NP-MRD: Showing NP-Card for applanatine B (NP0039931)

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Record Information

Version

2.0

Created at

2021-06-20 22:13:37 UTC

Updated at

2021-06-30 00:13:32 UTC

NP-MRD ID

NP0039931

Secondary Accession Numbers

None

Natural Product Identification

Common Name

applanatine B

Provided By

JEOL Database JEOL Logo

Description

[(1R,2S)-1-methoxy-5-(2-methoxyethyl)-2,4,6-trimethyl-2,3-dihydro-1H-inden-2-yl]methanol belongs to the class of organic compounds known as indanes. Indanes are compounds containing an indane moiety, which consists of a cyclopentane fused to a benzene ring. applanatine B is found in Ganoderma applanatum. applanatine B was first documented in 2010 (Fushimi, K., et al.). Based on a literature review very few articles have been published on [(1R,2S)-1-methoxy-5-(2-methoxyethyl)-2,4,6-trimethyl-2,3-dihydro-1H-inden-2-yl]methanol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212100133D          

 46 47  0  0  0  0            999 V2000
   -1.1109    4.8039    5.4320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6963    4.4144    4.1964 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8200    3.5716    3.4436 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5137    3.1926    2.1353 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6588    2.2864    1.2661 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2465    2.8553    0.3215 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3573    4.3452    0.1185 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0511    2.0233   -0.4732 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9511    0.6507   -0.3361 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0555    0.0844    0.5771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7386    0.8743    1.4106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6879    0.2220    2.3794 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1365   -1.4162    0.5047 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8039   -1.6469   -0.8787 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5843   -2.9705   -0.8820 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2868   -1.6882   -1.9764 C   0  0  2  0  0  0  0  0  0  0  0  0
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    1.7262   -0.4071   -1.0822 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9789   -0.6033   -0.4208 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0471    0.0839   -1.0546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9018    3.9259    6.0506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1913    5.3710    5.2584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8209    5.4439    5.9626 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1152    4.1075    3.2459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5836    2.6778    4.0319 H   0  0  0  0  0  0  0  0  0  0  0  0
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  8  6  2  0  0  0  0
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  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
M  END

     RDKit          3D

 46 47  0  0  0  0  0  0  0  0999 V2000
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   -1.6963    4.4144    4.1964 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8200    3.5716    3.4436 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652306212100133D          

 46 47  0  0  0  0            999 V2000
   -1.1109    4.8039    5.4320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6963    4.4144    4.1964 O   0  0  0  0  0  0  0  0  0  0  0  0
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  3 24  1  0  0  0  0
  3 25  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0039931

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])[C@]1(C([H])([H])[H])C([H])([H])C2=C(C([H])=C(C(=C2C([H])([H])[H])C([H])([H])C([H])([H])OC([H])([H])[H])C([H])([H])[H])[C@@]1([H])OC([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C17H26O3/c1-11-8-14-15(12(2)13(11)6-7-19-4)9-17(3,10-18)16(14)20-5/h8,16,18H,6-7,9-10H2,1-5H3/t16-,17+/m1/s1

> <INCHI_KEY>
SLJLUCPQAQEAOL-SJORKVTESA-N

> <FORMULA>
C17H26O3

> <MOLECULAR_WEIGHT>
278.392

> <EXACT_MASS>
278.188194697

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
33.263972176912475

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1R,2S)-1-methoxy-5-(2-methoxyethyl)-2,4,6-trimethyl-2,3-dihydro-1H-inden-2-yl]methanol

> <ALOGPS_LOGP>
2.82

> <JCHEM_LOGP>
3.0467300333333327

> <ALOGPS_LOGS>
-3.78

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.017216447658733

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7912695257940703

> <JCHEM_POLAR_SURFACE_AREA>
38.69

> <JCHEM_REFRACTIVITY>
82.2548

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.60e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(1R,2S)-1-methoxy-5-(2-methoxyethyl)-2,4,6-trimethyl-1,3-dihydroinden-2-yl]methanol

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 46 47  0  0  0  0  0  0  0  0999 V2000
   -1.1109    4.8039    5.4320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6963    4.4144    4.1964 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8200    3.5716    3.4436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5137    3.1926    2.1353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6588    2.2864    1.2661 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2465    2.8553    0.3215 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3573    4.3452    0.1185 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0511    2.0233   -0.4732 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9511    0.6507   -0.3361 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0555    0.0844    0.5771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7386    0.8743    1.4106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6879    0.2220    2.3794 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1365   -1.4162    0.5047 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8039   -1.6469   -0.8787 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5843   -2.9705   -0.8820 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2868   -1.6882   -1.9764 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2959   -1.8794   -3.2618 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7262   -0.4071   -1.0822 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9789   -0.6033   -0.4208 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0471    0.0839   -1.0546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9018    3.9259    6.0506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1913    5.3710    5.2584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8209    5.4439    5.9626 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1152    4.1075    3.2459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5836    2.6778    4.0319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7959    4.1009    1.5893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4821    2.7228    2.3479 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1708    4.5975   -0.5704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5703    4.7377   -0.3098 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5718    4.8527    1.0631 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7435    2.4451   -1.1958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4066   -0.8139    2.5922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6886    0.7346    3.3451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7017    0.2251    1.9671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8503   -1.8868    0.5590 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7610   -1.7812    1.3281 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9044   -3.8244   -0.7857 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2932   -3.0271   -0.0487 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1533   -3.0945   -1.8097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8736   -0.7638   -2.0085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9795   -2.5183   -1.7962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4365   -1.9284   -3.9008 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8546   -0.1611   -2.1428 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9628   -0.1117   -0.4901 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8705    1.1627   -1.0634 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1854   -0.2844   -2.0758 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  6  2  0
 18 19  1  0
  9 10  2  0
 19 20  1  0
 14 16  1  6
  5 11  2  0
 14 15  1  0
 11 10  1  0
 16 17  1  0
  6  5  1  0
 11 12  1  0
  9  8  1  0
  6  7  1  0
 10 13  1  0
  5  4  1  0
 13 14  1  0
  4  3  1  0
 14 18  1  0
  3  2  1  0
 18  9  1  0
  2  1  1  0
  8 31  1  0
 13 35  1  0
 13 36  1  0
 18 43  1  6
 20 44  1  0
 20 45  1  0
 20 46  1  0
 16 40  1  0
 16 41  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
 17 42  1  0
 12 32  1  0
 12 33  1  0
 12 34  1  0
  7 28  1  0
  7 29  1  0
  7 30  1  0
  4 26  1  0
  4 27  1  0
  3 24  1  0
  3 25  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
M  END

HEADER    PROTEIN                                 21-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-JUN-21         0                                  
HETATM    1  C   UNK     0      -1.111   4.804   5.432  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.696   4.414   4.196  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.820   3.572   3.444  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.514   3.193   2.135  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.659   2.286   1.266  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.247   2.855   0.322  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.357   4.345   0.119  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.051   2.023  -0.473  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.951   0.651  -0.336  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.056   0.084   0.577  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.739   0.874   1.411  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.688   0.222   2.379  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.137  -1.416   0.505  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.804  -1.647  -0.879  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.584  -2.970  -0.882  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.287  -1.688  -1.976  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.296  -1.879  -3.262  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.726  -0.407  -1.082  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.979  -0.603  -0.421  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.047   0.084  -1.055  0.00  0.00           C+0
HETATM   21  H   UNK     0      -0.902   3.926   6.051  0.00  0.00           H+0
HETATM   22  H   UNK     0      -0.191   5.371   5.258  0.00  0.00           H+0
HETATM   23  H   UNK     0      -1.821   5.444   5.963  0.00  0.00           H+0
HETATM   24  H   UNK     0       0.115   4.107   3.246  0.00  0.00           H+0
HETATM   25  H   UNK     0      -0.584   2.678   4.032  0.00  0.00           H+0
HETATM   26  H   UNK     0      -1.796   4.101   1.589  0.00  0.00           H+0
HETATM   27  H   UNK     0      -2.482   2.723   2.348  0.00  0.00           H+0
HETATM   28  H   UNK     0       1.171   4.598  -0.570  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.570   4.738  -0.310  0.00  0.00           H+0
HETATM   30  H   UNK     0       0.572   4.853   1.063  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.744   2.445  -1.196  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.407  -0.814   2.592  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.689   0.735   3.345  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.702   0.225   1.967  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.850  -1.887   0.559  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.761  -1.781   1.328  0.00  0.00           H+0
HETATM   37  H   UNK     0       0.904  -3.824  -0.786  0.00  0.00           H+0
HETATM   38  H   UNK     0       2.293  -3.027  -0.049  0.00  0.00           H+0
HETATM   39  H   UNK     0       2.153  -3.095  -1.810  0.00  0.00           H+0
HETATM   40  H   UNK     0      -0.874  -0.764  -2.009  0.00  0.00           H+0
HETATM   41  H   UNK     0      -0.980  -2.518  -1.796  0.00  0.00           H+0
HETATM   42  H   UNK     0      -0.437  -1.928  -3.901  0.00  0.00           H+0
HETATM   43  H   UNK     0       1.855  -0.161  -2.143  0.00  0.00           H+0
HETATM   44  H   UNK     0       4.963  -0.112  -0.490  0.00  0.00           H+0
HETATM   45  H   UNK     0       3.870   1.163  -1.063  0.00  0.00           H+0
HETATM   46  H   UNK     0       4.185  -0.284  -2.076  0.00  0.00           H+0
CONECT    1    2   21   22   23                                             
CONECT    2    3    1                                                       
CONECT    3    4    2   24   25                                             
CONECT    4    5    3   26   27                                             
CONECT    5   11    6    4                                                  
CONECT    6    8    5    7                                                  
CONECT    7    6   28   29   30                                             
CONECT    8    6    9   31                                                  
CONECT    9   10    8   18                                                  
CONECT   10    9   11   13                                                  
CONECT   11    5   10   12                                                  
CONECT   12   11   32   33   34                                             
CONECT   13   10   14   35   36                                             
CONECT   14   16   15   13   18                                             
CONECT   15   14   37   38   39                                             
CONECT   16   14   17   40   41                                             
CONECT   17   16   42                                                       
CONECT   18   19   14    9   43                                             
CONECT   19   18   20                                                       
CONECT   20   19   44   45   46                                             
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    3                                                            
CONECT   25    3                                                            
CONECT   26    4                                                            
CONECT   27    4                                                            
CONECT   28    7                                                            
CONECT   29    7                                                            
CONECT   30    7                                                            
CONECT   31    8                                                            
CONECT   32   12                                                            
CONECT   33   12                                                            
CONECT   34   12                                                            
CONECT   35   13                                                            
CONECT   36   13                                                            
CONECT   37   15                                                            
CONECT   38   15                                                            
CONECT   39   15                                                            
CONECT   40   16                                                            
CONECT   41   16                                                            
CONECT   42   17                                                            
CONECT   43   18                                                            
CONECT   44   20                                                            
CONECT   45   20                                                            
CONECT   46   20                                                            
MASTER        0    0    0    0    0    0    0    0   46    0   94    0
END

RDKit          3D

46 47  0  0  0  0  0  0  0  0999 V2000
   -1.1109    4.8039    5.4320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6963    4.4144    4.1964 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8200    3.5716    3.4436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5137    3.1926    2.1353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6588    2.2864    1.2661 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2465    2.8553    0.3215 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3573    4.3452    0.1185 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0511    2.0233   -0.4732 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9511    0.6507   -0.3361 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0555    0.0844    0.5771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7386    0.8743    1.4106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6879    0.2220    2.3794 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1365   -1.4162    0.5047 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8039   -1.6469   -0.8787 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5843   -2.9705   -0.8820 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2868   -1.6882   -1.9764 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2959   -1.8794   -3.2618 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7262   -0.4071   -1.0822 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9789   -0.6033   -0.4208 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0471    0.0839   -1.0546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9018    3.9259    6.0506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1913    5.3710    5.2584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8209    5.4439    5.9626 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1152    4.1075    3.2459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5836    2.6778    4.0319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7959    4.1009    1.5893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4821    2.7228    2.3479 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1708    4.5975   -0.5704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5703    4.7377   -0.3098 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5718    4.8527    1.0631 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7435    2.4451   -1.1958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4066   -0.8139    2.5922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6886    0.7346    3.3451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7017    0.2251    1.9671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8503   -1.8868    0.5590 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7610   -1.7812    1.3281 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9044   -3.8244   -0.7857 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2932   -3.0271   -0.0487 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1533   -3.0945   -1.8097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8736   -0.7638   -2.0085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9795   -2.5183   -1.7962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4365   -1.9284   -3.9008 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8546   -0.1611   -2.1428 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9628   -0.1117   -0.4901 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8705    1.1627   -1.0634 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1854   -0.2844   -2.0758 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  6  2  0
 18 19  1  0
  9 10  2  0
 19 20  1  0
 14 16  1  6
  5 11  2  0
 14 15  1  0
 11 10  1  0
 16 17  1  0
  6  5  1  0
 11 12  1  0
  9  8  1  0
  6  7  1  0
 10 13  1  0
  5  4  1  0
 13 14  1  0
  4  3  1  0
 14 18  1  0
  3  2  1  0
 18  9  1  0
  2  1  1  0
  8 31  1  0
 13 35  1  0
 13 36  1  0
 18 43  1  6
 20 44  1  0
 20 45  1  0
 20 46  1  0
 16 40  1  0
 16 41  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
 17 42  1  0
 12 32  1  0
 12 33  1  0
 12 34  1  0
  7 28  1  0
  7 29  1  0
  7 30  1  0
  4 26  1  0
  4 27  1  0
  3 24  1  0
  3 25  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₁₇H₂₆O₃

Average Mass

278.3920 Da

Monoisotopic Mass

278.18819 Da

IUPAC Name

[(1R,2S)-1-methoxy-5-(2-methoxyethyl)-2,4,6-trimethyl-2,3-dihydro-1H-inden-2-yl]methanol

Traditional Name

[(1R,2S)-1-methoxy-5-(2-methoxyethyl)-2,4,6-trimethyl-1,3-dihydroinden-2-yl]methanol

CAS Registry Number

Not Available

SMILES

[H]OC([H])([H])[C@]1(C([H])([H])[H])C([H])([H])C2=C(C([H])=C(C(=C2C([H])([H])[H])C([H])([H])C([H])([H])OC([H])([H])[H])C([H])([H])[H])[C@@]1([H])OC([H])([H])[H]

InChI Identifier

InChI=1S/C17H26O3/c1-11-8-14-15(12(2)13(11)6-7-19-4)9-17(3,10-18)16(14)20-5/h8,16,18H,6-7,9-10H2,1-5H3/t16-,17+/m1/s1

InChI Key

SLJLUCPQAQEAOL-SJORKVTESA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Ganoderma applanatum	JEOL database	Fushimi, K., et al, Tetrahedron 66, 9332 (2010).

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indanes. Indanes are compounds containing an indane moiety, which consists of a cyclopentane fused to a benzene ring.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Indanes

Sub Class

Not Available

Direct Parent

Indanes

Alternative Parents

Substituents

Indane
Ether
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
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	2.82	ALOGPS
logP	3.05	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	15.02	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	38.69 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	82.25 m³·mol⁻¹	ChemAxon
Polarizability	33.26 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

78438393

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

46918392

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Fushimi, K., et al. (2010). Fushimi, K., et al, Tetrahedron 66, 9332 (2010).. Tetrahedron.

Showing NP-Card for applanatine B (NP0039931)

MOL for NP0039931 (applanatine B)

3D MOL for NP0039931 (applanatine B)

3D SDF for NP0039931 (applanatine B)

3D-SDF for NP0039931 (applanatine B)

PDB for NP0039931 (applanatine B)

3D PDB for NP0039931 (applanatine B)

SMILES for NP0039931 (applanatine B)

INCHI for NP0039931 (applanatine B)

Structure for NP0039931 (applanatine B)

3D Structure for NP0039931 (applanatine B)