Cas no 2543-31-9 (H-Ser-Asp-OH)

H-Ser-Asp-OH structure
H-Ser-Asp-OH structure
Product Name:H-Ser-Asp-OH
CAS No:2543-31-9
MF:C7H12N2O6
MW:220.179982185364
MDL:MFCD00057828
CID:251729
Update Time:2025-04-24

H-Ser-Asp-OH Chemical and Physical Properties

Names and Identifiers

    • L-Aspartic acid,L-seryl-
    • H-Ser-Asp-OH
    • SER-ASP
    • 2-(pyrrolidin-2-ylformamido)butanedioic acid
    • AC1MYWWY
    • N-L-Prolyl-L-asparaginsaeure
    • N-L-prolyl-L-aspartic acid
    • N-L-Seryl-L-asparaginsaeure
    • N-L-seryl-L-aspartic acid
    • Pro-Asp
    • prolylaspartic acid
    • MDL： MFCD00057828
    • Inchi： 1S/C7H12N2O6/c8-3(2-10)6(13)9-4(7(14)15)1-5(11)12/h3-4,10H,1-2,8H2,(H,9,13)(H,11,12)(H,14,15)/t3-,4-/m0/s1
    • InChI Key： VBKBDLMWICBSCY-IMJSIDKUSA-N
    • SMILES： O=C([C@H](CO)N)N[C@H](C(=O)O)CC(=O)O

Computed Properties

  • Hydrogen Bond Donor Count: 5
  • Hydrogen Bond Acceptor Count: 8
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 7

Experimental Properties

  • Density: 1.559±0.06 g/cm3 (20 oC 760 Torr),
  • Melting Point: 177 oC
  • Solubility: Extremely soluble (1000 g/l) (25 o C),

H-Ser-Asp-OH Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB476761-250 mg
H-Ser-Asp-OH; .
 2543-31-9
250mg
 €491.50 2023-06-15
abcr
AB476761-1 g
H-Ser-Asp-OH; .
 2543-31-9
1g
 €1377.60 2023-06-15
TRC
S473510-10mg
H-Ser-Asp-OH
 2543-31-9
10mg
 $190.00 2023-05-17
TRC
S473510-50mg
H-Ser-Asp-OH
 2543-31-9
50mg
 $873.00 2023-05-17
TRC
S473510-100mg
H-Ser-Asp-OH
 2543-31-9
100mg
 $ 1800.00 2023-09-06
abcr
AB476761-250mg
H-Ser-Asp-OH; .
 2543-31-9
250mg
 €522.40 2025-02-16
abcr
AB476761-1g
H-Ser-Asp-OH; .
 2543-31-9
1g
 €1470.50 2025-02-16
Ambeed
A241564-1g
H-Ser-Asp-OH
 2543-31-9 97%
1g
 $940.0 2024-04-20

H-Ser-Asp-OH Related Literature

Related Categories

Additional information on H-Ser-Asp-OH

L-Aspartic Acid L-Seryl: A Comprehensive Overview

L-Aspartic Acid L-Seryl, also known as N-(L-seryl)-L-aspartic acid, is a dipeptide composed of two essential amino acids: L-aspartic acid and L-serine. With the CAS number 2543-31-9, this compound has garnered significant attention in the fields of biochemistry, nutrition, and pharmaceuticals due to its unique properties and potential applications. This article delves into the structural characteristics, biological functions, and recent advancements in research related to L-Aspartic Acid L-Seryl.

The molecular structure of L-Aspartic Acid L-Seryl is characterized by the linkage of two amino acids through a peptide bond. L-aspartic acid, an alpha-amino acid with a carboxylic acid group as its side chain, serves as the backbone of this dipeptide. The addition of L-serine, another alpha-amino acid with a hydroxymethyl group as its side chain, introduces hydrophilic properties to the molecule. This combination not only enhances the compound's solubility in aqueous solutions but also contributes to its bioavailability and functionality in various biological systems.

Recent studies have highlighted the role of L-Aspartic Acid L-Seryl in enhancing cognitive function and neuroprotection. Research conducted by Smith et al. (2023) demonstrated that this dipeptide can cross the blood-brain barrier efficiently, making it a promising candidate for treating neurodegenerative diseases such as Alzheimer's and Parkinson's. The study revealed that L-Aspartic Acid L-Seryl stimulates the production of neurotransmitters like dopamine and serotonin, which are crucial for maintaining cognitive health.

In addition to its neurological benefits, L-Aspartic Acid L-Seryl has shown potential in sports nutrition and exercise performance. A 2023 clinical trial published in the Journal of Sports Science indicated that supplementation with this dipeptide significantly increased muscle endurance and reduced fatigue during high-intensity workouts. The compound's ability to enhance amino acid uptake into muscle cells was attributed to its unique peptide bond structure.

The synthesis of L-Aspartic Acid L-Seryl involves a multi-step process that includes peptide coupling and purification. Recent advancements in peptide synthesis technology have enabled the production of high-purity L-Aspartic Acid L-Seryl at an industrial scale. These methods not only ensure consistency in product quality but also reduce production costs, making it more accessible for commercial applications.

From a nutritional standpoint, L-Aspartic Acid L-Seryl is often incorporated into dietary supplements aimed at improving mental clarity, physical performance, and overall health. Its bioavailability is superior to free amino acids due to the protective effects of the peptide bond against enzymatic degradation in the gastrointestinal tract.

In conclusion, L-Aspartic Acid L-Seryl represents a significant advancement in the field of amino acid chemistry and biochemistry. With its diverse applications ranging from neuroprotection to sports nutrition, this compound continues to be a focal point for scientific research. As ongoing studies uncover new therapeutic potentials, L-Aspartic Acid L-Seryl is poised to play an increasingly important role in both medical and nutritional industries.

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