhibits cancer cell migration, demonstrating anti-cancer activity.
        • $1,520
        10-14 weeks
        Size
        QTY
        Methanesulfonato(2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)(2'-amino-1,1'-biphenyl-2-yl)palladium(II)
        T646301445085-55-1
        Methanesulfonato(2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)(2'-amino-1,1'-biphenyl-2-yl)palladium(II) is a useful organic compound for research related to life sciences. The catalog number is T64630 and the CAS number is 1445085-55-1.
          7-10 days
          Inquiry
          TPMP-I-2
          T26285102660-13-9
          TPMP-I-2 has an anticancer effect of immunotoxins.
            6-8 weeks
            Inquiry
            Methanesulfonato(2-dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl)(2'-methylamino-1,1'-biphenyl-2-yl)palladium(II)
            T672581599466-85-9
            Methanesulfonato(2-dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl)(2'-methylamino-1,1'-biphenyl-2-yl)palladium(II) is a useful organic compound for research related to life sciences. The catalog number is T67258 and the CAS number is 1599466-85-9.
              7-10 days
              Inquiry
              Glyoxalase I inhibitor 2
              T626992314467-61-1
              Glyoxalase I inhibitor 2 (compound 26) is a potent inhibitor of glyoxalase I (GLO1) with an IC50 of 0.5 μM, and has potential applications in depression and anxiety studies.
              • $1,520
              6-8 weeks
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              QTY
              2’-O-Me-5-I-U-3’-phosphoramidite
              T75221
              2’-O-Me-5-I-U-3’-phosphoramidite, a purine nucleoside analog, exhibits extensive antitumor activity primarily against indolent lymphoid malignancies through mechanisms such as DNA synthesis inhibition and apoptosis induction, among others [1].
              • Inquiry Price
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              [Leu15]-Gastrin I human
              T876139024-57-2
              [Leu15]-Gastrin I human (Amino Acid Sequence Glp-Gly-Pro-Trp-Leu-Glu-Glu-Glu-Glu-Glu-Ala-Tyr-Gly-Trp-Leu-Asp-Phe-NH2) encodes for the protein [Leu15]-Gastrin I in human. In human chromosome, the gene GAST is localized on 17q21.2. G cells in the stomach antrum produces the precursor of [Leu15]-Gastrin I, progastrin.Progastrin undergoes cleavage and processing to yield gastrin, which is trophic for the entire gastrointestinal epithelium. Gastrin is essential for the growth of the digestive system and stimulates the production of gastric acid by parietal cells. Gastrin exerts its function through G-protein-coupled receptor called the cholecystokinin (CCK) or CCK-B receptor (CCK-BR). Gastrin release is stimulated by food, especially protein diet and is inhibited by very low pH. Atrophic gastritis, a Helicobacter pylori infection and long-term administration of proton pump inhibitors infection may cause overexpression of gastrin. Gastric adenocarcinoma show high levels of gastrin.
              • $71
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