10 Results for "

TXK

" in MedChemExpress (MCE) Product Catalog:
Products (10)

10 Results for "TXK" in MCE Product Catalog:

  • Isoforms Recommended:
  • Recombinant Proteins Recommended:
1
1 Cited Publications
Cat. No.: HY-139481
CAS No.: 1415823-49-2
Purity:  99.86%
TL-895 is a potent, orally active, ATP-competitive, and highly selective irreversible BTK inhibitor. TL-895 is active against recombinant BTK (average IC50: 1.5 nM) and inhibits only three additional kinases BLK, BMX (IC50 = 1.6 nM) and TXK with IC50 within tenfold of BTK activity. TL-895 inhibits BTK auto-phosphorylation at the Y223 phosphorylation site (IC50: 1-10 nM). The TL-895 effectively inhibits the production of inflammatory factors such as IL-8, IL-1β, MCP-1 and TNF-α by monocytes or macrophages, and reduces the chemotactic migration of MF cells towards SDF-1. TL-895 is used be for studies of chronic lymphocytic leukemia (CLL), myelofibrosis (MF), and B-cell malignancies .
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Cat. No.: HY-10644
CAS No.: 944795-06-6
Purity:  99.73%
Target:  

Src Btk Syk

Research Areas:  

Others

Lck inhibitor 2 is a bisanilino pyrimidine-derived tyrosine kinase inhibitor targeting LCK, BTK, LYN, SYK and TXK, with a Kd value of 10 nM against TXK .
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Cat. No.: HY-D2415
CAS No.: 2411845-57-1
BODIPY-FL staurosporine (Compound 8a) is a fluorescence probe based on staurosporine, exhibiting high specificity towards tyrosine kinases (TK) and tyrosine kinase-like (TKL) family kinases. BODIPY-FL staurosporine has the potential to develop binding assays for kinases that are not recommended for use with Kinase Tracer 236, such as PIM3, CDC42BPG, MAP2K7, TXK, and SIK3. BODIPY-FL staurosporine can be a powerful tool for analyzing kinase selectivity in kinase drug discovery .
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Cat. No.: HY-145373
CAS No.: 1643372-83-1
Target:  

Btk

Research Areas:  

Inflammation/Immunology

BMS-986143 is an orally active, reversible BTK inhibitor with an IC50 of 0.26 nM. BMS-986143 also inhibits TEC, BLK, BMX, TXK FGR, YES1, ITK with IC50s of 3 nM, 5 nM, 7 nM, 10 nM, 15 nM,19 nM, 21 nM, respectively. BMS-986143 can be used for the research of autoimmune diseases .
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Cat. No.: HY-174129
CAS No.: 2649008-95-5
Target:  

Btk Apoptosis

Research Areas:  

Cancer

TM471-1 is an orally active and covalent Bruton's tyrosine kinase (BTK) inhibitor with IC50 values of 1.3 nM (BTK WT), >40,000 nM (BTK C481S), 7.9 nM (TEC) and 12.4 nM (TXK). TM471-1 inhibits cell growth in vivo and in vitro, arrests cell cycle at G0/G1 phase and induces cell apoptosis .
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Cat. No.: HY-RS15285
Research Areas:  

Others

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

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Cat. No.: HY-RS28605
Research Areas:  

Others

Txk Rat Pre-designed siRNA Set A contains three designed siRNAs for Txk gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
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Cat. No.: HY-RS22085
Research Areas:  

Others

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

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Cat. No.: HY-P701655
Purity:  ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: TXK; Tyrosine-protein kinase TXK; Protein-tyrosine kinase 4; Resting lymphocyte kinase
Species:  
Source:  
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Cat. No.: HY-10644R
CAS No.: 944795-06-6
Target:  

Reference Standards Src

Research Areas:  

Inflammation/Immunology

Lck inhibitor 2 (Standard) is the analytical standard of Lck inhibitor 2 (HY-10644). This product is intended for research and analytical applications. Lck inhibitor 2 is a multi-target tyrosine kinase inhibitor with IC50s of 13nM, 9nM, 3nM, 26nM and 2nM for Lck, Btk, Lyn, Btk and Txk respectively.
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