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Fernene

PubChem CID: 441679

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Compound Synonyms Fernene, Fern-9(11)-ene, 1615-99-2, (3R,3aR,5aR,5bR,7aS,11aS,13aS,13bR)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,7a,9,10,11,13,13b-tetradecahydrocyclopenta[a]chrysene, CHEBI:5016, DTXSID40331608, C08625, Q27106625
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 0.0
Hydrogen Bond Donor Count 0.0
Pfizer 3 75 Rule False
Scaffold Graph Level C1CCC2C(C1)CCC1C2CCC2C3CCCC3CCC21
Np Classifier Class Fernane and Arborinane triterpenoids
Deep Smiles CC[C@H]CC[C@@H][C@]5C)CC[C@][C@@]6C)CC=C[C@@H]6CC[C@@H][C@]6C)CCCC6C)C))))))))))))))C)))))))))C
Heavy Atom Count 30.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level C1CCC2C(C1)CCC1C2CCC2C3CCCC3CCC21
Classyfire Subclass Triterpenoids
Isotope Atom Count 0.0
Molecular Complexity 741.0
Database Name cmaup_ingredients;imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 8.0
Iupac Name (3R,3aR,5aR,5bR,7aS,11aS,13aS,13bR)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,7a,9,10,11,13,13b-tetradecahydrocyclopenta[a]chrysene
Prediction Hob 1.0
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 10.5
Gsk 4 400 Rule False
Molecular Formula C30H50
Scaffold Graph Node Bond Level C1=C2C3CCCCC3CCC2C2CCC3CCCC3C2C1
Prediction Swissadme 0.0
Inchi Key ZHDRLFGZQZCZKX-BQOUFORSSA-N
Silicos It Class Poorly soluble
Fcsp3 0.9333333333333332
Logs -7.625
Rotatable Bond Count 1.0
Logd 6.3
Synonyms 7-fernene, 9(11)-fernene, fern-9(11)-ene, fernene, fernene, 9(11)-
Esol Class Poorly soluble
Functional Groups CC=C(C)C
Compound Name Fernene
Prediction Hob Swissadme 0.0
Exact Mass 410.391
Formal Charge 0.0
Monoisotopic Mass 410.391
Hydrogen Bond Acceptor Count 0.0
Molecular Weight 410.7
Gi Absorption False
Covalent Unit Count 1.0
Total Atom Stereocenter Count 8.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Esol -8.960726
Inchi InChI=1S/C30H50/c1-20(2)21-10-13-25-28(21,6)18-19-29(7)23-11-12-24-26(3,4)15-9-16-27(24,5)22(23)14-17-30(25,29)8/h14,20-21,23-25H,9-13,15-19H2,1-8H3/t21-,23+,24+,25-,27-,28-,29-,30+/m1/s1
Smiles CC(C)[C@H]1CC[C@@H]2[C@@]1(CC[C@]3([C@]2(CC=C4[C@@H]3CC[C@@H]5[C@@]4(CCCC5(C)C)C)C)C)C
Nring 5.0
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule False
Np Classifier Superclass Triterpenoids

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