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  3. Amino Acid Derivatives

Amino Acid Derivatives

Amino Acid Derivatives are bioactive molecules formed through chemical modifications or metabolic transformations of amino acids. They are widely present in living organisms and play crucial roles in physiological, psychological, and athletic performance.
The functions of these derivatives primarily include enhancing energy supply, regulating neurotransmitters, promoting fat metabolism, and reducing muscle damage. For example, creatine can increase muscle strength, enhance ATP resynthesis, and improve short-duration high-intensity exercise performance; tyrosine, as a precursor of dopamine and norepinephrine, helps enhance cognitive function and improve mood, particularly in sleep deprivation conditions, exhibiting anti-fatigue effects; carnitine facilitates fatty acid oxidation in the heart and skeletal muscles, improving endurance performance; HMB (β-hydroxy-β-methylbutyrate) reduces muscle breakdown and promotes muscle mass gain; while taurine exhibits antioxidant and antihypertensive properties and reduces oxidative stress induced by exercise.
Metabolic abnormalities or improper supplementation of amino acid derivatives may be associated with various diseases. For instance, tyrosine metabolism disorders can disrupt neurotransmitter balance, potentially leading to depression or stress-related disorders; elevated ADMA (asymmetric dimethylarginine) levels can inhibit nitric oxide synthesis, increasing the risk of cardiovascular diseases; carnitine deficiency is linked to certain genetic muscle disorders, impairing fat metabolism and energy production. Additionally, HMB may help slow muscle loss under specific conditions, while taurine intake is associated with improved cardiovascular health. Although some of the effects of these derivatives remain debated, they hold significant potential applications in sports nutrition, neurological regulation, and metabolic health.

Amino Acid Derivatives Related Products (1590):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-W000843
    (2S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(tert-butoxy)butanoic acid
    99.75%
    (2S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(tert-butoxy)butanoic acid is a threonine derivative.
    (2S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(tert-butoxy)butanoic acid
  • HY-W041992
    Fmoc-β-cyclopropyl-L-Alanine
    99.89%
    Fmoc-β-cyclopropyl-L-Alanine is an alanine derivative.
    Fmoc-β-cyclopropyl-L-Alanine
  • HY-W053705
    (S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-2,5-dihydro-1H-pyrrole-2-carboxylic acid
    98.52%
    (S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-2,5-dihydro-1H-pyrrole-2-carboxylic acid is a proline derivative.
    (S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-2,5-dihydro-1H-pyrrole-2-carboxylic acid
  • HY-W014259
    (S)-2-((tert-Butoxycarbonyl)amino)pent-4-ynoic acid
    (S)-2-((tert-Butoxycarbonyl)amino)pent-4-ynoic acid is a Glycine (HY-Y0966) derivative. (S)-2-((tert-Butoxycarbonyl)amino)pent-4-ynoic acid is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    (S)-2-((tert-Butoxycarbonyl)amino)pent-4-ynoic acid
  • HY-W013185
    Fmoc-β-HoVal-OH
    98.84%
    Fmoc-β-HoVal-OH is a valine derivative.
    Fmoc-β-HoVal-OH
  • HY-137875
    Hippuryl-His-Leu-OH hydrate
    99.58%
    Hippuryl-His-Leu-OH (N-Benzoyl-Gly-His-Leu) hydrate is a substrate for detecting the activity of angiotensin I converting enzyme. The His-Leu released by Hippuryl-His-Leu-OH hydrate can react with o-phtbaldialdehyde or Fluorescamine (HY-D0715) for fluorescence detection.
    Hippuryl-His-Leu-OH hydrate
  • HY-W011081
    Fmoc-Glu-OH
    99.41%
    Fmoc-Glu-OH is a glutamic acid derivative.
    Fmoc-Glu-OH
  • HY-131095
    Z-Glu-Tyr-OH
    99.17%
    Z-Glu-Tyr-OH can be used for synthesis of peptides on a solid support.
    Z-Glu-Tyr-OH
  • HY-N7403
    N-(3-Phenylpropionyl)glycine
    99.65%
    N-(3-Phenylpropionyl)glycine is a Glycine (HY-Y0966) derivative.
    N-(3-Phenylpropionyl)glycine
  • HY-W007720
    Fmoc-Ser-OH
    99.43%
    Fmoc-Ser-OH is a serine derivative.
    Fmoc-Ser-OH
  • HY-W005891
    H-D-Glu-OtBu
    ≥98.0%
    H-D-Glu-OtBu is a glutamic acid derivative.
    H-D-Glu-OtBu
  • HY-W006152
    (S)-Methyl 3-amino-2-((tert-butoxycarbonyl)amino)propanoate hydrochloride
    ≥98.0%
    (S)-Methyl 3-amino-2-((tert-butoxycarbonyl)amino)propanoate hydrochloride is an alanine derivative.
    (S)-Methyl 3-amino-2-((tert-butoxycarbonyl)amino)propanoate hydrochloride
  • HY-W016427
    H-Leu-OMe.HCl
    ≥98.0%
    H-Leu-OMe.HCl is a leucine derivative.
    H-Leu-OMe.HCl
  • HY-W013154
    Fmoc-Tic-OH
    99.83%
    Fmoc-Tic-OH is an amino acid derivative with an Fmoc protecting group, which can be used to synthesize bioactive peptide mimetics, such as the biotinylated derivative of the opioid receptor antagonist TIPP.
    Fmoc-Tic-OH
  • HY-P4093
    Cys-Penetratin
    99.94%
    Cys-Penetratin is a cell-penetrating peptide (CPP) with sequence of CRQIKIWFQNRRMKWKK.
    Cys-Penetratin
  • HY-W018062
    H-Sar-OtBu.HCl
    ≥98.0%
    H-Sar-OtBu.HCl is a Glycine (HY-Y0966) derivative.
    H-Sar-OtBu.HCl
  • HY-W014048
    Boc-N-Me-Ser-OH
    ≥98.0%
    Boc-N-Me-Ser-OH is a serine derivative.
    Boc-N-Me-Ser-OH
  • HY-W010724
    Fmoc-D-Cys(Trt)-OH
    99.37%
    Fmoc-D-Cys(Trt)-OH is a cysteine derivative.
    Fmoc-D-Cys(Trt)-OH
  • HY-22002
    N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-5-methyl-L-norleucine
    99.50%
    N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-5-methyl-L-norleucine is a leucine derivative.
    N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-5-methyl-L-norleucine
  • HY-Y0754
    Methyl L-histidinate dihydrochloride
    Methyl L-histidinate dihydrochloride is a histidine derivative.
    Methyl L-histidinate dihydrochloride