NP-MRD: Showing NP-Card for 2-[(3-{1,1,7,7a-tetramethyl-1ah,2h,4h,5h,6h,7h,7bh-cyclopropa[a]naphthalen-2-yl}-5-acetyl-2,4,6-trihydroxyphenyl)methyl]-6-acetyl-3,5-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one (NP0256280)

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Record Information

Version

2.0

Created at

2022-09-07 21:02:30 UTC

Updated at

2022-09-07 21:02:30 UTC

NP-MRD ID

NP0256280

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(3-{1,1,7,7a-tetramethyl-1ah,2h,4h,5h,6h,7h,7bh-cyclopropa[a]naphthalen-2-yl}-5-acetyl-2,4,6-trihydroxyphenyl)methyl]-6-acetyl-3,5-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one

Description

2-Acetyl-6-[(3-acetyl-5-{1,1,1b,2-tetramethyl-1H,1aH,1bH,2H,3H,4H,5H,7H,7aH-cyclopropa[a]naphthalen-7-yl}-2,4,6-trihydroxyphenyl)methyl]-3,5-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one belongs to the class of organic compounds known as aristolane sesquiterpenoids. These are sesquiterpenoids with a structure based on the aristolane skeleton. Aristolanes arise from the C6,C11 cyclization of the bicyclic eremophilane skeleton. 2-[(3-{1,1,7,7a-tetramethyl-1ah,2h,4h,5h,6h,7h,7bh-cyclopropa[a]naphthalen-2-yl}-5-acetyl-2,4,6-trihydroxyphenyl)methyl]-6-acetyl-3,5-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one is found in Dryopteris cycadina. 2-Acetyl-6-[(3-acetyl-5-{1,1,1b,2-tetramethyl-1H,1aH,1bH,2H,3H,4H,5H,7H,7aH-cyclopropa[a]naphthalen-7-yl}-2,4,6-trihydroxyphenyl)methyl]-3,5-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241518082D          

 42 46  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004241518082D          

 42 46  0  0  0  0            999 V2000
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    4.1482   -1.8917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7123   -1.1317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2485   -0.9196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5763   -1.6767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7237    1.0677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5432    0.9730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8711    0.2160    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0350    1.6355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8545    1.5408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3463    2.2033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0184    2.9604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1989    3.0550    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5102    3.6228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7724    3.9920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7457    4.4135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3297    3.5282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6576    2.7711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4771    2.6765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9688    3.3389    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8049    1.9194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1658    2.1087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4936    1.3516    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8215    4.1906    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7072    2.3926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7156    3.2175    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8876    2.4872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5598    3.2443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0515    3.9067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7402    3.3389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3959    1.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5763    1.9194    0.0000 O   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  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 10 14  1  0  0  0  0
  2 14  1  0  0  0  0
  6 14  1  0  0  0  0
 14 15  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 24 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 28 32  1  0  0  0  0
 21 32  1  0  0  0  0
 32 33  2  0  0  0  0
 27 34  1  0  0  0  0
 19 35  2  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 37 41  2  0  0  0  0
 16 41  1  0  0  0  0
 41 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0256280

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CCCC2=CC(C3C(C3(C)C)C12C)C1=C(O)C(CC2=C(O)C(C)(C)C(O)=C(C(C)=O)C2=O)=C(O)C(C(C)=O)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C34H42O8/c1-14-10-9-11-17-12-18(24-29(32(24,4)5)34(14,17)8)23-26(38)19(25(37)21(15(2)35)28(23)40)13-20-27(39)22(16(3)36)31(42)33(6,7)30(20)41/h12,14,18,24,29,37-38,40-42H,9-11,13H2,1-8H3

> <INCHI_KEY>
SAXKLAUHZWFAPW-UHFFFAOYSA-N

> <FORMULA>
C34H42O8

> <MOLECULAR_WEIGHT>
578.702

> <EXACT_MASS>
578.287968312

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
62.52278306298723

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(3-{1,1,7,7a-tetramethyl-1H,1aH,2H,4H,5H,6H,7H,7aH,7bH-cyclopropa[a]naphthalen-2-yl}-5-acetyl-2,4,6-trihydroxyphenyl)methyl]-6-acetyl-3,5-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one

> <ALOGPS_LOGP>
4.74

> <JCHEM_LOGP>
6.115692393333332

> <ALOGPS_LOGS>
-4.78

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
5.4752110576186865

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.0444675319101893

> <JCHEM_PKA_STRONGEST_BASIC>
-4.662106598337421

> <JCHEM_POLAR_SURFACE_AREA>
152.35999999999999

> <JCHEM_REFRACTIVITY>
162.5463

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.67e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(3-{1,1,7,7a-tetramethyl-1aH,2H,4H,5H,6H,7H,7bH-cyclopropa[a]naphthalen-2-yl}-5-acetyl-2,4,6-trihydroxyphenyl)methyl]-6-acetyl-3,5-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-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       3.891  -4.366   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.279  -2.953   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.749  -2.777   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.138  -1.363   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.055  -0.127   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.585  -0.303   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.503   0.933   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.033   0.756   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.645  -0.657   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.727  -1.893   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.257  -2.070   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.743  -3.531   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.796  -2.113   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.197  -1.717   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.809  -3.130   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.951   1.993   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.481   1.816   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       9.093   0.403   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       9.399   3.053   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.928   2.876   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.846   4.113   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.234   5.526   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.705   5.703   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      12.152   6.763   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.775   7.452   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      12.592   8.238   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      13.682   6.586   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      14.294   5.173   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      15.824   4.996   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      16.742   6.233   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      16.436   3.583   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      13.376   3.936   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      13.988   2.523   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      14.600   7.822   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       8.787   4.466   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       8.802   6.006   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       7.257   4.643   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       6.645   6.056   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       7.563   7.293   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       5.115   6.233   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       6.339   3.406   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       4.809   3.583   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   14                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   14                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   16                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9   11   14                                                  
CONECT   11   10    9   12   13                                             
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   10    2    6   15                                             
CONECT   15   14                                                            
CONECT   16    8   17   41                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   35                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   32                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26   27                                             
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   24   28   34                                                  
CONECT   28   27   29   32                                                  
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   28   21   33                                                  
CONECT   33   32                                                            
CONECT   34   27                                                            
CONECT   35   19   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38   41                                                  
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41   37   16   42                                                  
CONECT   42   41                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₄₂O₈

Average Mass

578.7020 Da

Monoisotopic Mass

578.28797 Da

IUPAC Name

2-[(3-{1,1,7,7a-tetramethyl-1H,1aH,2H,4H,5H,6H,7H,7aH,7bH-cyclopropa[a]naphthalen-2-yl}-5-acetyl-2,4,6-trihydroxyphenyl)methyl]-6-acetyl-3,5-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one

Traditional Name

2-[(3-{1,1,7,7a-tetramethyl-1aH,2H,4H,5H,6H,7H,7bH-cyclopropa[a]naphthalen-2-yl}-5-acetyl-2,4,6-trihydroxyphenyl)methyl]-6-acetyl-3,5-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one

CAS Registry Number

Not Available

SMILES

CC1CCCC2=CC(C3C(C3(C)C)C12C)C1=C(O)C(CC2=C(O)C(C)(C)C(O)=C(C(C)=O)C2=O)=C(O)C(C(C)=O)=C1O

InChI Identifier

InChI=1S/C34H42O8/c1-14-10-9-11-17-12-18(24-29(32(24,4)5)34(14,17)8)23-26(38)19(25(37)21(15(2)35)28(23)40)13-20-27(39)22(16(3)36)31(42)33(6,7)30(20)41/h12,14,18,24,29,37-38,40-42H,9-11,13H2,1-8H3

InChI Key

SAXKLAUHZWFAPW-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
Dryopteris cycadina	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aristolane sesquiterpenoids. These are sesquiterpenoids with a structure based on the aristolane skeleton. Aristolanes arise from the C6,C11 cyclization of the bicyclic eremophilane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Aristolane sesquiterpenoids

Alternative Parents

Substituents

Aristolane sesquiterpenoid
Alkyl-phenylketone
Acylphloroglucinol derivative
Acetophenone
Phenylketone
Benzenetriol
Phloroglucinol derivative
Aryl alkyl ketone
Aryl ketone
Benzoyl
Phenol
Monocyclic benzene moiety
Benzenoid
Vinylogous acid
Cyclic ketone
Ketone
Polyol
Enol
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	4.74	ALOGPS
logP	6.12	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	3.04	ChemAxon
pKa (Strongest Basic)	-4.7	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	152.36 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	162.55 m³·mol⁻¹	ChemAxon
Polarizability	62.52 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[(3-{1,1,7,7a-tetramethyl-1ah,2h,4h,5h,6h,7h,7bh-cyclopropa[a]naphthalen-2-yl}-5-acetyl-2,4,6-trihydroxyphenyl)methyl]-6-acetyl-3,5-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one (NP0256280)

MOL for NP0256280 (2-[(3-{1,1,7,7a-tetramethyl-1ah,2h,4h,5h,6h,7h,7bh-cyclopropa[a]naphthalen-2-yl}-5-acetyl-2,4,6-trihydroxyphenyl)methyl]-6-acetyl-3,5-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one)

3D MOL for NP0256280 (2-[(3-{1,1,7,7a-tetramethyl-1ah,2h,4h,5h,6h,7h,7bh-cyclopropa[a]naphthalen-2-yl}-5-acetyl-2,4,6-trihydroxyphenyl)methyl]-6-acetyl-3,5-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one)

3D SDF for NP0256280 (2-[(3-{1,1,7,7a-tetramethyl-1ah,2h,4h,5h,6h,7h,7bh-cyclopropa[a]naphthalen-2-yl}-5-acetyl-2,4,6-trihydroxyphenyl)methyl]-6-acetyl-3,5-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one)

3D-SDF for NP0256280 (2-[(3-{1,1,7,7a-tetramethyl-1ah,2h,4h,5h,6h,7h,7bh-cyclopropa[a]naphthalen-2-yl}-5-acetyl-2,4,6-trihydroxyphenyl)methyl]-6-acetyl-3,5-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one)

PDB for NP0256280 (2-[(3-{1,1,7,7a-tetramethyl-1ah,2h,4h,5h,6h,7h,7bh-cyclopropa[a]naphthalen-2-yl}-5-acetyl-2,4,6-trihydroxyphenyl)methyl]-6-acetyl-3,5-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one)

3D PDB for NP0256280 (2-[(3-{1,1,7,7a-tetramethyl-1ah,2h,4h,5h,6h,7h,7bh-cyclopropa[a]naphthalen-2-yl}-5-acetyl-2,4,6-trihydroxyphenyl)methyl]-6-acetyl-3,5-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one)

SMILES for NP0256280 (2-[(3-{1,1,7,7a-tetramethyl-1ah,2h,4h,5h,6h,7h,7bh-cyclopropa[a]naphthalen-2-yl}-5-acetyl-2,4,6-trihydroxyphenyl)methyl]-6-acetyl-3,5-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one)

INCHI for NP0256280 (2-[(3-{1,1,7,7a-tetramethyl-1ah,2h,4h,5h,6h,7h,7bh-cyclopropa[a]naphthalen-2-yl}-5-acetyl-2,4,6-trihydroxyphenyl)methyl]-6-acetyl-3,5-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one)

Structure for NP0256280 (2-[(3-{1,1,7,7a-tetramethyl-1ah,2h,4h,5h,6h,7h,7bh-cyclopropa[a]naphthalen-2-yl}-5-acetyl-2,4,6-trihydroxyphenyl)methyl]-6-acetyl-3,5-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one)

3D Structure for NP0256280 (2-[(3-{1,1,7,7a-tetramethyl-1ah,2h,4h,5h,6h,7h,7bh-cyclopropa[a]naphthalen-2-yl}-5-acetyl-2,4,6-trihydroxyphenyl)methyl]-6-acetyl-3,5-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one)