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Results for "

HAP1

" in MedChemExpress (MCE) Product Catalog:

13

Inhibitors & Agonists

4

Peptides

5

Antibodies

1

Click Chemistry

5

Oligonucleotides

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-170316

    Ras Cancer
    Ibetazol is a Importin β1 (KPNB1) inhibitor and nucleocytoplasmic transport disruptor. Ibetazol binds covalently to Cys585 of Importin β1, blocks both Importin β1-mediated direct transport and Importin α-dependent nuclear import processes, without affecting transport mediated by other nucleocytoplasmic transport proteins. Ibetazol induces cytoplasmic accumulation of Importin α1, and inhibits nuclear import of substrates carrying nuclear localization signals (NLS), including the NLS-cMyc reporter gene, RelA/p65 and SREBP1. Ibetazol triggers spindle malformation and chromosome misalignment by disrupting the mitotic function of Importin β1. Ibetazol inhibits the proliferation of cells expressing wild-type Importin β1. Ibetazol has a high activity-cytotoxicity window, lacks intrinsic fluorescence, and acts rapidly on nucleocytoplasmic transport processes. Ibetazol serves as a tool compound for investigating nuclear import processes specifically mediated by Importin β1 [1].
    Ibetazol
  • HY-P4096

    Bacterial Inflammation/Immunology
    HAP-1 is a synovial-targeted transduction peptide. HAP-1 facilitates specific internalization of protein complexes into human and rabbit synovial cells. HAP-1 fused to an antimicrobial peptide, (KLAK)2, to generate a proapoptotic peptide DP2 [1].
    HAP-1
  • HY-153119

    PROTACs PIKfyve Inflammation/Immunology
    TMX-4153 is a selective PIP4K2C PROTAC degrader. TMX-4153 induces PIP4K2C degradation in MOLT4 cells (DC50 = 24 nM) and HAP1 cells (DC50 = 361 nM). TMX-4153 can be used for the study of biological functions of PIP4K2C (immune modulation)-related diseases. (Pink: BTK ligand (HY-177432), Blue: VHL Ligand (HY-112078), Black: Linker) [1].
    TMX-4153
  • HY-174866

    Histone Acetyltransferase Epigenetic Reader Domain PROTACs Cancer
    BT-O2C is a highly selective p300 PROTAC degrader. BT-O2C can significantly degrade the level of p300 in HAP1 cells. BT-O2C has significant cytotoxicity in CIC:DUX4 sarcoma (CDS) cell lines (IC50 ranges from 152 to 221 nM) and significantly reduces the expression of CDS target genes (ETV1, ETV4, ETV5). BT-O2C can be used for research on cancer. (Pink: p300 Ligand (HY-174868); Blue: CRBN Ligand (HY-W023573); Black: Linker; CRBN Ligand+Linker (HY-174869)) [1].
    BT-O2C
  • HY-150221

    PARP Cancer
    DB008 is potent and selective PARP16 inhibitor with an IC50 value of 0.27 μM, containing an acrylamide electrophilic reagent. DB008 is membrane-permeable and marks PARP16 selectively [1]. DB008 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    DB008
  • HY-RS17886

    Small Interfering RNA (siRNA) Others

    Hap1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Hap1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Hap1 Mouse Pre-designed siRNA Set A
    Hap1 Mouse Pre-designed siRNA Set A
  • HY-RS24355

    Small Interfering RNA (siRNA) Others

    Hap1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Hap1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Hap1 Rat Pre-designed siRNA Set A
    Hap1 Rat Pre-designed siRNA Set A
  • HY-RS06000

    Small Interfering RNA (siRNA) Others

    HAP1 Human Pre-designed siRNA Set A contains three designed siRNAs for HAP1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    HAP1 Human Pre-designed siRNA Set A
    HAP1 Human Pre-designed siRNA Set A
  • HY-174296

    PI5P4K Others
    TMX-4102 is a highly selective phosphatidylinositol 5-phosphate 4-kinase type II gamma (PIP4K2C) binder. TMX-4102 has binding activity to PIP4K2C (Kd = 0.45 nM) and has no significant effect on other lipid and non-lipid kinases.TMX-4102 specifically binds to PIP4K2C, regulating its scaffold function rather than its enzymatic activity. TMX-4102 can be used as a tool molecule to study the biological function and potential therapeutic value of PIP4K2C [1].
    TMX-4102
  • HY-RS00815

    Small Interfering RNA (siRNA) Others

    APEX1 Human Pre-designed siRNA Set A contains three designed siRNAs for APEX1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    APEX1 Human Pre-designed siRNA Set A
    APEX1 Human Pre-designed siRNA Set A
  • HY-173281

    Methionine Adenosyltransferase (MAT) Cancer
    MAT2A-IN-24 (Compound 9) is an inhibitor of methionine adenosyltransferase 2a (MAT2a). The IC50 value for the inhibition of MAT2a is 20 nM, and the IC50 value for the antiproliferative activity against HAP1MTAP–/– cells is 10 nM. MAT2A-IN-24 can be used in the research field of tumor diseases associated with MTAP deficiency [1].
    MAT2A-IN-24
  • HY-180573

    Arf Family GTPase Cancer
    ART5537 is a selective EXO1 inhibitor with a IC50 of 3.4 nM and a Kd of 6.8 nM. ART5537 exerts cellular homologous recombination (HR) inhibition with EC50 of 7.2 nM in HAP1 parental cells. ART5537 shows >200-fold selectivity over a panel of the wider nuclease superfamily. ART5537 exerts biological effects that are exclusively driven by EXO1 inhibition. ART5537 demonstrates sensitization to ionizing radiation and synergy with Olaparib (HY-10162). ART5537 can be used for research in breast cancer and colorectal adenocarcinoma [1].
    ART5537
  • HY-RS21480

    Small Interfering RNA (siRNA) Others

    Apex1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Apex1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Apex1 Mouse Pre-designed siRNA Set A
    Apex1 Mouse Pre-designed siRNA Set A

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