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M  END
> <ID>
CHEBI:27931

> <NAME>
alpha-maltotriose

> <DEFINITION>
A maltotriose trisaccharide in which the glucose residue at the reducing end is in the pyranose ring form and has α configuration at the anomeric carbon atom..

> <STAR>
3

> <SECONDARY_ID>
CHEBI:43937; CHEBI:6672; CHEBI:25146

> <SYNONYM>
MALTOTRIOSE; Maltotriose; Amylotriose; alpha-maltotriose; alpha-D-Glcp-(1->4)-alpha-D-Glcp-(1->4)-alpha-D-Glcp

> <IUPAC_NAME>
alpha-D-glucopyranosyl-(1->4)-alpha-D-glucopyranosyl-(1->4)-alpha-D-glucopyranose

> <FORMULA>
C18H32O16; C18H32O16

> <MASS>
504.43710

> <MONOISOTOPIC_MASS>
504.16903

> <CHARGE>
0

> <SMILES>
OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@@H](O[C@H]3[C@H](O)[C@@H](O)[C@@H](O)O[C@@H]3CO)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O

> <INCHI>
InChI=1S/C18H32O16/c19-1-4-7(22)8(23)12(27)17(31-4)34-15-6(3-21)32-18(13(28)10(15)25)33-14-5(2-20)30-16(29)11(26)9(14)24/h4-29H,1-3H2/t4-,5-,6-,7-,8+,9-,10-,11-,12-,13-,14-,15-,16+,17-,18-/m1/s1

> <INCHIKEY>
FYGDTMLNYKFZSV-PXXRMHSHSA-N

> <BEILSTEIN_REGISTRY_NUMBER>
1275025

> <DRUGBANK_ACCESSION>
DB03277

> <KEGG_COMPOUND_ACCESSION>
C01835

> <PDBECHEM_ACCESSION>
MLR

$$$$