UCSF

ZINC04095490

Substance Information

In ZINC since Heavy atoms Benign functionality
November 7th, 2005 23 No

CAS Numbers: 14641-93-1 , 4482-75-1 , 6363-53-7 , 69-79-4 , [69-79-4]

Other Names:

1-alpha-d-glucopyranosyl-4-alpha-d-glucopyranose; 1-alpha-delta-Glucopyranosyl-4-alpha-delta-glucopyranose; 4-(alpha-D-glucopyranosido)-alpha-glucopyranose; 4-(alpha-D-glucosido)-D-glucose; 4-(alpha-delta-glucopyranosido)-alpha-glucopyranose; 4-(alpha-del

1-alpha-D-Glucopyranosyl-4-alpha-D-glucopyranose; 4-(alpha-D-Glucopyranosido)-alpha-glucopyranose; 4-(alpha-D-Glucosido)-D-glucose; 4-O-alpha-D-Glucopyranosyl-D-glucose; Advanctose 100; Cextromaltose; D-(+)-Maltose; D-Glucose, 4-O-alpha-D-glucopyranosyl-

1-alpha-D-Glucopyranosyl-4-alpha-D-glucopyranose; 4-(alpha-D-Glucopyranosido)-alpha-glucopyranose; 4-(alpha-D-Glucosido)-D-glucose; 4-O-alpha-D-Glucopyranosyl-D-glucose; AI3-09089; Advanctose 100; BRN 0093798; Cextromaltose; D-(+)-Maltose; D-Glucose, 4-O-

4-(alpha-D-glucopyranosido)-alpha-glucopyranose; 4-(alpha-D-glucosido)-D-glucose; 4-O-alpha-D-glucopyranosyl-D-glucopyranose; 4-O-alpha-D-glucopyranosyl-D-glucose; Cextromaltose; D-(+)-maltose; D-maltose; Malzzucker; alpha-D-Glcp-(1->4)-D-Glcp; alpha-malt

4-O-?-Glucopyranosyl-D-glucose monohydrate

4-O-alpha-D-glucopyranosyl-alpha-D-glucopyranose; Glcalpha1-4Glca; Glcalpha1-4Glcalpha; alpha-D-Glcp-(1->4)-alpha-D-Glcp; alpha-maltose

4-O-alpha-Glucopyranosyl-D-glucose monohydrate

4-O-^a-Glucopyranosyl-D-glucose monohydrate

4482-75-1; C00897; alpha-Malt sugar; alpha-Maltose

6363-53-7; D05373; Maltose 10 (TN); Maltose hydrate (JP16)

69-79-4; C00208; Malt sugar; Maltose; alpha-D-Glucopyranosyl-(1->4)-D-glucopyranose

69-79-4; D00044; Madoros (TN); Maltose (NF)

A-4-(b-d-galactosido)-d-glucose

alpha-maltose

CHEBI:43893; CHEBI:12340; CHEBI:22463; CHEBI:10300

CHEBI:6668; CHEBI:14568; CHEBI:25144

D-(+)-Maltose monohydrate

D-(+)-Maltose Monohydrate [6363-53-7]

D-(+)-Maltose monohydrate, 95%

D-MALTOSE MONOHYDRATE; [6363-53-7]

Linear maltodextrin;Maltodextrin;Maltodextrin(N);Maltodextrin(N-2)

Maltodextrin

MFCD00011684

MFCD00149343

Download: MOL2 SDF SMILES Flexibase

Physical Representations

Type pH range xlogP Des A‑Pol Apolar desolvation (kcal/mol) Des Pol Polar desolvation (kcal/mol) H Don H-bond donors H Acc H-bond acceptors Chg Net charge tPSA (Ų) MWT Molecular weight (g/mol) RB Rotatable bonds DL
Ref Reference (pH 7) -4.45 -17 -12.25 8 11 0 190 342.297 4

Vendor Notes

Note Type Comments Provided By
MP 119-121 °C (dec.)(lit.) Indofine
UniProt Database Links 3OAGR_CLOPH; 6P22_YEAST; AGLA_THEMA; AGLA_THENE; AGLB_KLEPN; AGLB_THEMA; AGLB_THENE; AGLE_RHIME; AGLF_RHIME; AGLG_RHIME; AGLK_RHIME; AGLR_RHIME; AGLU_ASPOR; AGLU_CANTS; AGLU_SULS9; ALGD_PSEAE; AMML_ASTMO; AMY1_DICT6; AMYA1_ASPOR; AMYB_BACCE; AMYB_BACCI; A ChEBI
Melting_Point ca 120? dec. Alfa-Aesar
Melting_Point ca 120° dec. Alfa-Aesar
Patent Database Links EP0806140; EP0864580; EP1057416; EP1254903; EP1319409; EP1352647; EP1428831; EP1674474; EP1787642; EP1834950; GB1474364; US2001008644; US2002068113; US2002086904; US2003072785; US2004048829; US2004166199; US2005008746; US2005079223; US2005131027; US200515 ChEBI
Patent Database Links EP0864580; EP0971025; EP1159962; EP1236754; EP1279676; EP1308171; EP1310254; EP1439187; EP1508331; EP1510215; EP1516615; EP1537858; EP1544297; EP1547472; EP1555318; EP1579771; EP1595533; EP1607087; EP1623723; EP1627573; EP1632778; EP1637597; EP1642904; EP ChEBI
SOLUBILITY H2O: 50 mg/mL Indofine
Reactome Database Links REACT_9403; REACT_9414; REACT_9424; REACT_9426; REACT_9475; REACT_9479; REACT_9506 ChEBI

Activity (Go SEA)

Direct Reactome Annotations (via ChEBI)

Description Species
Digestion of dietary carbohydrate
Trehalose biosynthesis

Analogs ( Draw Identity 99% 90% 80% 70% )