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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-32688
    Boc-Ser-OMe
    99.11%
    Boc-Ser-OMe is a serine derivative.
    Boc-Ser-OMe
  • HY-W008029
    H-Lys(Z)-OtBu.HCl
    99.93%
    H-Lys(Z)-OtBu.HCl is a lysine derivative.
    H-Lys(Z)-OtBu.HCl
  • HY-112716
    N-alpha-Tosyl-L-lysine chloromethyl ketone hydrochloride
    ≥99.0%
    N-alpha-Tosyl-L-lysine chloromethyl ketone (TLCK), a trypsin like protease inhibitor, sensitizes HeLa cells to Fas-mediated cell death.
    N-alpha-Tosyl-L-lysine chloromethyl ketone hydrochloride
  • HY-W041867
    Boc-Ser-OtBu
    ≥98.0%
    Boc-Ser-OtBu is a serine derivative.
    Boc-Ser-OtBu
  • HY-79106
    L-Biphenylalanine
    99.95%
    L-Biphenylalanine is a phenylalanine derivative.
    L-Biphenylalanine
  • HY-W008558
    Fmoc-N-Me-Leu-OH
    99.23%
    Fmoc-N-Me-Leu-OH, an N-Fmoc-N-methyl amino acid, is available for the peptide-coupling reaction.
    Fmoc-N-Me-Leu-OH
  • HY-W013726
    Fmoc-Phe(4-Br)-OH
    99.83%
    Fmoc-Phe(4-Br)-OH is a phenylalanine derivative that can be used for compound synthesis.
    Fmoc-Phe(4-Br)-OH
  • HY-W010782
    Fmoc-Lys(Z)-OH
    99.53%
    Fmoc-Lys(Z)-OH is a lysine derivative.
    Fmoc-Lys(Z)-OH
  • HY-W019676
    Boc-Tyr-OtBu
    99.68%
    Boc-Tyr-OtBu is a tyrosine derivative.
    Boc-Tyr-OtBu
  • HY-W008021
    Fmoc-D-Leu-OH
    99.93%
    Fmoc-D-Leu-OH is a leucine derivative.
    Fmoc-D-Leu-OH
  • HY-W008694
    N-Benzoyl-L-arginine ethyl ester hydrochloride
    98.18%
    N-Benzoyl-L-arginine ethyl ester hydrochloride is an arginine derivative.
    N-Benzoyl-L-arginine ethyl ester hydrochloride
  • HY-W013714
    Fmoc-Phe(4-I)-OH
    99.63%
    Fmoc-Phe(4-I)-OH is a phenylalanine derivative.
    Fmoc-Phe(4-I)-OH
  • HY-W048207
    N6-Propionyl-L-lysine
    99.86%
    N6-Propionyl-L-lysine is a lysine derivative.
    N6-Propionyl-L-lysine
  • HY-W006886
    Fmoc-(R)-2-(7-octenyl)Ala-OH
    98.85%
    Fmoc-(R)-2-(7-octenyl)Ala-OH is an amino acid derivative with an Fmoc protecting group that can be used to synthesize inhibitor peptides that combinatorially inactivate ErbB1, ErbB2, and ErbB3.
    Fmoc-(R)-2-(7-octenyl)Ala-OH
  • HY-W008986
    Fmoc-Lys(Ac)-OH
    99.79%
    Fmoc-Lys(Ac)-OH is a lysine derivative.
    Fmoc-Lys(Ac)-OH
  • HY-W013998
    Glycyl-L-phenylalanine
    99.74%
    Glycyl-L-phenylalanine is a phenylalanine derivative.
    Glycyl-L-phenylalanine
  • HY-W141821
    Fmoc-Phe(CF2PO3)-OH
    ≥98.0%
    Fmoc-Phe(CF2PO3)-OH is a phenylalanine derivative.
    Fmoc-Phe(CF2PO3)-OH
  • HY-W141858
    N-(3-Indolylacetyl)-L-alanine
    99.91%
    N-(3-Indolylacetyl)-L-alanine (Indoleacetylalanine) is an indoleacetylamino acid. N-(3-Indolylacetyl)-L-alanine appears to increase callus growth and reduces the ability of growths to differentiate into shoots of Phalaenopsis orchids.
    N-(3-Indolylacetyl)-L-alanine
  • HY-W041989
    Fmoc-Oic-OH
    99.72%
    Fmoc-Oic-OH is an amino acid derivative with an Fmoc protecting group, which can be used to synthesize bioactive peptide mimetics, such as [desArg10]HOE 140, which has bradykinin B1 antagonist activity.
    Fmoc-Oic-OH
  • HY-W041982
    Fmoc-Asp-OMe
    99.29%
    Fmoc-Asp-OMe is an aspartic acid derivative.
    Fmoc-Asp-OMe