23 Results for "

GLK

" in MedChemExpress (MCE) Product Catalog:
Products (23)

23 Results for "GLK" in MCE Product Catalog:

Cat. No.: HY-P9983
CAS No.: 166089-32-3
Synonyms: SGN-33; HuM-195; GLK-33 Antibody
Lintuzumab (HUM-195) is an anti-CD33 humanized monoclonal antibody. Lintuzumab reduces the production of TNFα-induced pro-inflammatory cytokines and chemokines by AML cells. Lintuzumab promotes tumor cell killing through antibody-dependent cellular cytotoxicity (ADCC) and phagocytosis (ADCP) activities against MDR and MDR+ AML cell lines and primary AML patient samples. Lintuzumab enhances survival and reduces tumor burden in mice .
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Cat. No.: HY-138742
CAS No.: 2320462-65-3
Purity:  99.33%
Target:  

MAP4K

Research Areas:  

Cancer

HPK1-IN-7 is a potent, orally active HPK1 (hematopoietic progenitor kinase 1, MAP4K1) inhibitor (IC50=2.6 nM) with excellent family and kinome selectivity. HPK1-IN-7 shows selectivity against IRAK4 (59 nM) and GLK (140 nM). HPK1-IN-7 shows robust efficacy against MC38 syngeneic tumor model in combination with anti-PD1 .
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Cat. No.: HY-144093
CAS No.: 2229042-24-2
Purity:  ≥98.0%
Target:  

MAP4K

Research Areas:  

Infection

HPK1/GLK-IN-1 is a HPK1 and GLK inhibitor. HPK1/GLK-IN-1 (compound 38) potently inhibits GLK with an IC50 of  33 nM . HPK1-IN-26 can be used for the research of animal pathogen infection .
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Cat. No.: HY-174357
Research Areas:  

Cancer

HPK1 ligand 3-dimethylph tetrahydropyridine is a Target Protein Ligand-Linker Conjugate. HPK1 ligand 3-dimethylph tetrahydropyridine can be used to synthesize PROTAC HPK1 Degrader-4 (HY-174135) .
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Cat. No.: HY-128663
CAS No.: 353484-37-4
Target:  

Parasite

Research Areas:  

Infection

GLK7-001 is a Trypanosoma cruzi glucokinase (TcGlcK) inhibitor. GLK7-001 has in vitro trypanocidal activity .
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Cat. No.: HY-P5566
CAS No.: 1225014-04-9
Target:  

Bacterial

Research Areas:  

Infection

GLK-19 is an antimicrobial peptide, and is active against E. coli (MIC: 10 μM) .
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Cat. No.: HY-RS24869
Research Areas:  

Others

Galk1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Galk1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS05331
Research Areas:  

Others

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

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Cat. No.: HY-RS08077
Research Areas:  

Others

MAP4K3 Human Pre-designed siRNA Set A contains three designed siRNAs for MAP4K3 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS05330
Research Areas:  

Others

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

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Cat. No.: HY-RS08078
Research Areas:  

Others

Map4k3 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Map4k3 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS05329
Research Areas:  

Others

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

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Cat. No.: HY-178097
Target:  

MAP4K

Research Areas:  

Cancer

HPK1-IN-62 is a selective and orally active HPK-1 inhibitor with an IC50 of 1.22 nM. HPK1-IN-62 significantly improves GLK selectivity (> 665-fold) and LCK selectivity (> 1095-fold). HPK1-IN-62 enhances T-cell activation and demonstrated synergistic effects when combined with anti-mPD-1 therapy in the MC38 tumor model, inhibiting a tumor growth. HPK1-IN-62 can be used in the researchs of colon cancer and cancer immunotherapy .
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Cat. No.: HY-179111
CAS No.: 3034320-17-4
Research Areas:  

Cancer

HPK1-IN-64 is a potent, selective, and orally active HPK1 inhibitor with an IC50 value of 1.9 nM. HPK1-IN-64 exhibits selectivity exceeding 100-fold, 80-fold, 300-fold, and 350-fold against off-target kinases such as GLK, MAP4K5, TBK1, and TNIK, respectively. HPK1-IN-64 inhibits SLP76 protein phosphorylation and IL-2 secretion. HPK1-IN-64 may be used in cancer research, such as for colorectal cancer .
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Cat. No.: HY-174135
Target:  

PROTACs MAP4K

Research Areas:  

Cancer

PROTAC HPK1 Degrader-4 (compound E3) is a selective and orally active PROTAC HPK1 degrader with a DC50 of 3.16 nM. PROTAC HPK1 Degrader-4 demonstrates >1000-fold selectivity over GLK. PROTAC HPK1 Degrader-4 promotes immune activation. PROTAC HPK1 Degrader-4 can be used for the study of colon cancer and lymphoma (Pink: ligand for target protein (HY-174355); Blue: ligand for E3 ligase CRBN (HY-45808); Black: Linker (HY-174356); Target protein ligand-linker Conjugate (HY-174357)) .
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Cat. No.: HY-P703250
Purity:  ≥ 80%, as determined by reducing SDS-PAGE.
Synonyms: Mitogen-activated protein kinase kinase kinase kinase 3; Germinal center kinase-related protein kinase; GLK; MAPK/ERK kinase kinase kinase 3; MEK kinase kinase 3; MEKKK 3; MAP4K3; RAB8IPL1; Homo sapiens; Human; GLK; Kinase; Serine/threonine-protein kinase; Transferase; 2.7.11.1
Species:  
Source:  
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Cat. No.: HY-RS18388
Research Areas:  

Others

Galk1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Galk1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-179727
PROTAC HPK1 Degrader-7 (compound D02) is a potent and selective PROTAC HPK1 degrader with an DC50 of 3.07 nM. PROTAC HPK1 Degrader-7 exhibits selectivity over GLK. PROTAC HPK1 Degrader-7 induces HPK1 degradation in a CRBN- and proteasome-dependent manner. PROTAC HPK1 Degrader-7 inhibits SLP-76 phosphorylation, induces IL-2 and IFN-γ secretion in human primary T cells. PROTAC HPK1 Degrader-7 can be used for immunology research .
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Cat. No.: HY-179338
Research Areas:  

Cancer

HPK1-IN-65 is a selective and orally active HPK1 inhibitor with an IC50 value of < 5 nM. HPK1-IN-65 inhibits HPK1 kinase activity and displays 1257-fold selectivity over the MAP4K kinase family member GLK. HPK1-IN-65 exhibits an IC50 of 92.3 nM for inhibiting pSLP76 phosphorylation. HPK1-IN-65 demonstrates an EC50 of 398 nM for stimulating IL-2 production. HPK1-IN-65 inhibits TCR-induced phosphorylation of SLP76 at Ser376 in a dose-dependent manner. HPK1-IN-65 can be further utilized for colorectal cancer research .
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Cat. No.: HY-P75790
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Hexokinase-4; HK4; Hexokinase-D; Glucokinase
Species:  
Source:  
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