Detail Information

Number mr1438
Declustering Potential(DP) 20
Collision Energy(CE) 20
Observed mass(Da)
Exact mass(Da)
Accurate mass error(ppm)
Molecular formula
Ionization model
Ret. Time(min) 1.72
Precursor ions(Q1) 133.0
Product ions(Q3) 74.0
Main fragments 74.0, 123.1, 112.1, 83.1
Compound L-Asparagine
Identification standard
class Amino acid
Organism
Reference
CV(%) 66.46
H2 0.75
ChEBI_ID CHEBI:17196
Agricola Citation Links
ArrayExpress Database Links
BRAND Names
Beilstein Registry Numbers 1723527;;
BioModels Database Links BIOMD0000000497;;BIOMD0000000496;;BIOMD0000000473;;BIOMD0000000472;;BIOMD0000000471;;BIOMD0000000470;;BIOMD0000000469;;
CAS Registry Numbers 70-47-3;;
COMe Database Links
ChEBI ID
ChEBI Name L-asparagine;;
Charge 0;;
Chinese Abstracts Citation Links
CiteXplore Citation Links
Definition An optically active form of asparagine having L-configuration.;;
DrugBank Database Links DB00174;;
Formulae C4H8N2O3;;
Gmelin Registry Numbers 3334;;
INN
IUPAC Names L-asparagine;;
InChI InChI=1S/C4H8N2O3/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H2,6,7)(H,8,9)/t2-/m0/s1;;
InChIKey DCXYFEDJOCDNAF-REOHCLBHSA-N;;
IntAct Database Links
IntEnz Database Links
KEGG COMPOUND Database Links
KEGG DRUG Database Links
KEGG GLYCAN Database Links
LIPID MAPS class Database Links
LIPID MAPS instance Database Links
Last Modified 27 Jan 2016;;
Mass 132.11800;;
MolBase Database Links
PDBeChem Database Links ASN;;
Patent Database Links WO2007097934;;WO2006086484;;WO2006004433;;WO2005010160;;US2007219157;;US2007202058;;US2007197430;;US2006223760;;US2005130881;;US2005085547;;US2004034080;;GB1585736;;EP1983044;;EP1938798;;EP1869977;;EP1762232;;EP1627884;;EP1616963;;EP1609462;;EP1568283;;EP
PubChem Database Links 8144629;;
PubMed Central Citation Links
PubMed Citation Links 7914846;;6198473;;24027187;;22513289;;21854356;;21800258;;19309105;;19212411;;18502700;;18052033;;17497286;;16844612;;16668324;;16368161;;16239337;;16190636;;16027730;;15911239;;15907185;;15875186;;15849197;;15835923;;15828851;;15284236;;15270080;;1499229
RESID Database Links
Reactome Database Links R-HSA-983162;;R-HSA-983158;;R-HSA-983150;;R-HSA-70599;;R-HSA-428007;;R-HSA-427998;;R-HSA-380227;;R-HSA-379996;;R-HSA-352191;;R-HSA-352182;;R-HSA-352174;;R-HSA-352119;;R-HSA-352108;;R-HSA-352059;;R-HSA-1247939;;R-HSA-1247927;;R-HSA-1247912;;R-HSA-1236970;;
Rhea Database Links
SABIO-RK Database Links 98;;917;;6996;;3220;;286;;1658;;1483;;13466;;10043;;
SMILES N[C@@H](CC(N)=O)C(O)=O;;
Secondary ChEBI ID CHEBI:21242;;CHEBI:13083;;CHEBI:6191;;CHEBI:40902;;
Star 3;;
Synonyms alpha-aminosuccinamic acid;;alpha-Aminosuccinamate;;alpha Amminosuccinamic acid;;alpha Amminosuccinamate;;a-Aminosuccinamic acid;;a-Aminosuccinamate;;N;;L-beta-Asparagine;;L-b-Asparagine;;L-aspartic acid beta-amide;;L-Aspartamine;;L-Asparagin;;L-2-aminosu
UM-BBD compID Database Links
UniProt Database Links U6BLZ9;;U6A629;;Q9ZZX1;;Q9ZWQ7;;Q9ZWA9;;Q9ZWA6;;Q9ZVX8;;Q9ZVC7;;Q9ZVC2;;Q9ZV65;;Q9ZV07;;Q9ZUA0;;Q9ZSD6;;Q9ZRA3;;Q9ZQC5;;Q9ZPY0;;Q9ZNT9;;Q9ZNQ8;;Q9ZMF4;;Q9ZLT1;;Q9ZLH6;;Q9ZLB9;;Q9ZKM6;;Q9ZE11;;Q9ZE09;;Q9ZCK8;;Q9Z9X0;;Q9Z9G8;;Q9Z9G6;;Q9Z8W5;;Q9Z581;;Q9Z578;
ChEBI Image