NP-MRD: Showing NP-Card for 9-[(2-{[3-hydroxy-4-({4-methoxy-7-oxofuro[3,2-g]chromen-9-yl}oxy)-2-methylbutan-2-yl]oxy}-3-methylbut-3-en-1-yl)oxy]-4-methoxyfuro[3,2-g]chromen-7-one (NP0300071)

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Record Information

Version

2.0

Created at

2022-09-10 12:16:06 UTC

Updated at

2022-09-10 12:16:06 UTC

NP-MRD ID

NP0300071

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9-[(2-{[3-hydroxy-4-({4-methoxy-7-oxofuro[3,2-g]chromen-9-yl}oxy)-2-methylbutan-2-yl]oxy}-3-methylbut-3-en-1-yl)oxy]-4-methoxyfuro[3,2-g]chromen-7-one

Description

9-[(2-{[3-Hydroxy-4-({4-methoxy-7-oxo-7H-furo[3,2-g]chromen-9-yl}oxy)-2-methylbutan-2-yl]oxy}-3-methylbut-3-en-1-yl)oxy]-4-methoxy-7H-furo[3,2-g]chromen-7-one belongs to the class of organic compounds known as 5-methoxypsoralens. These are psoralens containing a methoxy group attached at the C5 position of the psoralen group. 9-[(2-{[3-hydroxy-4-({4-methoxy-7-oxofuro[3,2-g]chromen-9-yl}oxy)-2-methylbutan-2-yl]oxy}-3-methylbut-3-en-1-yl)oxy]-4-methoxyfuro[3,2-g]chromen-7-one is found in Angelica dahurica. 9-[(2-{[3-Hydroxy-4-({4-methoxy-7-oxo-7H-furo[3,2-g]chromen-9-yl}oxy)-2-methylbutan-2-yl]oxy}-3-methylbut-3-en-1-yl)oxy]-4-methoxy-7H-furo[3,2-g]chromen-7-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241516462D          

 46 51  0  0  0  0            999 V2000
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  3 46  2  0  0  0  0
 42 46  1  0  0  0  0
M  END

     RDKit          3D

 78 83  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1533004241516462D          

 46 51  0  0  0  0            999 V2000
   -0.2934   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4210   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.2789   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2934  -10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0079  -11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0079  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8329  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1829  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0079  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2934  -13.2000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7224  -13.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7224  -14.0250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4368  -14.4375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4368  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7224  -15.6750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7224  -16.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0079  -16.9125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4368  -16.9125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1513  -16.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1513  -15.6750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8658  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5803  -15.6750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5803  -16.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8658  -14.4375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4789  -13.8855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1433  -13.1318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3228  -13.2180    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1513  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4210  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4210  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1355  -10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2934   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0780   -8.5049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5630   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0780   -7.1701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2934   -7.4250    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  1  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
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  2  0  0  0  0
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 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
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 24 25  1  0  0  0  0
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 29 30  1  0  0  0  0
 24 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 31 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 23 38  2  0  0  0  0
 34 38  1  0  0  0  0
 14 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 11 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 45 46  1  0  0  0  0
  3 46  2  0  0  0  0
 42 46  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0300071

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2C=COC2=C(OCC(O)C(C)(C)OC(COC2=C3OC=CC3=C(OC)C3=C2OC(=O)C=C3)C(C)=C)C2=C1C=CC(=O)O2

> <INCHI_IDENTIFIER>
InChI=1S/C34H32O12/c1-17(2)22(15-42-32-28-20(11-13-40-28)26(38-5)18-7-9-24(36)44-30(18)32)46-34(3,4)23(35)16-43-33-29-21(12-14-41-29)27(39-6)19-8-10-25(37)45-31(19)33/h7-14,22-23,35H,1,15-16H2,2-6H3

> <INCHI_KEY>
JXAVUIQDQXFQNF-UHFFFAOYSA-N

> <FORMULA>
C34H32O12

> <MOLECULAR_WEIGHT>
632.618

> <EXACT_MASS>
632.18937647

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
64.16819685032564

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
9-(2-hydroxy-3-{[1-({4-methoxy-7-oxo-7H-furo[3,2-g]chromen-9-yl}oxy)-3-methylbut-3-en-2-yl]oxy}-3-methylbutoxy)-4-methoxy-7H-furo[3,2-g]chromen-7-one

> <ALOGPS_LOGP>
4.38

> <JCHEM_LOGP>
4.136975433666665

> <ALOGPS_LOGS>
-4.72

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.224436228721427

> <JCHEM_PKA_STRONGEST_BASIC>
-2.555437099336183

> <JCHEM_POLAR_SURFACE_AREA>
145.26000000000005

> <JCHEM_REFRACTIVITY>
163.84109999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.21e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
9-(2-hydroxy-3-{[1-({4-methoxy-7-oxofuro[3,2-g]chromen-9-yl}oxy)-3-methylbut-3-en-2-yl]oxy}-3-methylbutoxy)-4-methoxyfuro[3,2-g]chromen-7-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -0.548 -10.780   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.786 -11.550   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.786 -13.090   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.120 -13.860   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.453 -13.090   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.787 -13.860   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.787 -15.400   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       6.121 -16.170   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0       3.453 -16.170   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.120 -15.400   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.786 -16.170   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       0.786 -17.710   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -0.548 -18.480   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.548 -20.020   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -1.881 -20.790   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.881 -22.330   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.421 -22.330   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.341 -22.330   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.881 -23.870   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -0.548 -24.640   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -3.215 -24.640   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -3.215 -26.180   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -4.549 -26.950   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.549 -28.490   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -3.215 -29.260   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -3.215 -30.800   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -1.881 -31.570   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -4.549 -31.570   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -5.882 -30.800   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -5.882 -29.260   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -7.216 -28.490   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -8.550 -29.260   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -8.550 -30.800   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -7.216 -26.950   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -8.361 -25.920   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -7.734 -24.513   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -6.203 -24.674   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -5.882 -26.180   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       0.786 -20.790   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       0.786 -22.330   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       2.120 -20.020   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -0.548 -15.400   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      -2.012 -15.876   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      -2.918 -14.630   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -2.012 -13.384   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -0.548 -13.860   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   46                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9    4   11                                                  
CONECT   11   10   12   42                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   39                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18   19                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   16   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   38                                                  
CONECT   24   23   25   30                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   24   31                                                  
CONECT   31   30   32   34                                                  
CONECT   32   31   33                                                       
CONECT   33   32                                                            
CONECT   34   31   35   38                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   23   34                                                  
CONECT   39   14   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39                                                            
CONECT   42   11   43   46                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45    3   42                                                  
MASTER        0    0    0    0    0    0    0    0   46    0  102    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₃₂O₁₂

Average Mass

632.6180 Da

Monoisotopic Mass

632.18938 Da

IUPAC Name

9-(2-hydroxy-3-{[1-({4-methoxy-7-oxo-7H-furo[3,2-g]chromen-9-yl}oxy)-3-methylbut-3-en-2-yl]oxy}-3-methylbutoxy)-4-methoxy-7H-furo[3,2-g]chromen-7-one

Traditional Name

9-(2-hydroxy-3-{[1-({4-methoxy-7-oxofuro[3,2-g]chromen-9-yl}oxy)-3-methylbut-3-en-2-yl]oxy}-3-methylbutoxy)-4-methoxyfuro[3,2-g]chromen-7-one

CAS Registry Number

Not Available

SMILES

COC1=C2C=COC2=C(OCC(O)C(C)(C)OC(COC2=C3OC=CC3=C(OC)C3=C2OC(=O)C=C3)C(C)=C)C2=C1C=CC(=O)O2

InChI Identifier

InChI=1S/C34H32O12/c1-17(2)22(15-42-32-28-20(11-13-40-28)26(38-5)18-7-9-24(36)44-30(18)32)46-34(3,4)23(35)16-43-33-29-21(12-14-41-29)27(39-6)19-8-10-25(37)45-31(19)33/h7-14,22-23,35H,1,15-16H2,2-6H3

InChI Key

JXAVUIQDQXFQNF-UHFFFAOYSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Angelica dahurica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 5-methoxypsoralens. These are psoralens containing a methoxy group attached at the C5 position of the psoralen group.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Furanocoumarins

Direct Parent

5-methoxypsoralens

Alternative Parents

Substituents

5-methoxypsoralen
Benzopyran
1-benzopyran
Benzofuran
Anisole
Alkyl aryl ether
Pyranone
Pyran
Benzenoid
Furan
Heteroaromatic compound
Lactone
Secondary alcohol
Organoheterocyclic compound
Ether
Dialkyl ether
Oxacycle
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
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	4.38	ALOGPS
logP	4.14	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	13.22	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	145.26 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	163.84 m³·mol⁻¹	ChemAxon
Polarizability	64.17 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

11050454

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 9-[(2-{[3-hydroxy-4-({4-methoxy-7-oxofuro[3,2-g]chromen-9-yl}oxy)-2-methylbutan-2-yl]oxy}-3-methylbut-3-en-1-yl)oxy]-4-methoxyfuro[3,2-g]chromen-7-one (NP0300071)

MOL for NP0300071 (9-[(2-{[3-hydroxy-4-({4-methoxy-7-oxofuro[3,2-g]chromen-9-yl}oxy)-2-methylbutan-2-yl]oxy}-3-methylbut-3-en-1-yl)oxy]-4-methoxyfuro[3,2-g]chromen-7-one)

3D MOL for NP0300071 (9-[(2-{[3-hydroxy-4-({4-methoxy-7-oxofuro[3,2-g]chromen-9-yl}oxy)-2-methylbutan-2-yl]oxy}-3-methylbut-3-en-1-yl)oxy]-4-methoxyfuro[3,2-g]chromen-7-one)

3D SDF for NP0300071 (9-[(2-{[3-hydroxy-4-({4-methoxy-7-oxofuro[3,2-g]chromen-9-yl}oxy)-2-methylbutan-2-yl]oxy}-3-methylbut-3-en-1-yl)oxy]-4-methoxyfuro[3,2-g]chromen-7-one)

3D-SDF for NP0300071 (9-[(2-{[3-hydroxy-4-({4-methoxy-7-oxofuro[3,2-g]chromen-9-yl}oxy)-2-methylbutan-2-yl]oxy}-3-methylbut-3-en-1-yl)oxy]-4-methoxyfuro[3,2-g]chromen-7-one)

PDB for NP0300071 (9-[(2-{[3-hydroxy-4-({4-methoxy-7-oxofuro[3,2-g]chromen-9-yl}oxy)-2-methylbutan-2-yl]oxy}-3-methylbut-3-en-1-yl)oxy]-4-methoxyfuro[3,2-g]chromen-7-one)

3D PDB for NP0300071 (9-[(2-{[3-hydroxy-4-({4-methoxy-7-oxofuro[3,2-g]chromen-9-yl}oxy)-2-methylbutan-2-yl]oxy}-3-methylbut-3-en-1-yl)oxy]-4-methoxyfuro[3,2-g]chromen-7-one)

SMILES for NP0300071 (9-[(2-{[3-hydroxy-4-({4-methoxy-7-oxofuro[3,2-g]chromen-9-yl}oxy)-2-methylbutan-2-yl]oxy}-3-methylbut-3-en-1-yl)oxy]-4-methoxyfuro[3,2-g]chromen-7-one)

INCHI for NP0300071 (9-[(2-{[3-hydroxy-4-({4-methoxy-7-oxofuro[3,2-g]chromen-9-yl}oxy)-2-methylbutan-2-yl]oxy}-3-methylbut-3-en-1-yl)oxy]-4-methoxyfuro[3,2-g]chromen-7-one)

Structure for NP0300071 (9-[(2-{[3-hydroxy-4-({4-methoxy-7-oxofuro[3,2-g]chromen-9-yl}oxy)-2-methylbutan-2-yl]oxy}-3-methylbut-3-en-1-yl)oxy]-4-methoxyfuro[3,2-g]chromen-7-one)

3D Structure for NP0300071 (9-[(2-{[3-hydroxy-4-({4-methoxy-7-oxofuro[3,2-g]chromen-9-yl}oxy)-2-methylbutan-2-yl]oxy}-3-methylbut-3-en-1-yl)oxy]-4-methoxyfuro[3,2-g]chromen-7-one)