NP-MRD: Showing NP-Card for 3-Hydroxy-5-methoxy-6,7-methylenedioxyflavanone (NP0055887)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 01:48:52 UTC

Updated at

2022-04-28 01:48:52 UTC

NP-MRD ID

NP0055887

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-Hydroxy-5-methoxy-6,7-methylenedioxyflavanone

Description

(2R,3R)-3-hydroxy-5-methoxy-6,7- methylenedioxyflavanone belongs to the class of organic compounds known as 5-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C5 atom of the flavonoid backbone (2R,3R)-3-hydroxy-5-methoxy-6,7- methylenedioxyflavanone is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. 3-Hydroxy-5-methoxy-6,7-methylenedioxyflavanone is found in Persicaria lapathifolia, Pisonia aculeata, Polygonum nodosum and Thanatephorus cucumeris. 3-Hydroxy-5-methoxy-6,7-methylenedioxyflavanone was first documented in 2018 (PMID: 29381070). Based on a literature review very few articles have been published on (2R,3R)-3-hydroxy-5-methoxy-6,7- methylenedioxyflavanone.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 37 40  0  0  0  0  0  0  0  0999 V2000
   -3.7910   -0.6506    2.0094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4495    0.4220    1.1747 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6936    0.3484    0.0374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2745    0.1254   -1.1922 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4608    0.0611   -2.3042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0916    0.2146   -2.2067 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4996    0.4387   -0.9783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3262    0.5021    0.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6818    0.7379    1.4157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3572    1.2788    2.3261 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7404    0.3274    1.5792 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2229    0.8189    2.7933 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5111    0.8846    0.4090 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8702    0.3155    0.2768 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4593   -0.4184    1.2535 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7317   -0.9201    1.0677 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4335   -0.6953   -0.0975 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8409    0.0458   -1.0860 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5763    0.5372   -0.8860 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8413    0.6011   -0.7923 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3165   -0.1716   -3.3940 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6340   -0.4123   -2.9423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5857   -0.0570   -1.5516 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9145   -0.6923    2.0309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3621   -1.6123    1.6963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4802   -0.3686    3.0483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4660    0.1608   -3.0952 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8031   -0.7771    1.5201 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9114    0.2127    3.5071 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5945    1.9782    0.5974 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9359   -0.6106    2.1707 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1537   -1.4944    1.8703 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4444   -1.1105   -0.2098 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3703    0.2292   -1.9942 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1366    1.1141   -1.6768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3919    0.1620   -3.4853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8005   -1.5256   -3.0285 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4 23  1  0
 23 22  1  0
 22 21  1  0
 21  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 11 13  1  0
 13 20  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
  8  3  1  0
 19 14  1  0
  5  4  1  0
 20  7  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
 22 36  1  0
 22 37  1  0
  6 27  1  0
 11 28  1  1
 12 29  1  0
 13 30  1  1
 15 31  1  0
 16 32  1  0
 17 33  1  0
 18 34  1  0
 19 35  1  0
M  END


  Mrv1652304282203482D          

 23 26  0  0  1  0            999 V2000
   -0.0734   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0734   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8580   -1.2680    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3429   -1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8580   -2.6029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -1.5229    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7845   -2.3479    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0701   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -3.5854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -2.7604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -3.5854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  1  9  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  3 13  1  0  0  0  0
 13 14  2  0  0  0  0
 12 15  1  1  0  0  0
 11 16  1  6  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 16 21  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0055887

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2OCOC2=CC2=C1C(=O)[C@H](O)[C@H](O2)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C17H14O6/c1-20-17-12-10(7-11-16(17)22-8-21-11)23-15(14(19)13(12)18)9-5-3-2-4-6-9/h2-7,14-15,19H,8H2,1H3/t14-,15+/m0/s1

> <INCHI_KEY>
MJAIKSJQFBNFDU-LSDHHAIUSA-N

> <FORMULA>
C17H14O6

> <MOLECULAR_WEIGHT>
314.293

> <EXACT_MASS>
314.079038171

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
30.843678241396958

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(11R,12R)-12-hydroxy-2-methoxy-11-phenyl-4,6,10-trioxatricyclo[7.4.0.0^{3,7}]trideca-1(9),2,7-trien-13-one

> <ALOGPS_LOGP>
1.27

> <JCHEM_LOGP>
1.8462077566666668

> <ALOGPS_LOGS>
-2.65

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.319246146526847

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.131198391326462

> <JCHEM_PKA_STRONGEST_BASIC>
-4.05279527519522

> <JCHEM_POLAR_SURFACE_AREA>
74.22000000000001

> <JCHEM_REFRACTIVITY>
78.91540000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.03e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(11R,12R)-12-hydroxy-2-methoxy-11-phenyl-4,6,10-trioxatricyclo[7.4.0.0^{3,7}]trideca-1(9),2,7-trien-13-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -0.137  -4.383   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.197  -5.153   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.530  -4.383   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.530  -2.843   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.197  -2.073   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.137  -2.843   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.602  -2.367   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -2.507  -3.613   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -1.602  -4.859   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       3.864  -2.073   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       5.198  -2.843   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.198  -4.383   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.864  -5.153   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.864  -6.693   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       6.531  -5.153   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.531  -2.073   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.531  -0.533   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.865   0.237   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.199  -0.533   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.199  -2.073   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.865  -2.843   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.197  -6.693   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.530  -7.463   0.000  0.00  0.00           C+0
CONECT    1    2    6    9                                                  
CONECT    2    1    3   22                                                  
CONECT    3    2    4   13                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8    1                                                       
CONECT   10    4   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13   15                                                  
CONECT   13   12    3   14                                                  
CONECT   14   13                                                            
CONECT   15   12                                                            
CONECT   16   11   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   16                                                       
CONECT   22    2   23                                                       
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₁₄O₆

Average Mass

314.2930 Da

Monoisotopic Mass

314.07904 Da

IUPAC Name

(11R,12R)-12-hydroxy-2-methoxy-11-phenyl-4,6,10-trioxatricyclo[7.4.0.0^{3,7}]trideca-1(9),2,7-trien-13-one

Traditional Name

(11R,12R)-12-hydroxy-2-methoxy-11-phenyl-4,6,10-trioxatricyclo[7.4.0.0^{3,7}]trideca-1(9),2,7-trien-13-one

CAS Registry Number

Not Available

SMILES

COC1=C2OCOC2=CC2=C1C(=O)[C@H](O)[C@H](O2)C1=CC=CC=C1

InChI Identifier

InChI=1S/C17H14O6/c1-20-17-12-10(7-11-16(17)22-8-21-11)23-15(14(19)13(12)18)9-5-3-2-4-6-9/h2-7,14-15,19H,8H2,1H3/t14-,15+/m0/s1

InChI Key

MJAIKSJQFBNFDU-LSDHHAIUSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Persicaria lapathifolia	LOTUS Database	35616633
Pisonia aculeata	LOTUS Database	35616633
Polygonum nodosum	Plant	KNApSAcK
Thanatephorus cucumeris	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 5-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C5 atom of the flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

O-methylated flavonoids

Direct Parent

5-O-methylated flavonoids

Alternative Parents

Substituents

5-methoxyflavonoid-skeleton
3-hydroxyflavonoid
Flavanone
Hydroxyflavonoid
Flavanonol
Flavan
Chromone
Chromane
1-benzopyran
Benzopyran
Benzodioxole
Anisole
Aryl alkyl ketone
Aryl ketone
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Secondary alcohol
Ketone
Organoheterocyclic compound
Oxacycle
Acetal
Ether
Organooxygen compound
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

monomethoxyflavanone (CHEBI:67372 )
extended flavonoid (CHEBI:67372 )
dihydroflavonols (CHEBI:67372 )

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.27	ALOGPS
logP	1.85	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	12.13	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	74.22 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	78.92 m³·mol⁻¹	ChemAxon
Polarizability	30.84 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

10305946

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21721856

PDB ID

Not Available

ChEBI ID

67372

Good Scents ID

Not Available

References

General References

Ayoub IM, Korinek M, Hwang TL, Chen BH, Chang FR, El-Shazly M, Singab ANB: Probing the Antiallergic and Anti-inflammatory Activity of Biflavonoids and Dihydroflavonols from Dietes bicolor. J Nat Prod. 2018 Feb 23;81(2):243-253. doi: 10.1021/acs.jnatprod.7b00476. Epub 2018 Jan 30. [PubMed:29381070 ]

Showing NP-Card for 3-Hydroxy-5-methoxy-6,7-methylenedioxyflavanone (NP0055887)

MOL for NP0055887 (3-Hydroxy-5-methoxy-6,7-methylenedioxyflavanone)

3D MOL for NP0055887 (3-Hydroxy-5-methoxy-6,7-methylenedioxyflavanone)

3D SDF for NP0055887 (3-Hydroxy-5-methoxy-6,7-methylenedioxyflavanone)

3D-SDF for NP0055887 (3-Hydroxy-5-methoxy-6,7-methylenedioxyflavanone)

PDB for NP0055887 (3-Hydroxy-5-methoxy-6,7-methylenedioxyflavanone)

3D PDB for NP0055887 (3-Hydroxy-5-methoxy-6,7-methylenedioxyflavanone)

SMILES for NP0055887 (3-Hydroxy-5-methoxy-6,7-methylenedioxyflavanone)

INCHI for NP0055887 (3-Hydroxy-5-methoxy-6,7-methylenedioxyflavanone)

Structure for NP0055887 (3-Hydroxy-5-methoxy-6,7-methylenedioxyflavanone)

3D Structure for NP0055887 (3-Hydroxy-5-methoxy-6,7-methylenedioxyflavanone)