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Results for "

STEAP1

" in MedChemExpress (MCE) Product Catalog:

10

Inhibitors & Agonists

3

Inhibitory Antibodies

2

Recombinant Proteins

4

Oligonucleotides

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-P990688

    AMG-509

    CD3 Cancer
    Xaluritamig (AMG-509) is a bispecific T cell engager and cytolytic agent with a Kd of 27.6 nM for human CD3ε. Xaluritamig binds to CD3ε via an anti-CD3 single-chain variable fragment (scFv) domain, and to STEAP1 via a bispecific anti-STEAP1 antigen-binding fragment (Fab) domain, thereby recruiting and activating T cells and forming a bridge between T cells and STEAP1-expressing cancer cells. Xaluritamig induces T cell-mediated redirected cytotoxicity, tumor cell lysis, cytokine release, CD8 + T cell activation and expansion, as well as tumor stasis or regression. Xaluritamig contains an Fc domain with no effector function, which prolongs serum half-life, exhibits only minimal activity against cells with low STEAP1 expression and normal cells, and shows extremely low target-related off-tumor toxicity in cynomolgus monkeys. Xaluritamig is used in STEAP1×CD3 XmAb 2+1 immunotherapy and in research on metastatic castration-resistant prostate cancer and Ewing sarcoma [1] .
    Xaluritamig
  • HY-P990673

    DSTP-3086S Antibody; RG-7450 Antibody

    ADC Antibody Transmembrane Glycoprotein Mitosis Cancer
    Vandortuzumab (DSTP-3086S Antibody; RG-7450 Antibody) is a humanized anti-STEAP1 IgG1 antibody and antimitotic agent that can be conjugated with MMAE (HY-15162) to form the antibody-drug conjugate (ADC) Vandortuzumab vedotin. Vandortuzumab vedotin specifically binds to STEAP1 and drives internalization of the complex, releasing the MMAE (HY-15162) payload intracellularly. After binding to tubulin, MMAE inhibits cell division and induces cell death. Vandortuzumab exhibits antitumor activity in preclinical xenograft models of prostate cancer and can be used for research related to metastatic castration-resistant prostate cancer (mCRPC) [1] .
    Vandortuzumab
  • HY-138632

    PROTACs Epigenetic Reader Domain PROTAC-Linker Conjugates for PAC Cancer
    PROTAC BRD4 Degrader linker conjugate is a linker-payload conjugate as well as a bifunctional degrader of BRD4 that binds to VHL, consisting of PROTAC and a linker. PROTAC BRD4 Degrader linker conjugate can be conjugated with STEAP1 and CLL1 antibodies to degrade BRD4 protein, with DC50 values of 0.86 nM and 7.6 nM, respectively. PROTAC BRD4 Degrader linker conjugate can be used in research related to prostate cancer and acute myeloid leukemia (BRD4 ligand: (HY-129939); VHL ligand: (HY-125845)) [1].\n




    PROTAC BRD4 Degrader linker conjugate
  • HY-RS13905

    Small Interfering RNA (siRNA) Others

    STEAP1 Human Pre-designed siRNA Set A contains three designed siRNAs for STEAP1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    STEAP1 Human Pre-designed siRNA Set A
    STEAP1 Human Pre-designed siRNA Set A
  • HY-RS16998

    Small Interfering RNA (siRNA) Others

    Steap1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Steap1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Steap1 Mouse Pre-designed siRNA Set A
    Steap1 Mouse Pre-designed siRNA Set A
  • HY-RS23441

    Small Interfering RNA (siRNA) Others

    Steap1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Steap1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Steap1 Rat Pre-designed siRNA Set A
    Steap1 Rat Pre-designed siRNA Set A
  • HY-138633

    PROTACs Epigenetic Reader Domain Cancer
    PROTAC BRD4 Degrader-10 (compound 8b) is a PROTAC connected by ligands for von Hippel-Lindau and BRD4. PROTAC BRD4 Degrader-10 can be conjugated with STEAP1 and CLL1 antibodies to degrade the BRD4 protein in PC3 prostate cancer cells, with a DC50 of 1.3 nM and 18 nM, respectively [1].
    PROTAC BRD4 Degrader-10
  • HY-138635

    PROTACs Epigenetic Reader Domain Cancer
    PROTAC BRD4 Degrader-12 (compound 9c) is a PROTAC connected by ligands for von Hippel-Lindau and BRD4. PROTAC BRD4 Degrader-12 can be conjugated with STEAP1 and CLL1 antibodies to degrade the BRD4 protein in PC3 prostate cancer cells, with a DC50 of 0.39 nM and 0.24 nM, respectively [1].
    PROTAC BRD4 Degrader-12
  • HY-P99528

    DSTP 3086S; RG 7450; MSTP2109A

    Antibody-Drug Conjugates (ADCs) Cancer
    Vandortuzumab vedotin (DSTP 3086S; RG 7450) is a STEAP1-targeted antibody-drug conjugate (ADC). Vandortuzumab vedotin binds specifically to STEAP1, triggers internalization of the conjugate complex, mediates intracellular release of monomethyl auristatin E, inhibits cell division, and induces cell death. Vandortuzumab vedotin exhibits antitumor activity in preclinical prostate cancer xenografts. Vandortuzumab vedotin can be used for the research of metastatic castration-resistant prostate cancer [1].
    Vandortuzumab vedotin
  • HY-RS13906

    Small Interfering RNA (siRNA) Others

    STEAP1B Human Pre-designed siRNA Set A contains three designed siRNAs for STEAP1B gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    STEAP1B Human Pre-designed siRNA Set A
    STEAP1B Human Pre-designed siRNA Set A

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