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Macrocarpal L

PubChem CID: 9847648

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Compound Synonyms Macrocarpal L, 327601-97-8, 5-[(1R)-1-[(1aS,3aS,4S,7R,7aR,7bS)-7-hydroxy-1,1,3a,7-tetramethyl-1a,2,3,4,5,6,7a,7b-octahydrocyclopropa[a]naphthalen-4-yl]-3-methylbutyl]-2,4,6-trihydroxybenzene-1,3-dicarbaldehyde, SCHEMBL2885673, CHEMBL3937802, 5-[(1R)-1-[(1aS,3aS,4S,7R,7aR,7bS)-Decahydro-7-hydroxy-1,1,3a,7-tetramethyl-1H-cyclopropa[a]naphthalen-4-yl]-3-methylbutyl]-2,4,6-trihydroxy-1,3-benzenedicarboxaldehyde, (+)-Macrocarpal L, AKOS032948195, CS-0023924
Topological Polar Surface Area 115.0
Hydrogen Bond Donor Count 4.0
Heavy Atom Count 34.0
Isotope Atom Count 0.0
Molecular Complexity 774.0
Database Name cmaup_ingredients;pubchem
Defined Atom Stereocenter Count 7.0
Iupac Name 5-[(1R)-1-[(1aS,3aS,4S,7R,7aR,7bS)-7-hydroxy-1,1,3a,7-tetramethyl-1a,2,3,4,5,6,7a,7b-octahydrocyclopropa[a]naphthalen-4-yl]-3-methylbutyl]-2,4,6-trihydroxybenzene-1,3-dicarbaldehyde
Prediction Hob 0.0
Xlogp 6.4
Molecular Formula C28H40O6
Prediction Swissadme 0.0
Inchi Key HWFSHYBHNVCQPE-XRTAJGAOSA-N
Fcsp3 0.7142857142857143
Logs -3.661
Rotatable Bond Count 6.0
Logd 4.326
Compound Name Macrocarpal L
Prediction Hob Swissadme 0.0
Exact Mass 472.282
Formal Charge 0.0
Monoisotopic Mass 472.282
Hydrogen Bond Acceptor Count 6.0
Molecular Weight 472.6
Covalent Unit Count 1.0
Total Atom Stereocenter Count 7.0
Total Bond Stereocenter Count 0.0
Esol -6.511644635294119
Inchi InChI=1S/C28H40O6/c1-14(2)11-15(20-23(32)16(12-29)22(31)17(13-30)24(20)33)18-8-10-28(6,34)25-21-19(26(21,3)4)7-9-27(18,25)5/h12-15,18-19,21,25,31-34H,7-11H2,1-6H3/t15-,18+,19+,21+,25-,27+,28-/m1/s1
Smiles CC(C)C[C@H]([C@@H]1CC[C@@]([C@H]2[C@]1(CC[C@H]3[C@@H]2C3(C)C)C)(C)O)C4=C(C(=C(C(=C4O)C=O)O)C=O)O
Nring 4.0
Defined Bond Stereocenter Count 0.0

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