NP-MRD: Showing NP-Card for (-)-(4S,5S,10R,20R)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde (NP0035664)

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Record Information

Version

2.0

Created at

2021-06-20 19:02:50 UTC

Updated at

2021-06-30 00:06:48 UTC

NP-MRD ID

NP0035664

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-(4S,5S,10R,20R)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde

Provided By

JEOL Database JEOL Logo

Description

(-)-(4S,5S,10R,20R)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde18,20-methyl acetal 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. (-)-(4S,5S,10R,20R)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde is found in Fraxinus sieboldiana. (-)-(4S,5S,10R,20R)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde was first documented in 2010 (Lin, S., et al.). Based on a literature review very few articles have been published on (-)-(4S,5S,10R,20R)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde18,20-methyl acetal.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202121023D          

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     RDKit          3D

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M  END


  Mrv1652306202121023D          

 54 57  0  0  0  0            999 V2000
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    0.3389    2.6269   -1.8069 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8873    1.0810   -2.4175 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5341    3.0232   -0.0357 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3067    4.0024    0.7653 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3063    2.0263    2.5445 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8823    1.4100    4.4923 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2421   -0.3014    4.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5439    0.8174    4.6431 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8603    0.1598    2.5362 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5924   -0.9813    2.0732 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0935    0.2878    0.9455 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1770   -1.0894    2.1584 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4585   -2.2011    0.1816 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9186   -2.0427    1.8568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1839   -1.1137    1.2271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8841   -2.4766    0.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0429   -0.9917   -1.5582 H   0  0  0  0  0  0  0  0  0  0  0  0
  9 10  1  0  0  0  0
 12 13  2  0  0  0  0
 21 20  2  0  0  0  0
 20 16  1  0  0  0  0
 16 14  2  0  0  0  0
 14 13  1  0  0  0  0
  8  6  1  0  0  0  0
 14 15  1  0  0  0  0
 11 12  1  0  0  0  0
 16 17  1  0  0  0  0
 24 23  1  0  0  0  0
 17 18  1  0  0  0  0
 23 22  1  0  0  0  0
 17 19  1  0  0  0  0
 22 21  1  0  0  0  0
  6  5  1  0  0  0  0
 12 21  1  0  0  0  0
 11  3  1  0  0  0  0
  6 24  1  0  0  0  0
 24 54  1  6  0  0  0
 11 10  1  6  0  0  0
  6  7  1  6  0  0  0
 11 24  1  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  0  0  0  0
  3  2  1  0  0  0  0
  9  8  1  0  0  0  0
  2  1  1  0  0  0  0
  9 36  1  0  0  0  0
  9 37  1  0  0  0  0
  8 34  1  0  0  0  0
  8 35  1  0  0  0  0
 10 38  1  0  0  0  0
 10 39  1  0  0  0  0
 23 52  1  0  0  0  0
 23 53  1  0  0  0  0
 22 50  1  0  0  0  0
 22 51  1  0  0  0  0
 20 49  1  0  0  0  0
 13 40  1  0  0  0  0
 15 41  1  0  0  0  0
 17 42  1  1  0  0  0
 18 43  1  0  0  0  0
 18 44  1  0  0  0  0
 18 45  1  0  0  0  0
 19 46  1  0  0  0  0
 19 47  1  0  0  0  0
 19 48  1  0  0  0  0
  5 29  1  0  0  0  0
  5 30  1  0  0  0  0
  3 28  1  1  0  0  0
  7 31  1  0  0  0  0
  7 32  1  0  0  0  0
  7 33  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
M  END
> <DATABASE_ID>
NP0035664

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C(C([H])=C2C(=C1[H])[C@]13C([H])([H])C([H])([H])C([H])([H])[C@](C([H])([H])[H])(C([H])([H])O[C@@]1([H])OC([H])([H])[H])[C@]3([H])C([H])([H])C2([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C21H30O3/c1-13(2)15-10-14-6-7-18-20(3)8-5-9-21(18,16(14)11-17(15)22)19(23-4)24-12-20/h10-11,13,18-19,22H,5-9,12H2,1-4H3/t18-,19+,20+,21-/m0/s1

> <INCHI_KEY>
UBQQOJDZHPQINO-BQJUDKOJSA-N

> <FORMULA>
C21H30O3

> <MOLECULAR_WEIGHT>
330.468

> <EXACT_MASS>
330.219494826

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
38.38597565101195

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,10S,11S,14R)-14-methoxy-11-methyl-5-(propan-2-yl)-13-oxatetracyclo[9.3.3.0^{1,10}.0^{2,7}]heptadeca-2,4,6-trien-4-ol

> <ALOGPS_LOGP>
4.72

> <JCHEM_LOGP>
5.132570628333333

> <ALOGPS_LOGS>
-5.35

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.711816737615457

> <JCHEM_PKA_STRONGEST_BASIC>
-4.013231727999051

> <JCHEM_POLAR_SURFACE_AREA>
38.69

> <JCHEM_REFRACTIVITY>
95.5281

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.48e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,10S,11S,14R)-5-isopropyl-14-methoxy-11-methyl-13-oxatetracyclo[9.3.3.0^{1,10}.0^{2,7}]heptadeca-2,4,6-trien-4-ol

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
   -2.1200    2.1229    2.4559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3960    1.2213    1.6318 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2721    1.6943    0.2879 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5430    1.6577   -0.3640 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0137    0.3356   -0.6053 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0502   -0.4865   -1.4856 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6583   -1.8828   -1.7111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8699    0.1806   -2.8770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1634    1.5335   -2.8498 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0455    1.5760   -1.9127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    0.9045   -0.5137 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1470    0.9176    0.2858 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8899    2.1070    0.4247 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0794    2.1402    1.1591 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7739    3.3138    1.2640 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5728    0.9986    1.7906 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8665    1.0228    2.5883 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6170    0.7166    4.0681 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9084    0.0650    2.0023 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8232   -0.1818    1.6713 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6169   -0.2325    0.9447 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9015   -1.5563    0.8737 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5474   -1.4610    0.4093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6478   -0.5504   -0.8208 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1720    1.6988    3.4623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1405    2.2586    2.0858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6074    3.0879    2.5140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9730    2.7499    0.3265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9851    0.4322   -1.1041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2074   -0.1595    0.3537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9254   -2.3686   -0.7668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9602   -2.5371   -2.2448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5760   -1.8192   -2.3073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8425    0.2981   -3.3717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2843   -0.4918   -3.5192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8397    1.7911   -3.8659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8753    2.3185   -2.5713 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3389    2.6269   -1.8069 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8873    1.0810   -2.4175 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5341    3.0232   -0.0357 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3067    4.0024    0.7653 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3063    2.0263    2.5445 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8823    1.4100    4.4923 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2421   -0.3014    4.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5439    0.8174    4.6431 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8603    0.1598    2.5362 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5924   -0.9813    2.0732 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0935    0.2878    0.9455 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1770   -1.0894    2.1584 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4585   -2.2011    0.1816 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9186   -2.0427    1.8568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1839   -1.1137    1.2271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8841   -2.4766    0.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0429   -0.9917   -1.5582 H   0  0  0  0  0  0  0  0  0  0  0  0
  9 10  1  0
 12 13  2  0
 21 20  2  0
 20 16  1  0
 16 14  2  0
 14 13  1  0
  8  6  1  0
 14 15  1  0
 11 12  1  0
 16 17  1  0
 24 23  1  0
 17 18  1  0
 23 22  1  0
 17 19  1  0
 22 21  1  0
  6  5  1  0
 12 21  1  0
 11  3  1  0
  6 24  1  0
 24 54  1  6
 11 10  1  6
  6  7  1  6
 11 24  1  0
  3  4  1  0
  5  4  1  0
  3  2  1  0
  9  8  1  0
  2  1  1  0
  9 36  1  0
  9 37  1  0
  8 34  1  0
  8 35  1  0
 10 38  1  0
 10 39  1  0
 23 52  1  0
 23 53  1  0
 22 50  1  0
 22 51  1  0
 20 49  1  0
 13 40  1  0
 15 41  1  0
 17 42  1  1
 18 43  1  0
 18 44  1  0
 18 45  1  0
 19 46  1  0
 19 47  1  0
 19 48  1  0
  5 29  1  0
  5 30  1  0
  3 28  1  1
  7 31  1  0
  7 32  1  0
  7 33  1  0
  1 25  1  0
  1 26  1  0
  1 27  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      -2.120   2.123   2.456  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.396   1.221   1.632  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.272   1.694   0.288  0.00  0.00           C+0
HETATM    4  O   UNK     0      -2.543   1.658  -0.364  0.00  0.00           O+0
HETATM    5  C   UNK     0      -3.014   0.336  -0.605  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.050  -0.487  -1.486  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.658  -1.883  -1.711  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.870   0.181  -2.877  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.163   1.534  -2.850  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.046   1.576  -1.913  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.171   0.905  -0.514  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.147   0.918   0.286  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.890   2.107   0.425  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.079   2.140   1.159  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.774   3.314   1.264  0.00  0.00           O+0
HETATM   16  C   UNK     0       3.573   0.999   1.791  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.867   1.023   2.588  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.617   0.717   4.068  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.908   0.065   2.002  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.823  -0.182   1.671  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.617  -0.233   0.945  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.902  -1.556   0.874  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.547  -1.461   0.409  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.648  -0.550  -0.821  0.00  0.00           C+0
HETATM   25  H   UNK     0      -2.172   1.699   3.462  0.00  0.00           H+0
HETATM   26  H   UNK     0      -3.140   2.259   2.086  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.607   3.088   2.514  0.00  0.00           H+0
HETATM   28  H   UNK     0      -0.973   2.750   0.327  0.00  0.00           H+0
HETATM   29  H   UNK     0      -3.985   0.432  -1.104  0.00  0.00           H+0
HETATM   30  H   UNK     0      -3.207  -0.160   0.354  0.00  0.00           H+0
HETATM   31  H   UNK     0      -2.925  -2.369  -0.767  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.960  -2.537  -2.245  0.00  0.00           H+0
HETATM   33  H   UNK     0      -3.576  -1.819  -2.307  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.842   0.298  -3.372  0.00  0.00           H+0
HETATM   35  H   UNK     0      -1.284  -0.492  -3.519  0.00  0.00           H+0
HETATM   36  H   UNK     0      -0.840   1.791  -3.866  0.00  0.00           H+0
HETATM   37  H   UNK     0      -1.875   2.318  -2.571  0.00  0.00           H+0
HETATM   38  H   UNK     0       0.339   2.627  -1.807  0.00  0.00           H+0
HETATM   39  H   UNK     0       0.887   1.081  -2.418  0.00  0.00           H+0
HETATM   40  H   UNK     0       1.534   3.023  -0.036  0.00  0.00           H+0
HETATM   41  H   UNK     0       3.307   4.002   0.765  0.00  0.00           H+0
HETATM   42  H   UNK     0       5.306   2.026   2.545  0.00  0.00           H+0
HETATM   43  H   UNK     0       3.882   1.410   4.492  0.00  0.00           H+0
HETATM   44  H   UNK     0       4.242  -0.301   4.220  0.00  0.00           H+0
HETATM   45  H   UNK     0       5.544   0.817   4.643  0.00  0.00           H+0
HETATM   46  H   UNK     0       6.860   0.160   2.536  0.00  0.00           H+0
HETATM   47  H   UNK     0       5.592  -0.981   2.073  0.00  0.00           H+0
HETATM   48  H   UNK     0       6.093   0.288   0.946  0.00  0.00           H+0
HETATM   49  H   UNK     0       3.177  -1.089   2.158  0.00  0.00           H+0
HETATM   50  H   UNK     0       1.458  -2.201   0.182  0.00  0.00           H+0
HETATM   51  H   UNK     0       0.919  -2.043   1.857  0.00  0.00           H+0
HETATM   52  H   UNK     0      -1.184  -1.114   1.227  0.00  0.00           H+0
HETATM   53  H   UNK     0      -0.884  -2.477   0.174  0.00  0.00           H+0
HETATM   54  H   UNK     0       0.043  -0.992  -1.558  0.00  0.00           H+0
CONECT    1    2   25   26   27                                             
CONECT    2    3    1                                                       
CONECT    3   11    4    2   28                                             
CONECT    4    3    5                                                       
CONECT    5    6    4   29   30                                             
CONECT    6    8    5   24    7                                             
CONECT    7    6   31   32   33                                             
CONECT    8    6    9   34   35                                             
CONECT    9   10    8   36   37                                             
CONECT   10    9   11   38   39                                             
CONECT   11   12    3   10   24                                             
CONECT   12   13   11   21                                                  
CONECT   13   12   14   40                                                  
CONECT   14   16   13   15                                                  
CONECT   15   14   41                                                       
CONECT   16   20   14   17                                                  
CONECT   17   16   18   19   42                                             
CONECT   18   17   43   44   45                                             
CONECT   19   17   46   47   48                                             
CONECT   20   21   16   49                                                  
CONECT   21   20   22   12                                                  
CONECT   22   23   21   50   51                                             
CONECT   23   24   22   52   53                                             
CONECT   24   23    6   54   11                                             
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    3                                                            
CONECT   29    5                                                            
CONECT   30    5                                                            
CONECT   31    7                                                            
CONECT   32    7                                                            
CONECT   33    7                                                            
CONECT   34    8                                                            
CONECT   35    8                                                            
CONECT   36    9                                                            
CONECT   37    9                                                            
CONECT   38   10                                                            
CONECT   39   10                                                            
CONECT   40   13                                                            
CONECT   41   15                                                            
CONECT   42   17                                                            
CONECT   43   18                                                            
CONECT   44   18                                                            
CONECT   45   18                                                            
CONECT   46   19                                                            
CONECT   47   19                                                            
CONECT   48   19                                                            
CONECT   49   20                                                            
CONECT   50   22                                                            
CONECT   51   22                                                            
CONECT   52   23                                                            
CONECT   53   23                                                            
CONECT   54   24                                                            
MASTER        0    0    0    0    0    0    0    0   54    0  114    0
END

RDKit          3D

54 57  0  0  0  0  0  0  0  0999 V2000
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    2.8232   -0.1818    1.6713 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6169   -0.2325    0.9447 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9015   -1.5563    0.8737 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5474   -1.4610    0.4093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6478   -0.5504   -0.8208 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -1.9602   -2.5371   -2.2448 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.2843   -0.4918   -3.5192 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.8753    2.3185   -2.5713 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3389    2.6269   -1.8069 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8873    1.0810   -2.4175 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5341    3.0232   -0.0357 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3067    4.0024    0.7653 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3063    2.0263    2.5445 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8823    1.4100    4.4923 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2421   -0.3014    4.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5439    0.8174    4.6431 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8603    0.1598    2.5362 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5924   -0.9813    2.0732 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0935    0.2878    0.9455 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1770   -1.0894    2.1584 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4585   -2.2011    0.1816 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9186   -2.0427    1.8568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1839   -1.1137    1.2271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8841   -2.4766    0.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0429   -0.9917   -1.5582 H   0  0  0  0  0  0  0  0  0  0  0  0
  9 10  1  0
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 21 20  2  0
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  8  6  1  0
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 11 12  1  0
 16 17  1  0
 24 23  1  0
 17 18  1  0
 23 22  1  0
 17 19  1  0
 22 21  1  0
  6  5  1  0
 12 21  1  0
 11  3  1  0
  6 24  1  0
 24 54  1  6
 11 10  1  6
  6  7  1  6
 11 24  1  0
  3  4  1  0
  5  4  1  0
  3  2  1  0
  9  8  1  0
  2  1  1  0
  9 36  1  0
  9 37  1  0
  8 34  1  0
  8 35  1  0
 10 38  1  0
 10 39  1  0
 23 52  1  0
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 22 50  1  0
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 20 49  1  0
 13 40  1  0
 15 41  1  0
 17 42  1  1
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 18 45  1  0
 19 46  1  0
 19 47  1  0
 19 48  1  0
  5 29  1  0
  5 30  1  0
  3 28  1  1
  7 31  1  0
  7 32  1  0
  7 33  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₀O₃

Average Mass

330.4680 Da

Monoisotopic Mass

330.21949 Da

IUPAC Name

(1R,10S,11S,14R)-14-methoxy-11-methyl-5-(propan-2-yl)-13-oxatetracyclo[9.3.3.0^{1,10}.0^{2,7}]heptadeca-2,4,6-trien-4-ol

Traditional Name

(1R,10S,11S,14R)-5-isopropyl-14-methoxy-11-methyl-13-oxatetracyclo[9.3.3.0^{1,10}.0^{2,7}]heptadeca-2,4,6-trien-4-ol

CAS Registry Number

Not Available

SMILES

[H]OC1=C(C([H])=C2C(=C1[H])[C@]13C([H])([H])C([H])([H])C([H])([H])[C@](C([H])([H])[H])(C([H])([H])O[C@@]1([H])OC([H])([H])[H])[C@]3([H])C([H])([H])C2([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C21H30O3/c1-13(2)15-10-14-6-7-18-20(3)8-5-9-21(18,16(14)11-17(15)22)19(23-4)24-12-20/h10-11,13,18-19,22H,5-9,12H2,1-4H3/t18-,19+,20+,21-/m0/s1

InChI Key

UBQQOJDZHPQINO-BQJUDKOJSA-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	4.72	ALOGPS
logP	5.13	ChemAxon
logS	-5.4	ALOGPS
pKa (Strongest Acidic)	10.71	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	38.69 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	95.53 m³·mol⁻¹	ChemAxon
Polarizability	38.39 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

26390206

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

70562

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 (-)-(4S,5S,10R,20R)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde (NP0035664)

MOL for NP0035664 ((-)-(4S,5S,10R,20R)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde)

3D MOL for NP0035664 ((-)-(4S,5S,10R,20R)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde)

3D SDF for NP0035664 ((-)-(4S,5S,10R,20R)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde)

3D-SDF for NP0035664 ((-)-(4S,5S,10R,20R)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde)

PDB for NP0035664 ((-)-(4S,5S,10R,20R)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde)

3D PDB for NP0035664 ((-)-(4S,5S,10R,20R)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde)

SMILES for NP0035664 ((-)-(4S,5S,10R,20R)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde)

INCHI for NP0035664 ((-)-(4S,5S,10R,20R)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde)

Structure for NP0035664 ((-)-(4S,5S,10R,20R)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde)

3D Structure for NP0035664 ((-)-(4S,5S,10R,20R)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde)