14 Results for "

MEK5

" in MedChemExpress (MCE) Product Catalog:
Products (14)

14 Results for "MEK5" in MCE Product Catalog:

  • Isoforms Recommended:
  • Targets Recommended:
10
10 Publications Verification
Cat. No.: HY-12056
CAS No.: 1265916-41-3
Purity:  99.93%
Target:  

MEK ERK

Research Areas:  

Cancer

BIX02189 is a potent and selective MEK5 inhibitor with an IC50 of 1.5 nM. BIX02189 also inhibits ERK5 catalytic activity with an IC50 of 59 nM.
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3
3 Cited Publications
Cat. No.: HY-12055
CAS No.: 334949-59-6
Purity:  99.85%
Target:  

MEK ERK

Research Areas:  

Cancer

BIX02188 is a potent MEK5-selective inhibitor with an IC50 of 4.3 nM. BIX02188 inhibits ERK5 catalytic activity, with an IC50 of 810 nM.
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2
2 Cited Publications
Cat. No.: HY-100115
CAS No.: 1784751-19-4
Purity:  99.85%
TA-02, an analog of SB 203580 (HY-10256), is a p38 MAPK inhibitor with an IC50 of 20 nM. TA-02 especially inhibits TGFBR-2. TA-02 exhibits similar cardiogenic properties as SB 203580 and SB 202190 (HY-10295) .
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1
1 Cited Publications
Cat. No.: HY-114189
CAS No.: 790186-68-4
Purity:  99.94%
Synonyms: UNC10225170
Target:  

MEK

Research Areas:  

Cancer

GW284543 (UNC10225170) is a selective MEK5 inhibitor. GW284543 reduces pERK5, and decreases endogenous MYC protein .
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Cat. No.: HY-148907
CAS No.: 2388506-83-8
Purity:  99.43%
CS640 (Compound 19) is a chemical probe and a calmodulin-dependent kinase inhibitor. CS640 inhibits CaMK1D, CaMK1B, CaMK1A, CaMK1G, MEK5, RIPK4, mLK3 and PIP5K1, with IC50 values of 8, 3, 1, 1, 25 nM, 5.69, 2.75 and 11.2 μM, respectively. CS640 blocks Aβ-induced hyperphosphorylation of tau protein at the Thr181 site, but fails to protect primary mouse cortical neurons from Aβ-induced toxic damage. CS640 is applicable to research related to Alzheimer's disease .
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Cat. No.: HY-E70747
Target:  

MEK

Research Areas:  

Cancer

MEK5 Recombinant Human Active Protein Kinase is a MAP/ERK kinase. MEK5 is thought to lie in an uncharacterized MAP kinase pathway, because MEK5 does not phosphorylate the ERK/MAP kinase family members ERK1, ERK2, ERK3, JNK/SAPK, or p38/HOG1, nor will Raf-1, c-Mos, or MEKK1 highly phosphorylate it .
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Cat. No.: HY-107622
CAS No.: 1094614-84-2
Target:  

ERK MEK

Research Areas:  

Metabolic Disease

(E/Z)-BIX02188 is a MEK5/ERK5 pathway inhibitor. (E/Z)-BIX02188 inhibits the catalytic function of purified MEK5 enzyme.(E/Z)-BIX02188 can be used for the role of MEK5/ERK5 pathway in various biological systems .
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Cat. No.: HY-114189A
CAS No.: 179246-08-3
Synonyms: UNC10225170 hydrochloride
Target:  

MEK

Research Areas:  

Cancer

GW284543 (UNC10225170) hydrochloride is a selective MEK5 inhibitor. GW284543 reduces pERK5, and decreases endogenous MYC protein .
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Cat. No.: HY-P83395
Synonyms: MAP2K5; MEK5; MKK5; PRKMK5; Dual specificity mitogen-activated protein kinase kinase 5; MAP kinase kinase 5; MAPKK 5; MAPK/ERK kinase 5; MEK 5

Host:  

Rabbit

Application:  

WB, ICC/IF

Reactivity:  

Human

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Cat. No.: HY-RS08043
Research Areas:  

Others

Map2k5 Rat Pre-designed siRNA Set A contains three designed siRNAs for Map2k5 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS08042
Research Areas:  

Others

Map2k5 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Map2k5 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS08041
Research Areas:  

Others

MAP2K5 Human Pre-designed siRNA Set A contains three designed siRNAs for MAP2K5 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-183856
CAS No.: 2570386-33-1
Target:  

MEK

Research Areas:  

Cancer

MEK4 IN-4 is a MEK4 inhibitor (IC50 = 0.041 μM) that inhibits the kinase catalytic activity of MEK4 via competitive blockade of ATP binding. MEK4 IN-4 can be used to investigate cell proliferative diseases and disorders associated with MEK4 activity, including cancer .
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Cat. No.: HY-100115R
CAS No.: 1784751-19-4
TA-02 (Standard) is the analytical standard of TA-02 (HY-100115). This product is intended for research and analytical applications. TA-02, an analog of SB 203580 (HY-10256), is a p38 MAPK inhibitor with an IC50 of 20 nM. TA-02 especially inhibits TGFBR-2. TA-02 exhibits similar cardiogenic properties as SB 203580 and SB 202190 (HY-10295) .
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