Detail Information

Number qtl-m1155
Declustering Potential(DP)
Collision Energy(CE)
Observed mass(Da)
Exact mass(Da)
Accurate mass error(ppm)
Molecular formula
Ionization model
Ret. Time(min)
Precursor ions(Q1) 181.1
Product ions(Q3) 135.1
Main fragments
Compound D-Mannosamine
Identification putative
class
Organism
Reference
CV(%)
H2
ChEBI_ID CHEBI:27503
Agricola Citation Links
ArrayExpress Database Links
BRAND Names
Beilstein Registry Numbers
BioModels Database Links
CAS Registry Numbers 2636-92-2;;14307-02-9;;
COMe Database Links
ChEBI ID
ChEBI Name aldehydo-D-mannosamine;;
Charge 0;;
Chinese Abstracts Citation Links
CiteXplore Citation Links
Definition A D-mannosamine in open-chain aldehydo-form.;;
DrugBank Database Links
Formulae C6H13NO5;;
Gmelin Registry Numbers
INN
IUPAC Names 2-amino-2-deoxy-D-mannose;;
InChI InChI=1S/C6H13NO5/c7-3(1-8)5(11)6(12)4(10)2-9/h1,3-6,9-12H,2,7H2/t3-,4-,5-,6-/m1/s1;;
InChIKey FZHXIRIBWMQPQF-KVTDHHQDSA-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 16 Jun 2014;;
Mass 179.17110;;
MolBase Database Links
PDBeChem Database Links
Patent Database Links WO2008142155;;US2007270496;;EP1995323;;EP1844784;;EP1731132;;
PubChem Database Links 8144501;;
PubMed Central Citation Links
PubMed Citation Links 20096904;;19309147;;16076127;;12596851;;
RESID Database Links
Reactome Database Links
Rhea Database Links
SABIO-RK Database Links 13590;;11631;;
SMILES [H]C(=O)[C@@H](N)[C@@H](O)[C@H](O)[C@H](O)CO;;
Secondary ChEBI ID CHEBI:4207;;CHEBI:21055;;
Star 3;;
Synonyms Manosamine;;D-ManN;;D-(+)-Mannosamine;;2-amino-2-deoxymannose;;
UM-BBD compID Database Links
UniProt Database Links P86922;;
ChEBI Image