| Number |
qtl-m0720 |
| Declustering Potential(DP) |
40 |
| Collision Energy(CE) |
30 |
| Observed mass(Da) |
577.1552 |
| Exact mass(Da) |
577.1552 |
| Accurate mass error(ppm) |
0.03 |
| Molecular formula |
C27H28O14 |
| Ionization model |
|
| Ret. Time(min) |
|
| Precursor ions(Q1) |
577.3 |
| Product ions(Q3) |
337.1 |
| Main fragments |
337.1, 545.2, 397.2, 207.2 |
| Compound |
Maysin |
| Identification |
putative |
| class |
Flavonoid |
| Organism |
|
| Reference |
Elliger et. al (1980) |
| CV(%) |
|
| H2 |
|
| ChEBI_ID |
CHEBI:70206 |
| Agricola Citation Links |
|
| ArrayExpress Database Links |
|
| BRAND Names |
|
| Beilstein Registry Numbers |
|
| BioModels Database Links |
|
| CAS Registry Numbers |
70255-49-1;; |
| COMe Database Links |
|
| ChEBI ID |
|
| ChEBI Name |
maysin;; |
| Charge |
0;; |
| Chinese Abstracts Citation Links |
|
| CiteXplore Citation Links |
|
| Definition |
A flavone C-glycoside that is luteolin attached to a disaccharide residue at position 6. It has been isolated from natural product Petrorhagia velutina and Zea mays and exhibits insecticidal and neuroprotecti |
| DrugBank Database Links |
|
| Formulae |
C27H28O14;; |
| Gmelin Registry Numbers |
|
| INN |
|
| IUPAC Names |
(6R)-2,6-anhydro-1-deoxy-5-O-(6-deoxy-alpha-D-mannopyranosyl)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-6-yl]-D-xylo-hex-3-ulose;; |
| InChI |
InChI=1S/C27H28O14/c1-8-20(33)23(36)26(41-27-24(37)22(35)19(32)9(2)39-27)25(38-8)18-14(31)7-16-17(21(18)34)13(30)6-15(40-16)10-3-4-11(28)12(29)5-10/h3-9,19,22-29,31-32,34-37H,1-2H3/t8-,9+,19+,22-,23+,24-,25+,26-,27+/m0/s1;; |
| InChIKey |
GKLSYIMLZDYQBJ-CGOKOBCESA-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 |
LMPK12110512;; |
| Last Modified |
14 Oct 2014;; |
| Mass |
576.50280;; |
| MolBase Database Links |
|
| PDBeChem Database Links |
|
| Patent Database Links |
KR20110026271;; |
| PubChem Database Links |
160712578;; |
| PubMed Central Citation Links |
|
| PubMed Citation Links |
24928367;;24286330;;21080643;;11332855;; |
| RESID Database Links |
|
| Reactome Database Links |
|
| Rhea Database Links |
|
| SABIO-RK Database Links |
|
| SMILES |
C[C@H]1O[C@H](O[C@H]2[C@H](O)C(=O)[C@H](C)O[C@@H]2c2c(O)cc3oc(cc(=O)c3c2O)-c2ccc(O)c(O)c2)[C@@H](O)[C@@H](O)[C@@H]1O;; |
| Secondary ChEBI ID |
|
| Star |
3;; |
| Synonyms |
|
| UM-BBD compID Database Links |
|
| UniProt Database Links |
|
| ChEBI Image |
 |
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