NP-MRD: Showing NP-Card for (3r)-8,9-bis[(3r)-7-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)-9,10-dioxocyclohexa[f]chromen-8-yl]-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexa[f]chromene-7,10-dione (NP0156971)

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Record Information

Version

2.0

Created at

2022-09-02 14:15:50 UTC

Updated at

2022-09-02 14:15:50 UTC

NP-MRD ID

NP0156971

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r)-8,9-bis[(3r)-7-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)-9,10-dioxocyclohexa[f]chromen-8-yl]-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexa[f]chromene-7,10-dione

Description

(3R)-8,9-bis[(3R)-7-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)-9,10-dioxo-3H,9H,10H-cyclohexa[f]chromen-8-yl]-3-methyl-3-(4-methylpent-3-en-1-yl)-3H,7H,10H-cyclohexa[f]chromene-7,10-dione belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. Based on a literature review very few articles have been published on (3R)-8,9-bis[(3R)-7-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)-9,10-dioxo-3H,9H,10H-cyclohexa[f]chromen-8-yl]-3-methyl-3-(4-methylpent-3-en-1-yl)-3H,7H,10H-cyclohexa[f]chromene-7,10-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022216152D          

 71 79  0  0  1  0            999 V2000
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M  END

     RDKit          3D

127135  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652309022216152D          

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M  END
> <DATABASE_ID>
NP0156971

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC[C@@]1(C)OC2=CC=C3C(O)=C(C(=O)C(=O)C3=C2C=C1)C1=C(C(=O)C2=C(C=CC3=C2C=C[C@@](C)(CCC=C(C)C)O3)C1=O)C1=C(O)C2=CC=C3O[C@](C)(CCC=C(C)C)C=CC3=C2C(=O)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C60H56O11/c1-31(2)13-10-25-58(7)28-22-34-40(69-58)19-16-37-43(34)53(64)47(49-52(63)39-18-21-42-36(45(39)55(66)57(49)68)24-30-60(9,71-42)27-12-15-33(5)6)46(50(37)61)48-51(62)38-17-20-41-35(44(38)54(65)56(48)67)23-29-59(8,70-41)26-11-14-32(3)4/h13-24,28-30,62-63H,10-12,25-27H2,1-9H3/t58-,59-,60-/m1/s1

> <INCHI_KEY>
RHQKAXXTUCIZNS-UPMPAGDASA-N

> <FORMULA>
C60H56O11

> <MOLECULAR_WEIGHT>
953.097

> <EXACT_MASS>
952.382262623

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
127

> <JCHEM_AVERAGE_POLARIZABILITY>
106.71572735816824

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3R)-8,9-bis[(3R)-7-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)-9,10-dioxo-3H,9H,10H-cyclohexa[f]chromen-8-yl]-3-methyl-3-(4-methylpent-3-en-1-yl)-3H,7H,10H-cyclohexa[f]chromene-7,10-dione

> <ALOGPS_LOGP>
5.40

> <JCHEM_LOGP>
11.191172187

> <ALOGPS_LOGS>
-7.49

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
9

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
5.60868387656264

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.751838776127865

> <JCHEM_PKA_STRONGEST_BASIC>
-4.443014584139558

> <JCHEM_POLAR_SURFACE_AREA>
170.56999999999996

> <JCHEM_REFRACTIVITY>
282.0747999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.06e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R)-8,9-bis[(3R)-7-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)-9,10-dioxocyclohexa[f]chromen-8-yl]-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexa[f]chromene-7,10-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0     -18.968  -2.130   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -18.701  -0.614   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -19.881   0.376   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -17.254  -0.087   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -16.074  -1.077   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -14.627  -0.550   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -13.447  -1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -14.627  -2.530   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -12.677  -2.874   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -11.137  -2.874   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -10.367  -1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -11.137  -0.206   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -10.367   1.127   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -8.827   1.127   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -8.057  -0.206   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -8.827  -1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -8.057  -2.874   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -8.827  -4.207   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -6.517  -2.874   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -5.747  -4.207   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -6.517  -5.541   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -8.057  -5.541   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -5.747  -6.875   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -6.517  -8.208   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -5.747  -9.542   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -4.207  -9.542   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -3.437  -8.208   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -4.207  -6.875   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -3.437  -5.541   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -1.897  -5.541   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -4.207  -4.207   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -3.606  -2.243   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -1.897  -8.208   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -1.127  -9.542   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -1.897 -10.876   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -0.450 -11.402   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -2.165 -12.392   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -0.985 -13.382   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -1.252 -14.899   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -2.700 -15.426   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -2.967 -16.942   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -3.879 -14.436   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      -3.437 -10.876   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      -5.747  -1.540   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -4.207  -1.540   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -3.437  -2.874   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      -3.276  -4.405   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      -1.897  -2.874   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -1.127  -4.207   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       0.413  -4.207   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       1.183  -2.874   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       0.413  -1.540   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      -1.127  -1.540   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      -1.897  -0.206   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0      -1.127   1.127   0.000  0.00  0.00           O+0
HETATM   56  C   UNK     0      -3.437  -0.206   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0      -4.207   1.127   0.000  0.00  0.00           O+0
HETATM   58  C   UNK     0       1.183  -0.206   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0       2.723  -0.206   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0       3.493  -1.540   0.000  0.00  0.00           C+0
HETATM   61  C   UNK     0       4.672  -2.530   0.000  0.00  0.00           C+0
HETATM   62  C   UNK     0       4.672  -0.550   0.000  0.00  0.00           C+0
HETATM   63  C   UNK     0       6.119  -1.077   0.000  0.00  0.00           C+0
HETATM   64  C   UNK     0       7.299  -0.087   0.000  0.00  0.00           C+0
HETATM   65  C   UNK     0       8.746  -0.614   0.000  0.00  0.00           C+0
HETATM   66  C   UNK     0       9.926   0.376   0.000  0.00  0.00           C+0
HETATM   67  C   UNK     0       9.014  -2.130   0.000  0.00  0.00           C+0
HETATM   68  O   UNK     0       2.723  -2.874   0.000  0.00  0.00           O+0
HETATM   69  C   UNK     0      -6.517  -0.206   0.000  0.00  0.00           C+0
HETATM   70  O   UNK     0      -5.747   1.127   0.000  0.00  0.00           O+0
HETATM   71  O   UNK     0     -12.677  -0.206   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   71                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13   71                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   69                                                  
CONECT   16   15   11   17                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   44                                                  
CONECT   20   19   21   31                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   28                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   43                                                  
CONECT   27   26   28   33                                                  
CONECT   28   27   23   29                                                  
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   20   32                                                  
CONECT   32   31                                                            
CONECT   33   27   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36   37   43                                             
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40                                                            
CONECT   43   35   26                                                       
CONECT   44   19   45   69                                                  
CONECT   45   44   46   56                                                  
CONECT   46   45   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46   49   53                                                  
CONECT   49   48   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50   52   68                                                  
CONECT   52   51   53   58                                                  
CONECT   53   52   48   54                                                  
CONECT   54   53   55   56                                                  
CONECT   55   54                                                            
CONECT   56   54   45   57                                                  
CONECT   57   56                                                            
CONECT   58   52   59                                                       
CONECT   59   58   60                                                       
CONECT   60   59   61   62   68                                             
CONECT   61   60                                                            
CONECT   62   60   63                                                       
CONECT   63   62   64                                                       
CONECT   64   63   65                                                       
CONECT   65   64   66   67                                                  
CONECT   66   65                                                            
CONECT   67   65                                                            
CONECT   68   60   51                                                       
CONECT   69   44   15   70                                                  
CONECT   70   69                                                            
CONECT   71   12    7                                                       
MASTER        0    0    0    0    0    0    0    0   71    0  158    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₆₀H₅₆O₁₁

Average Mass

953.0970 Da

Monoisotopic Mass

952.38226 Da

IUPAC Name

(3R)-8,9-bis[(3R)-7-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)-9,10-dioxo-3H,9H,10H-cyclohexa[f]chromen-8-yl]-3-methyl-3-(4-methylpent-3-en-1-yl)-3H,7H,10H-cyclohexa[f]chromene-7,10-dione

Traditional Name

(3R)-8,9-bis[(3R)-7-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)-9,10-dioxocyclohexa[f]chromen-8-yl]-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexa[f]chromene-7,10-dione

CAS Registry Number

Not Available

SMILES

CC(C)=CCC[C@@]1(C)OC2=CC=C3C(O)=C(C(=O)C(=O)C3=C2C=C1)C1=C(C(=O)C2=C(C=CC3=C2C=C[C@@](C)(CCC=C(C)C)O3)C1=O)C1=C(O)C2=CC=C3O[C@](C)(CCC=C(C)C)C=CC3=C2C(=O)C1=O

InChI Identifier

InChI=1S/C60H56O11/c1-31(2)13-10-25-58(7)28-22-34-40(69-58)19-16-37-43(34)53(64)47(49-52(63)39-18-21-42-36(45(39)55(66)57(49)68)24-30-60(9,71-42)27-12-15-33(5)6)46(50(37)61)48-51(62)38-17-20-41-35(44(38)54(65)56(48)67)23-29-59(8,70-41)26-11-14-32(3)4/h13-24,28-30,62-63H,10-12,25-27H2,1-9H3/t58-,59-,60-/m1/s1

InChI Key

RHQKAXXTUCIZNS-UPMPAGDASA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Naphthoquinone
1-naphthol
Benzopyran
Naphthalene
1-benzopyran
Aryl ketone
Quinone
Alkyl aryl ether
Benzenoid
Pyran
Vinylogous acid
Ketone
Cyclic ketone
Enol
Ether
Oxacycle
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organooxygen compound
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	5.4	ALOGPS
logP	11.19	ChemAxon
logS	-7.5	ALOGPS
pKa (Strongest Acidic)	4.75	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	170.57 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	282.07 m³·mol⁻¹	ChemAxon
Polarizability	106.72 Å³	ChemAxon
Number of Rings	9	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

4445046

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5281731

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3r)-8,9-bis[(3r)-7-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)-9,10-dioxocyclohexa[f]chromen-8-yl]-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexa[f]chromene-7,10-dione (NP0156971)

MOL for NP0156971 ((3r)-8,9-bis[(3r)-7-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)-9,10-dioxocyclohexa[f]chromen-8-yl]-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexa[f]chromene-7,10-dione)

3D MOL for NP0156971 ((3r)-8,9-bis[(3r)-7-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)-9,10-dioxocyclohexa[f]chromen-8-yl]-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexa[f]chromene-7,10-dione)

3D SDF for NP0156971 ((3r)-8,9-bis[(3r)-7-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)-9,10-dioxocyclohexa[f]chromen-8-yl]-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexa[f]chromene-7,10-dione)

3D-SDF for NP0156971 ((3r)-8,9-bis[(3r)-7-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)-9,10-dioxocyclohexa[f]chromen-8-yl]-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexa[f]chromene-7,10-dione)

PDB for NP0156971 ((3r)-8,9-bis[(3r)-7-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)-9,10-dioxocyclohexa[f]chromen-8-yl]-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexa[f]chromene-7,10-dione)

3D PDB for NP0156971 ((3r)-8,9-bis[(3r)-7-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)-9,10-dioxocyclohexa[f]chromen-8-yl]-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexa[f]chromene-7,10-dione)

SMILES for NP0156971 ((3r)-8,9-bis[(3r)-7-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)-9,10-dioxocyclohexa[f]chromen-8-yl]-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexa[f]chromene-7,10-dione)

INCHI for NP0156971 ((3r)-8,9-bis[(3r)-7-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)-9,10-dioxocyclohexa[f]chromen-8-yl]-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexa[f]chromene-7,10-dione)

Structure for NP0156971 ((3r)-8,9-bis[(3r)-7-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)-9,10-dioxocyclohexa[f]chromen-8-yl]-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexa[f]chromene-7,10-dione)

3D Structure for NP0156971 ((3r)-8,9-bis[(3r)-7-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)-9,10-dioxocyclohexa[f]chromen-8-yl]-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexa[f]chromene-7,10-dione)