NP-MRD: Showing NP-Card for 13-hydroxy-13-(hydroxymethyl)-2,6-dimethyltetracyclo[10.3.1.0¹,¹⁰.0²,⁷]hexadec-6-ene-5,8-dione (NP0328645)

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Record Information

Version

1.0

Created at

2022-09-12 12:18:05 UTC

Updated at

2022-09-12 12:18:05 UTC

NP-MRD ID

NP0328645

Secondary Accession Numbers

None

Natural Product Identification

Common Name

13-hydroxy-13-(hydroxymethyl)-2,6-dimethyltetracyclo[10.3.1.0¹,¹⁰.0²,⁷]hexadec-6-ene-5,8-dione

Description

13-Hydroxy-13-(hydroxymethyl)-2,6-dimethyltetracyclo[10.3.1.0¹,¹⁰.0²,⁷]Hexadec-6-ene-5,8-dione belongs to the class of organic compounds known as chamigranes. These are sesquiterpenoids characterized by a 1,1,5,9-tetramethylspiro[5,5]undecane skeleton, formally obtained by linking the C1-C6 and C6-C11 of farnesane together. They are predominantly isolated from algae. Based on a literature review very few articles have been published on 13-hydroxy-13-(hydroxymethyl)-2,6-dimethyltetracyclo[10.3.1.0¹,¹⁰.0²,⁷]Hexadec-6-ene-5,8-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 49 52  0  0  0  0  0  0  0  0999 V2000
   -4.5059   -0.8135    0.8835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4404    0.0158    0.2155 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2270   -0.4716    0.0410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9550   -1.8425    0.5229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8707   -2.6825    0.6081 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5498   -2.2224    0.9141 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3215   -1.6042   -0.1246 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8064   -1.7471    0.1424 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4310   -0.5965   -0.6137 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2566    0.1451   -1.2852 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2017   -0.1145   -0.2187 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6615    0.4925    1.0615 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9768    1.2302    0.9574 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0575    0.4464    0.2819 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7787    1.2904   -0.6066 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0901   -0.1265    1.2128 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7594    0.9018    1.9169 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1823    0.3200   -0.6411 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2843   -0.1034   -2.1264 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3384    1.7932   -0.6327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6143    2.3529   -0.0853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7094    1.3680   -0.2442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8343    1.6517   -0.7484 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8688   -1.6037    0.1588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1910   -1.2127    1.8455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3885   -0.1595    1.0146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4783   -3.3242    0.8093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3213   -1.9770    1.9483 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1352   -2.1447   -1.0766 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1807   -2.6780   -0.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0493   -1.7967    1.1992 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1161   -0.9405   -1.4162 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4706    1.1982   -1.4427 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0193   -0.3583   -2.2378 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8314   -0.3020    1.8480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0821    1.1701    1.5272 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3196    1.3923    2.0220 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8545    2.2519    0.5459 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2780    0.7090   -1.2375 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6870   -0.8718    1.9161 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8708   -0.5956    0.5796 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9549    1.6489    1.3286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7095    0.5535   -2.7797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1751   -1.1740   -2.2656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3669    0.1181   -2.3714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4480    2.3050   -0.1257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2469    2.2395   -1.6782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4343    2.5771    1.0073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8858    3.2921   -0.6187 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  1
 12 13  1  0
 13 14  1  0
 14 15  1  6
 14 16  1  0
 16 17  1  0
 11 18  1  0
 18 19  1  6
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22  2  1  0
 18  3  1  0
 11  7  1  0
 14  9  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  6 27  1  0
  6 28  1  0
  7 29  1  6
  8 30  1  0
  8 31  1  0
  9 32  1  6
 10 33  1  0
 10 34  1  0
 12 35  1  0
 12 36  1  0
 13 37  1  0
 13 38  1  0
 15 39  1  0
 16 40  1  0
 16 41  1  0
 17 42  1  0
 19 43  1  0
 19 44  1  0
 19 45  1  0
 20 46  1  0
 20 47  1  0
 21 48  1  0
 21 49  1  0
M  END


  Mrv1652309122214182D          

 23 26  0  0  0  0            999 V2000
    4.4260   -0.0478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8370    0.5299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0422    0.3086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8228   -0.4928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4074   -1.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0268   -0.7144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4403   -0.1303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5906   -0.3140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1529    0.4410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8533    0.6524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5889    0.7373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    1.6094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5438    1.9121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0535    1.2932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6578    1.8548    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8588    1.1141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1064    0.3272    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4532    0.8863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8940    1.4929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6590    1.6852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4538    1.9065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0428    1.3288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8375    1.5500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  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
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  7 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
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 11 18  1  0  0  0  0
  3 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0328645

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=C2C(=O)CC3CC4CC3(CCC4(O)CO)C2(C)CCC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H26O4/c1-11-14(21)3-4-17(2)16(11)15(22)8-12-7-13-9-18(12,17)5-6-19(13,23)10-20/h12-13,20,23H,3-10H2,1-2H3

> <INCHI_KEY>
KEIKTRADEAFSDO-UHFFFAOYSA-N

> <FORMULA>
C19H26O4

> <MOLECULAR_WEIGHT>
318.413

> <EXACT_MASS>
318.183109317

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
34.35564186817284

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
13-hydroxy-13-(hydroxymethyl)-2,6-dimethyltetracyclo[10.3.1.0^{1,10}.0^{2,7}]hexadec-6-ene-5,8-dione

> <JCHEM_LOGP>
1.517815636

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.313609287783958

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.699048784885647

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0753367394890914

> <JCHEM_POLAR_SURFACE_AREA>
74.6

> <JCHEM_REFRACTIVITY>
86.58939999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
13-hydroxy-13-(hydroxymethyl)-2,6-dimethyltetracyclo[10.3.1.0^{1,10}.0^{2,7}]hexadec-6-ene-5,8-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       8.262  -0.089   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.162   0.989   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.679   0.576   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.269  -0.920   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       6.360  -2.007   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       3.783  -1.334   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.689  -0.243   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.102  -0.586   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.285   0.823   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.593   1.218   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.966   1.376   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.530   3.004   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.015   3.569   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.100   2.414   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -1.228   3.462   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.603   2.080   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -2.065   0.611   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.579   1.654   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.536   2.787   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.963   3.146   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.447   3.559   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.546   2.480   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.030   2.893   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4   18                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   11                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10    7   12   18                                             
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9   15   16                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16                                                            
CONECT   18   11    3   19   20                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    2   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₆O₄

Average Mass

318.4130 Da

Monoisotopic Mass

318.18311 Da

IUPAC Name

13-hydroxy-13-(hydroxymethyl)-2,6-dimethyltetracyclo[10.3.1.0^{1,10}.0^{2,7}]hexadec-6-ene-5,8-dione

Traditional Name

13-hydroxy-13-(hydroxymethyl)-2,6-dimethyltetracyclo[10.3.1.0^{1,10}.0^{2,7}]hexadec-6-ene-5,8-dione

CAS Registry Number

Not Available

SMILES

CC1=C2C(=O)CC3CC4CC3(CCC4(O)CO)C2(C)CCC1=O

InChI Identifier

InChI=1S/C19H26O4/c1-11-14(21)3-4-17(2)16(11)15(22)8-12-7-13-9-18(12,17)5-6-19(13,23)10-20/h12-13,20,23H,3-10H2,1-2H3

InChI Key

KEIKTRADEAFSDO-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 chamigranes. These are sesquiterpenoids characterized by a 1,1,5,9-tetramethylspiro[5,5]undecane skeleton, formally obtained by linking the C1-C6 and C6-C11 of farnesane together. They are predominantly isolated from algae.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Chamigranes

Alternative Parents

Substituents

Chamigrane sesquiterpenoid
Cyclohexenone
Tertiary alcohol
Cyclic alcohol
Cyclic ketone
Ketone
1,2-diol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic 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	1.52	ChemAxon
pKa (Strongest Acidic)	13.7	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.6 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	86.59 m³·mol⁻¹	ChemAxon
Polarizability	34.36 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

162944003

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 13-hydroxy-13-(hydroxymethyl)-2,6-dimethyltetracyclo[10.3.1.0¹,¹⁰.0²,⁷]hexadec-6-ene-5,8-dione (NP0328645)

MOL for NP0328645 (13-hydroxy-13-(hydroxymethyl)-2,6-dimethyltetracyclo[10.3.1.0¹,¹⁰.0²,⁷]hexadec-6-ene-5,8-dione)

3D MOL for NP0328645 (13-hydroxy-13-(hydroxymethyl)-2,6-dimethyltetracyclo[10.3.1.0¹,¹⁰.0²,⁷]hexadec-6-ene-5,8-dione)

3D SDF for NP0328645 (13-hydroxy-13-(hydroxymethyl)-2,6-dimethyltetracyclo[10.3.1.0¹,¹⁰.0²,⁷]hexadec-6-ene-5,8-dione)

3D-SDF for NP0328645 (13-hydroxy-13-(hydroxymethyl)-2,6-dimethyltetracyclo[10.3.1.0¹,¹⁰.0²,⁷]hexadec-6-ene-5,8-dione)

PDB for NP0328645 (13-hydroxy-13-(hydroxymethyl)-2,6-dimethyltetracyclo[10.3.1.0¹,¹⁰.0²,⁷]hexadec-6-ene-5,8-dione)

3D PDB for NP0328645 (13-hydroxy-13-(hydroxymethyl)-2,6-dimethyltetracyclo[10.3.1.0¹,¹⁰.0²,⁷]hexadec-6-ene-5,8-dione)

SMILES for NP0328645 (13-hydroxy-13-(hydroxymethyl)-2,6-dimethyltetracyclo[10.3.1.0¹,¹⁰.0²,⁷]hexadec-6-ene-5,8-dione)

INCHI for NP0328645 (13-hydroxy-13-(hydroxymethyl)-2,6-dimethyltetracyclo[10.3.1.0¹,¹⁰.0²,⁷]hexadec-6-ene-5,8-dione)

Structure for NP0328645 (13-hydroxy-13-(hydroxymethyl)-2,6-dimethyltetracyclo[10.3.1.0¹,¹⁰.0²,⁷]hexadec-6-ene-5,8-dione)

3D Structure for NP0328645 (13-hydroxy-13-(hydroxymethyl)-2,6-dimethyltetracyclo[10.3.1.0¹,¹⁰.0²,⁷]hexadec-6-ene-5,8-dione)