Basic information
- Standard 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[C@H]4[C@H](O)[C@@H](O)[C@@H](O[C@H]5[C@H](O)[C@@H](O)[C@@H](O[C@H]6[C@H](O)[C@@H](O)C(O)O[C@@H]6CO)O[C@@H]5CO)O[C@@H]4CO)O[C@@H]3CO)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O- InChIKey
OCIBBXPLUVYKCH-LIGGPISVSA-N- Molecular formula
- C36H62O31
- Average molar mass
- 990.9 g/mol
Overview
Alpha-D-Glcp-(1->4)-alpha-D-Glcp-(1->4)-alpha-D-Glcp-(1->4)-alpha-D-Glcp-(1->4)-alpha-D-Glcp-(1->4)-D-Glcp is a maltohexaose hexasaccharide consisting of five alpha-D-glucopyranose residues and a D-glucopyranose residue joined in sequence by (14) glycosidic bonds.
Names & identifiers
- Preferred name
- alpha-D-Glcp-(1->4)-alpha-D-Glcp-(1->4)-alpha-D-Glcp-(1->4)-alpha-D-Glcp-(1->4)-alpha-D-Glcp-(1->4)-D-Glcp
- IUPAC
- (2R,3R,4S,5S,6R)-2-[(2R,3S,4R,5R,6R)-6-[(2R,3S,4R,5R,6R)-6-[(2R,3S,4R,5R,6R)-6-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2R,3S,4R,5R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
Names & synonyms
CHEBI:143182alpha-D-Glcp-(1->4)-alpha-D-Glcp-(1->4)-alpha-D-Glcp-(1->4)-alpha-D-Glcp-(1->4)-alpha-D-Glcp-(1->4)-D-GlcpRefChem:644330GlyTouCan:G03116ETG03116ETD-maltohexaoseMFCD00083650AmylohexaoseI<<-Maltohexaoseorb1220737SCHEMBL21752778Maltohexaose, >=65% (HPLC)
Show more names
MSK3264AKOS024319624OM06869AC-34522SY009619NS00074221C01936Glc(a1-4)Glc(a1-4)Glc(a1-4)Glc(a1-4)Glc(a1-4)Glc
Database identifiers
- PubChem CID
- 439606
- ChEBI
CHEBI:143182
Properties
Computed structural properties
- XLogP
- -13.3
- Topological polar surface area
- 506 Ų
- Hydrogen bond donors
- 20
- Hydrogen bond acceptors
- 31
- Rotatable bonds
- 16
- Heavy atoms
- 67
- Formal charge
- 0
- Complexity
- 1,510
Experimental & physicochemical properties
Collision Cross Section
279.97 Ų [M-H]- [CCS Type: DT; Method: stepped-field]
281.5 Ų [M+Na]+
Related reactions
1 records
Compound notes
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