NP-MRD: Showing NP-Card for 20-Nor-3alpha-acetoxy-12-hydroxy-abieta-5,7,9,11,13-pentaene (NP0007693)

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Record Information

Version

2.0

Created at

2020-12-09 04:30:22 UTC

Updated at

2021-07-15 16:58:17 UTC

NP-MRD ID

NP0007693

Secondary Accession Numbers

None

Natural Product Identification

Common Name

20-Nor-3alpha-acetoxy-12-hydroxy-abieta-5,7,9,11,13-pentaene

Provided By

NPAtlas

Description

20-Nor-3alpha-acetoxy-12-hydroxy-abieta-5,7,9,11,13-pentaene is found in Microcoleus. 20-Nor-3alpha-acetoxy-12-hydroxy-abieta-5,7,9,11,13-pentaene was first documented in 2008 (PMID: 18404301). Based on a literature review very few articles have been published on (2R)-6-hydroxy-1,1-dimethyl-7-(propan-2-yl)-1,2,3,4-tetrahydrophenanthren-2-yl acetate.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242119023D          

 50 52  0  0  0  0            999 V2000
    6.6125    1.1450    1.1565 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5477    0.8658    0.1605 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.2069    0.8062    0.4862 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1744    0.5415   -0.4415 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2227    1.6757   -0.6312 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0689    1.6696    0.3516 C   0  0  2  0  0  0  0  0  0  0  0  0
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    0.3957   -1.9579   -0.1385 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.0668   -0.9544    0.2849 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652306242119023D          

 50 52  0  0  0  0            999 V2000
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  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 14 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
  9 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 22  5  1  0  0  0  0
 21  8  1  0  0  0  0
 21 12  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  5 28  1  6  0  0  0
  6 29  1  0  0  0  0
  6 30  1  0  0  0  0
  7 31  1  0  0  0  0
  7 32  1  0  0  0  0
 10 33  1  0  0  0  0
 11 34  1  0  0  0  0
 13 35  1  0  0  0  0
 15 36  1  1  0  0  0
 16 37  1  0  0  0  0
 16 38  1  0  0  0  0
 16 39  1  0  0  0  0
 17 40  1  0  0  0  0
 17 41  1  0  0  0  0
 17 42  1  0  0  0  0
 19 43  1  0  0  0  0
 20 44  1  0  0  0  0
 23 45  1  0  0  0  0
 23 46  1  0  0  0  0
 23 47  1  0  0  0  0
 24 48  1  0  0  0  0
 24 49  1  0  0  0  0
 24 50  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0007693

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C(C([H])=C2C([H])=C([H])C3=C(C2=C1[H])C([H])([H])C([H])([H])[C@@]([H])(OC(=O)C([H])([H])[H])C3(C([H])([H])[H])C([H])([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C21H26O3/c1-12(2)16-10-14-6-8-18-15(17(14)11-19(16)23)7-9-20(21(18,4)5)24-13(3)22/h6,8,10-12,20,23H,7,9H2,1-5H3/t20-/m1/s1

> <INCHI_KEY>
VAOOUXRVYRUSNC-HXUWFJFHSA-N

> <FORMULA>
C21H26O3

> <MOLECULAR_WEIGHT>
326.436

> <EXACT_MASS>
326.188194697

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
38.40310189973475

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R)-6-hydroxy-1,1-dimethyl-7-(propan-2-yl)-1,2,3,4-tetrahydrophenanthren-2-yl acetate

> <ALOGPS_LOGP>
5.64

> <JCHEM_LOGP>
5.1538011673333335

> <ALOGPS_LOGS>
-5.77

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.250967945032867

> <JCHEM_PKA_STRONGEST_BASIC>
-5.25166182224426

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
95.8528

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.51e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-6-hydroxy-7-isopropyl-1,1-dimethyl-3,4-dihydro-2H-phenanthren-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 50 52  0  0  0  0  0  0  0  0999 V2000
    6.6125    1.1450    1.1565 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5477    0.8658    0.1605 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8174    0.6684   -1.0378 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2069    0.8062    0.4862 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1744    0.5415   -0.4415 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2227    1.6757   -0.6312 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0689    1.6696    0.3516 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3457    0.4295    0.2188 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0628   -0.7283   -0.0087 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3957   -1.9579   -0.1385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9716   -2.0483   -0.0446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6870   -0.9050    0.1809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0668   -0.9544    0.2849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8311    0.1647    0.5136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3144    0.1192    0.6200 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7020   -1.3461    0.6345 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9368    0.7647   -0.6012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1688    1.3657    0.6396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8657    2.5337    0.8710 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7724    1.4388    0.5378 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0283    0.3104    0.3091 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5167   -0.7685   -0.1219 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0598   -1.3744    1.1649 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8324   -1.8143   -1.2054 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9607    0.2386    1.6712 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4431    1.6920    0.6758 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1541    1.8498    1.8966 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6980    0.4121   -1.4093 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7618    2.6343   -0.4982 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7624    1.7149   -1.6381 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5921    2.6242    0.2532 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4967    1.6707    1.4047 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9457   -2.8702   -0.3169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4697   -3.0026   -0.1461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5718   -1.9266    0.1792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6482    0.5761    1.5582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7961   -1.4501    0.8834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5382   -1.8170   -0.3397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1570   -1.8564    1.4550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1426    1.2180   -1.2505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4981   -0.0138   -1.1770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6474    1.5510   -0.2853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8691    2.5315    0.9563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2756    2.3836    0.6419 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6515   -2.4181    1.2166 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1529   -1.4567    1.0631 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7336   -0.8320    2.0601 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9758   -2.8143   -0.7805 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7616   -1.4576   -1.6951 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0050   -1.7833   -1.9527 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 14 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  2  0
  9 22  1  0
 22 23  1  1
 22 24  1  0
 22  5  1  0
 21  8  1  0
 21 12  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  5 28  1  6
  6 29  1  0
  6 30  1  0
  7 31  1  0
  7 32  1  0
 10 33  1  0
 11 34  1  0
 13 35  1  0
 15 36  1  1
 16 37  1  0
 16 38  1  0
 16 39  1  0
 17 40  1  0
 17 41  1  0
 17 42  1  0
 19 43  1  0
 20 44  1  0
 23 45  1  0
 23 46  1  0
 23 47  1  0
 24 48  1  0
 24 49  1  0
 24 50  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       6.612   1.145   1.157  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.548   0.866   0.161  0.00  0.00           C+0
HETATM    3  O   UNK     0       5.817   0.668  -1.038  0.00  0.00           O+0
HETATM    4  O   UNK     0       4.207   0.806   0.486  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.174   0.542  -0.442  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.223   1.676  -0.631  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.069   1.670   0.352  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.346   0.430   0.219  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.063  -0.728  -0.009  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.396  -1.958  -0.139  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.972  -2.048  -0.045  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.687  -0.905   0.181  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.067  -0.954   0.285  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.831   0.165   0.514  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.314   0.119   0.620  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.702  -1.346   0.635  0.00  0.00           C+0
HETATM   17  C   UNK     0      -5.937   0.765  -0.601  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.169   1.366   0.640  0.00  0.00           C+0
HETATM   19  O   UNK     0      -3.866   2.534   0.871  0.00  0.00           O+0
HETATM   20  C   UNK     0      -1.772   1.439   0.538  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.028   0.310   0.309  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.517  -0.769  -0.122  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.060  -1.374   1.165  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.832  -1.814  -1.205  0.00  0.00           C+0
HETATM   25  H   UNK     0       6.961   0.239   1.671  0.00  0.00           H+0
HETATM   26  H   UNK     0       7.443   1.692   0.676  0.00  0.00           H+0
HETATM   27  H   UNK     0       6.154   1.850   1.897  0.00  0.00           H+0
HETATM   28  H   UNK     0       3.698   0.412  -1.409  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.762   2.634  -0.498  0.00  0.00           H+0
HETATM   30  H   UNK     0       1.762   1.715  -1.638  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.592   2.624   0.253  0.00  0.00           H+0
HETATM   32  H   UNK     0       1.497   1.671   1.405  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.946  -2.870  -0.317  0.00  0.00           H+0
HETATM   34  H   UNK     0      -1.470  -3.003  -0.146  0.00  0.00           H+0
HETATM   35  H   UNK     0      -3.572  -1.927   0.179  0.00  0.00           H+0
HETATM   36  H   UNK     0      -5.648   0.576   1.558  0.00  0.00           H+0
HETATM   37  H   UNK     0      -6.796  -1.450   0.883  0.00  0.00           H+0
HETATM   38  H   UNK     0      -5.538  -1.817  -0.340  0.00  0.00           H+0
HETATM   39  H   UNK     0      -5.157  -1.856   1.455  0.00  0.00           H+0
HETATM   40  H   UNK     0      -5.143   1.218  -1.250  0.00  0.00           H+0
HETATM   41  H   UNK     0      -6.498  -0.014  -1.177  0.00  0.00           H+0
HETATM   42  H   UNK     0      -6.647   1.551  -0.285  0.00  0.00           H+0
HETATM   43  H   UNK     0      -4.869   2.531   0.956  0.00  0.00           H+0
HETATM   44  H   UNK     0      -1.276   2.384   0.642  0.00  0.00           H+0
HETATM   45  H   UNK     0       2.652  -2.418   1.217  0.00  0.00           H+0
HETATM   46  H   UNK     0       4.153  -1.457   1.063  0.00  0.00           H+0
HETATM   47  H   UNK     0       2.734  -0.832   2.060  0.00  0.00           H+0
HETATM   48  H   UNK     0       2.976  -2.814  -0.781  0.00  0.00           H+0
HETATM   49  H   UNK     0       3.762  -1.458  -1.695  0.00  0.00           H+0
HETATM   50  H   UNK     0       2.005  -1.783  -1.953  0.00  0.00           H+0
CONECT    1    2   25   26   27                                             
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   22   28                                             
CONECT    6    5    7   29   30                                             
CONECT    7    6    8   31   32                                             
CONECT    8    7    9   21                                                  
CONECT    9    8   10   22                                                  
CONECT   10    9   11   33                                                  
CONECT   11   10   12   34                                                  
CONECT   12   11   13   21                                                  
CONECT   13   12   14   35                                                  
CONECT   14   13   15   18                                                  
CONECT   15   14   16   17   36                                             
CONECT   16   15   37   38   39                                             
CONECT   17   15   40   41   42                                             
CONECT   18   14   19   20                                                  
CONECT   19   18   43                                                       
CONECT   20   18   21   44                                                  
CONECT   21   20    8   12                                                  
CONECT   22    9   23   24    5                                             
CONECT   23   22   45   46   47                                             
CONECT   24   22   48   49   50                                             
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    5                                                            
CONECT   29    6                                                            
CONECT   30    6                                                            
CONECT   31    7                                                            
CONECT   32    7                                                            
CONECT   33   10                                                            
CONECT   34   11                                                            
CONECT   35   13                                                            
CONECT   36   15                                                            
CONECT   37   16                                                            
CONECT   38   16                                                            
CONECT   39   16                                                            
CONECT   40   17                                                            
CONECT   41   17                                                            
CONECT   42   17                                                            
CONECT   43   19                                                            
CONECT   44   20                                                            
CONECT   45   23                                                            
CONECT   46   23                                                            
CONECT   47   23                                                            
CONECT   48   24                                                            
CONECT   49   24                                                            
CONECT   50   24                                                            
MASTER        0    0    0    0    0    0    0    0   50    0  104    0
END

RDKit          3D

50 52  0  0  0  0  0  0  0  0999 V2000
    6.6125    1.1450    1.1565 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5477    0.8658    0.1605 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8174    0.6684   -1.0378 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2069    0.8062    0.4862 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1744    0.5415   -0.4415 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2227    1.6757   -0.6312 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0689    1.6696    0.3516 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3457    0.4295    0.2188 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0628   -0.7283   -0.0087 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3957   -1.9579   -0.1385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9716   -2.0483   -0.0446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6870   -0.9050    0.1809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0668   -0.9544    0.2849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8311    0.1647    0.5136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3144    0.1192    0.6200 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7020   -1.3461    0.6345 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9368    0.7647   -0.6012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1688    1.3657    0.6396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8657    2.5337    0.8710 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7724    1.4388    0.5378 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0283    0.3104    0.3091 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5167   -0.7685   -0.1219 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0598   -1.3744    1.1649 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8324   -1.8143   -1.2054 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9607    0.2386    1.6712 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4431    1.6920    0.6758 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1541    1.8498    1.8966 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6980    0.4121   -1.4093 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7618    2.6343   -0.4982 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7624    1.7149   -1.6381 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5921    2.6242    0.2532 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4967    1.6707    1.4047 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9457   -2.8702   -0.3169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4697   -3.0026   -0.1461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5718   -1.9266    0.1792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6482    0.5761    1.5582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7961   -1.4501    0.8834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5382   -1.8170   -0.3397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1570   -1.8564    1.4550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1426    1.2180   -1.2505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4981   -0.0138   -1.1770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6474    1.5510   -0.2853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8691    2.5315    0.9563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2756    2.3836    0.6419 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6515   -2.4181    1.2166 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1529   -1.4567    1.0631 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7336   -0.8320    2.0601 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9758   -2.8143   -0.7805 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7616   -1.4576   -1.6951 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0050   -1.7833   -1.9527 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 14 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  2  0
  9 22  1  0
 22 23  1  1
 22 24  1  0
 22  5  1  0
 21  8  1  0
 21 12  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  5 28  1  6
  6 29  1  0
  6 30  1  0
  7 31  1  0
  7 32  1  0
 10 33  1  0
 11 34  1  0
 13 35  1  0
 15 36  1  1
 16 37  1  0
 16 38  1  0
 16 39  1  0
 17 40  1  0
 17 41  1  0
 17 42  1  0
 19 43  1  0
 20 44  1  0
 23 45  1  0
 23 46  1  0
 23 47  1  0
 24 48  1  0
 24 49  1  0
 24 50  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
(2R)-6-Hydroxy-1,1-dimethyl-7-(propan-2-yl)-1,2,3,4-tetrahydrophenanthren-2-yl acetic acid	Generator
20-Nor-3a-acetoxy-12-hydroxy-abieta-5,7,9,11,13-pentaene	Generator
20-Nor-3α-acetoxy-12-hydroxy-abieta-5,7,9,11,13-pentaene	Generator
20-AHBP CPD	MeSH

Chemical Formula

C₂₁H₂₆O₃

Average Mass

326.4360 Da

Monoisotopic Mass

326.18819 Da

IUPAC Name

(2R)-6-hydroxy-1,1-dimethyl-7-(propan-2-yl)-1,2,3,4-tetrahydrophenanthren-2-yl acetate

Traditional Name

(2R)-6-hydroxy-7-isopropyl-1,1-dimethyl-3,4-dihydro-2H-phenanthren-2-yl acetate

CAS Registry Number

Not Available

SMILES

CC(C)C1=C(O)C=C2C(C=CC3=C2CC[C@@H](OC(C)=O)C3(C)C)=C1

InChI Identifier

InChI=1S/C21H26O3/c1-12(2)16-10-14-6-8-18-15(17(14)11-19(16)23)7-9-20(21(18,4)5)24-13(3)22/h6,8,10-12,20,23H,7,9H2,1-5H3/t20-/m1/s1

InChI Key

VAOOUXRVYRUSNC-HXUWFJFHSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Microcoleus	NPAtlas	18404301

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	5.64	ALOGPS
logP	5.15	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Acidic)	10.25	ChemAxon
pKa (Strongest Basic)	-5.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	95.85 m³·mol⁻¹	ChemAxon
Polarizability	38.4 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA015688

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78439798

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102393971

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Perez Gutierrez RM, Martinez Flores A, Vargas Solis R, Carmona Jimenez J: Two new antibacterial norabietane diterpenoids from cyanobacteria, Microcoleous lacustris. J Nat Med. 2008 Jul;62(3):328-31. doi: 10.1007/s11418-008-0238-z. Epub 2008 Mar 26. [PubMed:18404301 ]

Showing NP-Card for 20-Nor-3alpha-acetoxy-12-hydroxy-abieta-5,7,9,11,13-pentaene (NP0007693)

MOL for NP0007693 (20-Nor-3alpha-acetoxy-12-hydroxy-abieta-5,7,9,11,13-pentaene)

3D MOL for NP0007693 (20-Nor-3alpha-acetoxy-12-hydroxy-abieta-5,7,9,11,13-pentaene)

3D SDF for NP0007693 (20-Nor-3alpha-acetoxy-12-hydroxy-abieta-5,7,9,11,13-pentaene)

3D-SDF for NP0007693 (20-Nor-3alpha-acetoxy-12-hydroxy-abieta-5,7,9,11,13-pentaene)

PDB for NP0007693 (20-Nor-3alpha-acetoxy-12-hydroxy-abieta-5,7,9,11,13-pentaene)

3D PDB for NP0007693 (20-Nor-3alpha-acetoxy-12-hydroxy-abieta-5,7,9,11,13-pentaene)

SMILES for NP0007693 (20-Nor-3alpha-acetoxy-12-hydroxy-abieta-5,7,9,11,13-pentaene)

INCHI for NP0007693 (20-Nor-3alpha-acetoxy-12-hydroxy-abieta-5,7,9,11,13-pentaene)

Structure for NP0007693 (20-Nor-3alpha-acetoxy-12-hydroxy-abieta-5,7,9,11,13-pentaene)

3D Structure for NP0007693 (20-Nor-3alpha-acetoxy-12-hydroxy-abieta-5,7,9,11,13-pentaene)