18 Results for "

hexokinase 2

" in MedChemExpress (MCE) Product Catalog:
Products (18)

18 Results for "hexokinase 2" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-134929
CAS No.: 2454676-05-0
Purity:  99.91%
Synonyms: BNBZ; hexokinase 2 inhibitor 1
Target:  

Hexokinase Apoptosis

Research Areas:  

Cancer

Benitrobenrazide (BNBZ) is the orally active inhibitor for hexokinase 2 with an IC50 of 0.53 µM. Benitrobenrazide causes DNA damage, and exhibits antitumor effect .
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2
2 Cited Publications
Cat. No.: HY-155008
CAS No.: 3033812-84-6
Purity:  98.98%
Target:  

PROTACs Hexokinase

Research Areas:  

Cancer

PROTAC HK2 Degrader-1 is a PROTAC consisting of Lonidamine (HY-B0486) as a target protein Hexokinase 2 (HK2) inhibitor and Thalidomide (HY-14658) as a CRBN ligand-linked PROTAC. PROTAC HK2 Degrader-1 selectively inhibits the proliferation of breast cancer cells by forming a ternary complex through the ubiquitin-proteasome system to degrade Hexokinase 2 (HK2) protein leading to mitochondrial damage and cell death. PROTAC HK2 Degrader-1 effectively inhibits breast tumor growth and reduces the colonic side effects of cisplatin for breast cancer research .
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2
2 Cited Publications
Cat. No.: HY-139409A
CAS No.: 33068-19-8
Purity:  ≥98.0%
Research Areas:  

Cancer

2-Deoxy-D-glucose 6-phosphate disodium is an ATP-competitive, 2-deoxy-D-glucose non-competitive Hexokinase inhibitor, with a Ki value of 1.45 mM against bovine heart hexokinase. 2-Deoxy-D-glucose 6-phosphate disodium exerts ATP-competitive and 2-deoxy-D-glucose non-competitive inhibitory effects on bovine heart hexokinase. 2-DG inhibits glycolysis via the production and intracellular accumulation of 2-Deoxy-D-glucose 6-phosphate disodium, thereby inhibiting the functions of hexokinase and Glucose-6-phosphate isomerase, and inducing cell death. 2-Deoxy-D-glucose 6-phosphate disodium can be used in cancer-related research .
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Cat. No.: HY-175035
CAS No.: 3114833-48-3
Target:  

Hexokinase

Research Areas:  

Inflammation/Immunology Cancer

HK-2-IN-1 is a Hexokinase 2 (HK-2) inhibitor. HK-2-IN-1 exhibits a non-activating effect on human recombinant HK-2 enzyme. HK-2-IN-1 has anti-tumor activity, affecting immune cells in the tumor microenvironment. HK-2-IN-1 has immunomodulatory effects and is potentially useful in the study of cancers such as colon cancer, liver cancer, and breast cancer .
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Cat. No.: HY-N2126
CAS No.: 952068-57-4
Parishin E is a modulator of hexokinase 2, lactate dehydrogenase A, and silent information regulator 6 (sirtuin 6), and is also a component present in Gastrodia elata Blume . Parishin E reduces the expression of hexokinase 2 and lactate dehydrogenase A, thereby regulating the process of cellular glycolysis . Parishin E regulates the deacetylation mediated by silent information regulator 6 (Sirtuin 6), and inhibits histone 3 lactylation modifications at the H3K18la and H3K27la sites . Parishin E inhibits macrophage polarization . Parishin E alleviates LPS-induced inflammatory responses and suppresses the expression of pro-inflammatory cytokines . Parishin E exerts ameliorating effects on rheumatoid arthritis . Parishin E can be used in studies related to rheumatoid arthritis .
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Cat. No.: HY-P10108
Synonyms: Hxk2VBD peptide, cell-permeable
Target:  

Hexokinase

Research Areas:  

Neurological Disease

Hexokinase II VDAC binding domain peptide (Hxk2VBD peptide) is a cell-permeable hexokinase II VDAC binding domain. Hexokinase II VDAC binding domain peptide inhibits mitochondrial localization of hexokinase 2 (HXK2). Hexokinase II VDAC binding domain peptide inhibits neurotrophic factor-directed axon outgrowth .
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Cat. No.: HY-W000133
CAS No.: 31112-62-6
Synonyms: Amipaque
Target:  

Hexokinase

Research Areas:  

Neurological Disease

Metrizamide (Amipaque) is used as the contrast medium for angiography in neuroradiological investigations . Metrizamide inhibits human brain hexokinase .
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Cat. No.: HY-168717
CAS No.: 3056278-80-6
HK2-IN-2 (Compound 26) is a Hexokinase 2 inhibitor that demonstrates significant anti-tumor activity by targeting microtubules and Hexokinase 2, with an IC50 value of 0.764 μM against MD-MBA-231 cells. HK2-IN-2 effectively inhibits the activity of Hexokinase 2, leading to the accumulation of Reactive Oxygen Species and dysfunction of the mitochondrial membrane potential (MMP), thereby promoting apoptosis and blocking the cell cycle .
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Cat. No.: HY-139409
CAS No.: 3573-50-0
Research Areas:  

Cancer

2-Deoxy-D-glucose 6-phosphate disodium is an ATP-competitive and 2-deoxy-D-glucose non-competitive Hexokinase inhibitor, with a Ki value of 1.45 mM against bovine heart hexokinase. 2-Deoxy-D-glucose 6-phosphate disodium exerts ATP-competitive and 2-deoxy-D-glucose non-competitive inhibitory effects on bovine heart hexokinase. 2-DG inhibits glycolysis via the generation and intracellular accumulation of 2-Deoxy-D-glucose 6-phosphate disodium, thereby inhibiting the functions of hexokinase and Glucose-6-phosphate isomerase, and inducing cell death. 2-Deoxy-D-glucose 6-phosphate disodium can be used in cancer-related research .
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Cat. No.: HY-P703943
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: HK2; HKII; hexokinase 2; hexokinase-2, Muscle; hexokinase Type II; Phosphotransferase; hexokinase-2; HK II; Muscle Form hexokinase; HXK2; hexokinase-B
Species:  
Source:  
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Cat. No.: HY-P704013
Purity:  ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: HK2; HKII; hexokinase 2; hexokinase-2, Muscle; hexokinase Type II; Phosphotransferase; hexokinase-2; HK II; Muscle Form hexokinase; HXK2; hexokinase-B
Species:  
Source:  
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Cat. No.: HY-P703943Y
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: HK2; HKII; hexokinase 2; hexokinase-2, Muscle; hexokinase Type II; Phosphotransferase; hexokinase-2; HK II; Muscle Form hexokinase; HXK2; hexokinase-B
Species:  
Source:  
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Cat. No.: HY-P86604
Synonyms: HK2; hexokinase-2; hexokinase type II; HK II; Muscle form hexokinase

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF, IP, ELISA

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P700580
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: HK1; Glycolytic Enzyme; hexokinase 1; hexokinase IR; Brain Form hexokinase; hexokinase-2; hexokinase Type I; NEDVIBA; hexokinase-A; HK1-Tc; hexokinase-1; CNSHA5; hexokinase; HMSNR; HK1-Tb; RP79; HK1-Ta; NMSR; HKI; HXK1; Neuropathy, Hereditary Motor And Se
Species:  
Source:  
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Cat. No.: HY-P700581
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: HK1; Glycolytic Enzyme; hexokinase 1; hexokinase IR; Brain Form hexokinase; hexokinase-2; hexokinase Type I; NEDVIBA; hexokinase-A; HK1-Tc; hexokinase-1; CNSHA5; hexokinase; HMSNR; HK1-Tb; RP79; HK1-Ta; NMSR; HKI; HXK1; Neuropathy, Hereditary Motor And Se
Species:  
Source:  
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Cat. No.: HY-139409B
Research Areas:  

Cancer

2-Deoxy-D-glucose 6-phosphate sodium is an ATP-competitive, 2-deoxy-D-glucose non-competitive Hexokinase inhibitor, with a Ki value of 1.45 mM against bovine heart hexokinase. 2-Deoxy-D-glucose 6-phosphate sodium exerts ATP-competitive and 2-deoxy-D-glucose non-competitive inhibitory effects on bovine heart hexokinase. 2-DG inhibits glycolysis via the production and intracellular accumulation of 2-Deoxy-D-glucose 6-phosphate sodium, thereby inhibiting the functions of hexokinase and Glucose-6-phosphate isomerase, and inducing cell death. 2-Deoxy-D-glucose 6-phosphate sodium can be used in cancer-related research .
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Cat. No.: HY-183809
CAS No.: 3124329-46-7
Target:  

Hexokinase

Research Areas:  

Inflammation/Immunology

ZSW is a hexokinase 2 (HK2) inhibitor with human HK2 IC50 of 0.48 μM, human HK2 Ka of 252.00 μM, and selectivity over HK3 and GCK. ZSW binds directly to HK2, inhibits its enzymatic activity, modulates macrophage phenotypes through glycolysis inhibition, and inhibits NF-κB nuclear translocation by preventing IκBα phosphorylation and degradation. ZSW alleviates inflammatory bowel disease (IBD) and improves the intestinal inflammatory state of IBD mice. ZSW can be used for the research of inflammatory bowel disease .
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Cat. No.: HY-182243
CAS No.: 2748366-80-3
Research Areas:  

Cancer

HK2-IN-4 is a selective hexokinase 2 (HK2) inhibitor with an IC50 value of 0.79 μM and a Kd value of 0.41 μM. HK2-IN-4 blocks the interaction between HK2 and voltage-dependent anion channel 1 (VDAC1). HK2-IN-4 reduces lactate and ATP levels in cancer cells. HK2-IN-4 induces the production of apoptosis (apoptosis) markers in cancer cells, including increased p-AMPK/AMPK ratio and Bax levels, as well as decreased Bcl2 levels. HK2-IN-4 inhibits the proliferation of cancer cells with high HK2 expression. HK2-IN-4 can be used in research related to colorectal cancer and non-small cell lung cancer .
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