Np mrd loader

Record Information
Version2.0
Created at2021-06-22 17:27:50 UTC
Updated at2026-02-09 04:01:13 UTC
NP-MRD IDNP0043892
Natural Product DOIhttps://doi.org/10.57994/5876
Secondary Accession NumbersNone
Natural Product Identification
Common NameGriffinoid 4
DescriptionGriffinoid D belongs to the class of organic compounds known as 7-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone. Griffinoid 4 was first documented in 2013 (PMID: 23795891). Based on a literature review very few articles have been published on Griffinoid D.
Structure
Thumb
SynonymsNot Available
Chemical FormulaC16H16O5
Average Mass288.2990 Da
Monoisotopic Mass288.09977 Da
IUPAC NameNot Available
Traditional NameNot Available
CAS Registry NumberNot Available
SMILESNot Available
InChI Identifier
InChI=1S/C16H16O5/c1-20-16-8-15-10(7-13(16)19)3-5-14(21-15)9-2-4-11(17)12(18)6-9/h2,4,6-8,14,17-19H,3,5H2,1H3/t14-/m0/s1
InChI KeyINHFJIACOJCKGT-AWEZNQCLSA-N
Experimental Spectra
Spectrum TypeDescriptionDepositor EmailDepositor OrganizationDepositorDeposition DateView
Predicted Spectra
Not Available
Chemical Shift Submissions
Spectrum TypeDescriptionDepositor EmailDepositor OrganizationDepositorDeposition DateView
1D NMR1H NMR Spectrum (1D, 400.0, Chloroform-d, simulated)[email protected]Not AvailableNot Available2026-02-09View Spectrum
1D NMR13C NMR Spectrum (1D, 100.0, Chloroform-d, simulated)[email protected]Not AvailableNot Available2026-02-09View Spectrum
Species
Species of Origin
Species NameSourceReference
Combretum griffithii
      Not Available
Chemical Taxonomy
Description Belongs to the class of organic compounds known as 7-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassFlavonoids
Sub ClassO-methylated flavonoids
Direct Parent7-O-methylated flavonoids
Alternative Parents
Substituents
  • 7-methoxyflavonoid-skeleton
  • 3'-hydroxyflavonoid
  • 4'-hydroxyflavonoid
  • 6-hydroxyflavonoid
  • Hydroxyflavonoid
  • Flavan
  • 1-benzopyran
  • Chromane
  • Benzopyran
  • Phenol ether
  • Anisole
  • Catechol
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Alkyl aryl ether
  • Phenol
  • Benzenoid
  • Monocyclic benzene moiety
  • Organoheterocyclic compound
  • Oxacycle
  • Ether
  • Organooxygen compound
  • Organic oxygen compound
  • Hydrocarbon derivative
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic 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 PropertiesNot Available
HMDB IDNot Available
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDNot Available
KNApSAcK IDNot Available
Chemspider ID30824223
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound71746435
PDB IDNot Available
ChEBI IDNot Available
Good Scents IDNot Available
References
General References
  1. Moosophon P, Kanokmedhakul S, Kanokmedhakul K, Buayairaksa M, Noichan J, Poopasit K: Antiplasmodial and cytotoxic flavans and diarylpropanes from the stems of Combretum griffithii. J Nat Prod. 2013 Jul 26;76(7):1298-302. doi: 10.1021/np400266h. Epub 2013 Jun 24. [PubMed:23795891 ]
  2. DOI: 10.1021/np400266h
  3. PMID: 23795891