97 Results for "

AMPK kinase

" in MedChemExpress (MCE) Product Catalog:
Products (97)

97 Results for "AMPK kinase" in MCE Product Catalog:

  • Targets Recommended:
77
77 Publications Verification
Cat. No.: HY-10971
CAS No.: 1028486-01-2
Purity:  99.36%
Synonyms: MLN 8237
Research Areas:  

Cancer

Alisertib (MLN 8237) is an orally active and selective Aurora A kinase inhibitor (IC50=1.2 nM), which binds to Aurora A kinase resulting in mitotic spindle abnormalities, mitotic accumulation. Alisertib (MLN 8237) induces apoptosis and autophagy through targeting the AKT/mTOR/AMPK/p38 pathway in leukemic cells. Antitumor activity .
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48
48 Cited Publications
Cat. No.: HY-50662
CAS No.: 844499-71-4
Target:  

AMPK

Research Areas:  

Metabolic Disease

A-769662 is a AMP-activated protein kinase (AMPK) activator. A-769662 inhibits the function of the 26S proteasome by an AMPK-independent mechanism and leads to cell cycle arrest. A-769662 directly stimulates partially purified rat liver AMPK (EC50 = 0.8 μM) and inhibits fatty acid synthesis in primary rat hepatocytes (IC50 = 3.2 μM). A-769662 can alleviate the symptoms of metabolic diseases such as type 2 diabetes .
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44
44 Cited Publications
Cat. No.: HY-16966
CAS No.: 1884220-36-3
Target:  

ULK AMPK Autophagy Apoptosis

Research Areas:  

Cancer

SBI-0206965 is a potent, selective and cell permeable autophagy kinase ULK1 inhibitor with IC50s of 108 nM for ULK1 kinase and 711 nM for the highly related kinase ULK2. SBI-0206965 is also an AMPK inhibitor that can paradoxically increase Thr172 phosphorylation .
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42
42 Cited Publications
Cat. No.: HY-10249
CAS No.: 937174-76-0
Purity:  98.47%
Target:  

Akt AMPK Autophagy

Research Areas:  

Cancer

GSK-690693 is an ATP-competitive pan-Akt inhibitor with IC50s of 2 nM, 13 nM, 9 nM for Akt1, Akt2 and Akt3, respectively. GSK-690693 is also an AMPK inhibitor, affects Unc-51-like autophagy activating kinase 1 (ULK1) activity and robustly inhibits STING-dependent IRF3 activation .
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19
19 Cited Publications
Cat. No.: HY-19330
CAS No.: 1203494-49-8
Target:  

Pyruvate Kinase

Research Areas:  

Metabolic Disease Cancer

DASA-58 is a potential pyruvate kinase isozyme (PKM2) allosteric activator. DASA-58 can be used for the research of metabolism and kinds of cancer .
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18
18 Cited Publications
Cat. No.: HY-112083
CAS No.: 2377576-35-5
Purity:  99.66%
Target:  

AMPK

Research Areas:  

Cancer

BAY-3827, a chemical probe, is a potent and selective AMPK inhibitor with IC50 values of 1.4 nM at low (10 μM ATP concentration) and 15 nM at high (2 mM ATP concentration). BAY-3827 shows over 500-fold selectivity for most of the 331 kinases. BAY-3827 prevents phosphorylation of acetyl-CoA carboxylase 1 and shows strongest anti-proliferative activity in androgen-dependent prostate cancer cell lines .
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10
10 Cited Publications
Cat. No.: HY-N0281
CAS No.: 486-35-1
Synonyms: 7,8-Dihydroxycoumarin
Daphnetin (7,8-dihydroxycoumarin), one coumarin derivative can be found in plants of the Genus Daphne, is a potent, oral active protein kinase inhibitor, with IC50s of 7.67 μM, 9.33 μM and 25.01 μM for EGFR, PKA and PKC in vitro, respectively. Daphnetin triggers ROS-induced cell apoptosis and induces cytoprotective autophagy by modulating the AMPK/Akt/mTOR pathway. Daphnetin has anti-inflammation activitity and inhibits TNF-α, IL-1β, ROS, and MDA production. Daphnetin has schizontocidal activity against malaria parasites. Daphnetin can be used for rheumatoid arthritis , cancer and anti-malarian research .
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9
9 Cited Publications
Cat. No.: HY-148189
CAS No.: 2904601-67-6
Purity:  99.37%
Synonyms: LXY-05-029
Aldometanib (LXY-05-029) is an orally active aldolase inhibitor. Aldometanib can activate lysosomal adenosine monophosphate-activated protein kinase (AMPK) and decreases blood glucose. Aldometanib can be used for the research of metabolic homeostasis .
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8
8 Cited Publications
Cat. No.: HY-112769
CAS No.: 1219739-36-2
Purity:  98.92%
Target:  

AMPK

Research Areas:  

Metabolic Disease

EX229, a Benzimidazole derivative, is a potent and allosteric activator of AMP-activated protein kinase (AMPK), with Kds of 0.06 μM, 0.06 μM and 0.51 μM for α1β1γ1, α2β1γ1 and α1β2γ1 in biolayer interferometry, respectively.
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4
4 Cited Publications
Cat. No.: HY-N0772
CAS No.: 24699-16-9
Isomangiferin is an orally active xanthone C-glucoside, and its chemical structure is similar to Mangiferin (HY-N0290). Isomangiferin is an effective VEGFR-2 kinase inhibitor, which can induces cell apoptosis, inhibit the growth, metastasis and angiogenesis of breast cancer. Isomangiferin exerts anti-inflammatory effects by inhibiting the HMGB1/NLRP3/NF-κB signaling pathway, thereby improving the renal function indicators of diabetic mice. Isomangiferin exhibits inhibitory effects on various bacteria and herpes simplex virus type 1 (HSV-1). Isomangiferin promotes the migration and osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) and reduces cell apoptosis and the production of ROS by activating the AMPK/ACC pathway, thereby facilitating fracture healing .
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4
4 Cited Publications
Cat. No.: HY-N6631
CAS No.: 1621-56-3
Target:  

AMPK

Research Areas:  

Metabolic Disease Cancer

7-Methoxyisoflavone is an isoflavone derivative and also an activator of adenosine monophosphate-activated protein kinase (AMPK).
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3
3 Cited Publications
Cat. No.: HY-107988
CAS No.: 1219737-12-8
Purity:  98.03%
Target:  

AMPK

Research Areas:  

Metabolic Disease

MK-3903 is a potent and selective AMP-activated protein kinase (AMPK) activator with an EC50 of 8 nM.
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3
3 Cited Publications
Cat. No.: HY-12831
CAS No.: 1233082-79-5
Purity:  99.28%
Target:  

AMPK

Research Areas:  

Metabolic Disease

Ampkinone is an indirect AMP-activated protein kinase (AMPK) activator.
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3
3 Cited Publications
Cat. No.: HY-P0136
CAS No.: 125911-68-4
Target:  

AMPK

Research Areas:  

Metabolic Disease

SAMS peptide is a specific substrate for the AMP-activated protein kinase (AMPK).
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2
2 Cited Publications
Cat. No.: HY-115463
CAS No.: 1839150-63-8
Purity:  99.57%
Target:  

AMPK Apoptosis

Research Areas:  

Cancer

EB-3D is a potent and selective choline kinase α (ChoKα) inhibitor, with an IC50 of 1 μM for ChoKα1. EB-3D exerts effects on ChoKα expression, AMPK activation, apoptosis, endoplasmic reticulum stress and lipid metabolism. EB-3D exhibits a potent antiproliferative activity in a panel of T-leukemia cell lines. Anti-cancer activity .
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2
2 Cited Publications
Cat. No.: HY-124822
CAS No.: 73439-19-7
Purity:  99.73%
Target:  

AMPK

Research Areas:  

Metabolic Disease Cancer

COH-SR4 is an AMPK activator. COH-SR4 shows potent anti-proliferative activities against leukemia, melanoma, breast and lung cancers. COH-SR4 inhibits adipocyte differentiation via AMPK activation. COH-SR4 can be used for the research of obesity and related metabolic disorders .
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2
2 Cited Publications
Cat. No.: HY-P80541
Synonyms: PRKAA2; AMPK; AMPK2; 5'-AMP-activated protein kinase catalytic subunit alpha-2; AMPK subunit alpha-2; Acetyl-CoA carboxylase kinase; ACACA kinase; Hydroxymethylglutaryl-CoA reductase kinase; HMGCR kinase

Host:  

Rabbit

Application:  

WB, IP

Reactivity:  

Human

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2
2 Cited Publications
Cat. No.: HY-P76141
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: PRKAG1; 5'-AMP-Activated Protein kinase, Gamma-1 Subunit; Protein kinase AMP-Activated Non-Catalytic Subunit Gamma 1; AMPK Subunit Gamma-1; 5'-AMP-Activated Protein kinase Subunit Gamma-1; AMPK Gamma-1 Chain; Protein kinase, AMP-Activated, Gamma 1 Non-Cat
Species:  
Human
Source:  
Sf9 insect cells
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2
2 Cited Publications
Cat. No.: HY-P76143
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: PRKAG1; 5'-AMP-Activated Protein kinase, Gamma-1 Subunit; Protein kinase AMP-Activated Non-Catalytic Subunit Gamma 1; AMPK Subunit Gamma-1; 5'-AMP-Activated Protein kinase Subunit Gamma-1; AMPK Gamma-1 Chain; Protein kinase, AMP-Activated, Gamma 1 Non-Cat
Species:  
Human
Source:  
Sf9 insect cells
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1
1 Cited Publications
Cat. No.: HY-N6258
CAS No.: 6894-43-5
Kahweol is one of the consituents of the coffee from Coffea Arabica with anti-inflammatory anti-angiogenic, and anti-cancerous activities. Kahweol inhibits adipogenesis and increase glucose uptake by AMP-activated protein kinase (AMPK) activation. Kahweol induces apoptosis.
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