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219096

Sigma-Aldrich

D-Aspartic acid

99%, for peptide synthesis, ReagentPlus®

Sinonimo/i:

(R)-(−)-Aminosuccinic acid, (R)-2-Aminosuccinic acid

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About This Item

Formula condensata:
HO2CCH2CH(NH2)CO2H
Numero CAS:
1783-96-6
Peso molecolare:
133.10
Beilstein:
1723529
Numero CE:
217-234-6
Numero MDL:
MFCD00063081
Codice UNSPSC:
12352209
ID PubChem:
24853106
NACRES:
NA.22

Nome del prodotto

D-Aspartic acid, ReagentPlus®, 99%

Livello qualitativo

100

Nome Commerciale

ReagentPlus®

Saggio

99%

Stato

powder

Attività ottica

[α]20/D −24°, c = 2.3 in 6 M HCl

Purezza ottica

ee: 98% (GLC)

Impiego in reazioni chimiche

reaction type: solution phase peptide synthesis

Punto di fusione

>300 °C (lit.)

applicazioni

peptide synthesis

Stringa SMILE

N[C@H](CC(O)=O)C(O)=O

InChI

1S/C4H7NO4/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H,6,7)(H,8,9)/t2-/m1/s1
CKLJMWTZIZZHCS-UWTATZPHSA-N

Informazioni sul gene

rat ... Slc1a3(29483)

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Applicazioni


  • Metabolomics Analysis Identifies Differential Metabolites as Biomarkers for Acute Myocardial Infarction.: This study utilizes metabolomics to identify biomarkers for acute myocardial infarction, showcasing D-Aspartic acid′s role in amino acid metabolism and potential diagnostic applications. (Zhou et al., 2024).

Note legali

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Applicazioni

N° Catalogo
Descrizione
Determinazione del prezzo

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
WXBD4935V
WXBD2967V
MKCK2078
MKCG5712
MKCC0521

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Sigma-Aldrich

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D-Glutamine ≥98% (HPLC)

Sigma-Aldrich

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D-Glutamine

Noriko Fujii et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 879(29), 3141-3147 (2011-07-05)
Homochirality is essential for life. L-Amino acids are exclusively used as substrates for the polymerization and formation of peptides and proteins in living systems. However, d-amino acids, which are enantiomers of L-amino acids, were recently detected in various living organisms
Yuhei Mori et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 879(29), 3303-3309 (2011-06-04)
UV-B irradiation is one of the risk factors in age-related diseases. We have reported that biologically uncommon D-β-Asp residues accumulate in proteins from sun-exposed elderly human skin. A previous study also reported that carboxymethyl lysine (CML; one of the advanced
Ikuhiko Noji et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 879(29), 3310-3316 (2011-07-12)
Unusual amino acid residues such as L-β-aspartyl (Asp), D-α-Asp, and D-β-Asp have been detected in proteins and peptides such as α-crystallin in the lens and β-amyloid in the brain. These residues increase with age, and hence they are associated with
H Homma
Amino acids, 32(1), 3-11 (2006-06-07)
Recent investigations have shown that D-aspartate (D-Asp) plays an important physiological role(s) in the mammalian body. Here, several recent studies of free D-Asp metabolism in mammals, focusing on cellular localization in tissues, intracellular localization, biosynthesis, efflux, uptake and degradation are
Tadatoshi Kinouchi et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 879(29), 3349-3352 (2011-09-29)
The formation and accumulation of D-aspartate residue (D-Asp) in proteins caused by oxidative stress leads to dysfunction and/or denaturation of proteins, and is consequently responsible for aging-related misfolding diseases such as cataracts, prion disease, and Alzheimer's disease. We sought to
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