NP-MRD: Showing NP-Card for 7alpha,16-dihydroxy-abiet-15(17)-en-19-al (NP0041655)

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Record Information

Version

2.0

Created at

2021-06-20 23:31:18 UTC

Updated at

2021-06-30 00:16:17 UTC

NP-MRD ID

NP0041655

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7alpha,16-dihydroxy-abiet-15(17)-en-19-al

Provided By

JEOL Database JEOL Logo

Description

7alpha,16-dihydroxy-abiet-15(17)-en-19-al is found in Erythroxylum suberosum. 7alpha,16-dihydroxy-abiet-15(17)-en-19-al was first documented in 2012 (Nascimento, C. J., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212101313D          

 55 57  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652306212101313D          

 55 57  0  0  0  0            999 V2000
    3.3294    2.5450   -5.0766 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1045    2.0787   -4.0787 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.0075   -2.0962   -3.3968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0291   -1.1958   -3.3738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6788   -2.8463   -1.7398 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9685   -3.1005   -1.1765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8054   -0.7162   -0.4763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1310   -3.5639   -0.2866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8485   -3.1712    1.2648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8129   -1.9490   -0.0146 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1510   -4.2202    0.6476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6123   -1.8598    3.0011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9181   -0.5674    1.8549 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7530   -1.2460    3.1553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2544    0.1567    3.4373 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0916    0.9988    1.1926 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6366    0.7015    1.9746 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6961   -2.2639    0.0004 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1761   -1.0476    1.1810 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0335   -2.2806    1.6243 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 23  1  1  0  0  0
 20 19  1  0  0  0  0
  6  5  1  0  0  0  0
 22 14  1  0  0  0  0
  5 10  1  0  0  0  0
 22  8  1  0  0  0  0
  8  7  1  0  0  0  0
  9 10  1  0  0  0  0
  8 34  1  6  0  0  0
  6  7  1  0  0  0  0
 11 12  1  0  0  0  0
 14 13  1  0  0  0  0
 15 17  1  1  0  0  0
 22 21  1  0  0  0  0
  5  2  1  0  0  0  0
 13 11  1  0  0  0  0
 15 16  1  0  0  0  0
 21 20  1  0  0  0  0
  2  3  1  0  0  0  0
 11  9  1  0  0  0  0
  3  4  1  0  0  0  0
 14 15  1  0  0  0  0
  2  1  2  3  0  0  0
  8  9  1  0  0  0  0
 17 18  2  0  0  0  0
 15 19  1  0  0  0  0
 17 46  1  0  0  0  0
 14 42  1  6  0  0  0
 13 40  1  0  0  0  0
 13 41  1  0  0  0  0
 11 38  1  6  0  0  0
  9 35  1  1  0  0  0
  7 32  1  0  0  0  0
  7 33  1  0  0  0  0
 21 51  1  0  0  0  0
 21 52  1  0  0  0  0
 20 49  1  0  0  0  0
 20 50  1  0  0  0  0
 19 47  1  0  0  0  0
 19 48  1  0  0  0  0
 23 53  1  0  0  0  0
 23 54  1  0  0  0  0
 23 55  1  0  0  0  0
  6 30  1  0  0  0  0
  6 31  1  0  0  0  0
  5 29  1  1  0  0  0
 10 36  1  0  0  0  0
 10 37  1  0  0  0  0
 12 39  1  0  0  0  0
 16 43  1  0  0  0  0
 16 44  1  0  0  0  0
 16 45  1  0  0  0  0
  3 26  1  0  0  0  0
  3 27  1  0  0  0  0
  4 28  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0041655

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O3/c1-13(11-21)14-5-6-16-15(9-14)17(23)10-18-19(2,12-22)7-4-8-20(16,18)3/h12,14-18,21,23H,1,4-11H2,2-3H3/t14-,15-,16-,17+,18-,19+,20+/m0/s1

> <INCHI_KEY>
DXZARVMGCPQDSK-TUFIBKJQSA-N

> <FORMULA>
C20H32O3

> <MOLECULAR_WEIGHT>
320.473

> <EXACT_MASS>
320.23514489

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
37.46110468223061

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,4aR,4bS,7S,8aS,9R,10aR)-9-hydroxy-7-(3-hydroxyprop-1-en-2-yl)-1,4a-dimethyl-tetradecahydrophenanthrene-1-carbaldehyde

> <ALOGPS_LOGP>
2.74

> <JCHEM_LOGP>
2.667926006000001

> <ALOGPS_LOGS>
-3.94

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.76022052941361

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.884459503537816

> <JCHEM_PKA_STRONGEST_BASIC>
-0.6933339621656626

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
91.73349999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.68e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4aR,4bS,7S,8aS,9R,10aR)-9-hydroxy-7-(3-hydroxyprop-1-en-2-yl)-1,4a-dimethyl-dodecahydrophenanthrene-1-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 55 57  0  0  0  0  0  0  0  0999 V2000
    3.3294    2.5450   -5.0766 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1045    2.0787   -4.0787 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5909    2.3686   -3.9951 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9917    3.3845   -4.9028 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5825    1.1820   -2.9535 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2925    2.0042   -1.6895 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8793    1.1089   -0.5203 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6580    0.2242   -0.8538 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9329   -0.5918   -2.1465 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3421    0.3406   -3.3066 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7273   -1.4568   -2.5512 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3431   -0.6216   -2.9922 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2241   -2.3296   -1.3993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0942   -1.4892   -0.1413 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8772   -2.2577    0.9771 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2409   -2.7602    0.4491 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1566   -3.5220    1.4444 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0490   -3.8187    2.6175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1678   -1.3090    2.1622 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0576   -0.5569    2.6650 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7607    0.2024    1.5443 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1745   -0.6926    0.3443 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3245   -1.6235    0.8040 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7378    3.1456   -5.8845 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2673    2.3355   -5.1398 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1601    1.4625   -4.2258 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8694    2.7001   -2.9902 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4742    4.1742   -4.6713 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3848    0.4658   -2.7225 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4958    2.7331   -1.8880 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1762    2.5802   -1.3906 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7400    0.4883   -0.2481 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6633    1.7542    0.3371 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8315    0.9162   -1.0773 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7780   -1.2674   -1.9608 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5005    1.0008   -3.5498 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5487   -0.2621   -4.2003 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0075   -2.0962   -3.3968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0291   -1.1958   -3.3738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6788   -2.8463   -1.7398 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9685   -3.1005   -1.1765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8054   -0.7162   -0.4763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1310   -3.5639   -0.2866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8485   -3.1712    1.2648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8129   -1.9490   -0.0146 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1510   -4.2202    0.6476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6123   -1.8598    3.0011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9181   -0.5674    1.8549 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7530   -1.2460    3.1553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2544    0.1567    3.4373 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0916    0.9988    1.1926 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6366    0.7015    1.9746 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6961   -2.2639    0.0004 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1761   -1.0476    1.1810 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0335   -2.2806    1.6243 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 23  1  1
 20 19  1  0
  6  5  1  0
 22 14  1  0
  5 10  1  0
 22  8  1  0
  8  7  1  0
  9 10  1  0
  8 34  1  6
  6  7  1  0
 11 12  1  0
 14 13  1  0
 15 17  1  1
 22 21  1  0
  5  2  1  0
 13 11  1  0
 15 16  1  0
 21 20  1  0
  2  3  1  0
 11  9  1  0
  3  4  1  0
 14 15  1  0
  2  1  2  3
  8  9  1  0
 17 18  2  0
 15 19  1  0
 17 46  1  0
 14 42  1  6
 13 40  1  0
 13 41  1  0
 11 38  1  6
  9 35  1  1
  7 32  1  0
  7 33  1  0
 21 51  1  0
 21 52  1  0
 20 49  1  0
 20 50  1  0
 19 47  1  0
 19 48  1  0
 23 53  1  0
 23 54  1  0
 23 55  1  0
  6 30  1  0
  6 31  1  0
  5 29  1  1
 10 36  1  0
 10 37  1  0
 12 39  1  0
 16 43  1  0
 16 44  1  0
 16 45  1  0
  3 26  1  0
  3 27  1  0
  4 28  1  0
  1 24  1  0
  1 25  1  0
M  END

HEADER    PROTEIN                                 21-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-JUN-21         0                                  
HETATM    1  C   UNK     0       3.329   2.545  -5.077  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.104   2.079  -4.079  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.591   2.369  -3.995  0.00  0.00           C+0
HETATM    4  O   UNK     0       5.992   3.385  -4.903  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.583   1.182  -2.954  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.293   2.004  -1.690  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.879   1.109  -0.520  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.658   0.224  -0.854  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.933  -0.592  -2.147  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.342   0.341  -3.307  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.727  -1.457  -2.551  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.343  -0.622  -2.992  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.224  -2.330  -1.399  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.094  -1.489  -0.141  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.877  -2.258   0.977  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.241  -2.760   0.449  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.157  -3.522   1.444  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.049  -3.819   2.618  0.00  0.00           O+0
HETATM   19  C   UNK     0      -1.168  -1.309   2.162  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.058  -0.557   2.665  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.761   0.202   1.544  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.175  -0.693   0.344  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.325  -1.624   0.804  0.00  0.00           C+0
HETATM   24  H   UNK     0       3.738   3.146  -5.885  0.00  0.00           H+0
HETATM   25  H   UNK     0       2.267   2.336  -5.140  0.00  0.00           H+0
HETATM   26  H   UNK     0       6.160   1.462  -4.226  0.00  0.00           H+0
HETATM   27  H   UNK     0       5.869   2.700  -2.990  0.00  0.00           H+0
HETATM   28  H   UNK     0       5.474   4.174  -4.671  0.00  0.00           H+0
HETATM   29  H   UNK     0       4.385   0.466  -2.723  0.00  0.00           H+0
HETATM   30  H   UNK     0       2.496   2.733  -1.888  0.00  0.00           H+0
HETATM   31  H   UNK     0       4.176   2.580  -1.391  0.00  0.00           H+0
HETATM   32  H   UNK     0       3.740   0.488  -0.248  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.663   1.754   0.337  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.832   0.916  -1.077  0.00  0.00           H+0
HETATM   35  H   UNK     0       2.778  -1.267  -1.961  0.00  0.00           H+0
HETATM   36  H   UNK     0       1.500   1.001  -3.550  0.00  0.00           H+0
HETATM   37  H   UNK     0       2.549  -0.262  -4.200  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.008  -2.096  -3.397  0.00  0.00           H+0
HETATM   39  H   UNK     0      -1.029  -1.196  -3.374  0.00  0.00           H+0
HETATM   40  H   UNK     0      -0.679  -2.846  -1.740  0.00  0.00           H+0
HETATM   41  H   UNK     0       0.969  -3.100  -1.177  0.00  0.00           H+0
HETATM   42  H   UNK     0      -0.805  -0.716  -0.476  0.00  0.00           H+0
HETATM   43  H   UNK     0      -2.131  -3.564  -0.287  0.00  0.00           H+0
HETATM   44  H   UNK     0      -2.849  -3.171   1.265  0.00  0.00           H+0
HETATM   45  H   UNK     0      -2.813  -1.949  -0.015  0.00  0.00           H+0
HETATM   46  H   UNK     0       0.151  -4.220   0.648  0.00  0.00           H+0
HETATM   47  H   UNK     0      -1.612  -1.860   3.001  0.00  0.00           H+0
HETATM   48  H   UNK     0      -1.918  -0.567   1.855  0.00  0.00           H+0
HETATM   49  H   UNK     0       0.753  -1.246   3.155  0.00  0.00           H+0
HETATM   50  H   UNK     0      -0.254   0.157   3.437  0.00  0.00           H+0
HETATM   51  H   UNK     0       0.092   0.999   1.193  0.00  0.00           H+0
HETATM   52  H   UNK     0       1.637   0.702   1.975  0.00  0.00           H+0
HETATM   53  H   UNK     0       2.696  -2.264   0.000  0.00  0.00           H+0
HETATM   54  H   UNK     0       3.176  -1.048   1.181  0.00  0.00           H+0
HETATM   55  H   UNK     0       2.034  -2.281   1.624  0.00  0.00           H+0
CONECT    1    2   24   25                                                  
CONECT    2    5    3    1                                                  
CONECT    3    2    4   26   27                                             
CONECT    4    3   28                                                       
CONECT    5    6   10    2   29                                             
CONECT    6    5    7   30   31                                             
CONECT    7    8    6   32   33                                             
CONECT    8   22    7   34    9                                             
CONECT    9   10   11    8   35                                             
CONECT   10    5    9   36   37                                             
CONECT   11   12   13    9   38                                             
CONECT   12   11   39                                                       
CONECT   13   14   11   40   41                                             
CONECT   14   22   13   15   42                                             
CONECT   15   17   16   14   19                                             
CONECT   16   15   43   44   45                                             
CONECT   17   15   18   46                                                  
CONECT   18   17                                                            
CONECT   19   20   15   47   48                                             
CONECT   20   19   21   49   50                                             
CONECT   21   22   20   51   52                                             
CONECT   22   23   14    8   21                                             
CONECT   23   22   53   54   55                                             
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    3                                                            
CONECT   27    3                                                            
CONECT   28    4                                                            
CONECT   29    5                                                            
CONECT   30    6                                                            
CONECT   31    6                                                            
CONECT   32    7                                                            
CONECT   33    7                                                            
CONECT   34    8                                                            
CONECT   35    9                                                            
CONECT   36   10                                                            
CONECT   37   10                                                            
CONECT   38   11                                                            
CONECT   39   12                                                            
CONECT   40   13                                                            
CONECT   41   13                                                            
CONECT   42   14                                                            
CONECT   43   16                                                            
CONECT   44   16                                                            
CONECT   45   16                                                            
CONECT   46   17                                                            
CONECT   47   19                                                            
CONECT   48   19                                                            
CONECT   49   20                                                            
CONECT   50   20                                                            
CONECT   51   21                                                            
CONECT   52   21                                                            
CONECT   53   23                                                            
CONECT   54   23                                                            
CONECT   55   23                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  114    0
END

RDKit          3D

55 57  0  0  0  0  0  0  0  0999 V2000
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    0.1510   -4.2202    0.6476 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9181   -0.5674    1.8549 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7530   -1.2460    3.1553 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6366    0.7015    1.9746 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6961   -2.2639    0.0004 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1761   -1.0476    1.1810 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0335   -2.2806    1.6243 H   0  0  0  0  0  0  0  0  0  0  0  0
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 22 21  1  0
  5  2  1  0
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 15 16  1  0
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  2  3  1  0
 11  9  1  0
  3  4  1  0
 14 15  1  0
  2  1  2  3
  8  9  1  0
 17 18  2  0
 15 19  1  0
 17 46  1  0
 14 42  1  6
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 11 38  1  6
  9 35  1  1
  7 32  1  0
  7 33  1  0
 21 51  1  0
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 19 48  1  0
 23 53  1  0
 23 54  1  0
 23 55  1  0
  6 30  1  0
  6 31  1  0
  5 29  1  1
 10 36  1  0
 10 37  1  0
 12 39  1  0
 16 43  1  0
 16 44  1  0
 16 45  1  0
  3 26  1  0
  3 27  1  0
  4 28  1  0
  1 24  1  0
  1 25  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

(1S,4aR,4bS,7S,8aS,9R,10aR)-9-hydroxy-7-(3-hydroxyprop-1-en-2-yl)-1,4a-dimethyl-tetradecahydrophenanthrene-1-carbaldehyde

Traditional Name

(1S,4aR,4bS,7S,8aS,9R,10aR)-9-hydroxy-7-(3-hydroxyprop-1-en-2-yl)-1,4a-dimethyl-dodecahydrophenanthrene-1-carbaldehyde

CAS Registry Number

Not Available

SMILES

[H]OC([H])([H])C(=C([H])[H])[C@@]1([H])C([H])([H])C([H])([H])[C@@]2([H])[C@]([H])(C1([H])[H])[C@]([H])(O[H])C([H])([H])[C@@]1([H])[C@](C([H])=O)(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[C@]21C([H])([H])[H]

InChI Identifier

InChI=1S/C20H32O3/c1-13(11-21)14-5-6-16-15(9-14)17(23)10-18-19(2,12-22)7-4-8-20(16,18)3/h12,14-18,21,23H,1,4-11H2,2-3H3/t14-,15-,16-,17+,18-,19+,20+/m0/s1

InChI Key

DXZARVMGCPQDSK-TUFIBKJQSA-N

Experimental Spectra

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

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Erythroxylum suberosum	JEOL database	Nascimento, C. J., et al, Phytochem. Lett. 5, 401 (2012)

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	2.74	ALOGPS
logP	2.67	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	16.88	ChemAxon
pKa (Strongest Basic)	-0.69	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	3	ChemAxon
Refractivity	91.73 m³·mol⁻¹	ChemAxon
Polarizability	37.46 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

Not Available

References

General References

Nascimento, C. J., et al. (2012). Nascimento, C. J., et al, Phytochem. Lett. 5, 401 (2012). Phytochem..

Showing NP-Card for 7alpha,16-dihydroxy-abiet-15(17)-en-19-al (NP0041655)

MOL for NP0041655 (7alpha,16-dihydroxy-abiet-15(17)-en-19-al)

3D MOL for NP0041655 (7alpha,16-dihydroxy-abiet-15(17)-en-19-al)

3D SDF for NP0041655 (7alpha,16-dihydroxy-abiet-15(17)-en-19-al)

3D-SDF for NP0041655 (7alpha,16-dihydroxy-abiet-15(17)-en-19-al)

PDB for NP0041655 (7alpha,16-dihydroxy-abiet-15(17)-en-19-al)

3D PDB for NP0041655 (7alpha,16-dihydroxy-abiet-15(17)-en-19-al)

SMILES for NP0041655 (7alpha,16-dihydroxy-abiet-15(17)-en-19-al)

INCHI for NP0041655 (7alpha,16-dihydroxy-abiet-15(17)-en-19-al)

Structure for NP0041655 (7alpha,16-dihydroxy-abiet-15(17)-en-19-al)

3D Structure for NP0041655 (7alpha,16-dihydroxy-abiet-15(17)-en-19-al)