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Results for "

GAPDH

" in MedChemExpress (MCE) Product Catalog:

17

Inhibitors & Agonists

2

Biochemical Assay Reagents

1

Natural
Products

3

Recombinant Proteins

3

Antibodies

1

Click Chemistry

5

Oligonucleotides

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-P2804

    GADPH; G3PDH; Glyceraldehyde phosphate dehydrogenase

    Others Others
    Glyceraldehyde phosphate dehydrogenase (EC 1.2.1.12) is the target of anti-thymocyte and anti-apoptotic agents. Glyceraldehyde phosphate dehydrogenase catalyzes the chain oxidation of reduced nicotinamide adenine dinucleotide by perhydroxyl radicals .
    GAPDH, rabbit muscle
  • HY-147280

    GP-2250

    Apoptosis Cancer
    Misetionamide is an orally oxathiazin-like compound. Misetionamide is a glyceraldehyde-3-phosphate dehydrogenase (GAPDH) inhibitor with antineoplastic activity. Misetionamide can be used for the research of cancer .
    Misetionamide
  • HY-120838

    Koningic acid

    Caspase Infection Cancer
    Heptelidic acid (Koningic acid) is a sesquiterpene antibiotic . Heptelidic acid inhibits Etoposide-induced apoptosis via downregulation of caspases . Koningic acid (KA) is a specific GAPDH inhibitor with an IC50of 90 μM .
    Heptelidic acid
  • HY-157395

    Others Cancer
    malonyl-NAC increases cellular propylation, resulting in reduced endogenous GAPDH activity. malonyl-NAC increases GAPDH malonylation in cells and inhibits pyruvate kinase activity. In addition, malonyl-NAC limits the metabolism and proliferation of a highly glycolytic kidney cancer cell line harboring a tricarboxylic acid cycle mutation .
    malonyl-NAC
  • HY-16361A

    CGP3466B; CGP3446 maleate; TCH346 maleate

    Apoptosis Neurological Disease Metabolic Disease
    Omigapil maleate, an orally bioavailable GAPDH nitrosylation inhibitor, abrogates Aβ1-42-induced tau acetylation, memory impairment, and locomotor dysfunction in mice. Omigapil maleate has the potential for the research of Alzheimer's disease . Omigapil maleate (CGP3446B maleate) is a apoptosis inhibitor. Omigapil maleate can be used for the research of congenital muscular dystrophy (CMD) . Omigapil (maleate) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    Omigapil maleate
  • HY-D0849

    Iodoacetic acid sodium salt

    Biochemical Assay Reagents Metabolic Disease Inflammation/Immunology
    Sodium iodoacetate is a specific inhibitor of GAPDH and has glycolysis inhibitory activity. In addition, sodium iodoacetate can induce osteoarthritis and related pain models in experimental animals .
    Sodium iodoacetate
  • HY-RS05273

    Small Interfering RNA (siRNA) Others

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

    GAPDH Human Pre-designed siRNA Set A
    GAPDH Human Pre-designed siRNA Set A
  • HY-RS05274

    Small Interfering RNA (siRNA) Others

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

    GAPDHS Human Pre-designed siRNA Set A
    GAPDHS Human Pre-designed siRNA Set A
  • HY-123668

    Others Others
    KM05382 serves as an inhibitor of CDK9 and reduces the transcription of GAPDH.
    KM05382
  • HY-N3247

    Parasite Others
    Monomethyl kolavate is a Trypanosoma brucei GAPDH enzyme (TbGAPDH) inhibitor with theIC50 value of 2 µM .
    Monomethyl kolavate
  • HY-131921

    Biochemical Assay Reagents Endocrinology
    DL-Glyceraldehyde 3-phosphate diethyl acetal barium is an Aspartate Aminotransferase isozyme inhibitor .
    DL-Glyceraldehyde 3-phosphate diethyl acetal barium
  • HY-112758
    DLin-KC2-DMA
    4 Publications Verification

    Liposome Others
    DLin-KC2-DMA is an ionisable cationic lipid (pKa≈6) that is virtually non-toxic to antigen presenting cells (APCs). DLin-KC2-DMA produces significant siRNA-mediated gene silencing of GAPDH, when binds to lipid nanoparticles (LNP). DLin-KC2-DMA can be used in siRNA delivery studies .
    DLin-KC2-DMA
  • HY-161668

    Ligands for E3 Ligase Ferroptosis Cancer
    Ru-Poma is a Ru(II)-based photosensitizer, which attenuates Cisplatin (HY-17394)-resistant tumor through photodynamic therapy (PDT). Ru-Poma photodegrades CRBN through a Pomalidomide (HY-10984) moiety. Ru-Poma induces ferroptosis, through an increase in lipid peroxide, downregulation of GPX4 and GAPDH expression. Ru-Poma exhibits cytotoxicity in A549, with IC50 of 18.46 μM and 0.37 μM in dark and upon irradiation, respectively .
    Ru-Poma
  • HY-RS03616

    Small Interfering RNA (siRNA) Others
    Ddit4 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Ddit4 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Components

    Ddit4 siRNA-1: 5 nmol (HPLC)

    Ddit4 siRNA-2: 5 nmol (HPLC)

    Ddit4 siRNA-3: 5 nmol (HPLC)

    siRNA Negative Control: 5 nmol (HPLC)

    FAM-labeled siRNA Negative Control: 5 nmol (HPLC)

    GAPDH siRNA Positive Control: 5 nmol (HPLC)

    DDIT4L Human Pre-designed siRNA Set A
    DDIT4L Human Pre-designed siRNA Set A
  • HY-RS16258

    Small Interfering RNA (siRNA) Others
    Lipt1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Lipt1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.
    Components
    Lipt1 siRNA-1: 5 nmol (HPLC)
    Lipt1 siRNA-2: 5 nmol (HPLC)
    Lipt1 siRNA-3: 5 nmol (HPLC)
    siRNA Negative Control: 5 nmol (HPLC)
    FAM-labeled siRNA Negative Control: 5 nmol (HPLC)
    GAPDH siRNA Positive Control: 5 nmol (HPLC)
    Lipt1 Mouse Pre-designed siRNA Set A
    Lipt1 Mouse Pre-designed siRNA Set A
  • HY-123962
    G6PD activator AG1
    3 Publications Verification

    Others Metabolic Disease
    G6PD activator AG1 is a potent and selective glucose-6-phosphate dehydrogenase (G6PD) activator with an EC50 of 3 µΜ . G6PD activator AG1 reduces hemolysis of human erythrocytes .
    G6PD activator AG1
  • HY-132126

    SRPK Others
    SPHINX is a selective SRPK1 inhibitor with an IC50 value of 0.58 μM. SPHINX effectively reduces Choroidal Neovascularization (CNV) in vivo. SPHINX can be used for the research of (age-related macular degenaration) AMD .
    SPHINX

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