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Results for "

Thiazolidine

" in MedChemExpress (MCE) Product Catalog:

12

Inhibitors & Agonists

1

Peptides

1

Isotope-Labeled Compounds

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-I0144

    Drug Intermediate Others
    Thiazolidine is a five-membered heterocyclic compound containing sulfur and nitrogen heteroatoms. Thiazolidine is an important intermediate in organic synthesis. Thiazolidine derivatives possess diverse bioactivities, such as anti-tumor, antibacterial and insecticidal activities, and the capacity to reduce blood glucose levels .
    Thiazolidine
  • HY-B1265

    Cortisol 17-valerate

    Glucocorticoid Receptor Others
    Hydrocortisone 17-valerate (Cortisol 17-valerate) is a thiazolidine compound .
    Hydrocortisone 17-valerate
  • HY-B1169

    1,3-Thiazolidine-4-carboxylic acid

    Amino Acid Derivatives Cardiovascular Disease Cancer
    Timonacic (1,3-Thiazolidine-4-carboxylic acid) is an orally active thiol antioxidant. Timonacic has anti-aging and anti-hepatotoxic effects. Timonacic has a LD50 of 400 mg/kg for mice. Timonacic can be used in the research of liver diseases, gastrointestinal diseases, and cancer .
    Timonacic
  • HY-116073

    Biochemical Assay Reagents Metabolic Disease
    L-Penicillamine is a mechanism-based inhibitor of serine palmitoyltransferase by forming a pyridoxal-5 '-phosphate-thiazolidine adduct. L-Penicillamine is a metal chelating agent of intermediate strength .
    L-Penicillamine
  • HY-148332

    Prolyl Endopeptidase (PREP) Neurological Disease
    Z-Thioprolyl-Thiazolidine is a potent and specific prolyl endopeptidase inhibitor with an Ki value of 0.36 nM for bovine brain prolyl endopeptidase
    Z-Thioprolyl-Thiazolidine
  • HY-B1265R

    Glucocorticoid Receptor Others
    Hydrocortisone 17-valerate (Standard) is the analytical standard of Hydrocortisone 17-valerate. This product is intended for research and analytical applications. Hydrocortisone 17-valerate (Cortisol 17-valerate) is a thiazolidine compound .
    Hydrocortisone 17-valerate (Standard)
  • HY-W722107

    1,3-Thiazolidine-4-carboxylic acid-d4

    Isotope-Labeled Compounds Amino Acid Derivatives Cardiovascular Disease Cancer
    Timonacic-d4 (1,3-Thiazolidine-4-carboxylic acid-d4) is deuterium labeled Timonacic. Timonacic (1,3-Thiazolidine-4-carboxylic acid) is a thiol antioxidant. Timonacic has anti-aging and anti-hepatotoxic effects, and it can be used to study acute illnesses and liver diseases, by inducing reversal, it is also used in research on certain cancer cases .
    Timonacic-d4
  • HY-109887

    Biochemical Assay Reagents Others
    3-Bromoimidazo[1,2-a]pyridine-6-carbaldehyde is a biochemical reagent that can be used for the preparation of (5Z)-5-[(3-acetylimidazo[1,2-α]pyridin-6-yl) methylidene]-1,3-thiazolidine-2,4-dione .
    3-Bromoimidazo[1,2-a]pyridine-6-carbaldehyde
  • HY-130096

    ADC Linker Cancer
    Ald-Ph-amido-C2-nitrate (Example XXIVb) is a thiazolidine derivative, used as a noncleavable ADC linker .
    Ald-Ph-amido-C2-nitrate
  • HY-131050

    Bacterial Fungal Infection
    Aspergillus niger-IN-1 (Compound 17), a derivative of thiazolidine-2,4-dione, acts as an antimicrobial agent. Aspergillus niger-IN-1 exhibited antimicrobial activity against various bacterial and fungal strains, including Bacillus subtilis, Staphylococcus aureus, Klebsiella pneumonia, Escherichia coli, Salmonella typhi, Candida albicans and Aspergillus niger, with MIC values of 11.3, 5.65, 11.3, 5.65, 5.65, 5.65, and 5.65 μM/mL, respectively .
    Aspergillus niger-IN-1
  • HY-151934

    Apoptosis Cancer
    ERK-IN-6 (compound 6g) is an potent anti-proliferation agent against esophageal squamous cell carcinoma (ESCC). ERK-IN-6 induces cell apoptosis via ERK pathway. ERK-IN-6 can be used for the research of ESCC .
    ERK-IN-6
  • HY-117047

    Apoptosis Caspase Cancer
    ALC67 is a cytotoxic thiazolidine compound with an IC50 of approximately 5 μM against liver, breast cancer, colon cancer, and endometrial cancer cell lines. ALC67 induces apoptosis in cancer cells by activating caspase-9 and causing cell cycle arrest at the SubG1/G1 phase, via a pathway that is independent of death receptors. ALC67 can be used in cancer research .
    ALC67

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