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Results for "

PMM

" in MedChemExpress (MCE) Product Catalog:

5

Inhibitors & Agonists

1

Natural
Products

2

Recombinant Proteins

2

Oligonucleotides

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-112597A

    REN001; HPP593

    PPAR Inflammation/Immunology
    Mavodelpar (REN001) is a selective PPARδ agonist. Mavodelpar suppresses glomerular injury and renal fibrosis. Mavodelpar can be used for the research of primary mitochondrial myopathies (PMM) and long-chain fatty acid oxidation disorders (LC-FAOD) . Mavodelpar is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    Mavodelpar
  • HY-124890

    Others Metabolic Disease
    Thr101 is an inhibitor (IC50=2.9 μM) of phosphomannose isomerase (PMI).PMI can compete with phosphomannose mutase 2 (PMM2) for the binding site of Man-6-P and convert mannose-6-phosphate (Man-6-P) into fructose-6-phosphate (Fru-6-P) .Thr101 only specifically inhibits PMI and not PMM2. Thr101 can be used for research of congenital disorder of glycosylation type Ia (CDG-Ia) .
    Thr101
  • HY-RS10766

    Small Interfering RNA (siRNA) Others

    PMM1 Human Pre-designed siRNA Set A contains three designed siRNAs for PMM1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    PMM1 Human Pre-designed siRNA Set A
    PMM1 Human Pre-designed siRNA Set A
  • HY-RS10767

    Small Interfering RNA (siRNA) Others

    PMM2 Human Pre-designed siRNA Set A contains three designed siRNAs for PMM2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    PMM2 Human Pre-designed siRNA Set A
    PMM2 Human Pre-designed siRNA Set A
  • HY-N8374

    Parasite Infection
    Pheanthine (Compound 2) is an antiplasmodial agent, that inhibits chloroquine-resistant Plasmodium falciparum K-1 (IC50 is 0.8 μM) and chloroquine-sensitive P. falciparum strain NF54 A19A (IC50 of 0.03 μM). Pheanthine exhibits low cytotoxicity in human lung fibrosblast (MRC-5, IC50 is 11.2 μM) and macrophages (PMM, IC50 is 8 μM) .
    Pheanthine

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