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Dihydroreynosin

PubChem CID: 189086

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Compound Synonyms Dihydroreynosin, 32223-12-4, 1-Hydroxy-4(15),11(13)-eudesmadien-12,6-olide, 11-epi-Dihydroreynosin, 11Beta,13-Dihydroreynosin, 11beta,13-dihydro-reynosin, CHEMBL272177, 11-beta-H,13-Dihydroreynosin, DTXSID70954061, (3S,3aS,5aR,6R,9aS,9bS)-6-hydroxy-3,5a-dimethyl-9-methylidene-3a,4,5,6,7,8,9a,9b-octahydro-3H-benzo[g][1]benzofuran-2-one, 6-Hydroxy-3,5a-dimethyl-9-methylidenedecahydronaphtho[1,2-b]furan-2(3H)-one, (2S,5S,9R,10R)-10-Hydroxy-5,9-dimethyl-13-methylene-3-oxatricyclo[7.4.0.0<2,6>]tridecan-4-one, (3S,3aS,5aR,6R,9aS,9bS)-6-hydroxy-3,5a-dimethyl-9-methylene-3a,4,5,6,7,8,9a,9b-octahydro-3H-benzo[g]benzofuran-2-one, Naphtho(1,2-b)furan-2(3H)-one, decahydro-6-hydroxy-3,5a-dimethyl-9-methylene-, (3S-(3alpha,3aalpha,5abeta,6beta,9aalpha,9bbeta))-
Ghose Rule True
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 46.5
Hydrogen Bond Donor Count 1.0
Pfizer 3 75 Rule False
Scaffold Graph Level CC1CC2CCC3CCCC(C)C3C2C1
Np Classifier Class Eudesmane sesquiterpenoids
Deep Smiles C=CCC[C@H][C@][C@H]6[C@H]OC=O)[C@H][C@@H]5CC9)))C))))))C))O
Heavy Atom Count 18.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level CC1CCCC2CCC3CC(O)OC3C12
Classyfire Subclass Terpene lactones
Isotope Atom Count 0.0
Molecular Complexity 403.0
Database Name cmaup_ingredients;imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 6.0
Uniprot Id n.a.
Iupac Name (3S,3aS,5aR,6R,9aS,9bS)-6-hydroxy-3,5a-dimethyl-9-methylidene-3a,4,5,6,7,8,9a,9b-octahydro-3H-benzo[g][1]benzofuran-2-one
Prediction Hob 1.0
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 2.2
Gsk 4 400 Rule True
Molecular Formula C15H22O3
Scaffold Graph Node Bond Level C=C1CCCC2CCC3CC(=O)OC3C12
Prediction Swissadme 0.0
Inchi Key JWBPWNWPEVPCMJ-DMLGPZFASA-N
Silicos It Class Soluble
Fcsp3 0.8
Logs -5.161
Rotatable Bond Count 0.0
Logd 2.703
Synonyms dihydroreynosin
Esol Class Soluble
Functional Groups C=C(C)C, CO, COC(C)=O
Compound Name Dihydroreynosin
Prediction Hob Swissadme 0.0
Exact Mass 250.157
Formal Charge 0.0
Monoisotopic Mass 250.157
Hydrogen Bond Acceptor Count 3.0
Molecular Weight 250.33
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 6.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Esol -2.7465955999999996
Inchi InChI=1S/C15H22O3/c1-8-4-5-11(16)15(3)7-6-10-9(2)14(17)18-13(10)12(8)15/h9-13,16H,1,4-7H2,2-3H3/t9-,10-,11+,12+,13-,15-/m0/s1
Smiles C[C@H]1[C@@H]2CC[C@]3([C@@H](CCC(=C)[C@@H]3[C@H]2OC1=O)O)C
Nring 3.0
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Sesquiterpenoids

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  • 2. Outgoing r'ship FOUND_IN to/from Cardamine Impatiens (Plant) Rel Props:Source_db:npass_chem_all
  • 3. Outgoing r'ship FOUND_IN to/from Hopea Parviflora (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all
  • 4. Outgoing r'ship FOUND_IN to/from Ligusticum Jeholense (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all
  • 5. Outgoing r'ship FOUND_IN to/from Salvia Carduacea (Plant) Rel Props:Source_db:npass_chem_all
  • 6. Outgoing r'ship FOUND_IN to/from Saussurea Costus (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all
  • 7. Outgoing r'ship FOUND_IN to/from Scabiosa Atropurpurea (Plant) Rel Props:Source_db:npass_chem_all
  • 8. Outgoing r'ship FOUND_IN to/from Schisandra Henryi (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all
  • 9. Outgoing r'ship FOUND_IN to/from Scrophularia Lepidota (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all
  • 10. Outgoing r'ship FOUND_IN to/from Veratrum Album (Plant) Rel Props:Source_db:npass_chem_all
  • 11. Outgoing r'ship FOUND_IN to/from Yucca Aloifolia (Plant) Rel Props:Source_db:npass_chem_all