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Results for "

α-Hydroxyisovaleric acid

" in MedChemExpress (MCE) Product Catalog:

4

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3

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Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-W008150
    2-Hydroxy-3-methylbutanoic acid
    1 Publications Verification

    α-Hydroxyisovaleric acid

    		 Endogenous Metabolite Metabolic Disease
    2-Hydroxy-3-methylbutanoic acid is an α-hydroxy analogue of valine and a valine precursor that reduces urea excretion. 2-Hydroxy-3-methylbutanoic acid can promote the growth of chickens and rats, and is converted into valine in the body, participating in protein synthesis and maintaining nitrogen balance, thereby supporting animal growth and development. 2-Hydroxy-3-methylbutanoic acid has a more significant effect on the valine-deficient dietary model. 2-Hydroxy-3-methylbutanoic acid is mainly used in animal nutrition research to evaluate its potential application as a nitrogen source substitute in feed .
    2-Hydroxy-3-methylbutanoic acid
  • HY-30217
    (S)-2-Hydroxy-3-methylbutanoic acid

    L-alpha-Hydroxyisovaleric acid

    		 Drug Intermediate Others
    (S)-2-Hydroxy-3-methylbutanoic acid (L-alpha-Hydroxyisovaleric acid) is a synthetic intermediate useful for pharmaceutical synthesis .
    (S)-2-Hydroxy-3-methylbutanoic acid
  • HY-W008150R
    2-Hydroxy-3-methylbutanoic acid (Standard)

    α-Hydroxyisovaleric acid (Standard)

    		 Reference Standards Endogenous Metabolite Neurological Disease
    2-Hydroxy-3-methylbutanoic acid (Standard) is the analytical standard of 2-Hydroxy-3-methylbutanoic acid. This product is intended for research and analytical applications. 2-Hydroxy-3-methylbutanoic acid is a close structure analogue of GHB, which is a naturally occurring neurotransmitter and a psychoactive agent.
    2-Hydroxy-3-methylbutanoic acid (Standard)
  • HY-N6704
    Enniatin A1

    		ERK Apoptosis Cancer
    Enniatin A1 isolated from Fusarium mycotoxins is a cyclic hexadepsipeptide consisting of alternating D-α-hydroxyisovaleric acids and N-methyl-L-amino acids. Enniatin A1 possesses anticarcinogenic properties by induction of apoptosis and disruption of ERK signalling pathway. Enniatin A1 inhibits ACAT with an IC50 of 49 μM in rat liver microsomes .
    Enniatin A1

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