331 Results for "

kinase-3

" in MedChemExpress (MCE) Product Catalog:
Products (331)

331 Results for "kinase-3" in MCE Product Catalog:

  • Targets Recommended:
22
22 Publications Verification
Cat. No.: HY-16294
CAS No.: 603288-22-8
Target:  

GSK-3

Research Areas:  

Cancer

LY2090314 is a potent inhibitor of glycogen synthase kinase-3 (GSK-3) with IC50 values of 1.5 nM and 0.9 nM for GSK-3α and GSK-3β, respectively.
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8
8 Cited Publications
Cat. No.: HY-125402
CAS No.: 1601496-05-2
Purity:  99.18%
Synonyms: GSK'843
Target:  

RIP kinase Apoptosis

Research Areas:  

Inflammation/Immunology

GSK-843 (GSK'843) is a receptor-interacting protein kinase 3 (RIP3 or RIPK3) inhibitor, which binds RIP3 kinase domain with an IC50 of 8.6 nM, and inhibits kinase activity with an IC50 of 6.5 nM. GSK-843 can be used for the research of inflammation .
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6
6 Cited Publications
Cat. No.: HY-113914
CAS No.: 1034895-42-5
Purity:  99.13%
Synonyms: Elraglusib
Target:  

GSK-3 Apoptosis Autophagy

Research Areas:  

Cancer

9-ING-41 (Elraglusib) is a maleimide-based ATP-competitive and selective glycogen synthase kinase-3β (GSK-3β) inhibitor with an IC50 of 0.71 μM. 9-ING-41 significantly leads to cell cycle arrest, autophagy and apoptosis in cancer cells. 9-ING-41 has anticancer activity and has the potential for enhancing the antitumor effects of chemotherapeutic agents [3] .
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4
4 Cited Publications
Cat. No.: HY-P80393
Synonyms: MAP kinase 3; MAPK 3; ERK-1; p44-MAPK; MAP kinase 1; MAPK 1; ERK-2; p42-MAPK

Host:  

Rabbit

Application:  

WB, ICC/IF, IP, FC

Reactivity:  

Human, Mouse, Rat

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4
4 Cited Publications
Cat. No.: HY-114349
CAS No.: 2158197-70-5
Purity:  99.89%
Target:  

RIP kinase

Research Areas:  

Cardiovascular Disease Cancer

HS-1371 is a potent and ATP-competitive receptor-interacting protein kinase 3 (RIP3) inhibitor with an IC50 of 20.8 nM .
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4
4 Cited Publications
Cat. No.: HY-N2081
CAS No.: 83-95-4
Skimmianine is an orally active furoquiniline alkaloid present mainly in the Rutaceae family. Skimmianine has analgesic, antispastic, sedative, and anti-inflammatory properties. Skimmianine inhibits acetylcholinesterase (AChE) (IC50 = 8.6 μg/mL). Skimmianine exhibits cytotoxicity against a variety of cancer cell lines and genotoxicity. Skimmianine has antioxidant and anti-inflammatory effects on ischemia-reperfusion (IR) injury. Skimmianine exerts anti-inflammatory effects through activation of the phosphatidylinositol-3-kinase (PI3K)-protein kinase B (AKT) pathway. Skimmianine is neuroprotective by targeting the NF-κB activation pathway to prevent neuroinflammation. Skimmianine inhibits the release of histamine, intracellular Ca 2+ signaling and protein kinase C signaling [3] .
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3
3 Cited Publications
Cat. No.: HY-59090
CAS No.: 676596-65-9
Synonyms: 1-Akp
Target:  

GSK-3

1-Azakenpaullone (1-Akp) is a highly selective and ATP-competitive inhibitor of glycogen synthase kinase-3 β (GSK-3β), with an IC50 value of 18 nM .
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2
2 Cited Publications
Cat. No.: HY-P70178
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: FLT3; CD135 Antigen; Fms Related Receptor Tyrosine kinase 3; FLK-2; CD135; Growth Factor Receptor Tyrosine kinase Type III; STK1; Receptor Protein-Tyrosine kinase; FLK2; Fms-Related Tyrosine kinase 3; Fms-Like Tyrosine kinase 3; Fetal Liver kinase 2; Rece
Species:  
Source:  
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2
2 Cited Publications
Cat. No.: HY-P80820
Synonyms: GSK3B; Glycogen synthase kinase-3 beta; GSK-3 beta; Serine/threonine-protein kinase GSK3B

Host:  

Rabbit

Application:  

WB, IHC-F, IHC-P, ICC/IF

Reactivity:  

Human, Mouse, Rat

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2
2 Cited Publications
Cat. No.: HY-P81190
Synonyms: p-PERK(Thr980); PERK(Phospho Thr980); PERK(Phospho T980); mo(Thr980)/hu (Thr982)/rat (Thr974); HRI; HsPEK; Pancreatic eIF2-alpha kinase; PEK; PRKR like endoplasmic reticulum kinase; WRS; DKFZp781H1925; EC 2.7.11.1; EIF2AK3; Eukaryotic translation initiation factor 2 alpha kinase 3; Heme regulated EIF2 alpha kinase.

Host:  

Rabbit

Application:  

WB, IHC-P, IHC-F, ICC/IF, FC

Reactivity:  

Human, Mouse, Rat

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1
1 Cited Publications
Cat. No.: HY-P7111
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: FLT3LG; IMD125; Fms Related Receptor Tyrosine kinase 3 Ligand; FLG3L; Fms-Related Tyrosine kinase 3 Ligand; FLT3L; Fms Related Tyrosine kinase 3 Ligand; Flt3L; Flt3 Ligand; FL; SL Cytokine
Species:  
Source:  
CHO
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1
1 Cited Publications
Cat. No.: HY-P70563
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: FLT3LG; IMD125; Fms Related Receptor Tyrosine kinase 3 Ligand; FLG3L; Fms-Related Tyrosine kinase 3 Ligand; FLT3L; Fms Related Tyrosine kinase 3 Ligand; Flt3L; Flt3 Ligand; FL; SL Cytokine
Species:  
Source:  
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1
1 Cited Publications
Cat. No.: HY-P701821
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: STK3; Serine/Threonine-Protein kinase Krs-1; Serine/Threonine kinase 3; MST-2; MST2; Serine/Threonine kinase 3 (STE20 Homolog, Yeast); KRS1; Non-Specific Serine/Threonine Protein kinase; Mammalian STE20-Like Protein kinase 2; Epididymis Secretory Sperm Bi
Species:  
Source:  
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1
1 Cited Publications
Cat. No.: HY-P75236
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: EPHB2; Ephrin Type-B Receptor 2 Variant; Prev. EPHT3; Protein-Tyrosine kinase HEK5; Prev. DRT; Elk-Related Tyrosine kinase; Prev. ERK; ELK-Related Tyrosine kinase; Tyrosine-Protein kinase Receptor EPH-3; Eph Tyrosine kinase 3; Ephrin Type-B Receptor 2; EP
Species:  
Source:  
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1
1 Cited Publications
Cat. No.: HY-121035
CAS No.: 916440-85-2
Purity:  99.20%
Synonyms: 7-Bromoindirubin-3-Oxime
Target:  

CDK GSK-3

Research Areas:  

Neurological Disease

7BIO (7-Bromoindirubin-3-Oxime) is the derivate of indirubin. 7BIO (7-Bromoindirubin-3-Oxime) has inhibitory effects against cyclin-dependent kinase-5 (CDK5) and glycogen synthase kinase-3β (GSK3β). 7BIO (7-Bromoindirubin-3-Oxime) inhibits Aβ oligomer-induced neuroinflammation, synaptic impairments, tau hyper-phosphorylation, activation of astrocytes and microglia, and attenuates Aβ oligomer-induced cognitive impairments in mice [1].
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1
1 Cited Publications
Cat. No.: HY-104021
CAS No.: 2361146-30-5
Purity:  99.95%
Synonyms: GSK'840
Target:  

RIP kinase

Research Areas:  

Inflammation/Immunology

GSK840 (GSK'840) is a receptor-interacting protein kinase 3 (RIP3 or RIPK3) inhibitor, which binds RIP3 kinase domain with an IC50 of 0.9 nM, and inhibits kinase activity with an IC50 of 0.3 nM .
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1
1 Cited Publications
Cat. No.: HY-141480
CAS No.: 1448990-73-5
Purity:  99.22%
Target:  

GSK-3 Apoptosis

Research Areas:  

Cancer

GSK-3β inhibitor 3 is a potent, selective, irreversible and covalent inhibitor of Glycogen Synthase Kinase 3β (GSK-3β), with an IC50 of 6.6 μM. GSK-3β inhibitor 3 can be used for the research of acute promyelocytic leukemia .
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1
1 Cited Publications
Cat. No.: HY-153896
CAS No.: 2764850-23-7
Purity:  98.74%
Target:  

c-Met/HGFR

Research Areas:  

Cancer

LMTK3-IN-1 (compound C28) is an ATP-competitive inhibitor of lemur tyrosine kinase 3 (LMTK3) (Kd=2.5 μM),that acts by degrading LMTK3 via the ubiquitin-proteasome pathway. LMTK3-IN-1 shows anticancer activity in a variety of cancer cell lines and in vivo BC mouse models. LMTK3-IN-1 induces apoptosis in BC cell lines at 10-20 μM .
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Cat. No.: HY-108263
CAS No.: 179237-49-1
Purity:  97.02%
Synonyms: CGP52421
Target:  

FLT3

Research Areas:  

Cancer

3-Hydroxy Midostaurin (CGP 52421), a metabolite of PKC412, effectively inhibits FMS-like tyrosine kinase-3 (FLT3) autophosphorylation with IC50s of approximately 132 nM and 9.8 μM in culture medium and plasma, respectively. 3-Hydroxy Midostaurin is less selective but more cytotoxic than PKC412 .
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Cat. No.: HY-P2558
Target:  

GSK-3

Research Areas:  

Others

GSK3 Substrate, α, β subunit is peptide substrate for glycogen synthase kinase-3 (GSK-3) and can be used to measure GSK-3 activity .
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