NP-MRD: Showing NP-Card for 9alpha,13alpha-epidioxiabiet-8(14)-en-18-ol (NP0030996)

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Record Information

Version

2.0

Created at

2021-06-19 22:12:21 UTC

Updated at

2021-06-29 23:59:19 UTC

NP-MRD ID

NP0030996

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9alpha,13alpha-epidioxiabiet-8(14)-en-18-ol

Provided By

JEOL Database JEOL Logo

Description

(13R)-9,13-Epidioxyabieta-8(14)-ene-18-ol belongs to the class of organic compounds known as 1,2-dioxanes. These are organic compounds containing 1,2-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 2. 9alpha,13alpha-epidioxiabiet-8(14)-en-18-ol is found in Cedrus atlantica. 9alpha,13alpha-epidioxiabiet-8(14)-en-18-ol was first documented in 2005 (Barrero, A. F., et al.). Based on a literature review very few articles have been published on (13R)-9,13-Epidioxyabieta-8(14)-ene-18-ol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202100123D          

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     RDKit          3D

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  Mrv1652306202100123D          

 55 58  0  0  0  0            999 V2000
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    1.4129   -3.1963   -2.6229 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5296   -2.3544    0.1391 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4327    0.9500   -2.4818 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6512   -0.2778   -2.3671 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1603   -0.6205   -3.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9618    0.1415    1.0577 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4933    1.3226   -0.1201 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6497    0.1144   -0.3771 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3283    0.5350    1.2924 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5083   -1.6989    1.8037 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1407   -1.7613    1.1632 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4557   -3.4395   -2.0274 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6653   -2.9553   -0.8536 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8734   -1.7374   -1.8172 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7266   -3.9839    1.2496 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2190   -4.7260   -0.2749 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8484   -3.8983    1.8714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7542    1.2352   -2.5306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7177    1.7779   -0.8477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0023    1.2725   -2.5276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9520    1.9274   -0.8872 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 14  1  0  0  0  0
 13 12  1  0  0  0  0
 19 20  1  0  0  0  0
  6  5  2  0  0  0  0
  5  4  1  0  0  0  0
  4 21  1  0  0  0  0
 21 20  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 10 19  1  0  0  0  0
 10 11  1  6  0  0  0
  9  8  1  0  0  0  0
 15 17  1  0  0  0  0
  8  7  1  0  0  0  0
 19 22  1  1  0  0  0
  7  6  1  0  0  0  0
  4 23  1  0  0  0  0
 19  6  1  0  0  0  0
  4  2  1  1  0  0  0
 15  9  1  0  0  0  0
  2  1  1  0  0  0  0
 10 12  1  0  0  0  0
  2  3  1  0  0  0  0
 10  9  1  0  0  0  0
 17 18  1  0  0  0  0
 23 22  1  0  0  0  0
 13 42  1  0  0  0  0
 13 43  1  0  0  0  0
 14 44  1  0  0  0  0
 14 45  1  0  0  0  0
 12 40  1  0  0  0  0
 12 41  1  0  0  0  0
  9 36  1  1  0  0  0
  8 34  1  0  0  0  0
  8 35  1  0  0  0  0
  7 32  1  0  0  0  0
  7 33  1  0  0  0  0
  5 31  1  0  0  0  0
 21 54  1  0  0  0  0
 21 55  1  0  0  0  0
 20 52  1  0  0  0  0
 20 53  1  0  0  0  0
 16 46  1  0  0  0  0
 16 47  1  0  0  0  0
 16 48  1  0  0  0  0
 11 37  1  0  0  0  0
 11 38  1  0  0  0  0
 11 39  1  0  0  0  0
 17 49  1  0  0  0  0
 17 50  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
 18 51  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0030996

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])[C@]1(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[C@@]2(C([H])([H])[H])[C@@]1([H])C([H])([H])C([H])([H])C1=C([H])[C@]3(OO[C@@]21C([H])([H])C3([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O3/c1-14(2)19-10-11-20(23-22-19)15(12-19)6-7-16-17(3,13-21)8-5-9-18(16,20)4/h12,14,16,21H,5-11,13H2,1-4H3/t16-,17-,18-,19-,20+/m0/s1

> <INCHI_KEY>
NVECILAMICWAEO-VYJAJWGXSA-N

> <FORMULA>
C20H32O3

> <MOLECULAR_WEIGHT>
320.473

> <EXACT_MASS>
320.23514489

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
37.40229128222444

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1R,2S,6R,7S,12R)-2,6-dimethyl-12-(propan-2-yl)-13,14-dioxatetracyclo[10.2.2.0^{1,10}.0^{2,7}]hexadec-10-en-6-yl]methanol

> <ALOGPS_LOGP>
4.33

> <JCHEM_LOGP>
4.146815614666666

> <ALOGPS_LOGS>
-4.43

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.592277898462896

> <JCHEM_PKA_STRONGEST_BASIC>
-1.227441821316003

> <JCHEM_POLAR_SURFACE_AREA>
38.69

> <JCHEM_REFRACTIVITY>
90.81809999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.19e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(1R,2S,6R,7S,12R)-12-isopropyl-2,6-dimethyl-13,14-dioxatetracyclo[10.2.2.0^{1,10}.0^{2,7}]hexadec-10-en-6-yl]methanol

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 55 58  0  0  0  0  0  0  0  0999 V2000
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   -4.7577   -0.1947   -0.7751 C   0  0  1  0  0  0  0  0  0  0  0  0
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    0.9332   -0.6015   -1.0102 C   0  0  2  0  0  0  0  0  0  0  0  0
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    1.5433    0.2570    0.1353 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9864   -0.1003    0.4663 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0982   -1.5587    0.8877 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.6422   -0.3977   -1.0542 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1054    1.0033   -1.5194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6448    1.0780   -1.5098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1529   -0.5609    0.3043 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6309   -0.3606    0.3738 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.9894    0.6513   -0.1125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8181   -1.6014    0.8996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3798   -1.3336    0.1248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1702   -2.3463   -0.6707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3607   -2.0948   -2.2743 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4327    0.9500   -2.4818 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6512   -0.2778   -2.3671 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1603   -0.6205   -3.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9618    0.1415    1.0577 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4933    1.3226   -0.1201 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.3283    0.5350    1.2924 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5083   -1.6989    1.8037 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1407   -1.7613    1.1632 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4557   -3.4395   -2.0274 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6653   -2.9553   -0.8536 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8734   -1.7374   -1.8172 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7266   -3.9839    1.2496 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2190   -4.7260   -0.2749 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8484   -3.8983    1.8714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7542    1.2352   -2.5306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7177    1.7779   -0.8477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0023    1.2725   -2.5276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9520    1.9274   -0.8872 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 14  1  0
 13 12  1  0
 19 20  1  0
  6  5  2  0
  5  4  1  0
  4 21  1  0
 21 20  1  0
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 15 16  1  6
 10 19  1  0
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  9  8  1  0
 15 17  1  0
  8  7  1  0
 19 22  1  1
  7  6  1  0
  4 23  1  0
 19  6  1  0
  4  2  1  1
 15  9  1  0
  2  1  1  0
 10 12  1  0
  2  3  1  0
 10  9  1  0
 17 18  1  0
 23 22  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 14 45  1  0
 12 40  1  0
 12 41  1  0
  9 36  1  1
  8 34  1  0
  8 35  1  0
  7 32  1  0
  7 33  1  0
  5 31  1  0
 21 54  1  0
 21 55  1  0
 20 52  1  0
 20 53  1  0
 16 46  1  0
 16 47  1  0
 16 48  1  0
 11 37  1  0
 11 38  1  0
 11 39  1  0
 17 49  1  0
 17 50  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
 18 51  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0      -5.522   0.026  -2.085  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.758  -0.195  -0.775  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.307  -1.443  -0.067  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.215  -0.240  -0.949  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.700  -1.391  -1.785  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.361  -1.468  -1.859  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.609  -2.530  -2.583  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.646  -3.034  -1.859  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.185  -2.132  -0.719  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.933  -0.602  -1.010  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.574  -0.127  -2.339  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.543   0.257   0.135  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.986  -0.100   0.466  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.098  -1.559   0.888  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.614  -2.560  -0.192  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.699  -2.671  -1.287  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.495  -3.971   0.468  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.719  -4.404   1.052  0.00  0.00           O+0
HETATM   19  C   UNK     0      -0.642  -0.398  -1.054  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.105   1.003  -1.519  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.645   1.078  -1.510  0.00  0.00           C+0
HETATM   22  O   UNK     0      -1.153  -0.561   0.304  0.00  0.00           O+0
HETATM   23  O   UNK     0      -2.631  -0.361   0.374  0.00  0.00           O+0
HETATM   24  H   UNK     0      -5.248   0.976  -2.553  0.00  0.00           H+0
HETATM   25  H   UNK     0      -5.338  -0.777  -2.805  0.00  0.00           H+0
HETATM   26  H   UNK     0      -6.601   0.062  -1.898  0.00  0.00           H+0
HETATM   27  H   UNK     0      -4.989   0.651  -0.113  0.00  0.00           H+0
HETATM   28  H   UNK     0      -4.818  -1.601   0.900  0.00  0.00           H+0
HETATM   29  H   UNK     0      -6.380  -1.334   0.125  0.00  0.00           H+0
HETATM   30  H   UNK     0      -5.170  -2.346  -0.671  0.00  0.00           H+0
HETATM   31  H   UNK     0      -3.361  -2.095  -2.274  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.323  -2.138  -3.566  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.260  -3.388  -2.797  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.421  -4.026  -1.447  0.00  0.00           H+0
HETATM   35  H   UNK     0       1.413  -3.196  -2.623  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.530  -2.354   0.139  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.433   0.950  -2.482  0.00  0.00           H+0
HETATM   38  H   UNK     0       2.651  -0.278  -2.367  0.00  0.00           H+0
HETATM   39  H   UNK     0       1.160  -0.621  -3.220  0.00  0.00           H+0
HETATM   40  H   UNK     0       0.962   0.142   1.058  0.00  0.00           H+0
HETATM   41  H   UNK     0       1.493   1.323  -0.120  0.00  0.00           H+0
HETATM   42  H   UNK     0       3.650   0.114  -0.377  0.00  0.00           H+0
HETATM   43  H   UNK     0       3.328   0.535   1.292  0.00  0.00           H+0
HETATM   44  H   UNK     0       2.508  -1.699   1.804  0.00  0.00           H+0
HETATM   45  H   UNK     0       4.141  -1.761   1.163  0.00  0.00           H+0
HETATM   46  H   UNK     0       3.456  -3.439  -2.027  0.00  0.00           H+0
HETATM   47  H   UNK     0       4.665  -2.955  -0.854  0.00  0.00           H+0
HETATM   48  H   UNK     0       3.873  -1.737  -1.817  0.00  0.00           H+0
HETATM   49  H   UNK     0       1.727  -3.984   1.250  0.00  0.00           H+0
HETATM   50  H   UNK     0       2.219  -4.726  -0.275  0.00  0.00           H+0
HETATM   51  H   UNK     0       3.848  -3.898   1.871  0.00  0.00           H+0
HETATM   52  H   UNK     0      -0.754   1.235  -2.531  0.00  0.00           H+0
HETATM   53  H   UNK     0      -0.718   1.778  -0.848  0.00  0.00           H+0
HETATM   54  H   UNK     0      -3.002   1.272  -2.528  0.00  0.00           H+0
HETATM   55  H   UNK     0      -2.952   1.927  -0.887  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    5   21   23    2                                             
CONECT    5    6    4   31                                                  
CONECT    6    5    7   19                                                  
CONECT    7    8    6   32   33                                             
CONECT    8    9    7   34   35                                             
CONECT    9    8   15   10   36                                             
CONECT   10   19   11   12    9                                             
CONECT   11   10   37   38   39                                             
CONECT   12   13   10   40   41                                             
CONECT   13   14   12   42   43                                             
CONECT   14   13   15   44   45                                             
CONECT   15   14   16   17    9                                             
CONECT   16   15   46   47   48                                             
CONECT   17   15   18   49   50                                             
CONECT   18   17   51                                                       
CONECT   19   20   10   22    6                                             
CONECT   20   19   21   52   53                                             
CONECT   21    4   20   54   55                                             
CONECT   22   19   23                                                       
CONECT   23    4   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    7                                                            
CONECT   34    8                                                            
CONECT   35    8                                                            
CONECT   36    9                                                            
CONECT   37   11                                                            
CONECT   38   11                                                            
CONECT   39   11                                                            
CONECT   40   12                                                            
CONECT   41   12                                                            
CONECT   42   13                                                            
CONECT   43   13                                                            
CONECT   44   14                                                            
CONECT   45   14                                                            
CONECT   46   16                                                            
CONECT   47   16                                                            
CONECT   48   16                                                            
CONECT   49   17                                                            
CONECT   50   17                                                            
CONECT   51   18                                                            
CONECT   52   20                                                            
CONECT   53   20                                                            
CONECT   54   21                                                            
CONECT   55   21                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  116    0
END

RDKit          3D

55 58  0  0  0  0  0  0  0  0999 V2000
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   -4.7577   -0.1947   -0.7751 C   0  0  1  0  0  0  0  0  0  0  0  0
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    0.9332   -0.6015   -1.0102 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -1.1529   -0.5609    0.3043 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.9894    0.6513   -0.1125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8181   -1.6014    0.8996 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.1702   -2.3463   -0.6707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3607   -2.0948   -2.2743 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.6512   -0.2778   -2.3671 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1603   -0.6205   -3.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9618    0.1415    1.0577 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4933    1.3226   -0.1201 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6497    0.1144   -0.3771 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3283    0.5350    1.2924 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5083   -1.6989    1.8037 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1407   -1.7613    1.1632 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4557   -3.4395   -2.0274 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6653   -2.9553   -0.8536 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8734   -1.7374   -1.8172 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7266   -3.9839    1.2496 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2190   -4.7260   -0.2749 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8484   -3.8983    1.8714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7542    1.2352   -2.5306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7177    1.7779   -0.8477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0023    1.2725   -2.5276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9520    1.9274   -0.8872 H   0  0  0  0  0  0  0  0  0  0  0  0
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 13 12  1  0
 19 20  1  0
  6  5  2  0
  5  4  1  0
  4 21  1  0
 21 20  1  0
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 15 16  1  6
 10 19  1  0
 10 11  1  6
  9  8  1  0
 15 17  1  0
  8  7  1  0
 19 22  1  1
  7  6  1  0
  4 23  1  0
 19  6  1  0
  4  2  1  1
 15  9  1  0
  2  1  1  0
 10 12  1  0
  2  3  1  0
 10  9  1  0
 17 18  1  0
 23 22  1  0
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 13 43  1  0
 14 44  1  0
 14 45  1  0
 12 40  1  0
 12 41  1  0
  9 36  1  1
  8 34  1  0
  8 35  1  0
  7 32  1  0
  7 33  1  0
  5 31  1  0
 21 54  1  0
 21 55  1  0
 20 52  1  0
 20 53  1  0
 16 46  1  0
 16 47  1  0
 16 48  1  0
 11 37  1  0
 11 38  1  0
 11 39  1  0
 17 49  1  0
 17 50  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
 18 51  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₂O₃

Average Mass

320.4730 Da

Monoisotopic Mass

320.23514 Da

IUPAC Name

[(1R,2S,6R,7S,12R)-2,6-dimethyl-12-(propan-2-yl)-13,14-dioxatetracyclo[10.2.2.0^{1,10}.0^{2,7}]hexadec-10-en-6-yl]methanol

Traditional Name

[(1R,2S,6R,7S,12R)-12-isopropyl-2,6-dimethyl-13,14-dioxatetracyclo[10.2.2.0^{1,10}.0^{2,7}]hexadec-10-en-6-yl]methanol

CAS Registry Number

Not Available

SMILES

[H]OC([H])([H])[C@]1(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[C@@]2(C([H])([H])[H])[C@@]1([H])C([H])([H])C([H])([H])C1=C([H])[C@]3(OO[C@@]21C([H])([H])C3([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C20H32O3/c1-14(2)19-10-11-20(23-22-19)15(12-19)6-7-16-17(3,13-21)8-5-9-18(16,20)4/h12,14,16,21H,5-11,13H2,1-4H3/t16-,17-,18-,19-,20+/m0/s1

InChI Key

NVECILAMICWAEO-VYJAJWGXSA-N

Experimental Spectra

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

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Cedrus atlantica	JEOL database	Barrero, A. F., et al, Phytochemistry 66, 105 (2005)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1,2-dioxanes. These are organic compounds containing 1,2-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 2.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Dioxanes

Sub Class

1,2-dioxanes

Direct Parent

1,2-dioxanes

Alternative Parents

Substituents

Ortho-dioxane
Dialkyl peroxide
Oxacycle
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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
logP	4.33	ALOGPS
logP	4.15	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	18.59	ChemAxon
pKa (Strongest Basic)	-1.2	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	2	ChemAxon
Refractivity	90.82 m³·mol⁻¹	ChemAxon
Polarizability	37.4 Å³	ChemAxon
Number of Rings	4	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

9442195

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11267184

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Barrero, A. F., et al. (2005). Barrero, A. F., et al, Phytochemistry 66, 105 (2005) . Phytochem..

Showing NP-Card for 9alpha,13alpha-epidioxiabiet-8(14)-en-18-ol (NP0030996)

MOL for NP0030996 (9alpha,13alpha-epidioxiabiet-8(14)-en-18-ol)

3D MOL for NP0030996 (9alpha,13alpha-epidioxiabiet-8(14)-en-18-ol)

3D SDF for NP0030996 (9alpha,13alpha-epidioxiabiet-8(14)-en-18-ol)

3D-SDF for NP0030996 (9alpha,13alpha-epidioxiabiet-8(14)-en-18-ol)

PDB for NP0030996 (9alpha,13alpha-epidioxiabiet-8(14)-en-18-ol)

3D PDB for NP0030996 (9alpha,13alpha-epidioxiabiet-8(14)-en-18-ol)

SMILES for NP0030996 (9alpha,13alpha-epidioxiabiet-8(14)-en-18-ol)

INCHI for NP0030996 (9alpha,13alpha-epidioxiabiet-8(14)-en-18-ol)

Structure for NP0030996 (9alpha,13alpha-epidioxiabiet-8(14)-en-18-ol)

3D Structure for NP0030996 (9alpha,13alpha-epidioxiabiet-8(14)-en-18-ol)