NP-MRD: Showing NP-Card for Taxodone (NP0030297)

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Record Information

Version

2.0

Created at

2021-06-19 21:41:34 UTC

Updated at

2021-06-29 23:58:11 UTC

NP-MRD ID

NP0030297

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Taxodone

Provided By

JEOL Database JEOL Logo

Description

(4BS,8aS,9S)-4,9-dihydroxy-4b,8,8-trimethyl-2-(propan-2-yl)-3,4b,5,6,7,8,8a,9-octahydrophenanthren-3-one is also known as 6,11-dihydroxyabieta-7,9(11),13-trien-12-one. Taxodone is found in Salvia munzii, Salvia phlomoides and Taxodium distichum &. Taxodone was first documented in 2003 ( Rodrguez, B.). Based on a literature review very few articles have been published on (4bS,8aS,9S)-4,9-dihydroxy-4b,8,8-trimethyl-2-(propan-2-yl)-3,4b,5,6,7,8,8a,9-octahydrophenanthren-3-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192123413D          

 51 53  0  0  0  0            999 V2000
   -4.2864    1.7765   -2.5709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9870    1.9431   -1.0779 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0298    1.1758   -0.2551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5475    1.5650   -0.7821 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7243    0.1474    0.0452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4276   -0.9628    0.7420 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.9660   -0.1915    1.0832 C   0  0  1  0  0  0  0  0  0  0  0  0
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    4.0061   -1.8198    0.8193 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4966   -0.8834    3.0492 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3797    0.6307    1.3090 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2965    1.2204   -0.0852 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8740    1.6596   -0.4098 C   0  0  1  0  0  0  0  0  0  0  0  0
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    0.8148    3.1936   -1.4351 O   0  0  0  0  0  0  0  0  0  0  0  0
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  8  7  1  0  0  0  0
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M  END

     RDKit          3D

 51 53  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652306192123413D          

 51 53  0  0  0  0            999 V2000
   -4.2864    1.7765   -2.5709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9870    1.9431   -1.0779 C   0  0  1  0  0  0  0  0  0  0  0  0
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    2.6088    2.4751    0.2766 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8984    2.0805   -1.4222 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7200    0.1163   -2.4658 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3841   -1.3058   -1.4877 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0321   -0.7195   -1.6788 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2404    3.9329   -1.7317 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0  0  0  0
 22 23  2  0  0  0  0
  6  5  1  0  0  0  0
 15 16  1  0  0  0  0
 14 11  1  0  0  0  0
 11 10  1  0  0  0  0
 17 16  1  0  0  0  0
 17 10  1  0  0  0  0
  4  2  1  0  0  0  0
  7  6  2  0  0  0  0
 17 19  1  0  0  0  0
  2  1  1  0  0  0  0
  5  4  2  0  0  0  0
 20 19  2  0  0  0  0
  2  3  1  0  0  0  0
 20 21  1  0  0  0  0
 17 18  1  6  0  0  0
  8  9  1  0  0  0  0
 11 12  1  6  0  0  0
 15 14  1  0  0  0  0
 11 13  1  0  0  0  0
 22 20  1  0  0  0  0
 19  6  1  0  0  0  0
 10  8  1  0  0  0  0
  4 22  1  0  0  0  0
 10 35  1  1  0  0  0
  8 33  1  6  0  0  0
  7 32  1  0  0  0  0
  5 31  1  0  0  0  0
  2 27  1  1  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  3 28  1  0  0  0  0
  3 29  1  0  0  0  0
  3 30  1  0  0  0  0
  9 34  1  0  0  0  0
 15 44  1  0  0  0  0
 15 45  1  0  0  0  0
 14 42  1  0  0  0  0
 14 43  1  0  0  0  0
 16 46  1  0  0  0  0
 16 47  1  0  0  0  0
 21 51  1  0  0  0  0
 18 48  1  0  0  0  0
 18 49  1  0  0  0  0
 18 50  1  0  0  0  0
 12 36  1  0  0  0  0
 12 37  1  0  0  0  0
 12 38  1  0  0  0  0
 13 39  1  0  0  0  0
 13 40  1  0  0  0  0
 13 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0030297

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(C([H])=C(C1=O)C([H])(C([H])([H])[H])C([H])([H])[H])=C([H])[C@]([H])(O[H])[C@]1([H])[C@]2(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])C1(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O3/c1-11(2)13-9-12-10-14(21)18-19(3,4)7-6-8-20(18,5)15(12)17(23)16(13)22/h9-11,14,18,21,23H,6-8H2,1-5H3/t14-,18-,20+/m0/s1

> <INCHI_KEY>
QEAIMIKGLGBTSA-ADLFWFRXSA-N

> <FORMULA>
C20H28O3

> <MOLECULAR_WEIGHT>
316.441

> <EXACT_MASS>
316.203844762

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
36.557589581346576

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4bS,8aS,9S)-4,9-dihydroxy-4b,8,8-trimethyl-2-(propan-2-yl)-3,4b,5,6,7,8,8a,9-octahydrophenanthren-3-one

> <ALOGPS_LOGP>
3.49

> <JCHEM_LOGP>
3.3762397466666663

> <ALOGPS_LOGS>
-3.44

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.861201248599336

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.749222785777935

> <JCHEM_PKA_STRONGEST_BASIC>
-0.6725104100483489

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
94.42279999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.15e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
taxodone

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 51 53  0  0  0  0  0  0  0  0999 V2000
   -4.2864    1.7765   -2.5709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9870    1.9431   -1.0779 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0298    1.1758   -0.2551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5475    1.5650   -0.7821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1261    0.4067   -0.2496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7243    0.1474    0.0452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4276   -0.9628    0.7420 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9398   -1.3453    1.2059 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7805   -1.7515    2.5610 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9660   -0.1915    1.0832 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4365   -0.5754    1.5291 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0061   -1.8198    0.8193 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4966   -0.8834    3.0492 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3797    0.6307    1.3090 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2965    1.2204   -0.0852 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8740    1.6596   -0.4098 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8087    0.5315   -0.3145 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9990   -0.4022   -1.5390 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3369    1.0555   -0.4271 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0584    2.2373   -0.9515 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8148    3.1936   -1.4351 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5111    2.5915   -1.0915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7953    3.7163   -1.5035 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3087    2.0976   -2.7989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1848    0.7311   -2.8839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6083    2.3781   -3.1856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1223    3.0018   -0.8193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0616    0.1140   -0.5226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0306    1.5868   -0.4297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8230    1.2563    0.8176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8412   -0.3738   -0.0048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2155   -1.6531    1.0390 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2590   -2.2256    0.6409 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5117   -0.9668    3.0692 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6615    0.5654    1.8277 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1039   -1.6946   -0.2575 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0110   -2.0509    1.1944 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3933   -2.7081    1.0009 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5350   -0.9253    3.4005 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9858   -0.1111    3.6348 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0523   -1.8526    3.2935 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4198    0.3451    1.5131 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1355    1.4216    2.0318 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9587    2.0929   -0.1433 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6686    0.5098   -0.8296 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6088    2.4751    0.2766 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8984    2.0805   -1.4222 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7200    0.1163   -2.4658 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3841   -1.3058   -1.4877 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0321   -0.7195   -1.6788 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2404    3.9329   -1.7317 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
 22 23  2  0
  6  5  1  0
 15 16  1  0
 14 11  1  0
 11 10  1  0
 17 16  1  0
 17 10  1  0
  4  2  1  0
  7  6  2  0
 17 19  1  0
  2  1  1  0
  5  4  2  0
 20 19  2  0
  2  3  1  0
 20 21  1  0
 17 18  1  6
  8  9  1  0
 11 12  1  6
 15 14  1  0
 11 13  1  0
 22 20  1  0
 19  6  1  0
 10  8  1  0
  4 22  1  0
 10 35  1  1
  8 33  1  6
  7 32  1  0
  5 31  1  0
  2 27  1  1
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  9 34  1  0
 15 44  1  0
 15 45  1  0
 14 42  1  0
 14 43  1  0
 16 46  1  0
 16 47  1  0
 21 51  1  0
 18 48  1  0
 18 49  1  0
 18 50  1  0
 12 36  1  0
 12 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 13 41  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0      -4.286   1.777  -2.571  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.987   1.943  -1.078  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.030   1.176  -0.255  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.547   1.565  -0.782  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.126   0.407  -0.250  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.724   0.147   0.045  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.428  -0.963   0.742  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.940  -1.345   1.206  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.781  -1.752   2.561  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.966  -0.192   1.083  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.437  -0.575   1.529  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.006  -1.820   0.819  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.497  -0.883   3.049  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.380   0.631   1.309  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.297   1.220  -0.085  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.874   1.660  -0.410  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.809   0.532  -0.315  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.999  -0.402  -1.539  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.337   1.056  -0.427  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.058   2.237  -0.952  0.00  0.00           C+0
HETATM   21  O   UNK     0       0.815   3.194  -1.435  0.00  0.00           O+0
HETATM   22  C   UNK     0      -1.511   2.591  -1.091  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.795   3.716  -1.504  0.00  0.00           O+0
HETATM   24  H   UNK     0      -5.309   2.098  -2.799  0.00  0.00           H+0
HETATM   25  H   UNK     0      -4.185   0.731  -2.884  0.00  0.00           H+0
HETATM   26  H   UNK     0      -3.608   2.378  -3.186  0.00  0.00           H+0
HETATM   27  H   UNK     0      -4.122   3.002  -0.819  0.00  0.00           H+0
HETATM   28  H   UNK     0      -5.062   0.114  -0.523  0.00  0.00           H+0
HETATM   29  H   UNK     0      -6.031   1.587  -0.430  0.00  0.00           H+0
HETATM   30  H   UNK     0      -4.823   1.256   0.818  0.00  0.00           H+0
HETATM   31  H   UNK     0      -2.841  -0.374  -0.005  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.216  -1.653   1.039  0.00  0.00           H+0
HETATM   33  H   UNK     0       1.259  -2.226   0.641  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.512  -0.967   3.069  0.00  0.00           H+0
HETATM   35  H   UNK     0       1.662   0.565   1.828  0.00  0.00           H+0
HETATM   36  H   UNK     0       4.104  -1.695  -0.258  0.00  0.00           H+0
HETATM   37  H   UNK     0       5.011  -2.051   1.194  0.00  0.00           H+0
HETATM   38  H   UNK     0       3.393  -2.708   1.001  0.00  0.00           H+0
HETATM   39  H   UNK     0       4.535  -0.925   3.401  0.00  0.00           H+0
HETATM   40  H   UNK     0       2.986  -0.111   3.635  0.00  0.00           H+0
HETATM   41  H   UNK     0       3.052  -1.853   3.293  0.00  0.00           H+0
HETATM   42  H   UNK     0       5.420   0.345   1.513  0.00  0.00           H+0
HETATM   43  H   UNK     0       4.136   1.422   2.032  0.00  0.00           H+0
HETATM   44  H   UNK     0       4.959   2.093  -0.143  0.00  0.00           H+0
HETATM   45  H   UNK     0       4.669   0.510  -0.830  0.00  0.00           H+0
HETATM   46  H   UNK     0       2.609   2.475   0.277  0.00  0.00           H+0
HETATM   47  H   UNK     0       2.898   2.080  -1.422  0.00  0.00           H+0
HETATM   48  H   UNK     0       1.720   0.116  -2.466  0.00  0.00           H+0
HETATM   49  H   UNK     0       1.384  -1.306  -1.488  0.00  0.00           H+0
HETATM   50  H   UNK     0       3.032  -0.720  -1.679  0.00  0.00           H+0
HETATM   51  H   UNK     0       0.240   3.933  -1.732  0.00  0.00           H+0
CONECT    1    2   24   25   26                                             
CONECT    2    4    1    3   27                                             
CONECT    3    2   28   29   30                                             
CONECT    4    2    5   22                                                  
CONECT    5    6    4   31                                                  
CONECT    6    5    7   19                                                  
CONECT    7    8    6   32                                                  
CONECT    8    7    9   10   33                                             
CONECT    9    8   34                                                       
CONECT   10   11   17    8   35                                             
CONECT   11   14   10   12   13                                             
CONECT   12   11   36   37   38                                             
CONECT   13   11   39   40   41                                             
CONECT   14   11   15   42   43                                             
CONECT   15   16   14   44   45                                             
CONECT   16   15   17   46   47                                             
CONECT   17   16   10   19   18                                             
CONECT   18   17   48   49   50                                             
CONECT   19   17   20    6                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20   51                                                       
CONECT   22   23   20    4                                                  
CONECT   23   22                                                            
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    2                                                            
CONECT   28    3                                                            
CONECT   29    3                                                            
CONECT   30    3                                                            
CONECT   31    5                                                            
CONECT   32    7                                                            
CONECT   33    8                                                            
CONECT   34    9                                                            
CONECT   35   10                                                            
CONECT   36   12                                                            
CONECT   37   12                                                            
CONECT   38   12                                                            
CONECT   39   13                                                            
CONECT   40   13                                                            
CONECT   41   13                                                            
CONECT   42   14                                                            
CONECT   43   14                                                            
CONECT   44   15                                                            
CONECT   45   15                                                            
CONECT   46   16                                                            
CONECT   47   16                                                            
CONECT   48   18                                                            
CONECT   49   18                                                            
CONECT   50   18                                                            
CONECT   51   21                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  106    0
END

RDKit          3D

51 53  0  0  0  0  0  0  0  0999 V2000
   -4.2864    1.7765   -2.5709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9870    1.9431   -1.0779 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0298    1.1758   -0.2551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5475    1.5650   -0.7821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1261    0.4067   -0.2496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7243    0.1474    0.0452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4276   -0.9628    0.7420 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9398   -1.3453    1.2059 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7805   -1.7515    2.5610 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9660   -0.1915    1.0832 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4365   -0.5754    1.5291 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0061   -1.8198    0.8193 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4966   -0.8834    3.0492 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3797    0.6307    1.3090 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2965    1.2204   -0.0852 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8740    1.6596   -0.4098 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8087    0.5315   -0.3145 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9990   -0.4022   -1.5390 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3369    1.0555   -0.4271 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0584    2.2373   -0.9515 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8148    3.1936   -1.4351 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5111    2.5915   -1.0915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7953    3.7163   -1.5035 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3087    2.0976   -2.7989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1848    0.7311   -2.8839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6083    2.3781   -3.1856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1223    3.0018   -0.8193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0616    0.1140   -0.5226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0306    1.5868   -0.4297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8230    1.2563    0.8176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8412   -0.3738   -0.0048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2155   -1.6531    1.0390 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2590   -2.2256    0.6409 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5117   -0.9668    3.0692 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6615    0.5654    1.8277 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1039   -1.6946   -0.2575 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0110   -2.0509    1.1944 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3933   -2.7081    1.0009 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5350   -0.9253    3.4005 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9858   -0.1111    3.6348 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0523   -1.8526    3.2935 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4198    0.3451    1.5131 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1355    1.4216    2.0318 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9587    2.0929   -0.1433 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6686    0.5098   -0.8296 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6088    2.4751    0.2766 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8984    2.0805   -1.4222 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7200    0.1163   -2.4658 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3841   -1.3058   -1.4877 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0321   -0.7195   -1.6788 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2404    3.9329   -1.7317 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
 22 23  2  0
  6  5  1  0
 15 16  1  0
 14 11  1  0
 11 10  1  0
 17 16  1  0
 17 10  1  0
  4  2  1  0
  7  6  2  0
 17 19  1  0
  2  1  1  0
  5  4  2  0
 20 19  2  0
  2  3  1  0
 20 21  1  0
 17 18  1  6
  8  9  1  0
 11 12  1  6
 15 14  1  0
 11 13  1  0
 22 20  1  0
 19  6  1  0
 10  8  1  0
  4 22  1  0
 10 35  1  1
  8 33  1  6
  7 32  1  0
  5 31  1  0
  2 27  1  1
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  9 34  1  0
 15 44  1  0
 15 45  1  0
 14 42  1  0
 14 43  1  0
 16 46  1  0
 16 47  1  0
 21 51  1  0
 18 48  1  0
 18 49  1  0
 18 50  1  0
 12 36  1  0
 12 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 13 41  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Value	Source
6,11-Dihydroxyabieta-7,9(11),13-trien-12-one	Kegg

Chemical Formula

C₂₀H₂₈O₃

Average Mass

316.4410 Da

Monoisotopic Mass

316.20384 Da

IUPAC Name

(4bS,8aS,9S)-4,9-dihydroxy-4b,8,8-trimethyl-2-(propan-2-yl)-3,4b,5,6,7,8,8a,9-octahydrophenanthren-3-one

Traditional Name

taxodone

CAS Registry Number

Not Available

SMILES

[H]OC1=C2C(C([H])=C(C1=O)C([H])(C([H])([H])[H])C([H])([H])[H])=C([H])[C@]([H])(O[H])[C@]1([H])[C@]2(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])C1(C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C20H28O3/c1-11(2)13-9-12-10-14(21)18-19(3,4)7-6-8-20(18,5)15(12)17(23)16(13)22/h9-11,14,18,21,23H,6-8H2,1-5H3/t14-,18-,20+/m0/s1

InChI Key

QEAIMIKGLGBTSA-ADLFWFRXSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, acetone-d6, 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
Salvia munzii	LOTUS Database	35616633
Salvia phlomoides	LOTUS Database	35616633
Taxodium distichum	JEOL database	Rodrguez, B., Magn. Reson. Chem. 41, 741 (2003)

Chemical Taxonomy

Classification

Not classified

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	3.49	ALOGPS
logP	3.38	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	9.75	ChemAxon
pKa (Strongest Basic)	-0.67	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	94.42 m³·mol⁻¹	ChemAxon
Polarizability	36.56 Å³	ChemAxon
Number of Rings	3	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

C00003489

Chemspider ID

242416

KEGG Compound ID

C09196

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

Rodrguez, B. (2003). Rodrguez, B., Magn. Reson. Chem. 41, 741 (2003). Mag. Reson. Chem..

Showing NP-Card for Taxodone (NP0030297)

MOL for NP0030297 (Taxodone)

3D MOL for NP0030297 (Taxodone)

3D SDF for NP0030297 (Taxodone)

3D-SDF for NP0030297 (Taxodone)

PDB for NP0030297 (Taxodone)

3D PDB for NP0030297 (Taxodone)

SMILES for NP0030297 (Taxodone)

INCHI for NP0030297 (Taxodone)

Structure for NP0030297 (Taxodone)

3D Structure for NP0030297 (Taxodone)