NP-MRD: Showing NP-Card for 7-formyl-4-hydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalen]-6'-yl acetate (NP0240304)

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Record Information

Version

2.0

Created at

2022-09-07 00:05:40 UTC

Updated at

2022-09-07 00:05:40 UTC

NP-MRD ID

NP0240304

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-formyl-4-hydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalen]-6'-yl acetate

Description

7-Formyl-4-hydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,5',6',7',8',8'a-octahydro-2'H,3H-spiro[1-benzofuran-2,1'-naphthalene]-6'-yl acetate belongs to the class of organic compounds known as benzofurans. These are organic compounds containing a benzene ring fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. Based on a literature review very few articles have been published on 7-formyl-4-hydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,5',6',7',8',8'a-octahydro-2'H,3H-spiro[1-benzofuran-2,1'-naphthalene]-6'-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072202052D          

 31 34  0  0  0  0            999 V2000
    4.4702    2.5100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2055    2.1359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8972    2.5857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2493    1.3121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5577    0.8623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8223    1.2363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1307    0.7866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1744   -0.0373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5907    0.5457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9098   -0.4113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9535   -1.2352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2619   -1.6850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5266   -1.3109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8349   -1.7607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4828   -0.4871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7480   -0.8621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1643   -0.2791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3404   -0.3228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0336   -1.0582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1094    0.3688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2647    1.1041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1851    1.7957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0089    1.7520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0885    1.1478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4626    1.8832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0128    2.5748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5383    0.4562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3532    0.3277    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6014    0.0384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0750   -0.6370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4262    0.0534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
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 10 29  1  0  0  0  0
  5 29  1  0  0  0  0
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 29 31  1  0  0  0  0
M  END

     RDKit          3D

 65 68  0  0  0  0  0  0  0  0999 V2000
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   -0.8054   -1.4580    0.0020 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -3.5171    0.2079    1.8880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2804    0.1607    3.2554 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5422    0.9395    1.3256 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7605    0.9743   -0.0243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8792    1.7767   -0.5977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5572    2.3999    0.4457 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9095    0.2408   -0.8395 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1694    0.2992   -2.2731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9186   -0.4854   -2.8845 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8814   -0.4943   -0.2886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9279   -1.2853   -0.8912 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8378    0.7848   -1.9275 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -0.6780   -0.3735 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1325   -1.7430    1.3050 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9433   -2.5383   -0.0536 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3411   -4.0691   -0.4523 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.0950   -3.5238    0.3674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6579   -4.4561   -1.6335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7027   -2.9666   -1.9118 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.5254    2.5559   -1.2920 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1 34  1  0
M  END


  Mrv1652309072202052D          

 31 34  0  0  0  0            999 V2000
    4.4702    2.5100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2055    2.1359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8972    2.5857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2493    1.3121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5577    0.8623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8223    1.2363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1307    0.7866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.2647    1.1041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.0089    1.7520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4626    1.8832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.5383    0.4562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3532    0.3277    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6014    0.0384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0750   -0.6370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4262    0.0534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0240304

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CCC2C(C)(C)C(CCC2(C)C11CC2=C(O)C=C(CO)C(C=O)=C2O1)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H34O6/c1-14-6-7-20-23(3,4)21(30-15(2)28)8-9-24(20,5)25(14)11-17-19(29)10-16(12-26)18(13-27)22(17)31-25/h10,13-14,20-21,26,29H,6-9,11-12H2,1-5H3

> <INCHI_KEY>
QQTZGKRXYRFKIF-UHFFFAOYSA-N

> <FORMULA>
C25H34O6

> <MOLECULAR_WEIGHT>
430.541

> <EXACT_MASS>
430.235538815

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
47.420290971066414

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-formyl-4-hydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,5',6',7',8',8'a-octahydro-2'H,3H-spiro[1-benzofuran-2,1'-naphthalene]-6'-yl acetate

> <JCHEM_LOGP>
3.8378471436666652

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.871037548046402

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.433841409373982

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9541208275556254

> <JCHEM_POLAR_SURFACE_AREA>
93.06000000000002

> <JCHEM_REFRACTIVITY>
117.09579999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
7-formyl-4-hydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,6',7',8'-hexahydro-2'H,3H-spiro[1-benzofuran-2,1'-naphthalene]-6'-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       8.344   4.685   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.717   3.987   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      11.008   4.827   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       9.799   2.449   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       8.508   1.610   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.135   2.308   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.844   1.468   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.926  -0.070   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.836   1.019   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.298  -0.768   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.380  -2.306   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.089  -3.145   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.716  -2.447   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.425  -3.287   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.635  -0.909   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.263  -1.609   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.173  -0.521   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.635  -0.603   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.063  -1.975   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -0.204   0.688   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.494   2.061   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.346   3.352   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.883   3.270   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.032   2.143   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.730   3.515   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.891   4.806   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.872   0.852   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       4.393   0.612   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       8.589   0.072   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.473  -1.189   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.129   0.100   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   29                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10   15                                             
CONECT    9    8                                                            
CONECT   10    8   11   29                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    8   16   28                                             
CONECT   16   15   17                                                       
CONECT   17   16   18   27                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   24   17   28                                                  
CONECT   28   27   15                                                       
CONECT   29   10    5   30   31                                             
CONECT   30   29                                                            
CONECT   31   29                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Value	Source
7-Formyl-4-hydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,5',6',7',8',8'a-octahydro-2'H,3H-spiro[1-benzofuran-2,1'-naphthalene]-6'-yl acetic acid	Generator

Chemical Formula

C₂₅H₃₄O₆

Average Mass

430.5410 Da

Monoisotopic Mass

430.23554 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1CCC2C(C)(C)C(CCC2(C)C11CC2=C(O)C=C(CO)C(C=O)=C2O1)OC(C)=O

InChI Identifier

InChI=1S/C25H34O6/c1-14-6-7-20-23(3,4)21(30-15(2)28)8-9-24(20,5)25(14)11-17-19(29)10-16(12-26)18(13-27)22(17)31-25/h10,13-14,20-21,26,29H,6-9,11-12H2,1-5H3

InChI Key

QQTZGKRXYRFKIF-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzofurans. These are organic compounds containing a benzene ring fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzofurans

Sub Class

Not Available

Direct Parent

Benzofurans

Alternative Parents

Substituents

Coumaran
Benzofuran
1-hydroxy-2-unsubstituted benzenoid
Aryl-aldehyde
Alkyl aryl ether
Benzenoid
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Aromatic alcohol
Primary alcohol
Organooxygen compound
Carbonyl group
Aldehyde
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

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

162922516

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-formyl-4-hydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalen]-6'-yl acetate (NP0240304)

MOL for NP0240304 (7-formyl-4-hydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalen]-6'-yl acetate)

3D MOL for NP0240304 (7-formyl-4-hydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalen]-6'-yl acetate)

3D SDF for NP0240304 (7-formyl-4-hydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalen]-6'-yl acetate)

3D-SDF for NP0240304 (7-formyl-4-hydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalen]-6'-yl acetate)

PDB for NP0240304 (7-formyl-4-hydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalen]-6'-yl acetate)

3D PDB for NP0240304 (7-formyl-4-hydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalen]-6'-yl acetate)

SMILES for NP0240304 (7-formyl-4-hydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalen]-6'-yl acetate)

INCHI for NP0240304 (7-formyl-4-hydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalen]-6'-yl acetate)

Structure for NP0240304 (7-formyl-4-hydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalen]-6'-yl acetate)

3D Structure for NP0240304 (7-formyl-4-hydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,6',7',8'-hexahydro-2'h,3h-spiro[1-benzofuran-2,1'-naphthalen]-6'-yl acetate)