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Results for "

TCP

" in MedChemExpress (MCE) Product Catalog:

15

Inhibitors & Agonists

1

Peptides

5

Recombinant Proteins

5

Antibodies

4

Oligonucleotides

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-136522

    Histone Demethylase Apoptosis Cancer
    S2116, a N-alkylated tranylcypromine (TCP) derivative, is a potent lysine-specific demethylase 1 (LSD1) inhibitor. S2116 increases H3K9 methylation and reciprocal H3K27 deacetylation at super-enhancer regions. S2116 induces apoptosis in TCP-resistant T-cell acute lymphoblastic leukemia (T-ALL) cells by repressing transcription of the NOTCH3 and TAL1 genes. S2116 significantly retardes the growth of T-ALL cells in xenotransplanted mice .
    S2116
  • HY-136523

    Histone Demethylase Apoptosis Cancer
    S2157, a N-alkylated tranylcypromine (TCP) derivative, is a potent lysine-specific demethylase 1 (LSD1) inhibitor. S2157 increases H3K9 methylation and reciprocal H3K27 deacetylation at super-enhancer regions. S2157 induces apoptosis in TCP-resistant T-cell acute lymphoblastic leukemia (T-ALL) cells by repressing transcription of the NOTCH3 and TAL1 genes. S2157 efficiently pass through the blood-brain barrier and can almost completely eradicate CNS leukemia in mice transplanted with T-ALL cells .
    S2157
  • HY-103000
    HSF1A
    1 Publications Verification

    HSP Cardiovascular Disease Cancer
    HSF1A is a cell-permeable activator of heat shock transcription factor 1 (HSF1) . HSF1A also acts as a specific inhibitor of TRiC/CCT. Chaperonin TCP-1 ring complex (TRiC)/chaperonin containing TCP-1 (CCT) plays a pivotal role in toxin translocation and/or refolding .
    HSF1A
  • HY-D1420

    Fluorescent Dye Others
    TCP-BP-SFAC is a luminogenic molecule. TCP-BP-SFAC exhibits strong sky-blue delayed fluorescence in neat films, with photoluminescence (PL) peaks at ~483 nm and delayed fluorescence lifetimes of 5.4 to 5.7 μs .
    TCP-BP-SFAC
  • HY-108668

    P2X Receptor Others
    TC-P 262 is a potent P2X3 inhibitor. TC-P 262 shows inhibition by bindings to hP2X3. TC-P 262 has the potential for the research of rheumatoid arthritis, cough, and pain .
    TC-P 262
  • HY-161848

    Histone Demethylase Cancer
    TCP-MP-CA (compound 11a) is an inhibitor of LSD1 demethylation enzymatic via binding to LSD1/CoREST complex. TCP-MP-CA exhibits an inhibitory effect on osteoclastogenesis, with an IC50 value of 0.14 µM .
    TCP-MP-CA
  • HY-RS14321

    Small Interfering RNA (siRNA) Others

    TCP1 Human Pre-designed siRNA Set A contains three designed siRNAs for TCP1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    TCP1 Human Pre-designed siRNA Set A
    TCP1 Human Pre-designed siRNA Set A
  • HY-RS14322

    Small Interfering RNA (siRNA) Others

    TCP11 Human Pre-designed siRNA Set A contains three designed siRNAs for TCP11 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    TCP11 Human Pre-designed siRNA Set A
    TCP11 Human Pre-designed siRNA Set A
  • HY-RS14324

    Small Interfering RNA (siRNA) Others

    TCP11L2 Human Pre-designed siRNA Set A contains three designed siRNAs for TCP11L2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    TCP11L2 Human Pre-designed siRNA Set A
    TCP11L2 Human Pre-designed siRNA Set A
  • HY-RS14323

    Small Interfering RNA (siRNA) Others

    TCP11L1 Human Pre-designed siRNA Set A contains three designed siRNAs for TCP11L1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    TCP11L1 Human Pre-designed siRNA Set A
    TCP11L1 Human Pre-designed siRNA Set A
  • HY-P3319

    iGluR Neurological Disease
    β-Neuroprotectin is a (3H)TCP binding inhibitor with activity against NMDA-mediated neuronal cell death. β-Neuroprotectin can effectively inhibit the binding of [3H]TCP. β-Neuroprotectin provides neuroprotection at low concentrations against NMDA-induced neuronal cell death .
    β-Neuroprotectin
  • HY-148542

    SD-142

    Endogenous Metabolite Cardiovascular Disease Cancer
    EpoY (SD-142) acts as an irreversible inhibitor of the brain's primary tubulin tyrosine carboxypeptidase (TCP), a complex formed by vasohibin-1 (VASH1) and the small vasohibin binding protein (SVBP). By inhibiting TCP with an IC50 value of approximately 500 nM, EpoY effectively decreases levels of detyrosinated alpha-tubulin, which is crucial for microtubule dynamics and neuronal differentiation. This inhibition leads to significant differentiation defects and has been linked to underlying issues associated with cancer and cardiomyopathies.
    EpoY
  • HY-144758

    Histone Demethylase Monoamine Oxidase Cancer
    LSD1-IN-17 (compound 5b) is a potent LSD1 inhibitor. LSD1-IN-17 can inhibit LSD1-CoREST, MAO-A and MAO-B, with IC50 values of 0.005, 0.028, and 0.820 μM, respectively. LSD1-IN-17 displays cell growth arrest in prostate cancer LNCaP cells, with an IC50 of 17.2 μM .
    LSD1-IN-17
  • HY-144756

    Histone Demethylase Monoamine Oxidase Cancer
    LSD1-IN-15 (compound 1b) is a potent LSD1 inhibitor. LSD1-IN-15 can inhibit LSD1-CoREST, MAO-A and MAO-B, with IC50 values of 0.149, 0.028, and 0.327 μM, respectively. LSD1-IN-15 displays cell growth arrest in prostate cancer LNCaP cells, with an IC50 of 9.9 μM .
    LSD1-IN-15
  • HY-144757

    Histone Demethylase Monoamine Oxidase Cancer
    LSD1-IN-16 (compound 4b) is a potent LSD1 inhibitor. LSD1-IN-16 can inhibit LSD1-CoREST, MAO-A and MAO-B, with IC50 values of 0.015, 0.024, and 0.366 μM, respectively. LSD1-IN-16 displays cell growth arrest in prostate cancer LNCaP cells, with an IC50 of 15.2 μM .
    LSD1-IN-16

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