22 Results for "

OTUB1

" in MedChemExpress (MCE) Product Catalog:
Products (22)

22 Results for "OTUB1" in MCE Product Catalog:

  • Recombinant Proteins Recommended:
3
3 Cited Publications
Cat. No.: HY-151563
CAS No.: 2858800-98-1
Purity:  98.31%
Target:  

Deubiquitinase

Research Areas:  

Cancer

OTUB1/USP8-IN-1 is a potent dual OTUB1/USP8 inhibitor with IC50 values of 0.17 and 0.28 nM for OTUB1 and USP8, respectively. OTUB1/USP8-IN-1 can be used in research of cancer [1].
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3
3 Cited Publications
Cat. No.: HY-151563A
Purity:  99.56%
Target:  

Deubiquitinase

Research Areas:  

Cancer

OTUB1/USP8-IN-1 TFA is the TFA salt form of OTUB1/USP8-IN-1 (HY-151563). OTUB1/USP8-IN-1 TFA is a dual inhibitor for OTUB1/USP8, IC50 for OTUB1 and USP8 is 0.17 and 0.28 nM, respectively. OTUB1/USP8-IN-1 TFA inhibits proliferation of NSCLC cells. OTUB1/USP8-IN-1 TFA exhibits good pharmacokinetic characters in ICR mouse, and exhibits antitumor activity in H1975 xenograft mouse model [1].
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Cat. No.: HY-143345
CAS No.: 2094893-05-5
Purity:  99.22%
Target:  

Deubiquitinase

Research Areas:  

Cancer

EN523 is a OTUB1 recruiter. EN523 targets a non-catalytic allosteric cysteine C23 in the K48-ubiquitin-specific deubiquitinase OTUB1 [1].
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Cat. No.: HY-115878
CAS No.: 2858812-70-9
Purity:  98.87%
Target:  

CFTR

Research Areas:  

Others

NJH-2-057 is an EN523 OTUB1 recruiter linked to lumacaftor, a agent used to treat cystic fibrosis that binds ΔF508-CFTR.
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Cat. No.: HY-143344
CAS No.: 2858812-69-6
Purity:  98.23%
Target:  

DUBTACs CFTR

Research Areas:  

Inflammation/Immunology

NJH-2-056 is a deubiquitinase-targeting chimera (DUBTAC) linking the OTUB1 recruiter EN523 to the CFTR chaperone lumacaftor. NJH-2-056 can be used for cystic fibrosis research [1].
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Cat. No.: HY-144999
CAS No.: 2858812-91-4
Purity:  98.08%
Target:  

DUBTACs Wee1

Research Areas:  

Cancer

LEB-03-146 is a WEE1 DUBTAC (deubiquitinase-targeting chimera) linking AZD1775 (Adavosertib) to the OTUB1 recruiter EN523 through a PEG2 linker. LEB-03-146 shows significant WEE1 stabilization in HEP3B hepatoma cancer cells [1].
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Cat. No.: HY-162966
CAS No.: 3060519-67-4
Research Areas:  

Cancer

MS7829 is a deubiquitinase-targeting chimera (DUBTAC) that targets cGAS. MS7829 recruits OTUB1 to cGAS, binds covalently to OTUB1, stabilizes the protein abundance of cGAS, and activates the cGAS-STING-IRF3 innate immune signaling pathway in an OTUB1-dependent manner. MS7829 is applicable to cancer-related research [1].
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Cat. No.: HY-RS09869
Research Areas:  

Others

OTUB1 Human Pre-designed siRNA Set A contains three designed siRNAs for OTUB1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS16735
Research Areas:  

Others

Otub1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Otub1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS23172
Research Areas:  

Others

Otub1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Otub1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-143342
CAS No.: 2858812-89-0
Target:  

DUBTACs Wee1

Research Areas:  

Cancer

LEB-03-144 is a WEE1 DUBTAC (deubiquitinase-targeting chimera) linking AZD1775 (Adavosertib) to the OTUB1 recruiter EN523 through a C3 alkyl linker. LEB-03-144 shows significant WEE1 stabilization in HEP3B hepatoma cancer cells [1].
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Cat. No.: HY-143343
CAS No.: 2858812-88-9
Target:  

DUBTACs Wee1

Research Areas:  

Cancer

LEB-03-153 is a WEE1 DUBTAC (deubiquitinase-targeting chimera) linking AZD1775 (Adavosertib) to the OTUB1 recruiter EN523 through no linker [1].
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Cat. No.: HY-143340
CAS No.: 2858812-90-3
Target:  

DUBTACs Wee1

Research Areas:  

Cancer

LEB-03-145 is a WEE1 DUBTAC (deubiquitinase-targeting chimera) linking AZD1775 (Adavosertib) to the OTUB1 recruiter EN523 through a C5 alkyl linker [1].
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Cat. No.: HY-183724
CAS No.: 3060517-63-4
Target:  

Deubiquitinase

Research Areas:  

Inflammation/Immunology

MS8572 is a selective OTUB1 covalent ligand. MS8572 covalently modifies the noncatalytic cysteine 23 residue of OTUB1 and does not inhibit OTUB1 deubiquitinase activity. MS8572 can be used for development of deubiquitinase-targeting chimeras for targeted protein stabilization [1].
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Cat. No.: HY-183725
CAS No.: 3060520-82-0
Research Areas:  

Inflammation/Immunology

MS5128 is an OTUB1-based deubiquitinase-targeting chimera (DUBTAC) targeting CFTR. MS5128 recruits OTUB1 to CFTR to induce deubiquitination and stabilization of CFTR. MS5128 can be used for the research of cystic fibrosis [1]. (Blue: CFTR Ligand (HY-183724); Pink: OTUB1 Ligand (HY-13262); Black: Linker)
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Cat. No.: HY-P81738
Synonyms: OTUB1; OTB1; OTU1; HSPC263; Ubiquitin thioesterase OTUB1; Deubiquitinating enzyme OTUB1; OTU domain-containing ubiquitin aldehyde-binding protein 1; OTUBain-1; hOTU1; Ubiquitin-specific-processing protease OTUB1

Host:  

Rabbit

Application:  

WB, IP

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P81738A
Synonyms: OTUB1; OTB1; OTU1; HSPC263; Ubiquitin thioesterase OTUB1; Deubiquitinating enzyme OTUB1; OTU domain-containing ubiquitin aldehyde-binding protein 1; OTUBain-1; hOTU1; Ubiquitin-specific-processing protease OTUB1

Host:  

Rabbit

Application:  

WB, IP

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-185122
CAS No.: 3060520-53-5
Target:  

DUBTACs CFTR

Research Areas:  

Cancer

MS6178 is a MS5105-based CFTR deubiquitinase-targeted chimera (DUBTAC) that recruits OTUB1 to stabilize ΔF508-CFTR mutant protein in a concentration- and time-dependent manner, with an OTUB1-dependent effect and no impact on CFTR mRNA level. MS6178 can be used for the research of cancer [1].
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Cat. No.: HY-P75952
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Ubiquitin thioesterase OTUB1; OTUBain-1; OTUB1; OTB1; OTU1
Species:  
Source:  
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Cat. No.: HY-182350
CAS No.: 3081876-96-9
Target:  

DUBTACs FXR

Research Areas:  

Metabolic Disease

FXR DUBTAC modulator-1 is a deubiquitinase-targeting chimeric molecule (DUBTAC) that targets FXR, with a Ka value of 2.12e-5 M for FXR. FXR DUBTAC modulator-1 recruits the deubiquitinase OTUB1, binds to OTUB1 and forms a ternary complex with FXR, reduces the polyubiquitination level of FXR, prevents FXR degradation via the ubiquitin-proteasome pathway, and elevates the protein level of FXR. FXR DUBTAC modulator-1 can be used in the research of cholestatic liver injury [1].
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