NP-MRD: Showing NP-Card for 7-methoxy-8-[(1r,4r,6r)-6-[(1e)-2-(7-methoxy-2-oxochromen-8-yl)ethenyl]-4,6-dimethylcyclohex-2-en-1-yl]chromen-2-one (NP0193712)

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Record Information

Version

2.0

Created at

2022-09-04 11:14:52 UTC

Updated at

2022-09-04 11:14:52 UTC

NP-MRD ID

NP0193712

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-methoxy-8-[(1r,4r,6r)-6-[(1e)-2-(7-methoxy-2-oxochromen-8-yl)ethenyl]-4,6-dimethylcyclohex-2-en-1-yl]chromen-2-one

Description

7-Methoxy-8-[(1R,4R,6R)-6-[(E)-2-(7-methoxy-2-oxo-2H-chromen-8-yl)ethenyl]-4,6-dimethylcyclohex-2-en-1-yl]-2H-chromen-2-one belongs to the class of organic compounds known as coumarins and derivatives. These are polycyclic aromatic compounds containing a 1-benzopyran moiety with a ketone group at the C2 carbon atom (1-benzopyran-2-one). Based on a literature review very few articles have been published on 7-methoxy-8-[(1R,4R,6R)-6-[(E)-2-(7-methoxy-2-oxo-2H-chromen-8-yl)ethenyl]-4,6-dimethylcyclohex-2-en-1-yl]-2H-chromen-2-one.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309042213142D          

 36 40  0  0  1  0            999 V2000
    3.4862   -2.3988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2986   -2.5420    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5808   -3.3173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3933   -3.4605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6754   -4.2358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1451   -4.8678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4273   -5.6430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8970   -6.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0845   -6.1317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5542   -6.7637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8024   -5.3565    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3327   -4.7245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0505   -3.9493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2380   -3.8060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -3.0308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4256   -2.1123    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
    1.4289   -4.1250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 O   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  1  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
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  2  0  0  0  0
  3 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 16 15  1  1  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 24 36  2  0  0  0  0
 30 36  1  0  0  0  0
M  END


  Mrv1652309042213142D          

 36 40  0  0  1  0            999 V2000
    3.4862   -2.3988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2986   -2.5420    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5808   -3.3173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3933   -3.4605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6754   -4.2358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1451   -4.8678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4273   -5.6430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8970   -6.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0845   -6.1317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5542   -6.7637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8024   -5.3565    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3327   -4.7245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0505   -3.9493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2380   -3.8060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -3.0308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4256   -2.1123    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
    1.4289   -4.1250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 O   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  1  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
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  2  0  0  0  0
  3 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 16 15  1  1  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 24 36  2  0  0  0  0
 30 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0193712

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C2C=CC(=O)OC2=C1\C=C\[C@@]1(C)C[C@@H](C)C=C[C@H]1C1=C2OC(=O)C=CC2=CC=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C30H28O6/c1-18-5-10-22(27-24(34-4)12-7-20-9-14-26(32)36-29(20)27)30(2,17-18)16-15-21-23(33-3)11-6-19-8-13-25(31)35-28(19)21/h5-16,18,22H,17H2,1-4H3/b16-15+/t18-,22-,30-/m0/s1

> <INCHI_KEY>
RXFTXWCDRFJJIS-OLMWYFNHSA-N

> <FORMULA>
C30H28O6

> <MOLECULAR_WEIGHT>
484.548

> <EXACT_MASS>
484.188588622

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
50.744931577064094

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7-methoxy-8-[(1R,4R,6R)-6-[(E)-2-(7-methoxy-2-oxo-2H-chromen-8-yl)ethenyl]-4,6-dimethylcyclohex-2-en-1-yl]-2H-chromen-2-one

> <JCHEM_LOGP>
5.649003428333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.541929646437638

> <JCHEM_POLAR_SURFACE_AREA>
71.06

> <JCHEM_REFRACTIVITY>
141.2597

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
7-methoxy-8-[(1R,4R,6R)-6-[(E)-2-(7-methoxy-2-oxochromen-8-yl)ethenyl]-4,6-dimethylcyclohex-2-en-1-yl]chromen-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       6.508  -4.478   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       8.024  -4.745   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.551  -6.192   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.067  -6.460   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.594  -7.907   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.604  -9.087   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.131 -10.534   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.141 -11.713   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.624 -11.446   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.635 -12.626   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       7.098  -9.999   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       8.088  -8.819   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.561  -7.372   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.044  -7.105   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.518  -5.657   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.528  -3.943   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   13                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   12                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11    6   13                                                  
CONECT   13   12    3   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   23                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   16   24                                                  
CONECT   24   23   25   36                                                  
CONECT   25   24   26   28                                                  
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   25   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   36                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   24   30                                                  
MASTER        0    0    0    0    0    0    0    0   36    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₂₈O₆

Average Mass

484.5480 Da

Monoisotopic Mass

484.18859 Da

IUPAC Name

7-methoxy-8-[(1R,4R,6R)-6-[(E)-2-(7-methoxy-2-oxo-2H-chromen-8-yl)ethenyl]-4,6-dimethylcyclohex-2-en-1-yl]-2H-chromen-2-one

Traditional Name

7-methoxy-8-[(1R,4R,6R)-6-[(E)-2-(7-methoxy-2-oxochromen-8-yl)ethenyl]-4,6-dimethylcyclohex-2-en-1-yl]chromen-2-one

CAS Registry Number

Not Available

SMILES

COC1=CC=C2C=CC(=O)OC2=C1\C=C\[C@@]1(C)C[C@@H](C)C=C[C@H]1C1=C2OC(=O)C=CC2=CC=C1OC

InChI Identifier

InChI=1S/C30H28O6/c1-18-5-10-22(27-24(34-4)12-7-20-9-14-26(32)36-29(20)27)30(2,17-18)16-15-21-23(33-3)11-6-19-8-13-25(31)35-28(19)21/h5-16,18,22H,17H2,1-4H3/b16-15+/t18-,22-,30-/m0/s1

InChI Key

RXFTXWCDRFJJIS-OLMWYFNHSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumarins and derivatives. These are polycyclic aromatic compounds containing a 1-benzopyran moiety with a ketone group at the C2 carbon atom (1-benzopyran-2-one).

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Not Available

Direct Parent

Coumarins and derivatives

Alternative Parents

Substituents

Coumarin
Benzopyran
1-benzopyran
Anisole
Styrene
Alkyl aryl ether
Pyranone
Pyran
Benzenoid
Heteroaromatic compound
Lactone
Oxacycle
Ether
Organoheterocyclic compound
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

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	5.65	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	71.06 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	141.26 m³·mol⁻¹	ChemAxon
Polarizability	50.74 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163194488

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-methoxy-8-[(1r,4r,6r)-6-[(1e)-2-(7-methoxy-2-oxochromen-8-yl)ethenyl]-4,6-dimethylcyclohex-2-en-1-yl]chromen-2-one (NP0193712)

MOL for NP0193712 (7-methoxy-8-[(1r,4r,6r)-6-[(1e)-2-(7-methoxy-2-oxochromen-8-yl)ethenyl]-4,6-dimethylcyclohex-2-en-1-yl]chromen-2-one)

3D MOL for NP0193712 (7-methoxy-8-[(1r,4r,6r)-6-[(1e)-2-(7-methoxy-2-oxochromen-8-yl)ethenyl]-4,6-dimethylcyclohex-2-en-1-yl]chromen-2-one)

3D SDF for NP0193712 (7-methoxy-8-[(1r,4r,6r)-6-[(1e)-2-(7-methoxy-2-oxochromen-8-yl)ethenyl]-4,6-dimethylcyclohex-2-en-1-yl]chromen-2-one)

3D-SDF for NP0193712 (7-methoxy-8-[(1r,4r,6r)-6-[(1e)-2-(7-methoxy-2-oxochromen-8-yl)ethenyl]-4,6-dimethylcyclohex-2-en-1-yl]chromen-2-one)

PDB for NP0193712 (7-methoxy-8-[(1r,4r,6r)-6-[(1e)-2-(7-methoxy-2-oxochromen-8-yl)ethenyl]-4,6-dimethylcyclohex-2-en-1-yl]chromen-2-one)

3D PDB for NP0193712 (7-methoxy-8-[(1r,4r,6r)-6-[(1e)-2-(7-methoxy-2-oxochromen-8-yl)ethenyl]-4,6-dimethylcyclohex-2-en-1-yl]chromen-2-one)

SMILES for NP0193712 (7-methoxy-8-[(1r,4r,6r)-6-[(1e)-2-(7-methoxy-2-oxochromen-8-yl)ethenyl]-4,6-dimethylcyclohex-2-en-1-yl]chromen-2-one)

INCHI for NP0193712 (7-methoxy-8-[(1r,4r,6r)-6-[(1e)-2-(7-methoxy-2-oxochromen-8-yl)ethenyl]-4,6-dimethylcyclohex-2-en-1-yl]chromen-2-one)

Structure for NP0193712 (7-methoxy-8-[(1r,4r,6r)-6-[(1e)-2-(7-methoxy-2-oxochromen-8-yl)ethenyl]-4,6-dimethylcyclohex-2-en-1-yl]chromen-2-one)

3D Structure for NP0193712 (7-methoxy-8-[(1r,4r,6r)-6-[(1e)-2-(7-methoxy-2-oxochromen-8-yl)ethenyl]-4,6-dimethylcyclohex-2-en-1-yl]chromen-2-one)