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Cistanoside E

PubChem CID: 21632979

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Compound Synonyms Cistanoside E, 97400-08-3, (2S,3R,4R,5R,6S)-2-((2R,3R,4S,5R,6R)-3,5-dihydroxy-2-(2-(4-hydroxy-3-methoxyphenyl)ethoxy)-6-(hydroxymethyl)oxan-4-yl)oxy-6-methyloxane-3,4,5-triol, (2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-2-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-6-(hydroxymethyl)oxan-4-yl]oxy-6-methyloxane-3,4,5-triol, DTXSID601317773
Topological Polar Surface Area 188.0
Hydrogen Bond Donor Count 7.0
Heavy Atom Count 33.0
Isotope Atom Count 0.0
Molecular Complexity 596.0
Database Name cmaup_ingredients;npass_chem_all;pubchem
Defined Atom Stereocenter Count 10.0
Iupac Name (2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-2-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-6-(hydroxymethyl)oxan-4-yl]oxy-6-methyloxane-3,4,5-triol
Prediction Hob 0.0
Xlogp -1.6
Molecular Formula C21H32O12
Prediction Swissadme 0.0
Inchi Key KNVLNWLGXNQJNJ-MGXJDOAZSA-N
Fcsp3 0.7142857142857143
Logs -1.542
Rotatable Bond Count 8.0
Logd -1.371
Compound Name Cistanoside E
Prediction Hob Swissadme 0.0
Exact Mass 476.189
Formal Charge 0.0
Monoisotopic Mass 476.189
Hydrogen Bond Acceptor Count 12.0
Molecular Weight 476.5
Covalent Unit Count 1.0
Total Atom Stereocenter Count 10.0
Total Bond Stereocenter Count 0.0
Esol -1.4115904545454558
Inchi InChI=1S/C21H32O12/c1-9-14(24)16(26)17(27)21(31-9)33-19-15(25)13(8-22)32-20(18(19)28)30-6-5-10-3-4-11(23)12(7-10)29-2/h3-4,7,9,13-28H,5-6,8H2,1-2H3/t9-,13+,14-,15+,16+,17+,18+,19-,20+,21-/m0/s1
Smiles C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@H]2[C@@H]([C@H](O[C@H]([C@@H]2O)OCCC3=CC(=C(C=C3)O)OC)CO)O)O)O)O
Nring 3.0
Defined Bond Stereocenter Count 0.0

  • 1. Outgoing r'ship FOUND_IN to/from Leonurus Japonicus (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all
  • 2. Outgoing r'ship FOUND_IN to/from Phlomoides Rotata (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all