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Sachaliside

PubChem CID: 14048613

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Compound Synonyms Sachaliside, (E)-Triandrin, 132294-76-9, Sachaliside 1, Sachaliside, (-)-, UNII-7WNF6LR591, Triandrin, 7WNF6LR591, 19764-35-3, (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E)-3-(4-hydroxyphenyl)prop-2-enoxy]oxane-3,4,5-triol, beta-D-Glucopyranoside, 3-(4-hydroxyphenyl)-2-propenyl, (E)-, beta-D-Glucopyranoside, (2E)-3-(4-hydroxyphenyl)-2-propen-1-yl, beta-D-Glucopyranoside, 3-(4-hydroxyphenyl)-2-propen-1-yl, (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-(((E)-3-(4-hydroxyphenyl)allyl)oxy)tetrahydro-2H-pyran-3,4,5-triol, MEGxp0_001501, CHEMBL3581238, CHEBI:181987, AKOS040753896, AKOS040763037, NCGC00385488-01, HY-123286, Q27268953, .BETA.-D-GLUCOPYRANOSIDE, (2E)-3-(4-HYDROXYPHENYL)-2-PROPEN-1-YL, .BETA.-D-GLUCOPYRANOSIDE, 3-(4-HYDROXYPHENYL)-2-PROPENYL, (E)-, NCGC00385488-01_C15H20O7_beta-D-Glucopyranoside, (2E)-3-(4-hydroxyphenyl)-2-propen-1-yl
Topological Polar Surface Area 120.0
Hydrogen Bond Donor Count 5.0
Heavy Atom Count 22.0
Isotope Atom Count 0.0
Molecular Complexity 354.0
Database Name cmaup_ingredients;npass_chem_all;pubchem
Defined Atom Stereocenter Count 5.0
Iupac Name (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E)-3-(4-hydroxyphenyl)prop-2-enoxy]oxane-3,4,5-triol
Prediction Hob 1.0
Xlogp -0.4
Molecular Formula C15H20O7
Prediction Swissadme 1.0
Inchi Key CNNXMGXBAZQZDE-HHMSBIESSA-N
Fcsp3 0.4666666666666667
Logs -0.622
Rotatable Bond Count 5.0
Logd -0.176
Compound Name Sachaliside
Prediction Hob Swissadme 1.0
Exact Mass 312.121
Formal Charge 0.0
Monoisotopic Mass 312.121
Hydrogen Bond Acceptor Count 7.0
Molecular Weight 312.31
Covalent Unit Count 1.0
Total Atom Stereocenter Count 5.0
Total Bond Stereocenter Count 1.0
Esol -1.3898897818181817
Inchi InChI=1S/C15H20O7/c16-8-11-12(18)13(19)14(20)15(22-11)21-7-1-2-9-3-5-10(17)6-4-9/h1-6,11-20H,7-8H2/b2-1+/t11-,12-,13+,14-,15-/m1/s1
Smiles C1=CC(=CC=C1/C=C/CO[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)O
Nring 2.0
Defined Bond Stereocenter Count 1.0

  • 1. Outgoing r'ship FOUND_IN to/from Pinellia Ternata (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all