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Results for "

Meglumine

" in MedChemExpress (MCE) Product Catalog:

9

Inhibitors & Agonists

1

Biochemical Assay Reagents

1

Natural
Products

1

Isotope-Labeled Compounds

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-B0342

    Methylglucamine; Meglumin; Methylglucamin

    Biochemical Assay Reagents Cancer
    Meglumine (Methylglucamine) is an orally active amino sugar derived from sorbitol. Meglumine has anti-inflammatory and antitumor activity. Meglumine is often used as an excipient in active molecules and with iodinated compounds in contrast agents such as meglumine and meglumine iodide .
    <em>Meglumine</em>
  • HY-14814A
    Delafloxacin meglumine
    2 Publications Verification

    ABT492 Meglumine; RX-3341 Meglumine; WQ-3034 Meglumine

    Bacterial Antibiotic Infection
    Delafloxacin meglumine (ABT492 meglumine; RX-3341 meglumine; WQ-3034 meglumine) is a broad-spectrum fluoroquinolone antibiotic. Delafloxacin has a broad spectrum of activity that includes drug-resistant Staphylococcus aureus, Streptococcus pneumoniae, and Klebsiella pneumonia .
    Delafloxacin <em>meglumine</em>
  • HY-147402A

    D-0502 Meglumine

    Estrogen Receptor/ERR Cancer
    Taragarestrant (D-0502) meglumine is a potent, orally active and selective estrogen receptor degrader (SERD). Taragarestrant meglumine shows potent activity in various ER+ breast cancer cell lines and xenograft models .
    Taragarestrant <em>meglumine</em>
  • HY-42937

    Transcrocetin Meglumine; trans-Crocetin Meglumine

    iGluR Cancer
    Crocetin (Transcrocetin) meglumine, extracted from saffron (Crocus sativus L.), acts as an NMDA receptor antagonist with high affinity.
    Crocetin <em>meglumine</em>
  • HY-A0261A

    ICI-50123 Meglumine

    Cholecystokinin Receptor Endocrinology Cancer
    Pentagastrin (ICI-50123) meglumine is a potent, selective Cholecystokinin B (CCKB) receptor antagonists with IC50 values of 11 nM and 1100 nM for CCKB and CCKA, respectively. Pentagastrin meglumine enhances gastric mucosal defense mechanisms against acid and protects the gastric mucosa from experimental injury . .
    Pentagastrin <em>meglumine</em>
  • HY-B0386

    COX Inflammation/Immunology
    Flunixin meglumine is a cyclooxygenase (COX) inhibitor with IC50 values of 0.55 and 3.24 μM for COX-1 and COX-2, respectively. Flunixin meglumine shows anti-inflammatory effects .
    Flunixin <em>meglumine</em>
  • HY-14852A
    Tafamidis meglumine
    1 Publications Verification

    Fx-1006A

    Transthyretin (TTR) Neurological Disease
    Tafamidis meglumine (Fx-1006A) is a potent and selective transthyretin (TTR) stabilizer, shows comparable potency and efficacy to the mutumant homotetramers V30M-TTR, V122I-TTR and wild type WT-TTR, with EC50s of 2.7-3.2 μM. Tafamidis meglumine inhibits amyloidogenesis .
    Tafamidis <em>meglumine</em>
  • HY-W040217

    N-Oxodecyl Meglumine

    Biochemical Assay Reagents Others
    MEGA-10 (N-Oxodecyl meglumine) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    MEGA-10
  • HY-121046S

    COX Inflammation/Immunology
    Flunixin-d3 is the deuterium labeled Flunixin. Flunixin Meglumine is a potent inhibitor of COX used as analgesic agent with anti-inflammatory and antipyretic activity[1][2].
    Flunixin-d3

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