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Marmelolactone A

PubChem CID: 101282726

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Compound Synonyms Marmelolactone A, CHEBI:195778, DTXSID301144282, 74133-35-0, (3R,5S)-3-methyl-5-[(1E)-3-methylbuta-1,3-dienyl]oxolan-2-one, (3R,5S)-Dihydro-3-methyl-5-[(1E)-3-methyl-1,3-butadien-1-yl]-2(3H)-furanone
Ghose Rule True
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 26.3
Hydrogen Bond Donor Count 0.0
Pfizer 3 75 Rule False
Scaffold Graph Level CC1CCCC1
Deep Smiles CC=C)/C=C/[C@H]OC=O)[C@@H]C5)C
Heavy Atom Count 12.0
Classyfire Class Lactones
Scaffold Graph Node Level OC1CCCO1
Classyfire Subclass Gamma butyrolactones
Isotope Atom Count 0.0
Molecular Complexity 228.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 2.0
Iupac Name (3R,5S)-3-methyl-5-[(1E)-3-methylbuta-1,3-dienyl]oxolan-2-one
Veber Rule True
Classyfire Superclass Organoheterocyclic compounds
Xlogp 2.7
Gsk 4 400 Rule True
Molecular Formula C10H14O2
Scaffold Graph Node Bond Level O=C1CCCO1
Inchi Key VOJBXZDIFIJUKD-HOMPQPGZSA-N
Silicos It Class Soluble
Rotatable Bond Count 2.0
Synonyms marmelolactone a
Esol Class Soluble
Functional Groups C=C(C)/C=C/C, COC(C)=O
Compound Name Marmelolactone A
Exact Mass 166.099
Formal Charge 0.0
Monoisotopic Mass 166.099
Hydrogen Bond Acceptor Count 2.0
Molecular Weight 166.22
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 2.0
Total Bond Stereocenter Count 1.0
Lipinski Rule Of 5 True
Inchi InChI=1S/C10H14O2/c1-7(2)4-5-9-6-8(3)10(11)12-9/h4-5,8-9H,1,6H2,2-3H3/b5-4+/t8-,9-/m1/s1
Smiles C[C@@H]1C[C@H](OC1=O)/C=C/C(=C)C
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 1.0
Egan Rule True

  • 1. Outgoing r'ship FOUND_IN to/from Cydonia Oblonga (Plant) Rel Props:Reference:The Unani Pharmacopoeia of India Part-1 Volume-2