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Results for "

2-Pyridones

" in MedChemExpress (MCE) Product Catalog:

8

Inhibitors & Agonists

2

Natural
Products

1

Isotope-Labeled Compounds

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-Y0191
    α-Pyridone

    2-Pyridone

    		 Endogenous Metabolite Bacterial Infection
    α-Pyridone (2-Pyridone) is an antibacterial agent that plays an important role in the field of biochemical research. α-Pyridone can serve as a scaffold compound to synthesize a variety of active compounds .
    α-Pyridone
  • HY-W018171
    3,5,6-Trichloro-2-pyridinol
    1 Publications Verification

    TCPy

    		 Environmental Pollutants Herbicide Metabolic Disease Inflammation/Immunology
    3,5,6-Trichloro-2-pyridinol (TCPy) is a chloride of 2-pyridone with oral activity. 3,5,6-Trichloro-2-pyridinol is the main degradation product of the herbicide Triclopyr and the insecticides Chlorpyrifos and chlorpyrifos-methyl. 3,5,6-Trichloro-2-pyridinol is associated with attention deficit hyperactivity disorder (ADHD) and decreased testosterone levels. 3,5,6-Trichloro-2-pyridinol causes hearing loss, hepatotoxicity and nephrotoxicity in mice [2] .
    3,5,6-Trichloro-2-pyridinol
  • HY-122643
    NITD-916

    		Bacterial Infection
    NITD-916, a 4-hydroxy-2-pyridone derivative, is an orally active mycobacterial enoyl reductase InhA inhibitor with an IC50 of 570 nM. NITD-916 forms a ternary complex with InhA and NADH to block access to the fatty acyl substrate binding pocket. NITD-916 inhibition of InhA reduces the synthesis of mycolic acids and results in cell death. NITD-916 has potent anti-tuberculosis effects [2].
    NITD-916
  • HY-W128159
    N-Acetyl-2-pyrrolidone

    		Hemoglobin Cancer
    N-Acetyl-2-pyrrolidone (No.20) is an N-acetylated amide. N-Acetyl-2-pyrrolidone can induce the differentiation of mouse erythroleukemia cells and has the activity of stimulating proliferation. N-Acetyl-2-pyrrolidone can be used in the research of leukemia differentiation therapy .
    N-Acetyl-2-pyrrolidone
  • HY-19951A
    A-867191 hydrochloride

    		Bacterial Infection
    A-867191 hydrochloride is a 2-pyridone DNA gyrase inhibitor. A-867191 hydrochloride has antibacterial activity. A-867191 hydrochloride can be used for research on infections .
    A-867191 hydrochloride
  • HY-Y0191R
    α-Pyridone (Standard)

    2-Pyridone (Standard)

    		 Reference Standards Endogenous Metabolite Bacterial Infection Metabolic Disease
    α-Pyridone (Standard) is the analytical standard of α-Pyridone. This product is intended for research and analytical applications. α-Pyridone (2-Pyridone) is an antibacterial agent. α-Pyridone can be synthesized via the 1,4-addition of 2-(phenylsulfinyl)acetamide to α,β-unsaturated ketones followed by cyclization and sulfoxide elimination. α-Pyridone can also be used to synthesize a wide range of heterocyclic compounds [2].
    α-Pyridone (Standard)
  • HY-W018171R
    3,5,6-Trichloro-2-pyridinol (Standard)

    TCPy (Standard)

    		 Herbicide Reference Standards Others
    3,5,6-Trichloro-2-pyridinol (Standard) is the analytical standard of 3,5,6-Trichloro-2-pyridinol. This product is intended for research and analytical applications. 3,5,6-Trichloro-2-pyridinol (TCPy) is a chloride of 2-pyridone with oral activity. 3,5,6-Trichloro-2-pyridinol is the main degradation product of the herbicide Triclopyr and the insecticides Chlorpyrifos and chlorpyrifos-methyl. 3,5,6-Trichloro-2-pyridinol is associated with attention deficit hyperactivity disorder (ADHD) and decreased testosterone levels. 3,5,6-Trichloro-2-pyridinol causes hearing loss, hepatotoxicity and nephrotoxicity in mice.
    3,5,6-Trichloro-2-pyridinol (Standard)
  • HY-Y0191S
    α-Pyridone-d5

    2-Pyridone-d5

    		 Isotope-Labeled Compounds Bacterial Endogenous Metabolite Infection Metabolic Disease
    α-Pyridone-d5 (2-Pyridone-d5) is the deuterium labeled α-Pyridone (HY-Y0191). α-Pyridone (2-Pyridone) is an antibacterial agent. α-Pyridone can be synthesized via the 1,4-addition of 2-(phenylsulfinyl)acetamide to α,β-unsaturated ketones followed by cyclization and sulfoxide elimination. α-Pyridone can also be used to synthesize a wide range of heterocyclic compounds [2].
    α-Pyridone-d5

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