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(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(1S,2R,4S)-1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl]oxy]oxane-3,4,5-triol

PubChem CID: 21631069

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Compound Synonyms (-)-Borneol glucoside, XB182721, (1S,2R,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl-O-?-D-glucopyranoside, 88763-93-3
Topological Polar Surface Area 99.4
Hydrogen Bond Donor Count 4.0
Heavy Atom Count 22.0
Isotope Atom Count 0.0
Molecular Complexity 427.0
Database Name cmaup_ingredients;pubchem
Defined Atom Stereocenter Count 8.0
Iupac Name (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(1S,2R,4S)-1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl]oxy]oxane-3,4,5-triol
Prediction Hob 1.0
Xlogp 0.9
Molecular Formula C16H28O6
Prediction Swissadme 0.0
Inchi Key JMCFZBXJPGDESD-CQXYJALYSA-N
Fcsp3 1.0
Logs -1.825
Rotatable Bond Count 3.0
Logd 1.566
Compound Name (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(1S,2R,4S)-1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl]oxy]oxane-3,4,5-triol
Prediction Hob Swissadme 0.0
Exact Mass 316.189
Formal Charge 0.0
Monoisotopic Mass 316.189
Hydrogen Bond Acceptor Count 6.0
Molecular Weight 316.39
Covalent Unit Count 1.0
Total Atom Stereocenter Count 8.0
Total Bond Stereocenter Count 0.0
Esol -2.1832428
Inchi InChI=1S/C16H28O6/c1-15(2)8-4-5-16(15,3)10(6-8)22-14-13(20)12(19)11(18)9(7-17)21-14/h8-14,17-20H,4-7H2,1-3H3/t8-,9+,10+,11+,12-,13+,14-,16+/m0/s1
Smiles C[C@]12CC[C@H](C1(C)C)C[C@H]2O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O
Nring 3.0
Defined Bond Stereocenter Count 0.0

  • 1. Outgoing r'ship FOUND_IN to/from Ophiopogon Japonicus (Plant) Rel Props:Source_db:cmaup_ingredients