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Record Information
Version1.0
Created at2022-09-12 02:15:07 UTC
Updated at2022-09-12 02:15:07 UTC
NP-MRD IDNP0323061
Secondary Accession NumbersNone
Natural Product Identification
Common Name4-(acetyloxy)-3b-formyl-6,6,9a-trimethyl-1-oxo-3h,3ah,4h,5h,5ah,7h,8h,9h,9bh,10h-phenanthro[1,2-c]furan-10-yl acetate
Description9-(Acetyloxy)-10-formyl-2,6,6-trimethyl-14-oxo-13-oxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-15-en-17-yl acetate belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. 4-(acetyloxy)-3b-formyl-6,6,9a-trimethyl-1-oxo-3h,3ah,4h,5h,5ah,7h,8h,9h,9bh,10h-phenanthro[1,2-c]furan-10-yl acetate is found in Chromodoris hamiltoni. 9-(Acetyloxy)-10-formyl-2,6,6-trimethyl-14-oxo-13-oxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-15-en-17-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).
Structure
Thumb
Synonyms
ValueSource
9-(Acetyloxy)-10-formyl-2,6,6-trimethyl-14-oxo-13-oxatetracyclo[8.7.0.0,.0,]heptadec-15-en-17-yl acetic acidGenerator
9-(Acetyloxy)-10-formyl-2,6,6-trimethyl-14-oxo-13-oxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-15-en-17-yl acetic acidGenerator
Chemical FormulaC24H32O7
Average Mass432.5130 Da
Monoisotopic Mass432.21480 Da
IUPAC Name9-(acetyloxy)-10-formyl-2,6,6-trimethyl-14-oxo-13-oxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-15-en-17-yl acetate
Traditional Name9-(acetyloxy)-10-formyl-2,6,6-trimethyl-14-oxo-13-oxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-15-en-17-yl acetate
CAS Registry NumberNot Available
SMILES
CC(=O)OC1CC2C(C)(C)CCCC2(C)C2C(OC(C)=O)C=C3C(COC3=O)C12C=O
InChI Identifier
InChI=1S/C24H32O7/c1-13(26)30-17-9-15-16(11-29-21(15)28)24(12-25)19(31-14(2)27)10-18-22(3,4)7-6-8-23(18,5)20(17)24/h9,12,16-20H,6-8,10-11H2,1-5H3
InChI KeyXMGOKGYGXQDPSO-UHFFFAOYSA-N
Experimental Spectra
Not Available
Predicted Spectra
Spectrum TypeDescriptionDepositor IDDepositor OrganizationDepositorDeposition DateView
1D NMR13C NMR Spectrum (1D, 25 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 100 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 252 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 1000 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 50 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 200 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 75 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 300 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 101 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 400 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 126 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 500 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 151 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 600 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 176 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 700 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 201 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 800 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 226 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 900 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
Chemical Shift Submissions
Not Available
Species
Species of Origin
Species NameSourceReference
Chromodoris hamiltoniLOTUS Database
Chemical Taxonomy
Description Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassPrenol lipids
Sub ClassTerpene lactones
Direct ParentDiterpene lactones
Alternative Parents
Substituents
  • Diterpene lactone
  • Diterpenoid
  • Spongiane diterpenoid
  • 17-oxosteroid
  • Oxosteroid
  • Steroid
  • 16-oxasteroid
  • Tricarboxylic acid or derivatives
  • Gamma butyrolactone
  • Alpha,beta-unsaturated carboxylic ester
  • Enoate ester
  • Tetrahydrofuran
  • Carboxylic acid ester
  • Lactone
  • Organoheterocyclic compound
  • Oxacycle
  • Carboxylic acid derivative
  • Hydrocarbon derivative
  • Organic oxide
  • Organic oxygen compound
  • Carbonyl group
  • Organooxygen compound
  • Aldehyde
  • Aliphatic heteropolycyclic compound
Molecular FrameworkAliphatic heteropolycyclic compounds
External DescriptorsNot Available
Physical Properties
StateNot Available
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP2.43ALOGPS
logP2.28ChemAxon
logS-4.9ALOGPS
pKa (Strongest Basic)-6.4ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area95.97 ŲChemAxon
Rotatable Bond Count5ChemAxon
Refractivity110.65 m³·mol⁻¹ChemAxon
Polarizability45.4 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
HMDB IDNot Available
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound73798231
PDB IDNot Available
ChEBI IDNot Available
Good Scents IDNot Available
References
General References
  1. LOTUS database [Link]