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Macrocarpal H

PubChem CID: 10719242

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Compound Synonyms Macrocarpal H, 179388-53-5, 1,3-Benzenedicarboxaldehyde, 5-[(1S)-1-[(1S,4aS,6R,8aS)-decahydro-6-(1-hydroxy-1-methylethyl)-8a-methyl-4-methylene-1-naphthalenyl]-3-methylbutyl]-2,4,6-trihydroxy-, 5-[(1S)-1-[(1S,4aS,6R,8aS)-6-(2-hydroxypropan-2-yl)-8a-methyl-4-methylidene-1,2,3,4a,5,6,7,8-octahydronaphthalen-1-yl]-3-methylbutyl]-2,4,6-trihydroxybenzene-1,3-dicarbaldehyde, 3V5VQV46B4, CHEMBL518509, CHEBI:175710, HY-N3341, AKOS032948191, DA-55163, FS-10496, CS-0023942, 1,3-Benzenedicarboxaldehyde, 5-[1-[decahydro-6-(1-hydroxy-1-methylethyl)-8a-methyl-4-methylene-1-naphthalenyl]-3-methylbutyl]-2,4,6-trihydroxy-, [1S-[1(R*),4a,6,8a]]-, 5-[(1S)-1-[(1S,4aS,6R,8aS)-Decahydro-6-(1-hydroxy-1-methylethyl)-8a-methyl-4-methylene-1-naphthalenyl]-3-methylbutyl]-2,4,6-trihydroxy-1,3-benzenedicarboxaldehyde, 5-[(1S)-1-[(1S,4aS,6R,8aS)-Decahydro-6-(1-hydroxy-1-methylethyl)-8a-methyl-4-methylene-1-naphthalenyl]-3-methylbutyl]-2,4,6-trihydroxy-1,3-benzenedicarboxaldehyde
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 115.0
Hydrogen Bond Donor Count 4.0
Pfizer 3 75 Rule False
Scaffold Graph Level CC1CCC(CC2CCCCC2)C2CCCCC12
Np Classifier Class Phloroglucinol-terpene hybrids
Deep Smiles O=CccO)c[C@H][C@@H]CCC=C)[C@H][C@@]6C)CC[C@H]C6)CO)C)C)))))))))))CCC)C))))ccc6O))C=O)))O
Heavy Atom Count 34.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level CC1CCC(CC2CCCCC2)C2CCCCC12
Classyfire Subclass Sesquiterpenoids
Isotope Atom Count 0.0
Molecular Complexity 740.0
Database Name cmaup_ingredients;imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 5.0
Iupac Name 5-[(1S)-1-[(1S,4aS,6R,8aS)-6-(2-hydroxypropan-2-yl)-8a-methyl-4-methylidene-1,2,3,4a,5,6,7,8-octahydronaphthalen-1-yl]-3-methylbutyl]-2,4,6-trihydroxybenzene-1,3-dicarbaldehyde
Prediction Hob 0.0
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 6.0
Gsk 4 400 Rule False
Molecular Formula C28H40O6
Scaffold Graph Node Bond Level C=C1CCC(Cc2ccccc2)C2CCCCC12
Prediction Swissadme 0.0
Inchi Key OOAOETHJYYAVCC-GNLPDQNGSA-N
Silicos It Class Moderately soluble
Fcsp3 0.6428571428571429
Logs -4.143
Rotatable Bond Count 7.0
Logd 3.748
Synonyms macrocarpal h
Esol Class Poorly soluble
Functional Groups C=C(C)C, CO, cC=O, cO
Compound Name Macrocarpal H
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
Gi Absorption False
Covalent Unit Count 1.0
Total Atom Stereocenter Count 5.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Esol -6.244044635294119
Inchi InChI=1S/C28H40O6/c1-15(2)11-18(23-25(32)19(13-29)24(31)20(14-30)26(23)33)21-8-7-16(3)22-12-17(27(4,5)34)9-10-28(21,22)6/h13-15,17-18,21-22,31-34H,3,7-12H2,1-2,4-6H3/t17-,18+,21+,22+,28+/m1/s1
Smiles CC(C)C[C@@H]([C@@H]1CCC(=C)[C@H]2[C@]1(CC[C@H](C2)C(C)(C)O)C)C3=C(C(=C(C(=C3O)C=O)O)C=O)O
Nring 3.0
Np Classifier Biosynthetic Pathway Polyketides, Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Phloroglucinols

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