12 Results for "

TAOK2

" in MedChemExpress (MCE) Product Catalog:
Products (12)

12 Results for "TAOK2" in MCE Product Catalog:

227
227 Cited Publications
Art. -Nr.: HY-15141
CAS. Nr.: 62996-74-1
Reinheit:  99.52%
Synonyms: Antibiotic AM-2282; STS; AM-2282
Staurosporine is a potent, ATP-competitive and non-selective inhibitor of protein kinases with IC50s of 6 nM, 15 nM, 2 nM, and 3 nM for PKC, PKA, c-Fgr, and Phosphorylase kinase respectively. Staurosporine also inhibits TAOK2 with an IC50 of 3 μM. Staurosporine is an apoptosis inducer [2] .
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Art. -Nr.: HY-100491
CAS. Nr.: 1702259-66-2
Reinheit:  ≥98.0%
Target:  

FGFR

Forschungsgebiete:  

Cancer

H3B-6527 is an orally active, highly selective and covalent FGFR4 inhibitor with an IC50 of <1.2 nM. H3B-6527 has at least 250-fold selectivity over FGFR1-3 with IC50s of 320 nM, 1290 nM and 1060 nM respectively. H3B-6527 has potent anti-cancer activity .
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Art. -Nr.: HY-122232
CAS. Nr.: 422281-45-6
Target:  

Autophagy p62

Forschungsgebiete:  

Cancer

SW083688 is a selective TAOK2 inhibitor with an IC50 of 1.3 μM. SW083688 increases the abundance of p62 protein, inhibits autophagosome maturation, and blocks Autophagic flux. SW083688 is applicable for the research of non-small cell lung cancer and pancreatic cancer [2].
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Art. -Nr.: HY-15141R
CAS. Nr.: 62996-74-1
Synonyms: Antibiotic AM-2282 (Standard); STS (Standard); AM-2282 (Standard)
Staurosporine (Standard) is the analytical standard of Staurosporine. This product is intended for research and analytical applications. Staurosporine is a potent, ATP-competitive and non-selective inhibitor of protein kinases with IC50s of 6 nM, 15 nM, 2 nM, and 3 nM for PKC, PKA, c-Fgr, and Phosphorylase kinase respectively. Staurosporine also inhibits TAOK2 with an IC50 of 3 μM. Staurosporine is an apoptosis inducer[1][2][3][4][5].
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Art. -Nr.: HY-RS14199
Forschungsgebiete:  

Others

TAOK2 Human Pre-designed siRNA Set A contains three designed siRNAs for TAOK2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Art. -Nr.: HY-RS20110
Forschungsgebiete:  

Others

Taok2 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Taok2 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Art. -Nr.: HY-RS26614
Forschungsgebiete:  

Others

Taok2 Rat Pre-designed siRNA Set A contains three designed siRNAs for Taok2 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Art. -Nr.: HY-181281
Target:  

Ser/Thr Kinase

Forschungsgebiete:  

Neurological Disease Cancer

VU6080195 is a blood-brain barrier-permeable pan-TAOK activator. VU6080195 shows the highest potency against TAOK1 (EC50 = 270 nM), followed by TAOK3 (EC50 = 503 nM) and TAOK2 (EC50 = 1,376 nM). VU6080195 can be used for the research of diseases such as neurodevelopmental disorders, tauopathies and breast cancer .
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Art. -Nr.: HY-P701641
Reinheit:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: TAOK2; Serine/threonine-protein kinase TAO2; Kinase from chicken homolog C; hKFC-C; Prostate-derived sterile 20-like kinase 1; PSK-1; PSK1; Prostate-derived STE20-like kinase 1; Thousand and one amino acid protein kinase 2
Species:  
Source:  
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Art. -Nr.: HY-181280
Target:  

Ser/Thr Protease

Forschungsgebiete:  

Neurological Disease

VU6083859 is a blood-brain barrier-permeable TAOK1 inhibitor with an IC50 of 158 nM. VU6083859 selectively inhibits TAOK1, exhibits only weak or no activity against TAOK2 and TAOK3, and shows high selectivity for a variety of other kinases. VU6083859 is applicable to research related to neurodevelopmental disorders and tauopathies.
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Art. -Nr.: HY-181619
CAS. Nr.: 3114565-22-6
Target:  

MAP3K

TAO Kinase-IN-3 is a potent pan-TAOK (Thousand-And-One Kinase) inhibitor that specifically binds to and inhibits the kinase activities of TAOK1, TAOK2 and TAOK3 with Kd values of <0.17 nM, 0.34 nM, and 0.17 nM, respectively. TAO Kinase-IN-3 can be used to study Alzheimer's disease, primary tauopathies and related syndromes. In addition, TAO Kinase-IN-3 is also widely used in research on the mechanisms of cancer cachexia and the muscle atrophy it induces .
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Art. -Nr.: HY-100491R
CAS. Nr.: 1702259-66-2
Forschungsgebiete:  

Cancer

H3B-6527 (Standard) is the analytical standard of H3B-6527 (HY-100491). This product is intended for research and analytical applications. H3B-6527 is an orally active, highly selective and covalent FGFR4 inhibitor with an IC50 of <1.2 nM. H3B-6527 has at least 250-fold selectivity over FGFR1-3 with IC50s of 320 nM, 1290 nM and 1060 nM respectively. H3B-6527 has potent anti-cancer activity .
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