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CasNo: 1783-96-6
MF: C4H7NO4
Appearance: White or almost white crystalline powder
Biological Activity |
Endogenous NMDA receptor agonist with similar activity to the L-isomer (L-Aminosuccinic acid ). Also a non-metabolizable substrate for EAA uptake systems. Modulates melatonin synthesis in the pineal gland. |
Definition |
ChEBI: The D-enantiomer of aspartic acid. |
InChI:InChI=1/C8H12N2O8/c9-8(7(17)18,2-5(13)14)10-3(6(15)16)1-4(11)12/h3,10H,1-2,9H2,(H,11,12)(H,13,14)(H,15,16)(H,17,18)/t3?,8-/m1/s1
Microbial l-asparaginases which catalyze...
Human renal dipeptidase, an enzyme assoc...
All experimental procedures discussed co...
An age of a man from an ancient burial m...
Small-molecule chemistry and biochemical...
The kinetics of a racemization reaction ...
DL-Aspartic acid was resolved with high ...
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Human amyloid-β peptide 1-42 (Aβ) was su...
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We herein show the chiral recognition an...
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L-Aspartate oxidase from the thermophili...
Stereoselective inhibition of the nuclea...
Two new bromopyrrole peptides, haloircin...
Structure-guided engineering of Pseudomo...
In order to use the enantioseparation ca...
(R)-Asparagine
(2R)-aspartic acid
Conditions | Yield |
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With hydrogenchloride;
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With hydrogenchloride; at 85 ℃; for 19h;
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With hydrogenchloride; water; In methanol; at 110 ℃; for 24h; Inert atmosphere; Sealed tube;
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With L-asparaginase from Thermococcus gammatolerans EJ3; In aq. buffer; at 85 ℃; pH=8.5; pH-value; Solvent; Temperature; Kinetics; Enzymatic reaction;
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aspartic Acid
(2R)-aspartic acid
Conditions | Yield |
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durch Spaltung;
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With L-glutamic acid;
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mit Hilfe eines Enzym-Praeparats aus Crotalus adamanteus;
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man bringt die Pilze, mit denen sich eine Loesung von l-Asparaginsaeure beim Stehen an der Luft bedeckt, auf eine Loesung von dl-Asparaginsaeure;
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(R)-Asparagine
aspartic Acid
bromosuccinic acid
2-aminosuccinic acid diethyl ester
aspartic Acid
N-[(2,4,5-trichloro-phenoxy)-acetyl]-D-aspartic acid
N-[(4-chloro-2-methyl-phenoxy)-acetyl]-D-aspartic acid
N-[(2,4-dichloro-phenoxy)-acetyl]-D-aspartic acid