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Isoforms Recommended: UCHL1
Results for "

UCHL1

" in MedChemExpress (MCE) Product Catalog:

18

Inhibitors & Agonists

2

Fluorescent Dye

1

Biochemical Assay Reagents

1

Peptides

3

Recombinant Proteins

4

Antibodies

4

Click Chemistry

3

Oligonucleotides

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-161378

    Deubiquitinase Cancer
    UCHL1-IN-1 (Compound 46) is an inhibitor for Ubiquitin C-terminal Hydrolase L1 (UCHL1), with an IC50 of 5.1 μM. UCHL1-IN-1 can be used for cancer research [1].
    UCHL1-IN-1
  • HY-133118
    6RK73
    3 Publications Verification

    Deubiquitinase Cancer
    6RK73 is a covalent irreversible and specific UCHL1 inhibitor with an IC50 of 0.23 µM. 6RK73 shows almost no inhibition of UCHL3 (IC50=236 µM). 6RK73 specifically inhibit UCHL1 activity in breast cancer [1].
    6RK73
  • HY-154914

    Deubiquitinase Others
    GK16S is a UCHL1 chemogenomic probe. GK16S can be used as a complement to GK13S. GK16S and GK13S can be used to study UCHL1 function in cells [1]. GK16S is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    GK16S
  • HY-153627

    Deubiquitinase Cancer
    G13KS is a deubiquitinase UCHL1 ligand and inhibitor. G13KS inhibits recombinant and cellular UCHL1. G13KS reduces levels of monoubiquitin in human glioblastoma cells [1]. GK13S is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    GK13S
  • HY-16658
    Z-VAD(OMe)-FMK
    190+ Cited Publications

    Z-Val-Ala-Asp(OMe)-FMK

    Caspase Cancer
    Z-VAD(OMe)-FMK (Z-Val-Ala-Asp(OMe)-FMK) is a cell-permeable and irreversible pan-caspase inhibitor [1]. Z-VAD(OMe)-FMK is an ubiquitin carboxy-terminal hydrolase L1 (UCHL1) inhibitor. Z-VAD(OMe)-FMK irreversibly modifies UCHL1 by targeting the active site of UCHL1 .
    Z-VAD(OMe)-FMK
  • HY-12989

    Deubiquitinase Neurological Disease Cancer
    LDN-91946 is a potent, selective and uncompetitive ubiquitin C-terminal hydrolase-L1 (UCH-L1) inhibitor with a Ki app of 2.8 μM [1].
    LDN-91946
  • HY-RS16745

    Small Interfering RNA (siRNA) Others

    Uchl1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Uchl1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Uchl1 Mouse Pre-designed siRNA Set A
    Uchl1 Mouse Pre-designed siRNA Set A
  • HY-RS15400

    Small Interfering RNA (siRNA) Others

    UCHL1 Human Pre-designed siRNA Set A contains three designed siRNAs for UCHL1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    UCHL1 Human Pre-designed siRNA Set A
    UCHL1 Human Pre-designed siRNA Set A
  • HY-RS23182

    Small Interfering RNA (siRNA) Others

    Uchl1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Uchl1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Uchl1 Rat Pre-designed siRNA Set A
    Uchl1 Rat Pre-designed siRNA Set A
  • HY-E70627

    Deubiquitinase Neurological Disease
    Ubiquitin thiolesterase UCHL1 (EC 3.1.2.15) is a member of the ubiquitin carboxy-terminal hydrolase family of deubiquitinating enzymes. Ubiquitin thiolesterase UCHL1 functions as an ubiquitin ligase and a mono-ubiquitin stabilizer [1].
    Ubiquitin thiolesterase UCHL1
  • HY-D1726

    Deubiquitinase Cancer
    8RK59, a Bodipy probe, is a potent UCHL1 (ubiquitin C-terminal hydrolase L1) inhibitor, with an IC50 close to 1 μM. 8RK59 could penetrate and label living cells. BodipyFL-alkyne is coupled to the azide of 8RK64 (HY-148254) using copper(I)-mediated click chemistry, resulting in compound 8RK59 [1].
    8RK59
  • HY-P0110

    (Iso)-Z-Val-Ala-Asp(OMe)-FMK

    Caspase Cancer
    (Iso)-Z-VAD(OMe)-FMK ((Iso)-Z-Val-Ala-Asp(OMe)-FMK) is an isomer of the caspase and UCHL1 inhibitor Z-VAD(OMe)-FMK (HY-16658) [1].
    (Iso)-Z-VAD(OMe)-FMK
  • HY-138995
    IMP-1710
    1 Publications Verification

    Deubiquitinase Others
    IMP-1710 is a potent and selective deubiquitylating enzyme UCHL1 inhibitor with an IC50 value of 38 nM. IMP-1710 has antifibrotic activity. IMP-1710 is a UCHL1 probe to identify and quantify target proteins in intact human cells [1]. IMP-1710 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. IMP-1710 can be used in the research of idiopathic pulmonary fibrosis [1].
    IMP-1710
  • HY-16658B
    Z-VAD-FMK
    Maximum Cited Publications
    629 Publications Verification

    Z-VAD(OH)-FMK

    Caspase Apoptosis Cancer
    Z-VAD-FMK (Z-VAD(OH)-FMK) is a well-know pan caspase inhibitor, which does not inhibit ubiquitin carboxy-terminal hydrolase L1 (UCHL1) activity even at concentrations as high as 440 μM [1].
    Z-VAD-FMK
  • HY-18637
    LDN-57444
    15+ Cited Publications

    Deubiquitinase Apoptosis Neurological Disease
    LDN-57444 is a reversible, competitive and site-directed inhibitor of ubiquitin C-terminal hydrolase L1 (UCH-L1), with an IC50 of 0.88 μM and a Ki of 0.40 μM; LDN-57444 also suppresses UCH-L3 activity, with an IC50 of 25 μM.
    LDN-57444
  • HY-148254

    Deubiquitinase Cancer
    8RK64, a chemical probe, is a covalent UCHL1 inhibitor (IC50: 0.32 μM) [1]. 8RK64 is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
    8RK64
  • HY-16658BG

    Caspase Apoptosis Cancer
    Z-VAD-FMK (GMP) is Z-VAD-FMK (HY-16658B) in GMP grade. GMP-grade small molecules can be used as auxiliary reagents in cell therapy. Z-VAD-FMK (Z-VAD(OH)-FMK) is a well-know pan caspase inhibitor, which does not inhibit ubiquitin carboxy-terminal hydrolase L1 (UCHL1) activity even at concentrations as high as 440 μM [1].
    Z-VAD-FMK
  • HY-178124

    Deubiquitinase Neurological Disease Cancer
    Huib32 is a potent small-molecule inhibitor of USP32 (IC50 = 21.2 nM), exhibiting high selectivity over other closely related deubiquitinating enzymes (DUBs), such as USP8/10/16, UCHL1 and OTUB2. Huib32 reversibly inhibits USP32 by covalently binding to the active site Cys743, which enhances substrate ubiquitination, alters endosomal morphology, and mimics USP32 depletion. Huib32 can be used for breast, ovarian, and lung cancer and Alzheimer's and Parkinson’s diseases research [1].
    Huib32

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