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Isonuatigenin

PubChem CID: 12311129

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Compound Synonyms Isonuatigenin, (25S)-Isonuatigenin, Spirost-5-ene-3,25-diol, (3beta,25S)-, 7050-41-1, (1S,2S,3'S,4S,6R,7S,8R,9S,12S,13R,16S)-3',7,9,13-tetramethylspiro(5-oxapentacyclo(10.8.0.02,9.04,8.013,18)icos-18-ene-6,6'-oxane)-3',16-diol, (1S,2S,3'S,4S,6R,7S,8R,9S,12S,13R,16S)-3',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,6'-oxane]-3',16-diol, 22S,25S-Furospirost-5-en-3beta,25-diol
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 58.9
Hydrogen Bond Donor Count 2.0
Pfizer 3 75 Rule False
Scaffold Graph Level C1CCC2(CC1)CC1CC3C(CCC4C5CCCCC5CCC43)C1C2
Np Classifier Class Spirostane steroids
Deep Smiles O[C@H]CC[C@]C=CC[C@@H][C@@H]6CC[C@][C@H]6C[C@H][C@@H]5[C@H]C)[C@]O5)CC[C@]CO6))C)O))))))))))C))))))))C6))C
Heavy Atom Count 31.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level C1CCC2(CC3C(CC4C3CCC3C5CCCCC5CCC34)O2)OC1
Classyfire Subclass Triterpenoids
Isotope Atom Count 0.0
Molecular Complexity 794.0
Database Name cmaup_ingredients;imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 11.0
Iupac Name (1S,2S,3'S,4S,6R,7S,8R,9S,12S,13R,16S)-3',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,6'-oxane]-3',16-diol
Prediction Hob 1.0
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 4.4
Gsk 4 400 Rule False
Molecular Formula C27H42O4
Scaffold Graph Node Bond Level C1=C2CCCCC2C2CCC3C4CC5(CCCCO5)OC4CC3C2C1
Prediction Swissadme 0.0
Inchi Key NHBDEADLHQSGDF-SGKAZYAESA-N
Silicos It Class Moderately soluble
Fcsp3 0.925925925925926
Logs -4.883
Rotatable Bond Count 0.0
Logd 3.87
Synonyms isonuatigenin
Esol Class Moderately soluble
Functional Groups CC=C(C)C, CO, CO[C@@](C)(C)OC
Compound Name Isonuatigenin
Prediction Hob Swissadme 0.0
Exact Mass 430.308
Formal Charge 0.0
Monoisotopic Mass 430.308
Hydrogen Bond Acceptor Count 4.0
Molecular Weight 430.6
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 11.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Esol -5.307099800000001
Inchi InChI=1S/C27H42O4/c1-16-23-22(31-27(16)12-11-24(2,29)15-30-27)14-21-19-6-5-17-13-18(28)7-9-25(17,3)20(19)8-10-26(21,23)4/h5,16,18-23,28-29H,6-15H2,1-4H3/t16-,18-,19+,20-,21-,22-,23-,24-,25-,26-,27+/m0/s1
Smiles C[C@H]1[C@H]2[C@H](C[C@@H]3[C@@]2(CC[C@H]4[C@H]3CC=C5[C@@]4(CC[C@@H](C5)O)C)C)O[C@]16CC[C@](CO6)(C)O
Nring 6.0
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Steroids

  • 1. Outgoing r'ship FOUND_IN to/from Dendrobium Chrysanthum (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all
  • 2. Outgoing r'ship FOUND_IN to/from Solanum Sisymbriifolium (Plant) Rel Props:Reference:ISBN:9788185042053
  • 3. Outgoing r'ship FOUND_IN to/from Tacca Leontopetaloides (Plant) Rel Props:Reference:ISBN:9780387706375; ISBN:9788172363093; ISBN:9788185042145