1. Signaling Pathways
  2. Others
  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 (1560):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-W008016
    Fmoc-Tyr(tBu)-OH
    99.93%
    Fmoc-Tyr(tBu)-OH is a tyrosine derivative.
    Fmoc-Tyr(tBu)-OH
  • HY-P4632
    H-γ-Glu-Leu-OH
    99.67%
    H-γ-Glu-Leu-OH is a dipeptide consisting of γ-glutamic acid and leucine, terminated by a hydroxyl group.
    H-γ-Glu-Leu-OH
  • HY-W007706
    Fmoc-Thr(tBu)-OH
    99.92%
    Fmoc-Thr(tBu)-OH is a threonine derivative.
    Fmoc-Thr(tBu)-OH
  • HY-W007798
    Fmoc-Cys(Trt)-OH
    99.98%
    Fmoc-Cys(Trt)-OH is a cysteine derivative.
    Fmoc-Cys(Trt)-OH
  • HY-19821
    Fmoc-Ile-OH
    99.96%
    Fmoc-Ile-OH is an isoleucine derivative.
    Fmoc-Ile-OH
  • HY-101552A
    L,L-Dityrosine
    99.80%
    L,L-Dityrosine (o,o'-Dityrosine) is a constituent of acid hydrolysates of a number of biological materials, including the insect cuticular resilin.
    L,L-Dityrosine
  • HY-W041987
    Fmoc-L-Lys(Dde)-OH
    99.76%
    Fmoc-L-Lys(Dde)-OH is a lysine derivative.
    Fmoc-L-Lys(Dde)-OH
  • HY-W010836
    Fmoc-Bip(4,4')-OH
    99.76%
    Fmoc-Bip(4,4')-OH is an alanine derivative.
    Fmoc-Bip(4,4')-OH
  • HY-W011210
    Fmoc-Pra-OH
    99.93%
    Fmoc-Pra-OH is a Glycine (HY-Y0966) derivative. Fmoc-Pra-OH is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    Fmoc-Pra-OH
  • HY-Y1166
    N-(9-Fluorenylmethoxycarbonyl)glutamic acid α-tert-butyl ester
    99.93%
    N-(9-Fluorenylmethoxycarbonyl)glutamic acid α-tert-butyl ester is a glutamic acid derivative.
    N-(9-Fluorenylmethoxycarbonyl)glutamic acid α-tert-butyl ester
  • HY-I1111
    Fmoc-L-Val-OH
    99.93%
    Fmoc-L-Val-OH is a valine derivative.
    Fmoc-L-Val-OH
  • HY-W007941
    Fmoc-Ser(tBu)-OH
    99.98%
    Fmoc-Ser(tBu)-OH is a serine derivative.
    Fmoc-Ser(tBu)-OH
  • HY-79131
    Fmoc-Phe-OH
    99.90%
    Fmoc-Phe-OH is a phenylalanine derivative.
    Fmoc-Phe-OH
  • HY-W010714
    Fmoc-D-Gln(Trt)-OH
    99.76%
    Fmoc-D-Gln(Trt)-OH is a glutamine derivative.
    Fmoc-D-Gln(Trt)-OH
  • HY-Y0511
    N,N-Dimethylglycine
    ≥98.0%
    N,N-Dimethylglycine (Dimethylglycine), a natural N-methylated glycine, is a nutrient supplement and acts as an NMDAR glycine site partial agonist. N,N-Dimethylglycine is a methyl donor that can improve immunity, act as an antioxidant to prevent oxidative stress, and scavenge excess free radicals. N,N-Dimethylglycine has antidepressant-like and surfactant effects.
    N,N-Dimethylglycine
  • HY-W008876
    Fmoc-Pen(Trt)-OH
    99.93%
    Fmoc-Pen(Trt)-OH is an amino acid derivative with an Fmoc protecting group that can be used to synthesize the inhibitory cystine knot (ICK) peptide ProTx-II.
    Fmoc-Pen(Trt)-OH
  • HY-W010712
    Fmoc-His(Trt)-OH
    99.88%
    Fmoc-His (Trt)-OH is a histidine derivative. Fmoc-His(Trt)-OH has trityl (Trt) group to protect the side-chain of His. Fmoc-His(Trt)-OH has Fmoc group to protect -αNH2. Fmoc-His(Trt)-OH can be used for solid phase synthesis of peptides, providing protection against racemization and by-product formation.
    Fmoc-His(Trt)-OH
  • HY-W008079
    (S)-2-Amino-6-((tert-butoxycarbonyl)amino)hexanoic acid
    ≥98.0%
    (S)-2-Amino-6-((tert-butoxycarbonyl)amino)hexanoic acid is a lysine derivative.
    (S)-2-Amino-6-((tert-butoxycarbonyl)amino)hexanoic acid
  • HY-W010862
    Fmoc-Lys(Alloc)-OH
    99.77%
    Fmoc-Lys(Alloc)-OH is a lysine derivative.
    Fmoc-Lys(Alloc)-OH
  • HY-W004864
    Fmoc-(S)-2-(4-pentenyl)Ala-OH
    99.92%
    Fmoc-(S)-2-(4-pentenyl)Ala-OH is an amino acid derivative with an Fmoc protecting group, which can be used to synthesize biologically active secretin analogs.
    Fmoc-(S)-2-(4-pentenyl)Ala-OH