Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C4H7N2O3.Na |
Molecular Weight | 154.0997 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].N[C@@H](CC(N)=O)C([O-])=O
InChI
InChIKey=HKCPSLRXMHNTBX-DKWTVANSSA-M
InChI=1S/C4H8N2O3.Na/c5-2(4(8)9)1-3(6)7;/h2H,1,5H2,(H2,6,7)(H,8,9);/q;+1/p-1/t2-;/m0./s1
Molecular Formula | Na |
Molecular Weight | 22.9898 |
Charge | 1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C4H7N2O3 |
Molecular Weight | 131.11 |
Charge | -1 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Asparagine is a non-essential amino acid, which is synthesized in the human body from L-aspartate by Asparagine synthetase. Asparagine is required for the synthesis of many important cellular proteins in normal human cells. Many tumor cells do not have this capacity, due to a lack of the enzyme L-asparagine synthetase, and therefore require an exogenous supply of the amino acid. This amino acid participates in the functions of the brain and nervous system. Asparagine may come from food or be taken as a dietary supplement.
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Asparagine in blood plasma. | 1953 Jun 20 |
|
Diminished phenylketonuria in phenylpyruvic oligophrenia after administration of L-glutamine, L-glutamate or L-asparagine. | 1956 Jun |
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L-asparaginase and L-asparagine metabolism. | 1970 |
|
Mass spectrometric analysis of asparagine deamidation and aspartate isomerization in polypeptides. | 2010 Jun |
Sample Use Guides
500 mg or 1 capsule daily as a dietary supplement or as recommended by a healthcare practitioner.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/27126896
HeLa cells were treated with 0.1 mM asparagine and at this concentration, the amino acid promoted cancer cell proliferation in 3 times.
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 19:10:49 GMT 2023
by
admin
on
Sat Dec 16 19:10:49 GMT 2023
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Record UNII |
4JPN99S4S5
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Record Status |
Validated (UNII)
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Record Version |
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100000126281
Created by
admin on Sat Dec 16 19:10:49 GMT 2023 , Edited by admin on Sat Dec 16 19:10:49 GMT 2023
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ACTIVE MOIETY |
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