15 Results for "

UCHL3

" in MedChemExpress (MCE) Product Catalog:
Products (15)

15 Results for "UCHL3" in MCE Product Catalog:

  • Isoforms Recommended:
  • Recombinant Proteins Recommended:
20
20 Publications Verification
Cat. No.: HY-18637
CAS No.: 668467-91-2
Research Areas:  

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.
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6
6 Cited Publications
Cat. No.: HY-18638
CAS No.: 30675-13-9
Synonyms: 4,5,6,7-Tetrachloroindan-1,3-dione
Target:  

Deubiquitinase

Research Areas:  

Neurological Disease

TCID (4,5,6,7-Tetrachloroindan-1,3-dione) is a potent and selective neuronal ubiquitin C-terminal hydrolase (UCH-L3) inhibitor with an IC50 of 0.6 μM . TCID diminishes glycine transporter GlyT2 ubiquitination in brainstem and spinal cord primary neurons .
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4
4 Cited Publications
Cat. No.: HY-133118
CAS No.: 1895050-66-4
Purity:  98.41%
Target:  

Deubiquitinase

Research Areas:  

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 .
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1
1 Cited Publications
Cat. No.: HY-P71115
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Ubiquitin Carboxyl-Terminal Hydrolase Isozyme L3; UCH-L3; Ubiquitin Thioesterase L3; UCHL3
Species:  
Source:  
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Cat. No.: HY-149230
CAS No.: 2931509-15-6
Purity:  99.35%
Target:  

Deubiquitinase

Research Areas:  

Cancer

USP28-IN-4 is a USP28 inhibitor (IC50=0.04 μM) with high selectivity over USP2, USP7, USP8, USP9x, UCHL3 and UCHL5. USP28-IN-4 shows cytotoxicity against cancer cells, down-regulates the cellular level of c-Myc through ubiquitin-proteasome system. USP28-IN-4 also decreases the ankyrase-1/2 level in vitro. USP28-IN-4 enhance the sensitivity of colorectal cancer cells to Regorafenib (HY-10331) .
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Cat. No.: HY-RS15401
Research Areas:  

Others

UCHL3 Human Pre-designed siRNA Set A contains three designed siRNAs for UCHL3 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS17309
Research Areas:  

Others

Uchl3 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Uchl3 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS23764
Research Areas:  

Others

Uchl3 Rat Pre-designed siRNA Set A contains three designed siRNAs for Uchl3 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-149229
CAS No.: 2931509-14-5
Purity:  98.26%
Target:  

Deubiquitinase

Research Areas:  

Cancer

USP28-IN-3 is a USP28 inhibitor (IC50=0.1 μM) with high selectivity over USP2, USP7, USP8, USP9x, UCHL3 and UCHL5. USP28-IN-3 shows cytotoxicity against cancer cells, down-regulates the cellular level of c-Myc through ubiquitin-proteasome system. USP28-IN-3 also decreases the ankyrase-1/2 level in vitro. USP28-IN-3 enhance the sensitivity of colorectal cancer cells to Regorafenib (HY-10331) .
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Cat. No.: HY-149228
CAS No.: 2931509-11-2
Target:  

Deubiquitinase

Research Areas:  

Cancer

USP28-IN-2 is a USP28 inhibitor (IC50=0.3 μM) with high selectivity over USP2, USP7, USP8, USP9x, UCHL3 and UCHL5. USP28-IN-2 shows cytotoxicity against cancer cells, down-regulates the cellular level of c-Myc through ubiquitin-proteasome system. USP28-IN-2 also decreases the ankyrase-1/2 level in vitro. USP28-IN-2 enhance the sensitivity of colorectal cancer cells to Regorafenib (HY-10331) .
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Cat. No.: HY-P76119A
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: UCH-L3; Ubiquitin thioesterase L3; UCHL3
Species:  
Source:  
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Cat. No.: HY-P83066
Synonyms: UCH-L3; Ubiquitin thiolesterase L3; Ubiquitin carboxyl-terminal hydrolase isozyme L3; UCHL3

Host:  

Rabbit

Application:  

WB

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P76689
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Ubiquitin carboxyl-terminal hydrolase isozyme L3; UCH-L3; Ubiquitin thioesterase L3
Species:  
Rat
Source:  
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Cat. No.: HY-P87636
Synonyms: Ubiquitin carboxyl-terminal hydrolase isozyme L3, UCH-L3, Ubiquitin thioesterase L3, UCHL3

Host:  

Rabbit

Application:  

WB, IHC-P, IHC-F, IF-Tissue

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-182636
CAS No.: 1895049-73-6
MT16-001 is a cell-permeable UCHL1 inhibitor with an IC50 value of 580 nM. MT16-001 also exhibits considerable inhibitory activity against USP30, and shows selectivity for other UCH family deubiquitinases (DUBs) as well as the broader proteome. MT16-001 binds covalently to the cysteine residue at the active site of UCHL1, and forms covalent interactions with ALDH2, ALDH9A1 and GATD3A in intact cells. Meanwhile, as a cytotoxic agent, it displays a steep dose-response curve in human embryonic kidney cells. MT16-001 can be used for research on various cancers, liver fibrosis and pulmonary fibrosis .
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