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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 (1536):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-79165
    (2S)-2-[(tert-Butoxycarbonyl)amino]-3-(3,4-difluorophenyl)propionic acid
    98.02%
    (2S)-2-[(tert-Butoxycarbonyl)amino]-3-(3,4-difluorophenyl)propionic acid is a phenylalanine derivative.
    (2S)-2-[(tert-Butoxycarbonyl)amino]-3-(3,4-difluorophenyl)propionic acid
  • HY-W040432
    (S)-3-Amino-4-hydroxybutanoic acid
    (S)-3-Amino-4-hydroxybutanoic acid is a serine derivative.
    (S)-3-Amino-4-hydroxybutanoic acid
  • HY-W027251
    DL-Lysine Monohydrochloride
    DL-Lysine Monohydrochloride is a lysine derivative.
    DL-Lysine Monohydrochloride
  • HY-Y1856
    N-(tert-Butoxycarbonyl)-N-methyl-D-alanine
    N-(tert-Butoxycarbonyl)-N-methyl-D-alanine is an alanine derivative.
    N-(tert-Butoxycarbonyl)-N-methyl-D-alanine
  • HY-23185
    N-((Benzyloxy)carbonyl)-O-(tert-butyl)-L-threonine
    99.89%
    N-((Benzyloxy)carbonyl)-O-(tert-butyl)-L-threonine is a threonine derivative.
    N-((Benzyloxy)carbonyl)-O-(tert-butyl)-L-threonine
  • HY-W142073
    7-Methyl-DL-tryptophan
    99.52%
    7-Methyl-DL-tryptophan (7-Methyltryptophan) is an amino acid derivative, which is a key precursor for biosynthesis of many non-ribosomal peptide antibiotics. 7-Methyl-DL-tryptophan plays an important role in synthesis of high-efficiency antibacterial agents and analogues thereof.
    7-Methyl-DL-tryptophan
  • HY-W009630
    (R)-2-Amino-3-(3-(trifluoromethyl)phenyl)propanoic acid
    (R)-2-Amino-3-(3-(trifluoromethyl)phenyl)propanoic acid is a phenylalanine derivative.
    (R)-2-Amino-3-(3-(trifluoromethyl)phenyl)propanoic acid
  • HY-W003985
    N-Boc-3-(2-pyridyl)-L-alanine
    N-Boc-3-(2-pyridyl)-L-alanine is an alanine derivative.
    N-Boc-3-(2-pyridyl)-L-alanine
  • HY-W141842
    3-(2-Thienyl)-DL-alanine
    99.79%
    3-(2-Thienyl)-DL-alanine is an alanine derivative.
    3-(2-Thienyl)-DL-alanine
  • HY-W141918
    Gly-Leu-Tyr
    Gly-Leu-Tyr is a Glycine (HY-Y0966) derivative.
    Gly-Leu-Tyr
  • HY-W048722
    Fmoc-D-Thi-OH
    99.05%
    Fmoc-D-Thi-OH (Fmoc-D-2-Thienylalanine) is an amino acid derivative with an Fmoc protecting group, which can be used to synthesize AS-Z-P with thrombin inhibitory activity.
    Fmoc-D-Thi-OH
  • HY-Y0555A
    D-N-(Benzyloxycarbonyl)leucine
    99.05%
    D-N-(Benzyloxycarbonyl)leucine is a leucine derivative.
    D-N-(Benzyloxycarbonyl)leucine
  • HY-W007875
    Boc-Glu-OBzl
    Boc-Glu-OBzl is a glutamic acid derivative.
    Boc-Glu-OBzl
  • HY-W016340
    2-Amino-3-(4-fluorophenyl)propanoic acid
    ≥98.0%
    2-Amino-3-(4-fluorophenyl)propanoic acid is a phenylalanine derivative.
    2-Amino-3-(4-fluorophenyl)propanoic acid
  • HY-W016035
    (R)-3-(4-Bromophenyl)-3-((tert-butoxycarbonyl)amino)propanoic acid
    (R)-3-(4-Bromophenyl)-3-((tert-butoxycarbonyl)amino)propanoic acid is a phenylalanine derivative.
    (R)-3-(4-Bromophenyl)-3-((tert-butoxycarbonyl)amino)propanoic acid
  • HY-W014917
    H-D-Met-OMe.HCl
    H-D-Met-OMe.HCl is a Methionine (HY-13694) derivative.
    H-D-Met-OMe.HCl
  • HY-79417
    (S)-N-Methyl-N-methoxy-2-(tert-butoxycarbonylamino)-4-methylpentanamide
    (S)-N-Methyl-N-methoxy-2-(tert-butoxycarbonylamino)-4-methylpentanamide is a leucine derivative.
    (S)-N-Methyl-N-methoxy-2-(tert-butoxycarbonylamino)-4-methylpentanamide
  • HY-W008179
    Z-Ser-OMe
    98.98%
    Z-Ser-OMe is a serine derivative.
    Z-Ser-OMe
  • HY-41912B
    Boc-D-norleucine
    ≥98.0%
    Boc-D-norleucine (Boc-D-Nle-OH) is a leucine derivative that can be used for peptide synthesis.
    Boc-D-norleucine
  • HY-P2398
    Fmoc-Phe-Ser(psi(Me,Me)pro)-OH
    99.25%
    Fmoc-Phe-Ser(psi(Me,Me)pro)-OH is a dipeptide.
    Fmoc-Phe-Ser(psi(Me,Me)pro)-OH