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Eleutheroside C

PubChem CID: 9859136

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Compound Synonyms ELEUTHEROSIDE C, 15486-24-5, (2S,3R,4S,5R,6R)-2-ETHOXY-6-(HYDROXYMETHYL)OXANE-3,4,5-TRIOL, ELEUTHEROSIDEC, Ethyl a-D-galactoside, ethyl a-d-galactopyranoside, 1-Ethyl-beta-D-galactoside, SCHEMBL2446115, DTXSID50879263, CHEBI:228960, HY-N3802, ?-D-GALACTOPYRANOSIDE, ETHYL, AKOS032948775, DA-63309, FE158668, MS-23142, CS-0024249, G13203, Ethyl -D-galactoside, Ethyl -D-galactopyranoside
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 99.4
Hydrogen Bond Donor Count 4.0
Pfizer 3 75 Rule True
Scaffold Graph Level C1CCCCC1
Deep Smiles CCO[C@H]O[C@H]CO))[C@@H][C@@H][C@H]6O))O))O
Heavy Atom Count 14.0
Classyfire Class Organooxygen compounds
Scaffold Graph Node Level C1CCOCC1
Classyfire Subclass Carbohydrates and carbohydrate conjugates
Isotope Atom Count 0.0
Molecular Complexity 175.0
Database Name imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 5.0
Iupac Name (2S,3R,4S,5R,6R)-2-ethoxy-6-(hydroxymethyl)oxane-3,4,5-triol
Veber Rule True
Classyfire Superclass Organic oxygen compounds
Xlogp -1.8
Gsk 4 400 Rule True
Molecular Formula C8H16O6
Scaffold Graph Node Bond Level C1CCOCC1
Inchi Key WYUFTYLVLQZQNH-HNEXDWKRSA-N
Silicos It Class Soluble
Rotatable Bond Count 3.0
Synonyms ethyl alpha-d-galactopyranoside, ethyl α-d-galactopyranoside, ethyl-a-d-galactopyranoside, ethyl-alpha-d-galacto-pyranoside, ethyl-alpha-d-galactopyranoside, ethyl-alpha-d-galactoside
Esol Class Highly soluble
Functional Groups CO, CO[C@H](C)OC
Compound Name Eleutheroside C
Exact Mass 208.095
Formal Charge 0.0
Monoisotopic Mass 208.095
Hydrogen Bond Acceptor Count 6.0
Molecular Weight 208.21
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 5.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Inchi InChI=1S/C8H16O6/c1-2-13-8-7(12)6(11)5(10)4(3-9)14-8/h4-12H,2-3H2,1H3/t4-,5+,6+,7-,8+/m1/s1
Smiles CCO[C@@H]1[C@@H]([C@H]([C@H]([C@H](O1)CO)O)O)O
Defined Bond Stereocenter Count 0.0
Egan Rule False

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