NP-MRD: Showing NP-Card for (+)-(1R)-1,12-dihydroxy-20-norabieta-5(10),8,11,13-tetraene (NP0035669)

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Record Information

Version

2.0

Created at

2021-06-20 19:03:02 UTC

Updated at

2021-06-30 00:06:49 UTC

NP-MRD ID

NP0035669

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-(1R)-1,12-dihydroxy-20-norabieta-5(10),8,11,13-tetraene

Provided By

JEOL Database JEOL Logo

Description

(+)-(1R)-1,12-dihydroxy-20-norabieta-5(10),8,11,13-tetraene is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. (+)-(1R)-1,12-dihydroxy-20-norabieta-5(10),8,11,13-tetraene is found in Fraxinus sieboldiana. (+)-(1R)-1,12-dihydroxy-20-norabieta-5(10),8,11,13-tetraene was first documented in 2010 (Lin, S., et al.). Based on a literature review very few articles have been published on (+)-(1R)-1,12-dihydroxy-20-norabieta-5(10),8,11,13-tetraene.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202121033D          

 47 49  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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  Mrv1652306202121033D          

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 15 12  1  0  0  0  0
 20 21  1  0  0  0  0
 19 44  1  0  0  0  0
 19 45  1  0  0  0  0
 18 42  1  0  0  0  0
 18 43  1  0  0  0  0
 20 46  1  1  0  0  0
 13 32  1  0  0  0  0
 13 33  1  0  0  0  0
 14 34  1  0  0  0  0
 14 35  1  0  0  0  0
  5 29  1  0  0  0  0
  8 30  1  0  0  0  0
 10 31  1  0  0  0  0
  2 25  1  1  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  3 26  1  0  0  0  0
  3 27  1  0  0  0  0
  3 28  1  0  0  0  0
 16 36  1  0  0  0  0
 16 37  1  0  0  0  0
 16 38  1  0  0  0  0
 17 39  1  0  0  0  0
 17 40  1  0  0  0  0
 17 41  1  0  0  0  0
 21 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0035669

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C2=C(C([H])=C1C([H])(C([H])([H])[H])C([H])([H])[H])C([H])([H])C([H])([H])C1=C2[C@]([H])(O[H])C([H])([H])C([H])([H])C1(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C19H26O2/c1-11(2)13-9-12-5-6-15-18(14(12)10-17(13)21)16(20)7-8-19(15,3)4/h9-11,16,20-21H,5-8H2,1-4H3/t16-/m1/s1

> <INCHI_KEY>
VGYQUIDVXNWOOS-MRXNPFEDSA-N

> <FORMULA>
C19H26O2

> <MOLECULAR_WEIGHT>
286.415

> <EXACT_MASS>
286.193280077

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
34.192173480271336

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5R)-8,8-dimethyl-2-(propan-2-yl)-5,6,7,8,9,10-hexahydrophenanthrene-3,5-diol

> <ALOGPS_LOGP>
4.52

> <JCHEM_LOGP>
4.412144647666667

> <ALOGPS_LOGS>
-4.23

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.536455003114089

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.12355166289465

> <JCHEM_PKA_STRONGEST_BASIC>
-3.013147987544011

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
87.33149999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.70e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5R)-2-isopropyl-8,8-dimethyl-6,7,9,10-tetrahydro-5H-phenanthrene-3,5-diol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 47 49  0  0  0  0  0  0  0  0999 V2000
    3.1546    1.7211    1.7695 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7072    2.2223    1.7651 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5415    3.3986    0.7985 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7294    1.1015    1.4501 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7818    0.4253    0.2223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1114   -0.6181   -0.0782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1068   -0.9977    0.8392 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1581   -0.3177    2.0651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2530    0.7079    2.3623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3321    1.3423    3.5722 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0669   -2.0865    0.4819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7794   -2.9248   -0.5468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5002   -2.7416   -1.3454 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0462   -1.2865   -1.4230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6946   -4.0911   -0.9615 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8954   -5.4020   -1.1224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3678   -3.7542   -2.3105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7978   -4.3611    0.0954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4117   -3.0728    0.6296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3421   -2.2066    1.2930 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0370   -2.7779    2.5688 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8368    2.5199    2.0804 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2768    0.8855    2.4676 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4750    1.3792    0.7794 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5083    2.6118    2.7706 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7933    3.1234   -0.2314 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1943    4.2292    1.0884 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5093    3.7663    0.8034 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5270    0.7107   -0.5178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9016   -0.5873    2.8088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0451    0.9371    4.0925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6157   -3.1020   -2.3726 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2833   -3.3547   -0.8811 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9749   -1.2557   -1.8214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6877   -0.7289   -2.1173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1743   -5.3484   -1.9452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3395   -5.6421   -0.2085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5633   -6.2447   -1.3369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0933   -4.5261   -2.5926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6401   -3.6894   -3.1267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8990   -2.7969   -2.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3809   -4.9299    0.9377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5896   -4.9913   -0.3294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1929   -3.3267    1.3561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8927   -2.5190   -0.1848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7827   -1.2187    1.4712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3206   -3.4210    2.4253 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 20  1  0
 11 12  2  0
 19 18  1  0
 19 20  1  0
  7  8  1  0
  6  5  1  0
  5  4  2  0
  4  9  1  0
  9  8  2  0
 18 15  1  0
  9 10  1  0
 11  7  1  0
  4  2  1  0
 12 13  1  0
  2  1  1  0
 13 14  1  0
  2  3  1  0
 14  6  1  0
 15 16  1  6
  7  6  2  0
 15 17  1  0
 15 12  1  0
 20 21  1  0
 19 44  1  0
 19 45  1  0
 18 42  1  0
 18 43  1  0
 20 46  1  1
 13 32  1  0
 13 33  1  0
 14 34  1  0
 14 35  1  0
  5 29  1  0
  8 30  1  0
 10 31  1  0
  2 25  1  1
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
 16 36  1  0
 16 37  1  0
 16 38  1  0
 17 39  1  0
 17 40  1  0
 17 41  1  0
 21 47  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       3.155   1.721   1.770  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.707   2.222   1.765  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.542   3.399   0.799  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.729   1.101   1.450  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.782   0.425   0.222  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.111  -0.618  -0.078  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.107  -0.998   0.839  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.158  -0.318   2.065  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.253   0.708   2.362  0.00  0.00           C+0
HETATM   10  O   UNK     0      -0.332   1.342   3.572  0.00  0.00           O+0
HETATM   11  C   UNK     0      -2.067  -2.087   0.482  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.779  -2.925  -0.547  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.500  -2.742  -1.345  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.046  -1.287  -1.423  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.695  -4.091  -0.962  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.895  -5.402  -1.122  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.368  -3.754  -2.311  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.798  -4.361   0.095  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.412  -3.073   0.630  0.00  0.00           C+0
HETATM   20  C   UNK     0      -3.342  -2.207   1.293  0.00  0.00           C+0
HETATM   21  O   UNK     0      -3.037  -2.778   2.569  0.00  0.00           O+0
HETATM   22  H   UNK     0       3.837   2.520   2.080  0.00  0.00           H+0
HETATM   23  H   UNK     0       3.277   0.886   2.468  0.00  0.00           H+0
HETATM   24  H   UNK     0       3.475   1.379   0.779  0.00  0.00           H+0
HETATM   25  H   UNK     0       1.508   2.612   2.771  0.00  0.00           H+0
HETATM   26  H   UNK     0       1.793   3.123  -0.231  0.00  0.00           H+0
HETATM   27  H   UNK     0       2.194   4.229   1.088  0.00  0.00           H+0
HETATM   28  H   UNK     0       0.509   3.766   0.803  0.00  0.00           H+0
HETATM   29  H   UNK     0       1.527   0.711  -0.518  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.902  -0.587   2.809  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.045   0.937   4.093  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.616  -3.102  -2.373  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.283  -3.355  -0.881  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.975  -1.256  -1.821  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.688  -0.729  -2.117  0.00  0.00           H+0
HETATM   36  H   UNK     0      -1.174  -5.348  -1.945  0.00  0.00           H+0
HETATM   37  H   UNK     0      -1.339  -5.642  -0.209  0.00  0.00           H+0
HETATM   38  H   UNK     0      -2.563  -6.245  -1.337  0.00  0.00           H+0
HETATM   39  H   UNK     0      -4.093  -4.526  -2.593  0.00  0.00           H+0
HETATM   40  H   UNK     0      -2.640  -3.689  -3.127  0.00  0.00           H+0
HETATM   41  H   UNK     0      -3.899  -2.797  -2.272  0.00  0.00           H+0
HETATM   42  H   UNK     0      -3.381  -4.930   0.938  0.00  0.00           H+0
HETATM   43  H   UNK     0      -4.590  -4.991  -0.329  0.00  0.00           H+0
HETATM   44  H   UNK     0      -5.193  -3.327   1.356  0.00  0.00           H+0
HETATM   45  H   UNK     0      -4.893  -2.519  -0.185  0.00  0.00           H+0
HETATM   46  H   UNK     0      -3.783  -1.219   1.471  0.00  0.00           H+0
HETATM   47  H   UNK     0      -2.321  -3.421   2.425  0.00  0.00           H+0
CONECT    1    2   22   23   24                                             
CONECT    2    4    1    3   25                                             
CONECT    3    2   26   27   28                                             
CONECT    4    5    9    2                                                  
CONECT    5    6    4   29                                                  
CONECT    6    5   14    7                                                  
CONECT    7    8   11    6                                                  
CONECT    8    7    9   30                                                  
CONECT    9    4    8   10                                                  
CONECT   10    9   31                                                       
CONECT   11   20   12    7                                                  
CONECT   12   11   13   15                                                  
CONECT   13   12   14   32   33                                             
CONECT   14   13    6   34   35                                             
CONECT   15   18   16   17   12                                             
CONECT   16   15   36   37   38                                             
CONECT   17   15   39   40   41                                             
CONECT   18   19   15   42   43                                             
CONECT   19   18   20   44   45                                             
CONECT   20   11   19   21   46                                             
CONECT   21   20   47                                                       
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    2                                                            
CONECT   26    3                                                            
CONECT   27    3                                                            
CONECT   28    3                                                            
CONECT   29    5                                                            
CONECT   30    8                                                            
CONECT   31   10                                                            
CONECT   32   13                                                            
CONECT   33   13                                                            
CONECT   34   14                                                            
CONECT   35   14                                                            
CONECT   36   16                                                            
CONECT   37   16                                                            
CONECT   38   16                                                            
CONECT   39   17                                                            
CONECT   40   17                                                            
CONECT   41   17                                                            
CONECT   42   18                                                            
CONECT   43   18                                                            
CONECT   44   19                                                            
CONECT   45   19                                                            
CONECT   46   20                                                            
CONECT   47   21                                                            
MASTER        0    0    0    0    0    0    0    0   47    0   98    0
END

RDKit          3D

47 49  0  0  0  0  0  0  0  0999 V2000
    3.1546    1.7211    1.7695 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7072    2.2223    1.7651 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5415    3.3986    0.7985 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7294    1.1015    1.4501 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7818    0.4253    0.2223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1114   -0.6181   -0.0782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1068   -0.9977    0.8392 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1581   -0.3177    2.0651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2530    0.7079    2.3623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3321    1.3423    3.5722 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0669   -2.0865    0.4819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7794   -2.9248   -0.5468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5002   -2.7416   -1.3454 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0462   -1.2865   -1.4230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6946   -4.0911   -0.9615 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8954   -5.4020   -1.1224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3678   -3.7542   -2.3105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7978   -4.3611    0.0954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4117   -3.0728    0.6296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3421   -2.2066    1.2930 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0370   -2.7779    2.5688 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8368    2.5199    2.0804 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2768    0.8855    2.4676 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4750    1.3792    0.7794 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5083    2.6118    2.7706 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7933    3.1234   -0.2314 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1943    4.2292    1.0884 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5093    3.7663    0.8034 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5270    0.7107   -0.5178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9016   -0.5873    2.8088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0451    0.9371    4.0925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6157   -3.1020   -2.3726 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2833   -3.3547   -0.8811 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9749   -1.2557   -1.8214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6877   -0.7289   -2.1173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1743   -5.3484   -1.9452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3395   -5.6421   -0.2085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5633   -6.2447   -1.3369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0933   -4.5261   -2.5926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6401   -3.6894   -3.1267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8990   -2.7969   -2.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3809   -4.9299    0.9377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5896   -4.9913   -0.3294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1929   -3.3267    1.3561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8927   -2.5190   -0.1848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7827   -1.2187    1.4712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3206   -3.4210    2.4253 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 20  1  0
 11 12  2  0
 19 18  1  0
 19 20  1  0
  7  8  1  0
  6  5  1  0
  5  4  2  0
  4  9  1  0
  9  8  2  0
 18 15  1  0
  9 10  1  0
 11  7  1  0
  4  2  1  0
 12 13  1  0
  2  1  1  0
 13 14  1  0
  2  3  1  0
 14  6  1  0
 15 16  1  6
  7  6  2  0
 15 17  1  0
 15 12  1  0
 20 21  1  0
 19 44  1  0
 19 45  1  0
 18 42  1  0
 18 43  1  0
 20 46  1  1
 13 32  1  0
 13 33  1  0
 14 34  1  0
 14 35  1  0
  5 29  1  0
  8 30  1  0
 10 31  1  0
  2 25  1  1
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
 16 36  1  0
 16 37  1  0
 16 38  1  0
 17 39  1  0
 17 40  1  0
 17 41  1  0
 21 47  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₆O₂

Average Mass

286.4150 Da

Monoisotopic Mass

286.19328 Da

IUPAC Name

(5R)-8,8-dimethyl-2-(propan-2-yl)-5,6,7,8,9,10-hexahydrophenanthrene-3,5-diol

Traditional Name

(5R)-2-isopropyl-8,8-dimethyl-6,7,9,10-tetrahydro-5H-phenanthrene-3,5-diol

CAS Registry Number

Not Available

SMILES

[H]OC1=C([H])C2=C(C([H])=C1C([H])(C([H])([H])[H])C([H])([H])[H])C([H])([H])C([H])([H])C1=C2[C@]([H])(O[H])C([H])([H])C([H])([H])C1(C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C19H26O2/c1-11(2)13-9-12-5-6-15-18(14(12)10-17(13)21)16(20)7-8-19(15,3)4/h9-11,16,20-21H,5-8H2,1-4H3/t16-/m1/s1

InChI Key

VGYQUIDVXNWOOS-MRXNPFEDSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
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, 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, 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, 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, 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

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Fraxinus sieboldiana	JEOL database	Lin, S., et al, J. Nat. Prod. 73, 1914 (2010)

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	4.52	ALOGPS
logP	4.41	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	10.12	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	40.46 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	87.33 m³·mol⁻¹	ChemAxon
Polarizability	34.19 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

Not Available

Chemspider ID

26389421

KEGG Compound ID

Not Available

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

70569

Good Scents ID

Not Available

References

General References

Lin, S., et al. (2010). Lin, S., et al, J. Nat. Prod. 73, 1914 (2010). J. Nat. Prod..

Showing NP-Card for (+)-(1R)-1,12-dihydroxy-20-norabieta-5(10),8,11,13-tetraene (NP0035669)

MOL for NP0035669 ((+)-(1R)-1,12-dihydroxy-20-norabieta-5(10),8,11,13-tetraene)

3D MOL for NP0035669 ((+)-(1R)-1,12-dihydroxy-20-norabieta-5(10),8,11,13-tetraene)

3D SDF for NP0035669 ((+)-(1R)-1,12-dihydroxy-20-norabieta-5(10),8,11,13-tetraene)

3D-SDF for NP0035669 ((+)-(1R)-1,12-dihydroxy-20-norabieta-5(10),8,11,13-tetraene)

PDB for NP0035669 ((+)-(1R)-1,12-dihydroxy-20-norabieta-5(10),8,11,13-tetraene)

3D PDB for NP0035669 ((+)-(1R)-1,12-dihydroxy-20-norabieta-5(10),8,11,13-tetraene)

SMILES for NP0035669 ((+)-(1R)-1,12-dihydroxy-20-norabieta-5(10),8,11,13-tetraene)

INCHI for NP0035669 ((+)-(1R)-1,12-dihydroxy-20-norabieta-5(10),8,11,13-tetraene)

Structure for NP0035669 ((+)-(1R)-1,12-dihydroxy-20-norabieta-5(10),8,11,13-tetraene)

3D Structure for NP0035669 ((+)-(1R)-1,12-dihydroxy-20-norabieta-5(10),8,11,13-tetraene)