NP-MRD: Showing NP-Card for 7beta,16-dihydroxydehydroabietic acid (NP0032645)

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Record Information

Version

2.0

Created at

2021-06-19 23:23:40 UTC

Updated at

2021-06-30 00:01:58 UTC

NP-MRD ID

NP0032645

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7beta,16-dihydroxydehydroabietic acid

Provided By

JEOL Database JEOL Logo

Description

7beta,16-dihydroxydehydroabietic acid is found in Phlebiopsis gigantea and Trametes Versicolor. 7beta,16-dihydroxydehydroabietic acid was first documented in 2007 (van Beek, T. A., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202101233D          

 52 54  0  0  0  0            999 V2000
    5.5801    0.7226   -0.4783 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5276    1.0505    0.5841 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0221    0.6449    1.9837 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1691    1.1630    3.0023 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1899    0.4073    0.2483 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0408   -0.9758    0.1326 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7959   -1.5366   -0.1664 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6510   -0.7380   -0.3506 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7963    0.6646   -0.2533 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0599    1.2116    0.0542 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3746    1.6168   -0.3892 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0251    2.7026   -1.2456 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6559    0.9747   -0.9190 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8584   -0.4044   -0.2712 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7088   -1.3735   -0.7354 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6154   -1.6007   -2.2651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9338   -2.7441   -0.0434 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3333   -3.3093   -0.2679 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4107   -2.3639    0.2373 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3333   -0.9365   -0.3533 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9362   -0.8856   -1.7676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2261   -0.0653    0.5507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8791    0.8835    1.2356 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5191   -0.4486    0.5615 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5082    1.2704   -0.2816 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.2305    1.0056   -1.4775 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3903    2.1403    0.5864 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0843   -0.4415    2.1069 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0208    1.0558    2.1657 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2714    0.8318    2.8167 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8924   -1.6393    0.2642 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7473   -2.6172   -0.2700 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1517    2.2951    0.1359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5717    2.0299    0.6088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7642    3.3326   -1.2171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4885    1.6554   -0.7080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6311    0.9075   -2.0124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6850   -0.2578    0.8095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5017   -2.0724   -2.6858 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2212   -2.2688   -2.5089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4332   -0.6745   -2.8195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2168   -3.4913   -0.4039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7600   -2.6463    1.0370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4201   -4.2644    0.2642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4955   -3.5364   -1.3266 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.3940   -2.8093    0.0372 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.4148   -1.5257   -2.4769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9798   -1.2232   -1.7690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9488    0.1778    1.1814 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  5  2  0  0  0  0
 18 19  1  0  0  0  0
  5  6  1  0  0  0  0
 18 17  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
 19 20  1  0  0  0  0
 15 16  1  6  0  0  0
 15  8  1  0  0  0  0
 20 21  1  0  0  0  0
 14 13  1  0  0  0  0
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  5  2  1  0  0  0  0
 11  9  1  0  0  0  0
  2  3  1  0  0  0  0
 20 14  1  0  0  0  0
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  8  9  2  0  0  0  0
 22 24  1  0  0  0  0
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 22 23  2  0  0  0  0
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  9 10  1  0  0  0  0
  3  4  1  0  0  0  0
 11 12  1  0  0  0  0
 18 45  1  0  0  0  0
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 13 37  1  0  0  0  0
 13 38  1  0  0  0  0
 11 35  1  1  0  0  0
 10 34  1  0  0  0  0
  6 32  1  0  0  0  0
  7 33  1  0  0  0  0
 16 40  1  0  0  0  0
 16 41  1  0  0  0  0
 16 42  1  0  0  0  0
 21 49  1  0  0  0  0
 21 50  1  0  0  0  0
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  2 28  1  1  0  0  0
  3 29  1  0  0  0  0
  3 30  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
 24 52  1  0  0  0  0
  4 31  1  0  0  0  0
 12 36  1  0  0  0  0
M  END

     RDKit          3D

 52 54  0  0  0  0  0  0  0  0999 V2000
    5.5801    0.7226   -0.4783 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5276    1.0505    0.5841 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0221    0.6449    1.9837 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1691    1.1630    3.0023 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1899    0.4073    0.2483 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0408   -0.9758    0.1326 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7959   -1.5366   -0.1664 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6510   -0.7380   -0.3506 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7963    0.6646   -0.2533 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0599    1.2116    0.0542 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3746    1.6168   -0.3892 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0251    2.7026   -1.2456 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6559    0.9747   -0.9190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8584   -0.4044   -0.2712 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7088   -1.3735   -0.7354 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -2.3333   -3.3093   -0.2679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4107   -2.3639    0.2373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3333   -0.9365   -0.3533 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9362   -0.8856   -1.7676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2261   -0.0653    0.5507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8791    0.8835    1.2356 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5191   -0.4486    0.5615 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5082    1.2704   -0.2816 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8236   -0.3452   -0.4987 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.2212   -2.2688   -2.5089 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7600   -2.6463    1.0370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4201   -4.2644    0.2642 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652306202101233D          

 52 54  0  0  0  0            999 V2000
    5.5801    0.7226   -0.4783 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5276    1.0505    0.5841 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0221    0.6449    1.9837 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1691    1.1630    3.0023 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1899    0.4073    0.2483 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0408   -0.9758    0.1326 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7959   -1.5366   -0.1664 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6510   -0.7380   -0.3506 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7963    0.6646   -0.2533 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0599    1.2116    0.0542 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3746    1.6168   -0.3892 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0251    2.7026   -1.2456 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6559    0.9747   -0.9190 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -2.4955   -3.5364   -1.3266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3292   -2.3101    1.3324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3940   -2.8093    0.0372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9427    0.1342   -2.1666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4148   -1.5257   -2.4769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9798   -1.2232   -1.7690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9488    0.1778    1.1814 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  5  2  0  0  0  0
 18 19  1  0  0  0  0
  5  6  1  0  0  0  0
 18 17  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
 19 20  1  0  0  0  0
 15 16  1  6  0  0  0
 15  8  1  0  0  0  0
 20 21  1  0  0  0  0
 14 13  1  0  0  0  0
 14 39  1  1  0  0  0
 13 11  1  0  0  0  0
  5  2  1  0  0  0  0
 11  9  1  0  0  0  0
  2  3  1  0  0  0  0
 20 14  1  0  0  0  0
  2  1  1  0  0  0  0
 15 17  1  0  0  0  0
  8  9  2  0  0  0  0
 22 24  1  0  0  0  0
 15 14  1  0  0  0  0
 22 23  2  0  0  0  0
 20 22  1  1  0  0  0
  9 10  1  0  0  0  0
  3  4  1  0  0  0  0
 11 12  1  0  0  0  0
 18 45  1  0  0  0  0
 18 46  1  0  0  0  0
 19 47  1  0  0  0  0
 19 48  1  0  0  0  0
 17 43  1  0  0  0  0
 17 44  1  0  0  0  0
 13 37  1  0  0  0  0
 13 38  1  0  0  0  0
 11 35  1  1  0  0  0
 10 34  1  0  0  0  0
  6 32  1  0  0  0  0
  7 33  1  0  0  0  0
 16 40  1  0  0  0  0
 16 41  1  0  0  0  0
 16 42  1  0  0  0  0
 21 49  1  0  0  0  0
 21 50  1  0  0  0  0
 21 51  1  0  0  0  0
  2 28  1  1  0  0  0
  3 29  1  0  0  0  0
  3 30  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
 24 52  1  0  0  0  0
  4 31  1  0  0  0  0
 12 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0032645

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)[C@]1(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[C@@]2(C3=C(C([H])=C(C([H])=C3[H])[C@]([H])(C([H])([H])[H])C([H])([H])O[H])[C@@]([H])(O[H])C([H])([H])[C@@]12[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O4/c1-12(11-21)13-5-6-15-14(9-13)16(22)10-17-19(15,2)7-4-8-20(17,3)18(23)24/h5-6,9,12,16-17,21-22H,4,7-8,10-11H2,1-3H3,(H,23,24)/t12-,16+,17-,19-,20-/m1/s1

> <INCHI_KEY>
BETVGAOCAIJQOL-LBCCXEDWSA-N

> <FORMULA>
C20H28O4

> <MOLECULAR_WEIGHT>
332.44

> <EXACT_MASS>
332.198759382

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
37.484846856439816

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,4aS,9S,10aR)-9-hydroxy-7-[(2S)-1-hydroxypropan-2-yl]-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid

> <ALOGPS_LOGP>
2.89

> <JCHEM_LOGP>
3.159228774333333

> <ALOGPS_LOGS>
-3.58

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
14.38779590991825

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.336475683622019

> <JCHEM_PKA_STRONGEST_BASIC>
-2.634084231064856

> <JCHEM_POLAR_SURFACE_AREA>
77.76

> <JCHEM_REFRACTIVITY>
92.81119999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.80e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4aS,9S,10aR)-9-hydroxy-7-[(2S)-1-hydroxypropan-2-yl]-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 52 54  0  0  0  0  0  0  0  0999 V2000
    5.5801    0.7226   -0.4783 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5276    1.0505    0.5841 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0221    0.6449    1.9837 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1691    1.1630    3.0023 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1899    0.4073    0.2483 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0408   -0.9758    0.1326 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7959   -1.5366   -0.1664 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6510   -0.7380   -0.3506 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7963    0.6646   -0.2533 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0599    1.2116    0.0542 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3746    1.6168   -0.3892 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0251    2.7026   -1.2456 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6559    0.9747   -0.9190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8584   -0.4044   -0.2712 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7088   -1.3735   -0.7354 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6154   -1.6007   -2.2651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9338   -2.7441   -0.0434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3333   -3.3093   -0.2679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4107   -2.3639    0.2373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3333   -0.9365   -0.3533 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9362   -0.8856   -1.7676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2261   -0.0653    0.5507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8791    0.8835    1.2356 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5191   -0.4486    0.5615 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5082    1.2704   -0.2816 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8236   -0.3452   -0.4987 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2305    1.0056   -1.4775 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3903    2.1403    0.5864 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0843   -0.4415    2.1069 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0208    1.0558    2.1657 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2714    0.8318    2.8167 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8924   -1.6393    0.2642 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7473   -2.6172   -0.2700 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1517    2.2951    0.1359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5717    2.0299    0.6088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7642    3.3326   -1.2171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4885    1.6554   -0.7080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6311    0.9075   -2.0124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6850   -0.2578    0.8095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5017   -2.0724   -2.6858 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2212   -2.2688   -2.5089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4332   -0.6745   -2.8195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2168   -3.4913   -0.4039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7600   -2.6463    1.0370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4201   -4.2644    0.2642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4955   -3.5364   -1.3266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3292   -2.3101    1.3324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3940   -2.8093    0.0372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9427    0.1342   -2.1666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4148   -1.5257   -2.4769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9798   -1.2232   -1.7690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9488    0.1778    1.1814 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  5  2  0
 18 19  1  0
  5  6  1  0
 18 17  1  0
  6  7  2  0
  7  8  1  0
 19 20  1  0
 15 16  1  6
 15  8  1  0
 20 21  1  0
 14 13  1  0
 14 39  1  1
 13 11  1  0
  5  2  1  0
 11  9  1  0
  2  3  1  0
 20 14  1  0
  2  1  1  0
 15 17  1  0
  8  9  2  0
 22 24  1  0
 15 14  1  0
 22 23  2  0
 20 22  1  1
  9 10  1  0
  3  4  1  0
 11 12  1  0
 18 45  1  0
 18 46  1  0
 19 47  1  0
 19 48  1  0
 17 43  1  0
 17 44  1  0
 13 37  1  0
 13 38  1  0
 11 35  1  1
 10 34  1  0
  6 32  1  0
  7 33  1  0
 16 40  1  0
 16 41  1  0
 16 42  1  0
 21 49  1  0
 21 50  1  0
 21 51  1  0
  2 28  1  1
  3 29  1  0
  3 30  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
 24 52  1  0
  4 31  1  0
 12 36  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       5.580   0.723  -0.478  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.528   1.050   0.584  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.022   0.645   1.984  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.169   1.163   3.002  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.190   0.407   0.248  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.041  -0.976   0.133  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.796  -1.537  -0.166  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.651  -0.738  -0.351  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.796   0.665  -0.253  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.060   1.212   0.054  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.375   1.617  -0.389  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.025   2.703  -1.246  0.00  0.00           O+0
HETATM   13  C   UNK     0      -1.656   0.975  -0.919  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.858  -0.404  -0.271  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.709  -1.373  -0.735  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.615  -1.601  -2.265  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.934  -2.744  -0.043  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.333  -3.309  -0.268  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.411  -2.364   0.237  0.00  0.00           C+0
HETATM   20  C   UNK     0      -3.333  -0.937  -0.353  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.936  -0.886  -1.768  0.00  0.00           C+0
HETATM   22  C   UNK     0      -4.226  -0.065   0.551  0.00  0.00           C+0
HETATM   23  O   UNK     0      -3.879   0.884   1.236  0.00  0.00           O+0
HETATM   24  O   UNK     0      -5.519  -0.449   0.562  0.00  0.00           O+0
HETATM   25  H   UNK     0       6.508   1.270  -0.282  0.00  0.00           H+0
HETATM   26  H   UNK     0       5.824  -0.345  -0.499  0.00  0.00           H+0
HETATM   27  H   UNK     0       5.231   1.006  -1.478  0.00  0.00           H+0
HETATM   28  H   UNK     0       4.390   2.140   0.586  0.00  0.00           H+0
HETATM   29  H   UNK     0       5.084  -0.442   2.107  0.00  0.00           H+0
HETATM   30  H   UNK     0       6.021   1.056   2.166  0.00  0.00           H+0
HETATM   31  H   UNK     0       3.271   0.832   2.817  0.00  0.00           H+0
HETATM   32  H   UNK     0       3.892  -1.639   0.264  0.00  0.00           H+0
HETATM   33  H   UNK     0       1.747  -2.617  -0.270  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.152   2.295   0.136  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.572   2.030   0.609  0.00  0.00           H+0
HETATM   36  H   UNK     0      -0.764   3.333  -1.217  0.00  0.00           H+0
HETATM   37  H   UNK     0      -2.489   1.655  -0.708  0.00  0.00           H+0
HETATM   38  H   UNK     0      -1.631   0.908  -2.012  0.00  0.00           H+0
HETATM   39  H   UNK     0      -1.685  -0.258   0.810  0.00  0.00           H+0
HETATM   40  H   UNK     0      -1.502  -2.072  -2.686  0.00  0.00           H+0
HETATM   41  H   UNK     0       0.221  -2.269  -2.509  0.00  0.00           H+0
HETATM   42  H   UNK     0      -0.433  -0.675  -2.820  0.00  0.00           H+0
HETATM   43  H   UNK     0      -0.217  -3.491  -0.404  0.00  0.00           H+0
HETATM   44  H   UNK     0      -0.760  -2.646   1.037  0.00  0.00           H+0
HETATM   45  H   UNK     0      -2.420  -4.264   0.264  0.00  0.00           H+0
HETATM   46  H   UNK     0      -2.495  -3.536  -1.327  0.00  0.00           H+0
HETATM   47  H   UNK     0      -3.329  -2.310   1.332  0.00  0.00           H+0
HETATM   48  H   UNK     0      -4.394  -2.809   0.037  0.00  0.00           H+0
HETATM   49  H   UNK     0      -3.943   0.134  -2.167  0.00  0.00           H+0
HETATM   50  H   UNK     0      -3.415  -1.526  -2.477  0.00  0.00           H+0
HETATM   51  H   UNK     0      -4.980  -1.223  -1.769  0.00  0.00           H+0
HETATM   52  H   UNK     0      -5.949   0.178   1.181  0.00  0.00           H+0
CONECT    1    2   25   26   27                                             
CONECT    2    5    3    1   28                                             
CONECT    3    2    4   29   30                                             
CONECT    4    3   31                                                       
CONECT    5   10    6    2                                                  
CONECT    6    5    7   32                                                  
CONECT    7    6    8   33                                                  
CONECT    8    7   15    9                                                  
CONECT    9   11    8   10                                                  
CONECT   10    5    9   34                                                  
CONECT   11   13    9   12   35                                             
CONECT   12   11   36                                                       
CONECT   13   14   11   37   38                                             
CONECT   14   13   39   20   15                                             
CONECT   15   16    8   17   14                                             
CONECT   16   15   40   41   42                                             
CONECT   17   18   15   43   44                                             
CONECT   18   19   17   45   46                                             
CONECT   19   18   20   47   48                                             
CONECT   20   19   21   14   22                                             
CONECT   21   20   49   50   51                                             
CONECT   22   24   23   20                                                  
CONECT   23   22                                                            
CONECT   24   22   52                                                       
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    2                                                            
CONECT   29    3                                                            
CONECT   30    3                                                            
CONECT   31    4                                                            
CONECT   32    6                                                            
CONECT   33    7                                                            
CONECT   34   10                                                            
CONECT   35   11                                                            
CONECT   36   12                                                            
CONECT   37   13                                                            
CONECT   38   13                                                            
CONECT   39   14                                                            
CONECT   40   16                                                            
CONECT   41   16                                                            
CONECT   42   16                                                            
CONECT   43   17                                                            
CONECT   44   17                                                            
CONECT   45   18                                                            
CONECT   46   18                                                            
CONECT   47   19                                                            
CONECT   48   19                                                            
CONECT   49   21                                                            
CONECT   50   21                                                            
CONECT   51   21                                                            
CONECT   52   24                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  108    0
END

RDKit          3D

52 54  0  0  0  0  0  0  0  0999 V2000
    5.5801    0.7226   -0.4783 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5276    1.0505    0.5841 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0221    0.6449    1.9837 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1691    1.1630    3.0023 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1899    0.4073    0.2483 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0408   -0.9758    0.1326 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7959   -1.5366   -0.1664 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6510   -0.7380   -0.3506 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7963    0.6646   -0.2533 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0599    1.2116    0.0542 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3746    1.6168   -0.3892 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0251    2.7026   -1.2456 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6559    0.9747   -0.9190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8584   -0.4044   -0.2712 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7088   -1.3735   -0.7354 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6154   -1.6007   -2.2651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9338   -2.7441   -0.0434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3333   -3.3093   -0.2679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4107   -2.3639    0.2373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3333   -0.9365   -0.3533 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9362   -0.8856   -1.7676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2261   -0.0653    0.5507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8791    0.8835    1.2356 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5191   -0.4486    0.5615 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5082    1.2704   -0.2816 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8236   -0.3452   -0.4987 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2305    1.0056   -1.4775 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3903    2.1403    0.5864 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0843   -0.4415    2.1069 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0208    1.0558    2.1657 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2714    0.8318    2.8167 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8924   -1.6393    0.2642 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7473   -2.6172   -0.2700 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1517    2.2951    0.1359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5717    2.0299    0.6088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7642    3.3326   -1.2171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4885    1.6554   -0.7080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6311    0.9075   -2.0124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6850   -0.2578    0.8095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5017   -2.0724   -2.6858 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2212   -2.2688   -2.5089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4332   -0.6745   -2.8195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2168   -3.4913   -0.4039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7600   -2.6463    1.0370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4201   -4.2644    0.2642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4955   -3.5364   -1.3266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3292   -2.3101    1.3324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3940   -2.8093    0.0372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9427    0.1342   -2.1666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4148   -1.5257   -2.4769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9798   -1.2232   -1.7690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9488    0.1778    1.1814 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  5  2  0
 18 19  1  0
  5  6  1  0
 18 17  1  0
  6  7  2  0
  7  8  1  0
 19 20  1  0
 15 16  1  6
 15  8  1  0
 20 21  1  0
 14 13  1  0
 14 39  1  1
 13 11  1  0
  5  2  1  0
 11  9  1  0
  2  3  1  0
 20 14  1  0
  2  1  1  0
 15 17  1  0
  8  9  2  0
 22 24  1  0
 15 14  1  0
 22 23  2  0
 20 22  1  1
  9 10  1  0
  3  4  1  0
 11 12  1  0
 18 45  1  0
 18 46  1  0
 19 47  1  0
 19 48  1  0
 17 43  1  0
 17 44  1  0
 13 37  1  0
 13 38  1  0
 11 35  1  1
 10 34  1  0
  6 32  1  0
  7 33  1  0
 16 40  1  0
 16 41  1  0
 16 42  1  0
 21 49  1  0
 21 50  1  0
 21 51  1  0
  2 28  1  1
  3 29  1  0
  3 30  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
 24 52  1  0
  4 31  1  0
 12 36  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₈O₄

Average Mass

332.4400 Da

Monoisotopic Mass

332.19876 Da

IUPAC Name

(1R,4aS,9S,10aR)-9-hydroxy-7-[(2S)-1-hydroxypropan-2-yl]-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid

Traditional Name

(1R,4aS,9S,10aR)-9-hydroxy-7-[(2S)-1-hydroxypropan-2-yl]-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid

CAS Registry Number

Not Available

SMILES

[H]OC(=O)[C@]1(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[C@@]2(C3=C(C([H])=C(C([H])=C3[H])[C@]([H])(C([H])([H])[H])C([H])([H])O[H])[C@@]([H])(O[H])C([H])([H])[C@@]12[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C20H28O4/c1-12(11-21)13-5-6-15-14(9-13)16(22)10-17-19(15,2)7-4-8-20(17,3)18(23)24/h5-6,9,12,16-17,21-22H,4,7-8,10-11H2,1-3H3,(H,23,24)/t12-,16+,17-,19-,20-/m1/s1

InChI Key

BETVGAOCAIJQOL-LBCCXEDWSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃ (H), CDCl₃ + CD₃OD (C), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃ (H), CDCl₃ + CD₃OD (C), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃ (H), CDCl₃ + CD₃OD (C), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃ (H), CDCl₃ + CD₃OD (C), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃ (H), CDCl₃ + CD₃OD (C), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃ (H), CDCl₃ + CD₃OD (C), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃ (H), CDCl₃ + CD₃OD (C), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃ (H), CDCl₃ + CD₃OD (C), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃ (H), CDCl₃ + CD₃OD (C), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃ (H), CDCl₃ + CD₃OD (C), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃ (H), CDCl₃ + CD₃OD (C), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃ (H), CDCl₃ + CD₃OD (C), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃ (H), CDCl₃ + CD₃OD (C), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃ (H), CDCl₃ + CD₃OD (C), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃ (H), CDCl₃ + CD₃OD (C), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃ (H), CDCl₃ + CD₃OD (C), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃ (H), CDCl₃ + CD₃OD (C), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃ (H), CDCl₃ + CD₃OD (C), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃ (H), CDCl₃ + CD₃OD (C), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃ (H), CDCl₃ + CD₃OD (C), 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
Phlebiopsis gigantea	JEOL database	van Beek, T. A., et al, J. Nat. Prod. 70, 154 (2007)
Trametes Versicolor	JEOL database	van Beek, T. A., et al, J. Nat. Prod. 70, 154 (2007)

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	2.89	ALOGPS
logP	3.16	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	4.34	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	77.76 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	92.81 m³·mol⁻¹	ChemAxon
Polarizability	37.48 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

van Beek, T. A., et al. (2007). van Beek, T. A., et al, J. Nat. Prod. 70, 154 (2007) . J. Nat. Prod..

Showing NP-Card for 7beta,16-dihydroxydehydroabietic acid (NP0032645)

MOL for NP0032645 (7beta,16-dihydroxydehydroabietic acid)

3D MOL for NP0032645 (7beta,16-dihydroxydehydroabietic acid)

3D SDF for NP0032645 (7beta,16-dihydroxydehydroabietic acid)

3D-SDF for NP0032645 (7beta,16-dihydroxydehydroabietic acid)

PDB for NP0032645 (7beta,16-dihydroxydehydroabietic acid)

3D PDB for NP0032645 (7beta,16-dihydroxydehydroabietic acid)

SMILES for NP0032645 (7beta,16-dihydroxydehydroabietic acid)

INCHI for NP0032645 (7beta,16-dihydroxydehydroabietic acid)

Structure for NP0032645 (7beta,16-dihydroxydehydroabietic acid)

3D Structure for NP0032645 (7beta,16-dihydroxydehydroabietic acid)