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Results for "

GSTP1

" in MedChemExpress (MCE) Product Catalog:

15

Inhibitors & Agonists

3

Peptides

1

Natural
Products

6

Recombinant Proteins

2

Antibodies

2

Click Chemistry

3

Oligonucleotides

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-115673
    LAS17
    1 Publications Verification

    Glutathione S-transferase Cancer
    LAS17 is a potent and selective tyrosine-directed irreversible inhibitor for glutathione S-Transferase Pi (GSTP1) [1]. LAS17 inhibits GSTP1 activity with an IC50 of 0.5 μM . LAS17 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    LAS17
  • HY-13634A
    Ezatiostat
    Maximum Cited Publications
    7 Publications Verification

    TER199(free base); TLK199

    Glutathione S-transferase Apoptosis Cancer
    Ezatiostat (TER199 free base; TLK199) is a tripeptide analog of glutathione and is a selective and orally active glutathione S-transferase P1-1 (GSTP1) inhibitor. Ezatiostat leads to JNK activation by inhibiting GSTP1. Ezatiostat stimulates both lymphocyte production and bone marrow progenitor proliferation. Ezatiostat has the potential for myelodysplastic syndrome (MDS) treatment [1] .
    Ezatiostat
  • HY-RS05886

    Small Interfering RNA (siRNA) Others

    GSTP1 Human Pre-designed siRNA Set A contains three designed siRNAs for GSTP1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    GSTP1 Human Pre-designed siRNA Set A
    GSTP1 Human Pre-designed siRNA Set A
  • HY-RS16643

    Small Interfering RNA (siRNA)
    Gstp1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Gstp1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.
    Gstp1 Mouse Pre-designed siRNA Set A
    Gstp1 Mouse Pre-designed siRNA Set A
  • HY-RS23077

    Small Interfering RNA (siRNA) Others
    Gstp1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Gstp1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
    Gstp1 Rat Pre-designed siRNA Set A
    Gstp1 Rat Pre-designed siRNA Set A
  • HY-160455

    Glutathione S-transferase Cancer
    GSTP1-1 inhibitor 1 (compound 6b) is an irreversible, long-acting, glutathione S-transferase inhibitor with an IC50 of 21 μM targeting GSTP1-1 . GSTP1-1 is a key tumor suppressor target, and GSTP1-1 inhibitor 1 has potential anticancer activity [1].
    GSTP1-1 inhibitor 1
  • HY-169058

    Glutathione S-transferase Cancer
    GSTP1-1 inhibitor 2 (Compound 5g) is an hGSTP1-1 (glutathione S-transferase P1-1) inhibitor with an IC50 value of 12.2 μM. GSTP1-1 inhibitor 2 exhibits significant cytotoxicity against DU-145, PC3, and MCF-7 cell lines, with CC50 values of 36.6 μM, 11.9 μM, and 17.4 μM, respectively. It can be used in cancer research [1].
    GSTP1-1 inhibitor 2
  • HY-13634

    TER199; TLK199 hydrochloride

    Glutathione S-transferase Apoptosis Cancer
    Ezatiostat hydrochloride (TER199; TLK199 hydrochloride) is a tripeptide analog of glutathione and is a selective and orally active glutathione S-transferase P1-1 (GSTP1) inhibitor. Ezatiostat hydrochloride leads to JNK activation by inhibiting GSTP1. Ezatiostat hydrochloride stimulates both lymphocyte production and bone marrow progenitor proliferation. Ezatiostat hydrochloride has the potential for myelodysplastic syndrome (MDS) treatment [1] .
    Ezatiostat hydrochloride
  • HY-N11778

    Bacterial Infection
    Bequinostatin C is a naphthoquinone originally isolated from Streptomyces and a glutathione S-transferase pi 1 (GSTP1) inhibitor (IC50=40 μg/mL for human GSTP1).
    Bequinostatin C
  • HY-145413

    Glutathione S-transferase Cancer
    BRD2889 is an analog of the alkaloid piperlongumine. BRD2889 is a robust modulator of the GSTP1-ISCU axis in pulmonary hypertension (PH) [1]. BRD2889 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    BRD2889
  • HY-135318
    NBDHEX
    1 Publications Verification

    Apoptosis Autophagy Glutathione S-transferase Cancer
    NBDHEX is a potent glutathione S-transferase P1-1 (GSTP1-1) inhibitor. NBDHEX induces apoptosis of tumor cells. NBDHEX acts as an anticancer agent by inhibiting GSTs catalytic activity, avoiding inconvenience of the inhibitor extrusion from the cell by specific pumps and disrupting the interaction between the GSTP1-1 and key signaling effectors. NBDHEX can also act as late-phase autophagy inhibitor [1] .
    NBDHEX
  • HY-16123

    DNA Alkylator/Crosslinker Cancer
    Canfosfamide (hydrochloride) is a prodrug that upon activation by glutathione s-transferase P1-1 (GSTP1-1) yields an anticancer alkylating agent and a glutathione derivative.
    Canfosfamide hydrochloride
  • HY-112534
    GSTO-IN-2
    2 Publications Verification

    Glutathione S-transferase Cancer
    GSTO-IN-2 is a glutathione S-transferase inhibitor with IC50s of 3.6, 16.3, and 1.4 μM for GSTA2, GSTM1, and GSTP1-1.
    GSTO-IN-2
  • HY-13634B
    TLK117
    1 Publications Verification

    TER117

    Glutathione S-transferase Inflammation/Immunology Cancer
    TLK117, the active metabolite of TLK199, selective inhibits Glutathione S-transferase P11 (GSTP1-1) with a Ki of 0.4 μM for GSTP. TLK117 also competitively inhibits glyoxalase I with a Ki of 0.56 μM.
    TLK117
  • HY-132913

    Biochemical Assay Reagents Cancer
    Cyclopropenone probe 1 can specifically and efficiently modify a triple-negative breast cancer driver, glutathione S-transferase pi-1 (GSTP1), by covalently binding at the catalytic active site. Cyclopropenone probe 1 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    Cyclopropenone probe 1

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