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LX-1

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Natural
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Oligonucleotides

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-163940
    LX1

    		Aldose Reductase Androgen Receptor Cancer
    LX1 is an anti-prostate cancer compound that targets androgen receptor (AR), AR variants and steroidogenic enzyme AKR1C3. LX1 inhibits the enzymatic activity of AKR1C3, reduces the conversion of androstenedione to testosterone and reduces the expression of AR and AR-V7 and downregulates their target genes. LX1 overcomes the resistance of tumor cells to Enzalutamide (HY-70002), and the combination with Enzalutamide (HY-70002) further inhibits tumor growth [1].
    LX1
  • HY-N14139
    Dioxamycin

    		Bacterial Infection Cancer
    Dioxamycin has anti-Gram-positive bacterial activity. Dioxamycin can inhibit Staphylococcus aureus 209P with a MIC of 3.12 μg/mL. Dioxamycin inhibits the growth of L1210, P388, IMC, LX-1 and SC-6 cells with IC50s (μg/mL) of 2.7, 1.4, 6.0, 2.0 and 2.5, respectively [1].
    Dioxamycin
  • HY-RS19841
    Slc22a1 Mouse Pre-designed siRNA Set A

    		Small Interfering RNA (siRNA) Others

    Slc22a1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Slc22a1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Slc22a1 Mouse Pre-designed siRNA Set A
    Slc22a1 Mouse Pre-designed siRNA Set A

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