NP-MRD: Showing NP-Card for Okanin 3,4,3',4'-tetramethyl ether (NP0054671)

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Record Information

Version

2.0

Created at

2022-04-28 00:57:16 UTC

Updated at

2022-04-28 00:57:16 UTC

NP-MRD ID

NP0054671

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Okanin 3,4,3',4'-tetramethyl ether

Description

Okanin 3,4,3',4'-tetramethyl ether belongs to the class of organic compounds known as 2'-hydroxychalcones. These are organic compounds containing chalcone skeleton that carries a hydroxyl group at the 2'-position. Thus, okanin 3,4,3',4'-tetramethyl ether is considered to be a flavonoid. Okanin 3,4,3',4'-tetramethyl ether is found in Bidens torta. Based on a literature review very few articles have been published on Okanin 3,4,3',4'-tetramethyl ether.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 46  0  0  0  0  0  0  0  0999 V2000
    6.8949    2.4373   -0.1366 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5324    1.0897   -0.0955 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2371    0.6093   -0.1004 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1279    1.4237   -0.1475 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8410    0.8640   -0.1494 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6328   -0.4932   -0.1054 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3175   -1.0972   -0.1063 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1842   -0.4301   -0.1486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1123   -1.1325   -0.1457 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1505   -2.4004   -0.1020 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3817   -0.4312   -0.1915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4482    0.9411   -0.2407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6683    1.6162   -0.2848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8345    0.8877   -0.2788 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0342    1.5856   -0.3233 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0950    2.9794   -0.3730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8169   -0.4994   -0.2299 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0172   -1.1769   -0.2263 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7328   -1.5299    0.9189 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5920   -1.1192   -0.1877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5323   -2.5074   -0.1381 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7886   -1.2831   -0.0584 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0572   -0.7606   -0.0554 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1639   -1.5940   -0.0077 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9670   -2.9937    0.0380 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8039    2.5526    0.5074 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1353    3.1283    0.2729 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1748    2.7243   -1.1734 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2483    2.5014   -0.1832 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9999    1.5553   -0.1877 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2457   -2.1837   -0.0695 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2400    0.6447   -0.1853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5448    1.5351   -0.2464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6659    2.6930   -0.3225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6593    3.3736   -1.3286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4246    3.3964    0.4324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0917    3.3704   -0.1680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9182   -0.6290    1.5637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7387   -1.8784    0.6104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1910   -2.2627    1.5368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3807   -3.0565   -0.1331 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6086   -2.3615   -0.0236 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6213   -3.3876   -0.9505 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2382   -3.2581    0.8204 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9704   -3.4426    0.2186 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 23  2  0
 23 24  1  0
 24 25  1  0
 23 22  1  0
 22  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 20  2  0
 20 21  1  0
 20 17  1  0
 17 18  1  0
 18 19  1  0
 17 14  2  0
 14 15  1  0
 15 16  1  0
 14 13  1  0
 13 12  2  0
  6  5  1  0
  5  4  2  0
  4  3  1  0
 12 11  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
 25 43  1  0
 25 44  1  0
 25 45  1  0
 22 42  1  0
  7 31  1  0
  8 32  1  0
 21 41  1  0
 19 38  1  0
 19 39  1  0
 19 40  1  0
 16 35  1  0
 16 36  1  0
 16 37  1  0
 13 34  1  0
 12 33  1  0
  5 30  1  0
  4 29  1  0
M  END


  Mrv1652304282202572D          

 25 26  0  0  0  0            999 V2000
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    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
  4  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  0  0  0  0
  3 21  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  0  0  0  0
  1 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0054671

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(OC)C=C(\C=C\C(=O)C2=C(O)C(OC)=C(OC)C=C2)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H20O6/c1-22-15-9-6-12(11-17(15)24-3)5-8-14(20)13-7-10-16(23-2)19(25-4)18(13)21/h5-11,21H,1-4H3/b8-5+

> <INCHI_KEY>
BOYAGHNMYQPGKZ-VMPITWQZSA-N

> <FORMULA>
C19H20O6

> <MOLECULAR_WEIGHT>
344.363

> <EXACT_MASS>
344.125988364

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
36.77483961736928

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-3-(3,4-dimethoxyphenyl)-1-(2-hydroxy-3,4-dimethoxyphenyl)prop-2-en-1-one

> <ALOGPS_LOGP>
3.58

> <JCHEM_LOGP>
3.6060749246666663

> <ALOGPS_LOGS>
-4.34

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.33777834972447

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.718789015053646

> <JCHEM_PKA_STRONGEST_BASIC>
-4.313939723640605

> <JCHEM_POLAR_SURFACE_AREA>
74.22000000000001

> <JCHEM_REFRACTIVITY>
94.7107

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.57e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-3-(3,4-dimethoxyphenyl)-1-(2-hydroxy-3,4-dimethoxyphenyl)prop-2-en-1-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       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       6.668 -10.010   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667 -13.860   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334 -14.630   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.000 -13.860   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.000 -12.320   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.334 -14.630   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -2.667 -13.860   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.334 -16.170   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -0.000 -16.940   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.002  -7.700   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       8.002  -4.620   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
CONECT    1    2    6   24                                                  
CONECT    2    1    3   22                                                  
CONECT    3    2    4   21                                                  
CONECT    4    3    5    7                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1                                                       
CONECT    7    4    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   19                                                  
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15   11                                                       
CONECT   17   14   18                                                       
CONECT   18   17                                                            
CONECT   19   13   20                                                       
CONECT   20   19                                                            
CONECT   21    3                                                            
CONECT   22    2   23                                                       
CONECT   23   22                                                            
CONECT   24    1   25                                                       
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₀O₆

Average Mass

344.3630 Da

Monoisotopic Mass

344.12599 Da

IUPAC Name

(2E)-3-(3,4-dimethoxyphenyl)-1-(2-hydroxy-3,4-dimethoxyphenyl)prop-2-en-1-one

Traditional Name

(2E)-3-(3,4-dimethoxyphenyl)-1-(2-hydroxy-3,4-dimethoxyphenyl)prop-2-en-1-one

CAS Registry Number

Not Available

SMILES

COC1=C(OC)C=C(\C=C\C(=O)C2=C(O)C(OC)=C(OC)C=C2)C=C1

InChI Identifier

InChI=1S/C19H20O6/c1-22-15-9-6-12(11-17(15)24-3)5-8-14(20)13-7-10-16(23-2)19(25-4)18(13)21/h5-11,21H,1-4H3/b8-5+

InChI Key

BOYAGHNMYQPGKZ-VMPITWQZSA-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
Bidens torta	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2'-hydroxychalcones. These are organic compounds containing chalcone skeleton that carries a hydroxyl group at the 2'-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Linear 1,3-diarylpropanoids

Sub Class

Chalcones and dihydrochalcones

Direct Parent

2'-Hydroxychalcones

Alternative Parents

Substituents

2'-hydroxychalcone
Cinnamylphenol
Methoxyphenol
Dimethoxybenzene
O-dimethoxybenzene
Benzoyl
Phenol ether
Styrene
Phenoxy compound
Aryl ketone
Anisole
Methoxybenzene
1-hydroxy-4-unsubstituted benzenoid
Phenol
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Acryloyl-group
Alpha,beta-unsaturated ketone
Vinylogous acid
Enone
Ketone
Ether
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Chalcones and dihydrochalcones (LMPK12120183 )

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	3.58	ALOGPS
logP	3.61	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	7.72	ChemAxon
pKa (Strongest Basic)	-4.3	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	7	ChemAxon
Refractivity	94.71 m³·mol⁻¹	ChemAxon
Polarizability	36.77 Å³	ChemAxon
Number of Rings	2	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

C00006971

Chemspider ID

4528609

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5380306

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Okanin 3,4,3',4'-tetramethyl ether (NP0054671)

MOL for NP0054671 (Okanin 3,4,3',4'-tetramethyl ether)

3D MOL for NP0054671 (Okanin 3,4,3',4'-tetramethyl ether)

3D SDF for NP0054671 (Okanin 3,4,3',4'-tetramethyl ether)

3D-SDF for NP0054671 (Okanin 3,4,3',4'-tetramethyl ether)

PDB for NP0054671 (Okanin 3,4,3',4'-tetramethyl ether)

3D PDB for NP0054671 (Okanin 3,4,3',4'-tetramethyl ether)

SMILES for NP0054671 (Okanin 3,4,3',4'-tetramethyl ether)

INCHI for NP0054671 (Okanin 3,4,3',4'-tetramethyl ether)

Structure for NP0054671 (Okanin 3,4,3',4'-tetramethyl ether)

3D Structure for NP0054671 (Okanin 3,4,3',4'-tetramethyl ether)